Lasik PDF
Lasik PDF
edited by
Dimitri T. Azar
Massachusetts Eye and Ear Infirmary
Schepens Eye Research Institute
and Harvard Medical School
Boston, Massachusetts, U.S.A.
Douglas D. Koch
Cullen Eye Institute
Baylor College of Medicine
Houston, Texas, U.S.A.
ISBN: 0-8247-0797-4
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Preface
For decades, the majority of ophthalmologists have been embarrassed by and highly
suspicious of refractive surgery, at times with good justification. They have been repelled
by its tactics in patient recruitment, uneasy about its seemingly cavalier use without long-
term data, eager to defend its unsuspecting victims, and deeply concerned that its short-
term benefits are outweighed by its burdensome long-term consequences. And so the words
of Germont, uttered pursuant to the most dramatic moment in Verdis La Traviata, echo the
extreme and oftentimes passionate contempt expressed by so many colleagues and close
friends towards academically oriented ophthalmologists who marched among the van-
guards of laser refractive surgeons. Their repudiation was not unlike Germonts scorn of
his son Alfredo for offending Violetta and for making himself worthy of disdain:
v
vi Preface
This book is the first in a series dedicated to Refractive Surgery by Marcel Dekker,
Inc. It will most certainly be judged by many as just another LASIK book. While there is
abundant coverage of the topic in other books, this volume has several unique features. Its
coverage of LASIK is relatively comprehensive, in that it is not limited to LASIK history,
surgical techniques, complications, and their management. New aspects of lasers, optics,
refraction, diagnostics, and instrumentation are combined with the science and general
principles of LASIK, and indications for its use. Although not meant to be encyclopedic,
key references abound. They are intended to serve as a guide to the literature on the topic.
Thus, this book is not so much a chronicle of LASIK, as an attempt to serve as a source of
information relevant to clinical practice.
We are indebted to the students, residents, and colleagues who have made valuable
contributions to this book. Several have included original work and analysis in their chap-
ters. It is evident that the authors have attended diligently to their assignments. We are
grateful for their effort in integrating the sometimes limited information in peer-reviewed
literature with the knowledge derived from their clinical experiences and interactions with
colleagues. We hope that this has resulted in a text that is both clinically relevant and as ev-
idence-based as possible.
We thank Dr. Geoffrey Greenwood and Elizabeth Curione of Marcel Dekker, Inc.,
for their commitment to this project and Drs. Tsubota, Boxer Wachler, Hoang-Xuan, Ang,
and Gatinel for their assistance in future books in this series. Special thanks go to Leona
Greenhill, for her editorial assistance, and to Rhonda Harris, who managed this project with
care and precision. Her attention to detail and her dedication have enabled us to work co-
herently in the face of adversity.
We take the opportunity to acknowledge the pioneering surgeons and researchers in
the field of refractive surgery. Their work and vision have provided the basis not only for
current refractive developments that we can offer to our patients, but also for future ad-
vances to be made by the next generation of thoughtful contributors to this important field.
Dimitri T. Azar
Douglas D. Koch
Contents
Preface v
Contributors xi
2. History of LASIK 21
Ioannis Pallikaris and Thekla Papadaki
4. Microkeratomes 57
Sandeep Kakaria, Thanh Hoang-Xuan, and Dimitri T. Azar
24. Bioptics: Combined LASIK and Phakic Intraocular Lens Surgery 329
Jos L. Gell, Mercedes Vzquez, Fortino Velasco, and Felicidad Manero
Index 495
Contributors
Ron Afshari Adelman, M.D. Massachusetts Eye and Ear Infirmary, Boston, Mas-
sachusetts, and Yale University Eye Center, New Haven, Connecticut, U.S.A.
Natalie A. Afshari Cornea Service, Duke University Eye Center, Durham, North Car-
olina, U.S.A.
Esen Karamursel Akpek, M.D. Cornea and External Disease Service, The Wilmer Eye
Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, U.S.A.
Rana Altan-Yaycioglu, M.D. Cornea and External Disease Service, The Wilmer Eye In-
stitute, Johns Hopkins University School of Medicine, Baltimore, Maryland, U.S.A.
Balamurali K. Ambati, M.D. Massachusetts Eye and Ear Infirmary and Department of
Opthalmology, Harvard Medical School, Boston, Massachusetts, U.S.A.
Robert T. Ang, M.D. Cornea and Refractive Surgery Service, Massachusetts Eye and
Ear Infirmary and Harvard Medical School, Boston, Massachusetts, U.S.A., and Asian Eye
Institute, Makati, The Philippines
Dimitri T. Azar, M.D. Cornea and Refractive Surgery Service, Massachusetts Eye and
Ear Infirmary, Schepens Eye Research Institute, and Harvard Medical School, Boston,
Massachusetts, U.S.A.
Brian S. Boxer Wachler, M.D. Refractive Surgery Service, Jules Stein Eye Institute at
UCLA, Los Angeles, California, U.S.A.
Margaret Chang Columbia University College of Physicians and Surgeons, New York,
New York, U.S.A.
Chun Chen Chen, M.D. Cornea and Refractive Surgery Service, Massachusetts Eye and
Ear Infirmary, Schepens Eye Research Institute, and Harvard Medical School, Boston,
Massachusetts, U.S.A.
Marsha C. Cheung Massachusetts Eye and Ear Infirmary and Harvard Medical School,
Boston, Massachusetts, U.S.A.
Kathryn Colby, M.D., Ph.D. Cornea and Refractive Surgery Service, Department of
Opthalmology, Massachusetts Eye and Ear Infirmary, Schepens Eye Research Institute,
and Harvard Medical School, Boston, Massachusetts, U.S.A.
Samir G. Farah, M.D. Massachusetts Eye and Ear Infirmary, Boston, Massachusetts,
U.S.A.
Liane Clamen Glazer, M.D. Massachusetts Eye and Ear Infirmary and Department of
Ophthalmology, Harvard Medical School, Boston, Massachusetts, U.S.A.
Sandeep Jain, M.D. Cornea and Refractive Surgery Service, Massachusetts Eye and Ear
Infirmary, Schepens Eye Research Institute, and Harvard Medical School, Boston, Mas-
sachusetts, U.S.A.
Roselyn Jeun, O.D. Massachusetts Eye and Ear Infirmary, Boston, Massachusetts,
U.S.A.
Contributors xiii
Jeffrey Johnson, O.D. Massachusetts Eye and Ear Infirmary, and Department of Oph-
thalmology, Harvard Medical School, Boston, Massachusetts, U.S.A.
Bilal F. Khan, M.D. Massachusetts Eye and Ear Infirmary and Department of Ophthal-
mology, Harvard Medical School, Boston, Massachusetts, U.S.A.
William J. Lahners, M.D. University of South Florida, Tampa, and Center for Sight,
Sarasota, Florida, U.S.A.
Jae Bum Lee Cornea and Refractive Surgery Service, Massachusetts Eye and Ear Infir-
mary, Schepens Eye Research Institute, and Harvard Medical School, Boston, Mas-
sachusetts, U.S.A.
Naoyuki Maeda, M.D. Departments of Ophthalmology and Medical Robotics and Im-
age Sciences, Osaka University Medical School, Osaka, Japan
Samir A. Melki, M.D., Ph.D. Cornea and Refractive Surgery Service, Massachusetts
Eye and Ear Infirmary, and Boston Cornea Center, Harvard Medical School, Boston, Mas-
sachusetts, U.S.A.
Manjula Misra, M.D. Cullen Eye Institute, Baylor College of Medicine, Houston,
Texas, U.S.A.
Jonathan D. Primack, M.D. Massachusetts Eye and Ear Infirmary, Boston, Mas-
sachusetts, U.S.A.
xiv Contributors
Cinthia E. Proano, M.D. Cornea and Refractive Surgery Service, Massachusetts Eye
and Ear Infirmary and Harvard Medical School, Boston, Massachusetts, U.S.A.
Manolette R. Roque, M.D. Massachusetts Eye and Ear Infirmary and Department of
Ophthalmology, Harvard Medical School, Boston, Massachusetts, U.S.A.
Walter J. Stark, M.D. Cornea, Cataract and Refractive Services, The Wilmer Eye Insti-
tute, Johns Hopkins University School of Medicine, Baltimore, Maryland, U.S.A.
Leon Strauss, M.D., Ph.D. The Wilmer Eye Institute, Johns Hopkins University School
of Medicine, Baltimore, Maryland, U.S.A.
Rodrigo Torres Massachusetts Eye and Ear Infirmary and Harvard Medical School,
Boston, Massachusetts, U.S.A.
Li Wang, M.D. Cullen Eye Institute, Baylor College of Medicine, Houston, Texas,
U.S.A.
Nan Wang Cullen Eye Institute, Baylor College of Medicine, Houston, Texas, U.S.A.
Patrick C. Yeh Cornea and Refractive Surgery Service, Massachusetts Eye and Ear In-
firmary, Schepens Eye Research Institute, and Harvard Medical School, Boston, Mas-
sachusetts, U.S.A.
Emily Yeung, M.D. Massachusetts Eye and Ear Infirmary, Schepens Eye Research In-
stitute, and Harvard Medical School, Boston, Massachusetts, U.S.A.
Laser in-situ keratomileusis (LASIK) involves creating a corneal flap so that midstromal
tissue can be ablated directly and reshaped with an excimer laser beam (1,2). The proce-
dure allows the ophthalmologist to surgically reshape the cornea in an attempt to obviate
the need for corrective lenses (Fig. 1.1). LASIK is a modification of Colombian Jos Bar-
raquers ingenious innovations. In 1949, Barraquer first described his technique, and in
1964 he published clinical results of his attempts to achieve emmetropia by shaving and re-
shaping the cornea (35). With Barraquers technique of keratomileusis (i.e., carving the
cornea), a lamellar button (lenticule) of the patients cornea was excised with a manual mi-
crokeratome. Barraquer then reshaped the lenticule so that the central corneal curvature
was flattened and the refractive power of the cornea decreased. He then replaced the lentic-
ule in position, either with or without sutures. Barraquers specific attempts to correct my-
opia were called cryolathe keratomileusis, because they involved freezing and reshaping
the removed lenticule with a cryolathe.
Troutman and Swinger introduced cryolathe keratomileusis to the United States in
1977 (6). While keratomileusis produced good results when performed by experienced sur-
geons, the procedure was technically very difficult and the results were therefore variable
(711). Innovations to this procedure, however, eventually led to the creation of the more
highly refined procedure of LASIK.
The introduction of the excited dimer (excimer) 193 nm UV laser allowed for the
1
2 Glazer and Azar
Figure 1.1 Schematic diagram of emmetropia. In emmetropia, the far point is optical infinity, and
the secondary focal point (F2) is at the retina. Parallel rays of light focus on the retina. (From
Ref. 115.)
corrected visual acuity (BCVA) are rare (1,18,19). In addition, with improved instrumen-
tation and increasing surgeon experience, LASIK complication rates continue to fall.
Figure 1.2 Schematic diagrams of myopia and hyperopia. In myopia, the far point is in front of
the eye (top), and the secondary focal point (F2) is anterior to the retina, in the vitreous (middle). In
hyperopia (bottom), the rays of light are in focus at a point behind the retina. (From Ref. 115.)
between the two focal lines is the circle of least confusion. A proper refractive correction
will place the circle of least confusion on the retina.
While astigmatism is clinically detectable in up to 95% of eyes, astigmatism of less
than 0.50 diopters rarely requires optical correction (22). However, 10% of the general pop-
ulation has naturally occurring astigmatism greater than 1 D. Since an astigmatic refractive
error of 1.00 to 2.00 D can decrease uncorrected vision to the 20/30 to 20/50 level, this de-
gree of astigmatism causes an unacceptably poor quality of uncorrected visual acuity
(23,24).
Regular astigmatism refers to corneal curvatures that are different but symmetrical,
with principal meridians 90 degrees away from each other. For regular astigmatism, one
Refractive Errors and Their Treatment 5
can achieve a refractive correction with cylindrical or spherocylindrical lenses. LASIK can
correct regular astigmatism by removing more tissue from the steeper side of the cornea.
Irregular astigmatism refers to a condition in which the principal meridians change
from point to point across the pupil, or in which the amount of astigmatism changes from
one point to another. Examples of irregular astigmatism include keratoconus or traumatic
corneal scars. LASIK is contraindicated in eyes with irregular astigmatism. Often, rigid
contact lenses are the best way to improve the visual acuity for eyes with irregular astig-
matism. The use of Zernike polynomials to analyze the wavefront in patients with irregu-
lar astigmatism has allowed, at least in theory, the incorporation of this information into the
laser treatment algorithm in LASIK and paved the way for custom corneal treatments.
Presbyopia refers to the age-related loss of accommodative response. Presbyopia typ-
ically sets in at approximately 40 years of age. The condition results from either a loss of
lens elasticity or an anatomic change in the position of the lens equator to the ciliary body
position. Presbyopia is an important issue to discuss during the informed consent of pa-
tients seeking refractive surgery. Some physicians give their patient the option of monovi-
sion, in which one eye is corrected for near vision and the other for distance vision.
Figure 1.3 Myopic automated lamellar keratoplasty. (A) A microkeratome is used to create a
hinged flap in the cornea. (B) A second microkeratome is used to remove a parallel-faced disc of tis-
sue from the corneal bed. (C) The initial flap is replaced, leaving a flattened central cornea. (From
Ref. 116.)
193 nm argon fluoride (ArF) excimer laser. Like LASIK, PRK utilizes the excimer laser to
flatten the cornea by ablating the central cornea. Unlike LASIK, no corneal flap is made;
rather, the central corneal epithelium is simply removed with a spatula or with the laser it-
self (Fig. 1.5). While there are three distinct techniques for performing excimer laser PRK
for myopia, the most widely used technique applies wide-area surface ablation with a large-
diameter beam. Most of the published results of PRK are based on PRK performed in this
manner. It is primarily in Europe that PRK is performed with the two other techniques:
scanning slit and flying spot lasers. A modification of PRK, first performed at the Mas-
sachusetts Eye and Ear Infirmary by Azar and Abad in 1996, was the use of 20% alcohol
to create an epithelial flap which was repositioned to cover the stromal ablation bed. Since
then, several investigators have started to use this laser epithelial keratomileusis (LASEK)
technique, but it is not clear whether LASEK offers any advantages over PRK.
PRK has been shown to be safe and efficacious for the treatment of low to moderate
myopia. Several national studies of PRK demonstrated that 90 to 100% of patients had
20/40 or better uncorrected visual acuity, and 78 to 98% had postoperative refractions
within 1.0 D of the target outcome (3234). Refractive results of PRK in patients with more
than 6 D of myopia tend to be highly variable and undergo more regression. Another dis-
advantage of PRK is a prolonged recovery time: while the corneal epithelium is healing,
Refractive Errors and Their Treatment 7
Figure 1.4 Hyperopic automated lamellar keratoplasty. (A) A hinged flap, approximately 70% of
corneal thickness, is created with a microkeratome. (B) Intraocular pressure displaces the very thin
posterior layer and overlying flap anteriorly, causing central corneal steepening. The original shape
of the cornea is shown with dotted lines. (From Ref. 116.)
patients may experience discomfort and blurry vision. In addition, potential complications
include postoperative haze, halos, induced astigmatism, diplopia, and keratitis (32,3537).
Although PRK was the first widely accepted laser vision correction procedure, it has
been largely supplanted by LASIK as the refractive procedure of choice not just for high
myopia but even for low and moderate myopia. This is partly because LASIK provides
faster visual rehabilitation and decreased time for wound healing (3843).
While LASIK is often the refractive procedure of choice for myopes, PRK may be
preferable to LASIK for patients who are hesitant to undergo incisional surgery, or for pa-
tients who have contraindications to LASIK. Such contraindications would include corneal
Figure 1.5 Schematic illustration of photorefractive keratectomy. The excimer laser is used to re-
move anterior stroma (left), causing corneal flattening (middle). The region of tissue subtraction is
designated by the shaded area. (From Ref. 115.)
8 Glazer and Azar
thinning, in which less than 200 to 250 microns of tissue would be left in the corneal bed,
and epithelial anterior basement membrane dystrophy, because this carries the risk of ep-
ithelial ingrowth. PRK is also competitive with LASIK in the arena of treatment for low
hyperopia. A recent review of 65 eyes with 1.00 to 4.00 D of hyperopia documented
that 92% of the eyes were within 1.00 D of the intended manifest SE at 18 months fol-
low-up (44). Other reports support the use of hyperopic PRK (H-PRK) for treating low de-
grees of hyperopia (4548). H-PRK for the treatment of higher degrees of hyperopia is less
predictable and may result in greater regression (45).
One can alter the shape, and thus the refractive index, of the cornea by adding material ei-
ther to the surface of the cornea or into the corneal stroma. Epikeratoplasty involves adding
a lenticule with power (i.e., carved donor tissue) to the deepithelialized surface of Bow-
mans layer. Also called epikeratophakia or lamellar keratoplasty, this technique has
proven problematical. First, the refractive results have been disappointing: only 33% of
eyes achieved 20/40 or better uncorrected visual acuity, 15% lost two or more lines of best
corrected visual acuity (BCVA), and regression was more than 2 D in 17.6% of patients at
5 months follow-up (4951). Secondly, 2.53.5% of patients who underwent this proce-
dure had delayed reepithelialization, which in some cases led to infections and graft melt-
ing (49,5255). Almost 8% of grafts had to be removed due to failure of epithelialization,
haze, glare, irregular astigmatism, epithelial ingrowth, epithelial interface cysts, melt, in-
fection, stromal infiltrates, and wound dehiscence (49,5354,5657). After the lenticules
were removed, many patients were left with central corneal scarring and loss of BCVA
(58,59). Because of the disappointing outcomes and unfortunate complications, epikerato-
plasty has been abandoned as a technique for the correction of myopia. However, epiker-
atoplasty is still occasionally used to diminish the myopia and irregular astigmatism of ker-
atoconus or other corneal thinning disorders (60). This procedure is also sometimes used
for the treatment of pediatric and adult aphakia.
Keratophakia is a procedure in which a lens is placed within the corneal stroma to al-
ter the corneas refractive power. While lenses used to be fashioned from donor human
corneas (homoplastic), these lenses had variable outcomes and a high incidence of compli-
cations (61). Keratophakic lenses are now fashioned exclusively from synthetic materials
(alloplastic).
The intrastromal corneal ring segment (ICRS), approved in the United States in April
1999, is a keratophakic technique to correct for low myopia (1.00 to 3.00 D with an
astigmatic component of 1.00 D or less). The ICRS consists of two 160 degree polymethyl
methacrylate (PMMA) segments placed in two pockets of the peripheral stroma, thereby
inducing peripheral steepening and indirectly causing central corneal flattening (Fig. 1.6).
The procedure is unique in that it retains the potential to be adjusted or reversed.
Two-year results of the phase II and phase III FDA trial analyzed 358 patient eyes.
At 24 months after surgery, 97% of the eyes had an UCVA of 20/40 or better, 76% were
20/20 or better, and 55% were 20/16 or better. In addition, 93% were within 1.00 D range,
and 73% were within 0.50 D range (62).
Potential disadvantages with the procedure include accidental perforation into the an-
terior chamber, surface perforation of the epithelium anteriorly, and induced astigmatism,
which can result from postoperative movement of the intracorneal ring segments (63).
Refractive Errors and Their Treatment 9
Figure 1.7 The development of radial and astigmatic keratotomy. Illustrations of Lanss studies
showing peripheral corneal bulging (A) and subsequent scarring (B) after astigmatic keratotomy (C)
and radial keratotomy (D). (From Ref. 117.)
The PERK study showed that 10 years after surgery, 53% of the patients had 20/20
or better uncorrected vision, 85% had 20/40 or better, and 63% of patients younger than 40
years old were spectacle-independent. Low myopes did better than moderate myopes: 94%
of patients with low myopia (2.00 to 3.12 D) had an uncorrected visual acuity (UCVA)
of 20/40 or better, while 79% of moderate myopes (3.25 to 4.37) had 20/40 or better
UCVA. The 10-year PERK results also revealed a long-term instability of refractive errors:
Refractive Errors and Their Treatment 11
43% of eyes demonstrated a hyperopic shift of one diopter or more (71). Of note, the PERK
study employed eight-incision surgery (Fig. 1.8). In lower myopes, the four oblique inci-
sions may be sufficient to achieve the desired result.
The concept of standardized RK was introduced by Casebeer in the early 1990s. Us-
ing his cookbook method, even novice surgeons have been able to perform RK, but the
safety and stability of this approach was controversial, for it was not studied with the same
rigor that was used in the PERK study (7275).
Approximately 250,000 RK operations were performed each year in the United
States in the early 1990s (7176). There were advantages of RK over more modern forms
of refractive surgery; RK utilized relatively inexpensive equipment, the procedure did not
involve incisions in the optical zone, and RK had more long-term follow-up data than sev-
eral other contemporary refractive procedures. In the early days of excimer laser surgery,
RK was generally reserved for patients who had low and moderate myopia (up to 5 D) who
Figure 1.8 Eight-incision radial keratotomy. A diagram highlights the optical zone (top) and the
central flattening (middle) after performing an RK with eight incisions (bottom). (From Ref. 117.)
12 Glazer and Azar
were willing to accept initial undercorrections because they had the best long-term results
with RK.
b. Incisional Surgery: Astigmatic Keratotomy
Astigmatic keratotomy (AK) is a procedure that attempts to correct astigmatic refractive er-
rors in patients with greater than 1.5 D of astigmatism. AK involves performing arcuate or
transverse (also called tangential, or T) incisions that parallel the limbus, flattening the
meridian in which they are placed and steepening the unincised meridian 90 degrees away.
The first AK was performed by Schiotz, a Norwegian ophthalmologist, in 1885. He
performed a 3.5 mm penetrating incision at the limbus in the steep meridian of a post
cataract patient. The patients astigmatism was reduced from 19.5 to 7 D (77). Since then,
many incision configurations and techniques have been described, with variable outcomes
(7880). In general, deeper and longer incisions produce greater effect, but cuts greater
than 75 degrees are not recommended. In addition, the effects of the cuts increase with age.
Both new instruments and nomograms for AK such as Lindstroms have improved results
(Fig. 1.9).
c. Incisional Surgery: Hexagonal Keratotomy
The first incisional surgery for the treatment of hyperopia was performed by Mendez in
1985 (8182). Discussion of this procedure is included for historical purposes. Mendezs
hexagonal keratotomy procedure consisted of making circumferential connecting
hexagonal peripheral cuts around a 4.5 to 6.0 mm optical zone (Fig. 1.10). The central
cornea then bulged forward, correcting the hyperopia. Although the procedure was re-
ported to be successful in early studies, it was soon discovered that intersecting incisions
caused corneal instability with poor predictability and fluctuating refractive results. In ad-
dition, many patients experienced excessive scarring at the incisions and induced astig-
matism (83).
Figure 1.9 Lindstroms nomogram for astigmatic keratotomy. (From Ref. 118.)
Refractive Errors and Their Treatment 13
In 1989, Jensen and Mendez attempted to improve upon the technique with shorter,
nonintersecting hexagonal incisions (84). Despite these modifications, corneal scarring,
optical aberrations, irregular astigmatism, perforation after minimal trauma, keratitis, and
endophthalmitis were complications that plagued this procedure (8587). It was soon de-
termined that hexagonal keratotomy was an unpredictable, unsafe surgical procedure
with a high complication rate . . . (87). As such, the procedure has largely been aban-
doned.
d. Thermal Surgery
Thermal keratoplasty (TK) was first performed by Lans in 1898 to treat astigmatism (64).
Lans applied thermal energy via a cautery to alter the structure of the corneal stromal col-
lagen and change the anterior corneal curvature. Heat was later applied by means of radio
frequency waves with instruments like the Los Alamos thermal keratoplasty probe (88).
Because it was difficult to control the amount of energy applied, TK using simple cauter-
ies and probes resulted in unpredictable results and regression (89,90).
Interest in TK was rekindled with the introduction of lasers that could heat the cornea
in a more controlled manner. In 1990, Seiler first reported the use of the holmium:yttrium
aluminum garnet (Ho:YAG) laser for hyperopia, a technique called laser thermokerato-
plasty (LTK) (91). Ho:YAG LTK delivers infrared radiation that is focused on the mid-
stroma, thereby avoiding damage to the epithelium. Two types of Ho:YAG LTK delivery
systems were developed: contact and noncontact.
Contact LTK was performed by applanating the cornea with a probe that applied en-
ergy pulses to achieve local, peripheral flattening and subsequent central steepening. In the
early 1990s, the procedure underwent Food and Drug Administration (FDA) trials. Re-
gression and undercorrection plagued the procedure, and contact LTK was withdrawn from
US FDA trials (92).
Noncontact LTK is performed by projecting simultaneously up to eight spots onto
the cornea through a slit lamp-mounted fiberoptic delivery system. FDA phase Iia clini-
cal trials with two years of follow-up showed a mean change in refraction of 0.53 to
1.48 D, with UCVA at two years improved by one or more lines of Snellen visual acu-
ity in 19 (73%) of 26 treated eyes (93). The problem with noncontact LTK is regression.
Studies have shown 31.5 to 40% regression (94,95). Another problem apparent with LTK
is the induction of irregular astigmatism (95,96). Despite these imperfections, noncontact
14 Glazer and Azar
Ho:YAG LTK recently received approval by the FDA. Some investigators are attempt-
ing to improve upon the current pulsed Ho:YAG LTK with a new continuous wave diode
laser that can achieve similar effects on the cornea, without the peaks and troughs of the
pulsed laser (97).
e. Orthokeratology
Orthokeratology is the programmed application of contact lenses to reduce or eliminate re-
fractive anomalies, primarily myopia. An orthokeratology lens is flatter, looser, and larger
than a conventional lens. Theoretically, the lens mechanically alters the central corneal
contour over time. In 1963, Grant and May introduced this practice to the United States.
They fitted a rigid PMMA lens that was 0.37 diopters flatter than the patients flattest
corneal median. As the cornea flattened, new lenses were applied, each time 0.37 D flatter
than the flattest meridian. The patients wore their lenses for 12 to 15 hours a day and were
followed at regular intervals. During the first phase of treatment, the adaptive phase, an av-
erage of six pairs of lenses was prescribed over a period of 18 to 24 months. When unaided
vision reached 20/20 or refraction stabilized to plano 0.50 diopters, the retainer phase be-
gan and patients would then wear a retainer lens to maintain the permanence of the proce-
dure (98,99).
While many anecdotal reports describe the myopia-reducing benefits of orthokera-
tology, there are no scientific studies to support claims that this practice is a viable alterna-
tive to refractive surgery. For example, one randomized, controlled clinical trial did demon-
strate an improvement in uncorrected visual acuity from 20/100 to 20/50 in 36.6% of the
orthokeratology group compared with 20.8% of the cosmetic lens wearers who improved
the same amount. However this trial had no long-term follow up; results were from data at
the very end of the 14 month (on average) treatment period (100).
versible, it can correct higher refractive errors than LASIK and other types of refractive
surgeries, and it can be performed by most ophthalmologists. In addition, phakic IOLs,
while currently used to treat myopia, may soon be approved to correct hyperopia. A recent
Phase I trial of silicone plate posterior chamber lenses, implanted in hyperopes, reported
100% of patients with 20/40 or better UCVA, and 70% with 20/20 or better UCVA (113).
The field of refractive surgery has changed significantly since Sato introduced radial
keratotomy and Barraquer performed his first cryolathe keratomileusis. Advances in instru-
mentation, and in research and understanding of the eye and wound healing, and constant
surgical innovation, will surely keep the field changing and improving as the years progress.
In the twenty-first century, LASIK has crossed the genre from medical procedure to
star-endorsed miracle treatment. The public is familiar with the litany of celebrities who
have had success with the procedure. When a sports celebrity or an eye surgeon is willing
to bet with such high stakes, perhaps the general public feels more comfortable taking a risk
as well. More than one million Americans have had LASIK procedures, and predictions es-
timate that 1.2 million Americans will undergo LASIK in the year 2001 (2).
Some decry LASIK as a shift from disease-driven to demand-driven procedures.
There are, however, individuals (such as athletes, firefighters, and military personnel) for
whom spectacles or contact lenses are hindering or even dangerous. In addition, people
with a high degree of myopia may find glasses to be inadequate due to image minification,
or they may be intolerant of contact lenses. The visual disability of high myopes can reduce
their quality of life so much that some studies suggest that refractive surgery for high my-
opes should be provided under health plans like Great Britains National Health Service.
Figure 1.11 Phakic IOLs. Drawings illustrating the three major types of phakic intraocular lenses
in use today. (From Ref. 119.)
16 Glazer and Azar
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Refractive Errors and Their Treatment 19
IOANNIS PALLIKARIS
University of Crete Medical School and University Hospital of Heraklion
Heraklion, Crete, Greece
THEKLA PAPADAKI
Vardinoyannion Eye Institute of Crete, University of Crete Medical School
Heraklion, Crete, Greece
A. INTRODUCTION
Modern lamellar refractive surgery has its roots in the pioneer work of Professor Jos Ig-
nacio Barraquer of Colombia. In 1949, Barraquer suggested that by adding or removing
corneal tissue, it was possible to manipulate surgically the curvature of the air/tear film in-
terface, where the two thirds of the refractive power of the eye is located (1). From the very
beginning, he realized the importance of preserving each layer of the cornea, and so corneal
lamellar techniques started to develop.
During the past 50 years, lamellar corneal refractive surgery has undergone a long
evolutionary process. Various different methods have been suggested to remove and/or
shape corneal tissue, in order to enhance the accuracy and predictability of lamellar proce-
dures. Laser in situ keratomileusis (LASIK) is the most recent step in this process and com-
bines well-established lamellar surgical techniques with the precision of excimer laser pho-
toablation. Although it enjoys, at present, great popularity among refractive surgeons,
LASIK is still a developing procedure in terms of technique and perioperative patient man-
agement.
In this chapter we are going to follow the steps that led from Barraquers first exper-
iments to LASIK. Reviewing the history of refractive surgery is essential, because it pro-
vides the fundamental principles which form the basis for better understanding and
refining the currently used techniques.
21
22 Pallikaris and Papadaki
Figure 2.1 Myopic keratomileusis (MKM). A lamellar corneal disc approximately 300 m in
depth is created (lamellar keratectomy) and tissue is removed from the residual stromal bed (refrac-
tive keratectomy). Once the disc is replaced, the anterior corneal surface is flattened, thus reducing
the refractive power of the eye and correcting myopia. (Reprinted with permission from D. T. Azar.
Refractive Surgery. Appleton & Lange, 1997.)
History of LASIK 23
Figure 2.2 Free keratomileusis. The dyed corneal disc is placed on the lathe, epithelial side down,
and frozen by liquid nitrogen (A). A frozen tool is then used to lathe the disc (B). (Courtesy of Dr.
Jos Ignacio Barraquer.)
mal surface was then lathed with more tissue removed from the center than the periphery
in the myopic cases so as to flatten the central corneal curvature (Fig. 2.2). For hyperopic
correction the disc was treated in the opposite way to achieve steepening of the central
corneal curvature (Fig. 2.3). After thawing, the carved disc was placed back on to the
cornea and held in place with sutures. This was the first time a part of a human organ was
removed from the body to alter its function and then returned.
Barraquer also thought he could achieve steepening of the central corneal curvature
more effectively by implanting a preprocessed stomal tissue lenticle (allograft) within the
recipients stroma (5). To create the lenticle, a lamellar corneal disc was resected from fresh
or preserved donors cornea, using a microkeratome. The epithelium, Bowmans layer and
the anterior stroma were removed. The remaining stromal tissue was preserved by a vari-
ety of means (refrigeration, freezing, and freeze drying) and processed on the lathe in a way
Figure 2.3 Freeze keratomileusis for myopia and hyperopia. As more tissue is removed centrally
than peripherally (A), the plano corneal disc is converted to a concave (negative) lens, capable of
correcting myopia. For hyperopic correction, more tissue is removed from the periphery of the disc
to achieve steepening of the central curvature (B). (Courtesy of Dr. Jos Ignacio Barraquer.)
24 Pallikaris and Papadaki
Figure 2.4 Keratophakia (KF) is the procedure in which a corneal lenticle is removed from a
donors cornea. After a lamellar resection is performed on the recipients cornea, the lenticule is in-
serted underneath the resected corneal cap. As the cap is sutured back, a new steepend anterior
corneal curvature is formed. (Reprinted with permission from D. T. Azar. Refractive Surgery. Ap-
pleton & Lange, 1997.)
similar to that in F-KM, to create a converge lenticle capable of correcting aphakia and high
hyperopia. Keratophakia (KF) was the term employed to describe the procedure in which
a lamellar keratectomy was performed on the recipients cornea, the lenticle was placed in-
trastromally, and the lamellar disc was sutured in place (Fig. 2.4). The lenticle diameter and
thickness varied, depending on the initial refractive error and the target correction. KF was
first reported in 1958 as having the potential to correct aphakia (5). With this report Barra-
quer introduced his work to the ophthalmic community.
The first report on F-MKM followed in 1967 (2). First results revealed visual im-
provement in 80% of the patients and indicated that refinement of the procedure should pro-
ceed. Over the next decade significant advantages in the cutting and shaping of the tissue
improved the predictability of the procedure but could not help overcome its major draw-
backs. These were the use of very complicated technology and the steep learning curve re-
quired for the procedure, together with the prolonged visual recovery time and the high rate
of complications such as scarring and irregular astigmatism (6).
Troutman and Swinger brought the concepts of KF and KM to the United States in 1978
(7). KF attracted the attention of the ophthalmic community as a possible solution for the
treatment of aphakia after cataract extraction (810). However, with the advent of IOL tech-
nology, interest in KF subsided. Though early results on MKM were encouraging (11,12), the
technical difficulty, the steep learning curve, and the potential of sight-threatening complica-
tions, which were attributed mainly to tissue damage during freezing and lathing (1215), dis-
couraged many ophthalmic surgeons, and the technique failed to be popularized.
In an attempt to simplify lamellar refractive surgery and make it safer, Kaufman,
Werblin, and Klyce of the Louisiana State University Eye Center introduced epiker-
atophakia (epikeratoplasty or epi) in 1979 (1618). The procedure involved deepithelial-
ization of the recipient cornea and preparation of a peripheral annular partial-thickness ker-
atotomy. A lyophilized preshaped corneal tissue lenticle (consisting of Bowmans layer
and the anterior stroma) was reconstituted and sutured into the keratotomy site, creating a
new shape for the anterior corneal surface (Fig. 2.5). The major advantage of this proce-
dure was that it avoided the problems of using a microkeratome to cut across the optical
zone and lathing the corneal tissue intraoperatively (19). Epi was intended for use in the
History of LASIK 25
treatment of aphakia, high myopia, or hyperopia (20,21). Plano epilenticles were also em-
ployed to flatten the cornea in keratoconus and provide a more regular surface for contact
lens wear (22). Unfortunately, the initial reports proved that the procedure was neither pre-
dictable nor safe (2324). The most common complications of epi included irregular astig-
matism, persistent epithelial defects, and delayed visual recovery (2527). These were
mainly attributed to the heavy processing of the graft tissue (28). Several modifications of
the initial procedure were employed (2930), among them the application of nonfreezing
techniques to shape the graft lenticle (31). Altman reported on using a spot excimer laser
beam to shape the corneal tissue, mounted on a movable platform (32). Buratto and Ferrari
used the BarraquerKrumeichSwinger technique (described below) to shape epilenticles
without freezing. Predictability was still low, but visual recovery was significantly faster
than with regular freezing techniques (33). Despite the efforts, epi never gained approval
from the FDA and was withdrawn from the market (34). However, the ease of epi compared
to MKM prompted the development of nonfreeze keratomileusis techniques.
The BarraquerKrumeichSwinger (BKS) refractive system was introduced in 1985
(35). This included an improved microkeratome (the BKS 1000), a set of dies, and a suc-
tion stand. The microkeratome was used to excise a lamellar corneal disc. The disc was then
placed epithelial side down on one of the suction dies, and the second refractive cut was
performed on the stromal aspect of the disc, using the microkeratome. The curvatures of the
dies varied, depending on the amount of the attempted correction of myopia or hyperopia
(Figs. 2.6 and 2.7). When a convex die was used, the keratome removed a central part of
the stroma, thus flattening the anterior surface of the cornea. For hyperopia correction, the
lenticle was placed on a concave die, and the microkeratome removed a peripheral portion
of the stroma, steepening the central cornea. The sculptured lamellar disc was finally su-
tured back to the bed. Despite its technical difficulty, nonfreeze keratomileusis proved to
have a major advantage: the rapid and comfortable visual recovery of the patients. This was
Figure 2.5 Epikeratophakia or epikeratoplasty. A preprocessed donor lenticle is fixed onto the
corneal surface. A peripheral circumferential keratectomy allows fixation of the lenticle into the host
cornea. For correction of hyperopia (right), a positive lens is used to steepen the anterior corneal cur-
vature. A negative lens (left), on the contrary, would flatten the anterior corneal curvature, resulting
in correction of myopia. (Reprinted with permission from D. T. Azar. Refractive Surgery. Appleton
& Lange, 1997.)
26 Pallikaris and Papadaki
Figure 2.7 The BarraquerKrumeichSwinger (BKS) system for nonfreeze keratomileusis. The
BKS microkeratome and the suction stand.
History of LASIK 27
As mentioned previously, Barraquer introduced KM in situ in the late 1940s (1) but
had to abandon the technique very soon due to the many technical difficulties inherent in
the use of a manual microkeratome. Ruiz and Rowsey revised the idea of KM in situ in the
late 1980s, taking advantage of the BKS system cutting properties (37). The initial kerate-
ctomy was performed as in the BKS technique. Subsequently, by using suction rings of dif-
ferent heights, Ruiz would perform the refractive cut on the stromal bed instead of the stro-
mal aspect of the disc. The thickness of the cut was proportional to the degree of myopia to
be corrected and was calculated using a nomogram that Ruiz proposed. The advantage of
the procedure, compared to classic KM, was that carving the stromal bed allowed for larger
optical zones and widened the range of potential correction (38,39). In 1987, Leo Bores
performed the first KM in situ in the US (40) and initiated the investigation of the tech-
nique. KM in situ with the use of a manual microkeratome, however, was reported as be-
ing not technically safe, precise, or predictable and was adopted by a very small number of
surgeons (38,39). The desire to improve the reproductability and accuracy of the in situ
technique prompted research in developing new improved microkeratomes (41).
In the late 1980s, Luis Ruiz gave impulse to lamellar refractive surgery, by develop-
ing an automated geared microkeratome (Fig. 2.8). A suction device stabilized the ker-
atome head on the eye, and the speed of the keratome passage could be controlled using a
foot pedal, so that more even, consistent cuts were obtained. The microkeratome would
also automatically reverse at the end of the procedure, without disturbing the lamellar cut.
This automatic corneal shaper (ACS) led to the introduction of automated lamellar kerato-
plasty (ALK) in the field of lamellar refractive corneal surgery. The procedure involved re-
section of the initial lamellar disc using ASC. For myopic corrections a second, plano re-
fractive cut was subsequently performed on the bed. The depth of the second cut was
adjusted by altering the height of the suction ring. In the end the anterior lamellar disc was
replaced on the stromal bed, with or without sutures (Fig. 2.9). In hyperopic ALK no re-
fractive cut was performed, as the initial cut generated ectasia of the residual stroma ade-
quate to correct up to 6 diopters of hyperopia. This ectasia was maintained after the ante-
rior lamellar disc was replaced. For higher hyperopic corrections, homoplastic ALK was
Figure 2.8 The Ruiz automated microkeratome is geared, so that the same motor that moves the
blade also drives the microkeratome across the eye.
28 Pallikaris and Papadaki
Figure 2.9 The Automated Lamellar Keratoplasty (ALK) is based on the same concept as ker-
atomileusis in situ. The use of the automated microkeratome has increased dramatically the safety and
effectiveness of the procedure. This photo shows the actual corneal bed after the two lamellar resec-
tions. The even sharp concentric borders of the lamellar cuts, as well as the smooth surface of the re-
maining stroma, are evident. (Reprinted with permission from J. Machat. Excimer Laser Refractive
Surgery. Slack, 1996.)
invented (42). The procedure involved excision of a small, very thin anterior lamellar disc,
which was discarded and replaced by a 300400 m thick donor lenticle (processed also
using ACS).
ALK has been a breakthrough in lamellar surgery. The total operative time was re-
duced, and the procedure could be safely performed under topical anesthesia. Recovery time
improved. ALK became very popular, as many surgeons who found it difficult to use the
manual microkeratomes adopted ACS. The first clinical trials on ALK revealed its advan-
tages: ease of use, rapid visual recovery, stability of refraction, and efficacy in th correction
of high myopia (43). There were major disadvantages, however; a relatively high rate for
irregular astigmatism (2%) and poor predictability of the procedure (within 2 D) (44). The
latter was attributed to the imprecision of the depth obtained with the second lamellar
resection. It became obvious that ALK could never overcome its inherent drawback: the re-
fractive cut was not truly refractiveit was resection of a plano disc from the stromal bed.
Investigators now started exploring ways to improve the accuracy of the second refractive
cut. That time coincides with the beginning of the excimer laser era in ophthalmology.
xenon bromide with an electron beam gun. In 1976, argon fluoride (ArF) was found to lase
at 193.3 nm when excited in an electron beam (45).
The first laboratory excimer lasers required a great amount of energy to excite the
rare gashalide complex. Therefore their usefulness for biological experiments was lim-
ited. Later on, it was shown to be possible to achieve laser action in a more compact device,
using a transverse electrical discharge as the energy source. Tachisto made the first com-
mercial system in 1979 (45). Within only a year, excimer lasers improved in reliability and
output energy and became suitable for general laboratory use. As a consequence, research
on the possible applications of excimer lasers and their potential hazards started to evolve.
The United States Air Force (USAF) School of Aerospace Medicine started investi-
gating the use of these new lasers on the eye. In 1981, Taboada reported that ArF laser light
produces an immediate but temporary indentation of the corneal epithelium, which takes
on the shape of the beam, without causing any opacification to the adjacent epithelium or
stroma (46,47).
IBM researcher R. Srinivasan further studied the interaction of a 193 nm laser with
organic materials. He suggested the term photoablative decompensation (later referred to
as photoablation) to describe the mechanism of ablation with the 193 nm excimer lasers,
and by creating grooves in human hair he demonstrated the high precision of the ablation
technique. He suggested the possibility of optical control of the corneal surface by remov-
ing tissue and set the basis for further studies (48).
Stephen Trokel first experimented on the cornea with excimer photoablation and de-
scribed its surgical potential. In 1983 Trokel reported, UV light at 193 nm, ablated corneal
tissue at a predictable rate, producing minimal thermal damage to the surrounding tissues
(49). These properties of excimer laser photoablation are the foundation of excimer laser
refractive surgery. Separate patents on photorefractive keratectomy (PRK) were filed by
Stephen Trokel and Francis LEsperance. Studies on animal corneas as early as 1984 re-
vealed that only 5 m of corneal tissue had to be removed to lower the refractive power
of a 4 mm corneal optical zone by 1 D (50). Early attempts to perform phototherapeutic ker-
atectomy (PTK) showed that the ablated surface would heal without scarring (51,52).
Thus the ophthalmologic community overcame the belief that the preservation of Bow-
mans membrane was essential to preserve corneal topography and clarity. Based on that
evidence, the use of the excimer laser to alter directly the cornea curvature was made pos-
sible and PRK was introduced. In 1985, Theo Seiler of Germany was the first to perform
excimer laser PTK in a sighted eye (53). Laser companies such as Meditec GmbH (Ger-
many), VISX (Santa Clara, CA), and Summit Technologies (Waltham, MA) began to
emerge. In 1987 Francis LEsperance performed the first PRK in the U.S. on a blind eye
(53). In 1988, FDA clinical trials on PRK began. Marguerite McDonald achieved the first
successful refractive correction with PRK in a normally sighted myope, as part of an FDA
trial (54). At the same time, C. Munnerlyn and his colleagues published a computer-based
algorithm that relates ablation zone diameter and thickness to the required amount of diop-
tric change (50).
In 1995 FDA issued approval of the Summit and VISX lasers for PTK and the Sum-
mit laser for PRK. In 1996 FDA approved the VISX laser for PRK (53).
As the use of the 193 nm excimer laser in refractive surgery increased, it was revealed
that, for the correction of more than 6 D of myopia, PRK resulted in significant central
corneal haze, regression of the refractive effect, and poor predictability (55). To achieve
more accurate corrections of high myopia, investigators began to use the excimer laser in
combination with intrastromal techniques.
30 Pallikaris and Papadaki
D. LASIK DEVELOPMENT
As a modality, LASIK was designed and developed at the University of Crete. In 1988,
Ioannis Pallikaris and colleagues introduced the term laser in situ keratomileusis (LASIK)
to describe excimer laser ablation performed under a hinged corneal flap (Fig. 2.10) (56).
Pureskin first suggested the idea of raising a corneal flap and removing stromal tissue from
the bed, back in 1967. He attempted to create the flap manually and cut out the in situ part
with a trephine in a procedure that he termed stromectomy (57).
In LASIK the automated microkeratome is used to create a hinged corneal disc (i.e.,
flap), which consists of epithelium Bowmans layer and anterior stroma. The laser beam is
then applied directly to the stroma, to remove a predetermined amount of tissue, depending
on the target correction. Once ablation is completed, the flap is repositioned and held in
place with the action of the endothelial pump (Fig. 2.11).
The idea for the LASIK procedure was based on the histological observation that dur-
ing surface photoablation (PRK) the corneal neural network is also ablated and takes sev-
eral months to reconstitute (58). The initial hypothesis was that destruction of both Bow-
mans layer and the superficial corneal nerves during PRK would have an adverse effect on
the healing response. It was thus theorized that creation of a flap instead of a lamellar disc
would assure better fitting of tissues after the ablation and would not affect the anatomic
integrity of the cornea mainly by preserving Bowmans layer and the superficial corneal
nervous net. Other important advantages would be reduction of surgical manipulations and
total time required for the operation (56).
Figure 2.10 The first published diagram for LASIK. (Pallikaris 1989.)
History of LASIK 31
Figure 2.11 In laser in situ keratomileusis (LASIK) for hyperopia, the automated microkeratome
is used to create a hinged corneal disc (i.e., flap), which consists of epithelium and anterior stroma.
The laser beam is then applied directly to the stroma to remove a predetermined amount of tissue, de-
pending on the target correction. Once ablation is completed, the flap is repositioned and held in place
with the action of the endothelial pump. (Reprinted with permission from D. T. Azar. Refractive
Surgery. Appleton & Lange, 1997.)
Figure 2.12 The first animal studies to determine wound healing after LASIK. University of
Crete, 1987.
32 Pallikaris and Papadaki
Figure 2.13 Excimer laser intrastromal keratomileusis. After the lamellar cap is harvested (A), it
is positioned, epithelial side down, under the laser beam for photoablation (B). The ablated disc (C)
is then sutured back in place (D). (Courtesy of Dr. Lucio Buratto.)
mal study in which an erbium-Yag laser was successfully used to remove the stroma from
a lamellar bed as well as the corneal surface. Peymans work, however, focused on the use
of the erbium-Yag laser for experimental PRK (59).
In 1990 Lucio Buratto independently attempted to use the excimer laser to perform the
second cut in KM. He introduced the technique of excimer laser intrastromal keratomileusis
or photokeratomileusis (PKM), in which a 300 m thick lamellar disc was excised, inverted,
and ablated on its stromal aspect (Lucio Buratto, personal communication: First International
Meeting on Keratomileusis, Venice, Italy, June 1990) (Fig. 2.13). First results on a large
series of human eyes proved that this technique was effective for myopia up to 25 D, yet not
safe (60). The complication rate was comparable to that of MKM, and so PKM was finally
abandoned in favor of LASIK.
E. LASIK MILESTONES
In June 1989, the first LASIK on a blind human eye was performed in the University of
Crete, as part of an unofficial blind eye protocol. A specially modified BKS 1000 micro-
keratome was used for the operation.
Human studies begun in 1990 (61,63). The first blind eye study accessed the effect
of flap creation on both the corneal healing response and the topographic pattern. It was re-
History of LASIK 33
vealed that, three months following the flap technique, corneal transparency was main-
tained and no significant irregular astigmatism was noted on corneal topography. The
safety of sutureless LASIK was also suggested at that time (61). It was recognized that ad-
equate adhesion between the flap and the stromal bed was possible even without sutures.
The absence of irregular astigmatism, the elimination of sutures, and the invention of the
automated geared microkeratome by Luis Ruiz (described previously) were the three most
important developments that made LASIK widely accepted.
In 1992, Stephen Slade and Stephen Brint performed the first LASIK in the U.S.
In 1993, Slade used the automated microkeratome to create the flap. He termed the
procedure excimer ALK (E-ALK) or flap and zap (64).
In 1994, Pallikaris and colleagues published their early experience in the use of
LASIK on sighted eyes, as well as the first study comparing LASIK and PRK (65,66).
LASIK proved superior to PRK in terms of stability and predictability for the correction of
myopia greater than 10 diopters.
In 1997, Buratto suggested the downup LASIK, which involves positioning the flap
hinge superiorly instead of nasally. This modification of the procedure was thought to min-
imize the risk for flap dislodgment during the early postoperative term. A superior hinge
would also allow for wider ablation profiles, which are crucial in cases of hyperopic and
astigmatic corrections. The advantages of downup LASIK over the classic technique are
currently under investigation (67).
In 1999, the FDA approved the Summit Excimer Laser (Summit Technologies,
Waltham, Mass.) for use in LASIK (68).
G. FUTURE TRENDS
For the foreseeable future, LASIK should remain the surgical treatment of choice for low
and moderate refractive errors. The most serious alternative to LASIK may be the use of
phakic intraocular lenses for high and moderate myopia.
For LASIK to be the first-choice procedure in the correction of high ametropias, its
accuracy and postoperative quality of vision must improve to reach that of an IOL implan-
tation (93). Continuous evolution in the field of microkeratome and excimer laser technol-
ogy is the only way to achieve that goal.
Currently there is great interest in refining refractive surgery by identifying and re-
ducing optical aberrations that degrade the optical image and limit visual acuity potential
(94). Corneal topography guided ablations and wavefront technology are used to develop
customized laser ablation patterns in an effort to improve optical performance after pho-
toablation. The primary results of their application are encouraging (95, 96). Possibly, as
the use of customized ablation increases, we will be able to improve the best-corrected
visual acuity in many eyes.
It has been suggested recently that many variables play a role in the surgical effect
obtained after LASIK (91). Currently used nomograms are far from perfect, as they con-
sider only the depth and the diameter of the ablation zone. Improved nomograms that in-
corporate multiple variables are under development and will soon be available in clinical
practice. We hope that their application will increase the accuracy of the procedure.
One area of advancement in LASIK may also be the development of nonexcimer
lasers to cut corneal flaps, which could reduce or eliminate microkeratome-related compli-
cations.
Furthermore, intrastromal ablation with picolasers may eliminate the need for the mi-
crokeratome. Solid-state picosecond lasers are infrared lasers that can penetrate tissues
without being absorbed. Thus such lasers can theoretically achieve intrastromal ablation
without disturbing the overlying epithelium and Bowmans layer. Animal studies are by far
encouraging, but extensive investigation is required before picosecond laser intrastromal
ablation becomes an acceptable keratorefractive procedure (97).
Continuing evolution in the current techniques is the only way to approach the ultimate
goal, which should be to offer our patients better vision in terms of quality and quantity.
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3
Lasers in LASIK
Basic Aspects
RODRIGO TORRES
Massachusetts Eye and Ear Infirmary and Harvard Medical School,
Boston, Massachusetts, U.S.A.
ROBERT T. ANG
Massachusetts Eye and Ear Infirmary and Harvard Medical School,
Boston, Massachusetts, U.S.A., and Asian Eye Institute, Makati, The Philippines
DIMITRI T. AZAR
Massachusetts Eye and Ear Infirmary, Schepens Eye Research Institute,
and Harvard Medical School, Boston, Massachusetts, U.S.A.
beam is perfectly homogeneous, the distribution of energy within the beam is uni-
form.
Coherence, monochromatic light waves perfectly in phase and parallel.
femtosecond, 1015 seconds; picosecond, 1012 seconds; nanosecond, 10-9 seconds.
Figure 3.1 The electromagnetic spectrum. The 193 nm argon fluoride (ArF) excimer laser falls in
the ultraviolet portion of the spectrum. (From Ref. 62.) [Color in original.]
Lasers in LASIK 41
Figure 3.2 The argon fluoride excimer laser demonstrates high absorption and low penetration
properties within the corneal surface. (From Ref. 63.)
absorb the radiant energy (Fig. 3.2). Other atoms are simply unaffected by the photons and
let them pass by. By manipulating the frequency of light, we can choose whether we want
the energy to affect water or biological tissue. Effectively, we can pick our molecular
targets.
Lasers used in LASIK utilize ultraviolet wavelengths around 200 nm (0.2 m),
falling in the UV-C range of the spectrum. The dominant chromophore in cornea for the
193 nm and 213 nm wavelengths within this range is the peptide bond linking adjacent
amino acids in collagen (3). Photons at these wavelengths carry in the range of 6.4 eV of
energy each, an amount exceeding that in typical peptide bonds. The bonds are broken by
the photon interaction. Ideally this process occurs with very little thermal generation, be-
cause the energy is used primarily in breaking bonds. The resulting fragments occupy a
greater volume than the single polymer from which they originated and are imparted some
kinetic energy from the irradiation. Both of these factors contribute to supersonic ejection
of the material from the corneal surface (4,5). This process has been referred to as photo-
chemical ablation, ablative photodecomposition (6), and photoablation (79). The choice
of frequency determines whether photovaporization, photothermal shrinkage, or photo-
chemical ablation occurs.
b. Homogeneity
A uniform distribution of energy in the beam cross section is termed beam homogeneity.
Because no laser leaves the resonator with a uniform distribution, it is important to charac-
terize the beam homogeneity. In the absence of homogeneity, ablation rates are expected to
vary over the treatment zone, resulting in irregular tissue removal (10). Prior to beam ma-
nipulation, a gaussian distribution for the excimer laser is expected. With gaussian beam
profiles, central overcorrection and peripheral undercorrection within the ablation zone
have been reported (1113). These distortions have been associated with the use of small
ablation diameters and a nonuniform gaussian beam profile which is hotter centrally
(12,14).
42 Torres et al.
c. Irradiance
Irradiance is central to studies of ablative threshold and ablative rate. The photoablative
threshold at 193 nm wavelength is a minimum irradiance of 50 mJ/cm2. At values lower
than this, appreciable ablation is not observed.
Photoablative rate is also a function of the irradiance. The relationship between ab-
lation rate and irradiance differs for different electromagnetic wavelengths. At 193 nm, the
photoablative rate increases appreciably as the irradiance increases from 50 mJ/cm2 (the
photoablative threshold) to 150 mJ/cm2; at irradiances greater than 150 mJ/cm2, the pho-
toablative rate tends to plateau for this wavelength (15). At 249 nm, however, the pho-
toablative rate does not plateau but continues to increase logarithmically as the irradiance
increases (Fig. 3.3).
The relationship between ablation rate and irradiance is important in refractive
surgery. Because there is significant pulse-to-pulse variation in irradiance, the ablation rate
must be fairly consistent despite this variability. The ablation rate to irradiance curve for
the 193 nm wavelength is favorable because this curve plateaus at an irradiance of 150
mJ/cm2.
Another important property related to ablation rate is ablation efficiency, which is the
ablation rate divided by the irradiance. Maximizing ablation efficiency minimizes excess
energy, which would otherwise contribute to shock waves, photochemical effects, and
heating of sites local and distant to irradiation (16). The 160180 mJ/cm2 irradiance range
is efficient for corneal ablation. At this range, ablation rates of 0.210.27 m per pulse for
the VISX laser and 0.26 m per pulse for the Summit laser have been confirmed (17).
d. Intensity
Irradiance is a measure of the amount of energy imparted onto a surface area, and intensity
is a measure of the rate at which energy is imparted onto a surface area. Imparting energy
at a rate greater than the rate at which it is absorbed by photoablation results in heating of
Figure 3.3 At irradiances greater than 150 mJ/cm2, the curve plateaus for the 193 nm wavelength.
The ablation rate remains fairly consistent despite a variability in irradiance. (From Ref. 15.)
Lasers in LASIK 43
collateral tissue. This heating can result in energy transduction into corneal surface shock
waves, an undesirable outcome.
Figure 3.4 The three approaches to excimer laser photoablation. (a) Scanning slit. (b) Large or
broad beam. (c) Flying spot. (From Ref. 64.)
Lasers in LASIK 45
smaller beam allows for ablation to occur at energy outputs less than those required for
wide field ablation. Reduced acoustic shock waves and smoother ablative surfaces are pos-
sible compared with wide area ablation. Beam uniformity and homogeneity are much im-
proved because of the smaller beam cross section. The incidence of steep central islands is
much lower using the scanning slit approach. In contrast to wide area ablation, there are no
optical zone (the size of the treated area) limitations for photorefractive keratectomy (PRK)
or phototherapeutic keratectomy (PTK) with the scanning slit approach.
Disadvantages of the scanning slit technique include increased dependence upon
complicated scanning systems and a longer operating time, compared with wide field ab-
lation. Consequently, eye tracking and fixation become a concern with the scanning slit.
Some systems using this approach include the Nidek EC-5000 and the Meditec MEL
60.
Laser heads can come in solid, liquid and gas phases. Liquid lasers have no immediate ap-
plication to photorefractive refractive surgery. Gas lasers investigated for refractive surgery
include the CO2 and the excimer lasers, the latter being the most useful for refractive
surgery.
46 Torres et al.
tions in velocity dependent on the energy of ablation and the wavelength of the radiation.
Pressures of up to 100 atmospheres can be generated, making corneal damage possible
from shock waves. Thermal denaturation of surface collagen can result in pseudomem-
brane formation, currently considered a local protective effect (33). Structural changes be-
neath the corneal surface following ablation include stromal vacuoles and an increased
number of keratocytes in later stages of wound healing (34).
Particulate ejection occurs as ablative decomposition renders polymers into multiple
heated polymeric fragments that occupy a larger volume (Fig. 3.5). This forces particles
into the air in a supersonic expanding plume (35) (Fig. 3.6). Particles in the plume include
H2O radicals, simple carbons, hydrocarbons, and some alkanes (36,37). The plume ejection
results in a recoil surface wave that travels at several meters per second, although as yet this
wave has not been demonstrated to induce corneal injury (38).
Corneal surface heating occurs secondary to ablative decomposition. Theoretically,
ablative decomposition channels energy into breaking peptide bonds and not into heat, but
the average corneal temperature has been observed to increase by 20C during ablation
(39). In theory, this increase in temperature could induce keratocyte injury.
Accuracy of the 193 nm excimer beam ablation. The 193 nm wavelength has subcel-
lular levels of accuracy for photoablative decomposition. Typical ablation rates are
0.210.27 m per pulse, which translates to roughly one twenty-eighth of the diameter of
Figure 3.5 As laser energy is absorbed (a) peptide bonds are broken (b), resulting in increase in
volume and subsequent ejection of particles (c). (From Ref. 7.)
48 Torres et al.
Figure 3.6 During excimer laser ablation of the cornea, the ejection of particles into the air is vis-
ible as an expanding plume. (From Ref. 35.)
a red blood cell (7 m) of ablation per pulse. In a dramatic demonstration of the precision
of the excimer laser, Srinivasan in 1983 used the ArF excimer to create grooves in a human
hair strand (Fig. 3.7). Light microscopy of ablated areas show clean edges with no de-
tectable traces of cellular injury other than in pale-staining cytoplasm of cells bordering the
ablation.
One feature of this subcellular ablation is the formation of a pseudomembrane, which
can be about 100 nm thick and is present at the ablation site. There is no cell membrane at
this site, but the pseudomembrane is thought to provide a barrier to the passage of water as
well as possibly provide a scaffolding for wound reepithelialization. On electron mi-
croscopy the pseudomembrane appears as a condensation of electron-dense material (40).
Figure 3.7 The clean, sharp edges of the grooves created by the excimer laser on a human hair
demonstrate the accuracy and precision of the laser. (From Ref. 5.)
Lasers in LASIK 49
Not all corneas form pseudomembranes. It is not known what causes pseudomembrane for-
mation, but the thermal effect and the uncoupling of organic double bonds during pho-
toablation have been proposed as contributing to the phenomenon (41).
The 193 nm wavelength has the useful property of a relatively constant ablative rate
at irradiances near the commonly used values of 160180 mJ/cm2. Because of this plateau,
pulse-to-pulse variability in irradiance does not drastically affect the ablative rate, allow-
ing for predictable ablative depths.
b. Other Advantages of the Excimer: Strong Beams with Large
Diameters
An important advantage of the excimer ArF laser is the ability to produce a homogeneous,
large-diameter beam (~6 mm), at ablative irradiances, capable of treating the entire optical
zone simultaneously. This was especially important earlier in photorefractive surgery when
eye tracking, eye fixation, and beam scanning made scanning slit and flying spot technolo-
gies more challenging to develop. As these technologies improve, reliance on large beam
diameters may diminish, opening the door to nonexcimer laser types that initially were im-
practical for refractive purposes.
c. Disadvantages of Excimer Systems
Nonexcimer laser systems are desirable in the future owing to the several potential disadvan-
tages of excimer laser systems. One disadvantage is the risk of toxic gas exposure. The gases
are consumed by laser utilization and must be changed frequently, increasing the risk. The
large size of the laser head and high energy requirements are also undesirable. Optics for
beam homogenization can be complex and require frequent replacement. Finally, because the
193 nm wavelength is absorbed so avidly by cornea, the laser does not allow for intrastromal
refractive surgery. This necessitates mechanical flap lifting for LASIK. Although there is cur-
rently no widely used alternatives to this approach for keratomileusis, in the future it would
be desirable to minimize the invasiveness of the procedure with intrastromal keratomileusis.
2. Solid-State Lasers
Although the excimer gas lasers have made by far the most important contribution to
photorefractive surgery, some solid-state lasers are showing promise for use in this capac-
ity. Keeping in mind that the goal for refractive surgery is to change the shape of the cornea
with precision and little collateral damage, it is important to remember that ablative
decomposition is only one way to attain this goal. Any tissue-altering modality (photodis-
ruption, photovaporization, collagen shrinking, photospallation) that alters tissue struc-
ture in a precise, localized, and predictable fashion has potential as a tool for refractive
surgery.
a. Wavelength-Modulated Nd:YAG and Nd:YLF Lasers
The Nd:YAG and Nd:YLF lasers are infrared solid-state lasers. The active media are the
neodymium-doped crystals of either yttrium-aluminum-garnet or yttrium-lithium-fluoride.
The Nd:YAG and Nd:YLF lasers have fundamental wavelengths of 1064 nm and 1053 nm,
respectively. When raised to the fifth harmonic, the wavelengths become 213 nm and 211
nm, respectively. These are very close to the 193 nm ArF excimer wavelength, suggesting
that these lasers may be suitable for photoablative decomposition. Histological studies
show that the damage zone created by the 213 nm Nd:YAG laser is less than 1 m, which
50 Torres et al.
is similar to the results with the ArF laser (42). Furthermore, PRK with the 213 nm laser
produces smooth surfaces and transitions, with a reepithelialization rate and histopatho-
logical findings similar to the results with the 193 nm excimer laser PRK in rabbit studies
(43). This evidence supports the possibility that 213 nm photoablative decomposition is
feasible and safe.
b. Mutagenicity of the 213 nm Wavelength
The question of mutagenicity at the 213 nm wavelength has been addressed by in vitro stud-
ies (44). These studies measured free radical production in bovine corneas and in vitro bac-
terial survival following 193 and 213 nm irradiation at subablative irradiances. Evidence
suggests that free radical production and species were identical for the two lasers, but the
213 nm wavelength clearly demonstrated increased bacterial cytotoxicity. If the differences
in cytotoxicity apply to mammalian cells, corneal fibroblasts responsible for collagen re-
pair would be much more affected by 213 nm irradiation (45). In vivo studies in rabbits do
not provide clear evidence as to the safety of the 213 nm wavelength in PRK. In one study,
the 213 nm radiation was found comparable to the 193 nm radiation (43), but in another
study, the results were significantly worse at 213 nm (46). Increased postoperative compli-
cations observed in the latter study could be partially explained if the 213 nm wavelength
were cytotoxic to mammalian keratocytes. More studies on the mutagenicity of the 213 nm
wavelength will be an interesting area of future work.
In summary, the frequency-quintupled solid-state lasers do show promise as tools for
refractive surgery. A solid-state laser on the market functioning at the 211 to 213 nm wave-
length range is the Novatec Lightblade flying spot laser. Although these lasers are not
as energy efficient as excimers, they show comparable ablative efficiency. As energy
efficiencies of these systems improve, they may become available as wide-area ablation
lasers, which would decrease operative time, improve intraoperative corneal hydration, and
possibly produce superior surgical results. Also, as flying spot and eye tracking technology
develop further, low-energy, small-beam solid-state lasers can also be expected to produce
superior results. Although not as clinically developed, solid-state lasers have several ad-
vantages over the excimers. The frequency-quintupled Nd:YAG laser is less expensive and
more compact than the ArF laser and does not require the use of toxic gases. Furthermore,
solid-state lasers can provide increased reliability, robustness of design, safety, and lower
operating costs than gas or dye lasers.
c. Nd:Glass (Femtosecond) Lasers
The Nd:glass lasers have been investigated for their ability to generate femtosecond pulses.
The technology for such generation has only recently become feasible. Because these
pulses provide a much higher power output and a much shorter exposure time, they require
only one-fourth to one-tenth the energy to produce corneal photodisruption compared with
picosecond and nanosecond infrared laser pulses (47,48). By utilizing less radiant energy,
the secondary shock wave and cavitation bubble size are reduced, allowing for closer pack-
ing of laser pulses and more contiguous photodisruption.
In a study using femtosecond pulses from a Nd:glass laser to produce an intrastromal
spiral ablation in porcine and primate cadaver eyes, the pulses were focused 150200 m
below the surface epithelium of the cornea and scanned in a spiral pattern to create a plane
(49). The plane was extended to the surface to create a flap, and mechanical tissue plane
separation was used to grade the contiguity of the intrastromal ablation. The results indi-
cated that many of the shortcomings of picosecond technology (including incomplete tis-
Lasers in LASIK 51
sue cutting, poor dissection, and surface quality) are significantly improved when the pulse
duration is further reduced into the femtosecond region. The femtosecond pulses allow for
very small cavitation bubbles, approximately 12 m, which in turn allow for closer place-
ment of pulses and smoother tissue dissection (47). Although results are encouraging, in
vivo systems that closely reproduce the clinical situation must be investigated to establish
clinical efficacy. An in vivo study in rabbits concluded that intrastromal photodisruption
with femtosecond lasers produced consistent changes in corneal thickness without loss of
corneal transparency (50). The study did not evaluate changes in corneal topography or
specular microscopy, although no damage to the corneal endothelium was seen on histo-
logic sections. This laser is now being used to create LASIK flaps in patients undergoing
LASIK surgery with good results.
Advances in ultrafast laser design and the development of powerful laser diodes have
finally made low-cost, reliable, diode-pumped, femtosecond laser systems possible (51).
Femtosecond lasers are solid-state, enjoying all of the advantages of solid-state lasers over
excimer lasers. Because infrared radiation is transmitted by corneal tissue (unlike excimer
193 nm radiation), infrared femtosecond lasers could allow for intrastromal refractive
surgery that obviates the need for mechanical flap creation or epithelial disruption (50). It
will be exciting to follow the advances in femtosecond laser technology and the applica-
tions it offers for corneal flap cutting, laser keratomileusis, corneal implant placement, and
possible intrastromal keratectomy.
availability of fluorine for stimulated emission. This reduces laser action. To maintain pu-
rity, the gas must be either constantly cleaned or frequently replaced. Cleansing of the gas
involves precipitation of contaminants using a cryogenic device and liquid nitrogen. Alter-
natively, the chamber can be cleansed by flushing it with fresh gas to replace the contami-
nated gas. Improvements in laser construction have reduced the need for cryogenic gas pu-
rification and prolonged the lifetime of a single gas fill (6).
2. Calibration Techniques
It is important to check the laser ablation rate prior to surgery because if the output is too
high, overcorrection is likely. If the output is compromised, undercorrection is a risk. This
checking process is referred to as calibration. Calibration methods are generally based on
measurement of energy (energy models) or measurement of ablation (ablation models). En-
ergy models use direct measurement of the energy output of the laser with meters, which is
accurate only within 15% due to the extraordinarily high output of lasers (53). Further-
more, calibration of these meters requires sophisticated equipment that is difficult to use
routinely in the field. For these reasons, the ablation models (ablation of Wratten filters,
PMMA blanks, scanning profilometry) are used most frequently.
One approach to calibration involves ablation of a piece of plastic, forming a lens.
The plastic used is PMMA, or polymethyl methacrylate, the plastic used for contact lenses.
The power of the formed lens can be tested with a lensometer to assess laser irradiance,
laser alignment, and laser beam profile. Distortions of the lens can indicate poor laser light
distribution within the beam (6). Another approach to calibration involves counting the
number of pulses necessary to perforate a plastic Wratten filter. This approach can be mod-
ified to ablate only 90% of the thickness of the plastic. The quality of light transmission
through the plastic can be grossly assessed for uniformity.
The VISX laser is calibrated based on preoperative ablations performed on a PMMA
block. Then the laser is reprogrammed to adjust the ablation rate to the desired value. The
Summit laser can be checked by doing a 90% gelatin film ablation. The Chiron-Technolas
laser is reprogrammed after counting the number of pulses needed to perforate a special
foil. The Coherent-Schwind laser also uses a gelatin film for calibration, with reprogram-
ming based on the number of pulses required for 1090% perforation of the film. The
LaserSight laser uses a patented device, ex-calibur, which employs commercially available
corneal topography systems (54).
Broad beam excimer laser ablations are usually characterized by a relatively uniform
distribution of surface power within the treated zone (55). Nonetheless, the hypothesis that
corneal stromal ablation shape exactly matches the laser beam profile has been shown to be
invalid (56). Rather, in uniform beams the ablation rate varies with the ablation diameter.
This fact must be taken into account when attempting to calibrate by an energy model ap-
proach. Failure to correct for this variance can lead to central undercorrections and periph-
eral overcorrections, a phenomenon termed steep central islands. The underlying causes for
spatially variable ablation rates across a uniform beam are unclear but may include differ-
ential hydration of the cornea, redeposition of ablated material as it lifts from the surface,
photospallation effects, dependence upon proximity to an unablated area, and persistent ab-
lation fog overlying the stromal surface.
Modifying the ablation algorithm to accommodate the spatial variance of corneal ab-
lation has produced spherical enucleated eye PRK ablations. By analyzing the postopera-
tive topography of PRK patients, the ablation algorithm was modified to produce a more
spherical ablation in situ (56).
Lasers in LASIK 53
rent laser systems, but the tracking is based on lower sampling frequencies, and with
equally good outcomes.
A recent study used the LADARVision system to treat one eye of each of 102 patients
with 1.5 to 6.25 D of spherical myopia (60). There was a 93% 1-year follow-up. The
follow-up results reported uncorrected visual acuity of 20/40 or better in 99% of eyes,
20/20 or better in 70% of eyes, and BCVA of 20/25 in 100% of eyes. One eye lost two lines
of BCVA (20/12.5 preoperative to 20/20 postoperative). No eyes lost more than two lines
of BCVA, and corneal haze was trace or better for all patients. Results were within 0.50
D of desired correction in 75% of eyes and within 1.00 D in 93% of eyes. The results of
this study were at least comparable, if not better, than those of a previous wide beam ex-
cimer laser clinical trial in which 63% of myopic eyes (baseline 1 to 6 D; n 342)
achieved visual acuity of 20/20 and 68% were within 0.50 D of the desired refraction
(57,61). The tracking systems on other laser platforms have also shown improved centra-
tion and improved visual outcomes (See ch. 14).
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4
Microkeratomes
SANDEEP KAKARIA
Cornell University Medical Center, New York, New York, U.S.A
THANH HOANG-XUAN
Fondation Ophtalmologique Adolphe de Rothschild, and Paris University,
Paris, France
DIMITRI T. AZAR
Massachusetts Eye and Ear Infirmary, Schepens Eye Research Institute,
and Harvard Medical School, Boston, Massachusetts, U.S.A.
A. INTRODUCTION
Microkeratomes have evolved from suction rings and moving blades that were difficult to
operate to more user-friendly devices currently utilized in LASIK refractive surgery. The
early microkeratomes used by Jos Ignacio Barraquer were limited to the treatment of high
myopia. Barraquers technique, involving the creation of a central lenticule with a manual
microkeratome, freezing this section, and carving the deep portion with a lathe, according
to the amount of refractive error, had several technical limitations and was associated with
numerous complications. Complications of this technique resulted from difficulties in mas-
tering the microkeratome and cryolathe and included lenticular damage, persistent corneal
haze, irregular astigmatism, under- and over-correction, and regression (1). Innovations to
address this problem, including Swingers technique, in which he did not freeze the back
side of the lenticule (14), and Ruizs in situ method for manually removing corneal stroma
deep to the flap (5), were particularly important milestones that led to the development of
current microkeratomes.
Burrato used argon-fluoride excimer laser ablation, previously reported for surface
ablation by Trokel (6), in combination with the microkeratome on the deep portion of the
lenticule (7). Pallikaris demonstrated that in situ ablation and refractive correction could be
57
58 Kakaria et al.
performed on the remaining stromal bed (8). With these advances and the increasing pop-
ularity of the excimer laser, the microkeratome still had its place, but it was no longer used
for reshaping. Instead, its primary purpose was the creation of the corneal flap.
The microkeratomes of today have become safer and have been proven successful in
performing corneal lamellar cuts; however, complications with their use continue to occur.
These complications have been decreasing with surgical experience, advancements, and
design elements incorporated into newer microkeratomes. The current microkeratomes are
by no means close to being free of complications, nor do they approximately an ideal mi-
crokeratome, which would optimize the following parameters: safety, ease of use and ster-
ilization, reliability, moderate increase in IOP and minimal structural deformation during
surgery, smooth beds, regular edges, reproducible thickness, sufficient hinge width, suction
ring stability, and reasonable cost of hardware and disposables. Although currently used
microkeratomes incorporate several features of the ideal microkeratome, they nevertheless
sacrifice some obviously useful features in order to achieve others.
Typical components of a modern microkeratome system include the following (9):
Motor
Microkeratome head
Applanator lenses to measure the diameter of the exposed cornea
Vacuum fixation ring used to secure the eye
Flap stop ring, which limits the travel of the microkeratome head through the fixation
ring
Foot switch
B. MICROKERATOME TYPES
Although microkeratomes share several similarities, they can be divided into five basic cat-
egories:
1. Nondisposable horizontal
A. Gear driven
B. Automated sliding
C. Manual
2. Nondisposable vertical
A. Automated
B. Manual
3. Disposable
A. Cable driven
B. Turbine driven
C. Gear driven
4. Water jet
5. Laser microkeratomes (picosecond)
Figure 4.1 Hinge location. (A) Nasal hinge. The keratomileusis occurred in the temporal-to-nasal
direction. (B) Superior hinge.
include the Moria LSK-1, the SCMD Turbokeratome by New United Development Cor-
poration, and the Med-Logics Manual.
The automated sliding microkeratomes (SKBM, B.B.-I-T-I, Allergan, and Nidek)
have virtually displaced all other horizontal microkeratomes in this category because they
are surgeon-independent reliable units that require minimal assembly during surgery and
have relatively high reproducibility of flap thickness.
1. Basics
Horizontal microkeratomes are derived from the original design by Barraquer. During the
keratomileusis procedure, the turbines or electric motors of these instruments are located
horizontally or to the side of the eye. Cuts are usually made with nasal hinges (Fig. 4.1A),
although it is possible to position narrow versions of these microkeratomes to create supe-
rior hinges.
Figure 4.2 Gears vs. sliding mechanism in nondisposable horizontal microkeratomes. (A) The
gears of the ACS head move through the geared tracks of the suction ring. (B) The SCMD slides
through its track without the assistance of gears.
60
Figure 4.3 Other examples of nondisposable horizontal microkeratomes. Note that the microkeratome motor is not directly above the
operating surface. (A) Moria Lamellar System for Keratoplasty-1. (B) Summit Krumeich-Barraquer. (C) Med-Logics Microkeratome.
(D) Innovative Optics Innovatome. (E) LaserSight Technologies Ultrashaper.
Kakaria et al.
Microkeratomes 61
2. Design
Automated horizontal microkeratomes may advance through the use of rotating gears be-
tween the microkeratome head and the suction ring (Fig. 4.2A) or through gearless sliding of
the microkeratome head on the suction ring. Manual microkeratomes primarily consist of
gearless sliding of the microkeratome head on the suction ring (Fig. 4.2B).
Gear-driven microkeratomes may have an increased likelihood of jamming due to
operative debris and may also be more difficult to clean between procedures. Sliding de-
signs may decrease these complications. The instances of microkeratome head slippage
from the suction ring tracks in the manual microkeratomes have been practically eliminated
in the newer automated sliding horizontal designs.
The ACS is a gear-driven nondisposable horizontal microkeratome, while the other in-
struments in this category utilize the sliding mechanism (Figs. 4.2B and 4.3). The Moria
LSK-1 and the SCMD, both manual microkeratomes, run on a gas-turbine mechanism, while
the others use an electric motor. Multiple flap sizes and depths are available. Technical fea-
tures of individual nondisposable horizontal microkeratomes may be seen in Table 1.
3. Safety Issues
The original SCS microkeratome uses multiple components to ensure appropriate depths
and flap size. Although this may allow flexibility, the incomplete, inappropriate tightening
of this instrument may result in free caps (if stop is not screwed properly) or corneal per-
foration (if the depth plate is not tightened or mistakenly not inserted). Care must be taken
Depth 160 and 180 mm 130, 160, 180 160 and 180 160
Mechanism Gear driven Sliding Sliding Sliding
Automated/manual Automated Automated Automated Automated
Advance rate 3.7 mm/s 0.13.0 mm/s 3.5 mm/s
Motor Electric Electric Electric Electric
in the use of all microkeratomes to ensure that a variable depth plate is tightened to the
proper level or that fixed depth plates are always inserted prior to keratomileusis.
1. Basics
In nondisposable vertical microkeratomes, the motor lies directly vertical or above the eye,
rather than to the side of the eye. This instrument may be used to create a superior hinge
(Fig. 1B). Vertical microkeratomes are equipped with a rotating head that travels to create
the surgical arc (flap).
2. Designs
The primary difference between the two popular vertical microkeratomes is the presence
of a geared track on the Hansatome compared to the smooth track of the Carriazo-Barra-
quer (Fig. 4.4). As with the ACS, the geared track may cause this instrument to be more
susceptible to jamming from debris; however, it provides the microkeratome with more
torque (torqueforce* distance). Greater torque allows the microkeratome to perform its
keratomileusis with minimal assistance from the surgeon. The Carrazo-Barraquers lack
Microkeratomes 63
Figure 4.4 Examples of nondisposable vertical microkeratomes. Note that the microkeratome
motor is directly above the operating surface. (A) The geared outer track of the Hansatome suction
ring. (B) The smooth outer track of the Carriazo-Barraquer suction ring. (C) Fully assembled
Hansatome with suction ring, plate, and head. (D) Fully assembled Carriazo-Barraquer with suction
ring and head. Note the microkeratome head in B is smaller than A. The M-2 Moria Microkeratome
has virtually replaced the Carriazo-Barraquer microkeratome because it avoids the problem of flap
thickness variability.
of an outside gear, and hence its inferior torque, may require the surgeon to push the mi-
crokeratome head gently to initiate keratomileusis. This causes the automatic version of
the Carriazo-Barraquer microkeratome to have a manual component.
Both the Hansatome and the Carriazo-Barraquer operate at high oscillation speeds,
close to 15,000 rpm. The Hansatome has a faster advancement rate, while the Carriazo-Bar-
raquer has a greater selection of flap diameters. Technical features of nondisposable verti-
cal microkeratomes appear in Table 2.
3. Safety Issues
The Hansatome has made a few advancements over the ACS. First of all, it will not oper-
ate if the plate is not inserted. Second, the number of gears is reduced and they are better
covered from debris. The Carriazo-Barraquer does not require a plate to be inserted and can
fit in narrower spaces. In addition, it may produce a hinge in any peripheral corneal loca-
tion.
E. DISPOSABLE MICROKERATOMES
These microkeratomes include the Refractive Technologies Flapmaker, the LaserSight
Technologies Unishaper, and the Moria LSK-1 Disposable.
1. Basics
These are horizontal microkeratomes that have the advantage of requiring no assembly, dis-
assembly, or cleaning. Each microkeratome head, blade, and suction ring combination is
sterile, used once, and then discarded.
2. Designs
In disposables, the blade is preassembled in the head, and the head is engaged in the track.
The head and suction ring are made of clear plastic, and the instruments operate by utiliz-
ing a sliding (cable driven or turbine driven) or a gear driven mechanism (Fig. 4.5).
The Moria LSK-1 Disposable is a manual microkeratome and uses the same con-
trol unit as the other Moria microkeratomes. The Flapmaker and Unishaper are auto-
mated and use electric motors. Technical features of disposable microkeratomes appear
in Table 3.
3. Safety Issues
Disposable systems have the advantage of requiring fewer components to be set up by the
surgeon; they also have improved sterility, thus decreasing the chance of operational error
or surgical infection. In addition, the clear plastic of the disposable systems ensures good
visibility for the keratomileusis procedure.
Figure 4.5 Examples of disposable microkeratomes. Note the pre-engaged plastic suction ring
and head. See the smooth tracks of A and B and the geared track in C. (A) Refractive Technologies
Flapmaker. (B) Moria LSK-1 disposable. (C) LaserSight Unishaper.
1. Basics
The theory behind the water systems is that blades cause collateral tissue damage, while a
beam of water can precisely cut between layers without leaving debris and provoking min-
imal wound response. In addition, the hydrokeratome can perform the cut without requir-
ing an increase in intraocular pressure.
2. Designs
The Medjet Hydroblade Keratome uses a 30 m beam, and advances at 6.7 mm/s. It has a
fixed depth plate and can produce superior, temporal, or nasal hinges. The Medjet Hy-
drorefractive Keratectomy (HRK) System is a water system that makes a bi-hinged flap
with a C-shaped needle. The system attempts to ablate without the need of a laser. Instead,
the shape and pressure of the template can be changed, along with the scan rate, in order to
remove different amounts of tissue. The Visijet Hydrokeratome is also a water jet system
that uses a 36 m beam and advances at 6.7 mm/s. It has a variable depth plate of 120200
m and a clear applanation lens for good visualization.
G. LASER MICROKERATOMES
These instruments include the Novatek Laser Microkeratome and the IntraLase Microker-
atome. The Novatek microkeratome has not been used clinically, whereas the IntraLase
Microkeratome (picosecond MK) has been in clinical use since early 2000 with outstand-
ing results.
1. Basics
Laser systems create a precise flap with a laser or perform an intrastromal cavitation by
carving a corneal lenticule with a laser beam. The vapor and fluid residues from intrastro-
mal ablations dissipate a few hours after surgery.
2. Designs
The IntraLase Laser Microkeratome depends upon femtosecond pulses, so less energy is
needed to photodisrupt corneal tissue, thus allowing more localized effects. It also allows
a wide variety of corneal flap shapes. It also depends on an applanation plate to ensure con-
sistent flap thickness. The Novatec Laser Systems Laser Microkeratome is expected to
have eye tracking systems to monitor eye movements, giving a three-dimensional map for
the lasers location within the cornea. The IntraLase Microkeratome has been continously
upgraded, so as to allow complete versatility and reproducibility, and may become the most
commonly used system for corneal flaps in the future.
H. OTHER MICROKERATOMES
The Ophthalmic Technologies Inc./Loktal Medical Clear Corneal Molder allows for cor-
rection without photoablation. It can perform convex or concave cuts, thus correcting for
Microkeratomes 67
myopia and hyperopia. It has minimal vibration, allowing use of steel or diamond blades.
It also has gearless tracks, is a manual microkeratome, and has separate motors for oscilla-
tion and advancement. It is adjustable, 1500 m in depth, and the standard is fixed at 180
m. Its blade speed is also adjustable to 24,000 rpm. It has a viewing window and auto-
matically stops if suction is lost. In addition, it only cuts in forward motion.
Mastel Precision Surgical Instruments Buzard Barraqueratome has a diamond blade
and needs no assembly. It provides good visualization of the flap and is compact, so it can
fit small eyes. It has a two-chambered vacuum, which acts on the cornea and sclera to al-
low for a lower IOP. The depth plate is fixed at 160 m and the instrument makes nasally
oriented flaps.
Hanna also makes a microkeratome. This instrument relies upon rotational motion
and is known for the formation of a smooth bed.
I. DISCUSSION
Micro- # of Incomplete Perorated Short Sliding wrinkles Free Flap Thin Decentered
First author keratome eyes cut lenticule flap flap (striae) cap melt flap flap Cumulative
First and foremost, a suitable microkeratome should have a low level of flap complications.
These complications depend on a multitude of factors, including experience and microker-
atome safety features. As refractive surgeons know, there is a steep learning curve for
LASIK, and regardless of microkeratome brand complications will decrease with time.
However, complications may be more apt to occur in certain microkeratomes
(1238). Farahs work quantitates flap complications, and by including data from further
studies, one may see the number of flap complications that have occurred with different mi-
crokeratome designs (1), specifically the ACS and the Hansatome (Table 4). In these stud-
ies, serious flap-related complications occurred in 4% of the ACS cases and 1% of the
Hansatome cases. The Hansatome studies contained less severe complications. There were
no free caps in the 440 eyes analyzed, and 10 of the 20 complications were a decentered
flap. Flap decentration appears to be an inherent possibility in the Hansatome cases. Of-
tentimes, suction ring application causes movement of the globe. The suction must be
stopped and the area recentered. However, in some cases, scleral indentation occurs when
the ring fixes on the globe on the first cut attempt and the indentation may prevent adjust-
ment (12). In these cases, a different suction ring or repeated attempts at recentration will
solve the problem.
Consistent flap thickness is also important in performing LASIK. Most surgeons aim
to leave a minimum of 250 m of residual cornea after ablation to prevent irreversible
corneal edema. For patients whose residual corneal thickness is predicted to be close to 250
m, according to refractive correction and preoperative pachymetry, a predictable flap
thickness is essential. Many microkeratome companies have performed studies to indicate
consistent flap thickness. Summits two studies showed varied results on flap thickness.
A 12 eye study with the Summit KrumeichBarraquer microkeratome indicated a 190
17 m cut with the 160 m head, while a 24 eye study indicated a 164 13 m cut with
the same head. One study involving 93 eyes that underwent LASIK with the Moria LSK-1
microkeratome indicated that the 160 m head averaged 159 28 m (13). Pinedas work
on 25 eyes reveals a 117 17 m cut with the ACS, and his 21 eye study shows a 127
29 m cut with the Hansatome; both studies attempted a 160 m cut (14). Pinedas work
and our experience indicate that the ACS and Hansatome provide cuts that are more often
thinner than expected.
In addition to consistent flap thickness, design features that offer good visibility are
an asset to all surgeons, especially those who are still in the steep portion of the learning
curve (1538). Proper visibility allows the beginner to learn correctly the positions and
technical details of microkeratome operation and aids the expert in avoiding debris in the
surgical path. Also, designs that are slim have benefits, since they can fit into the widest va-
riety of patients, such as those with narrow eyes or redundant eyelid skin.
Microkeratomes that rely on fixed depth plates, rather than heads that can achieve
variable depths, are preferable. First, if a surgeon needs to cut at a different depth, he or she
may still do so using a different head. Second, human error may occur when inserting the
depth plate into variable depth systems, thus leading to corneal perforation with high in-
traocular pressure. Such a complication may cause damage to various structures in the eye,
including the iris, the ciliary body, and the lens (37).
Finally, safety features such as alarms, automatic shut-sown buttons, or suction dis-
plays are very beneficial. If the microkeratome continues forward progress after suction is
lost, an irregular cap can occur with a cut through the central cornea. Scarring in this loca-
tion would be in the visual axis.
As for future methods to perform lamellar cuts, more accurate blades with consistent
Microkeratomes 69
depths can be expected, along with laser systems that may cause less corneal disturbance.
Time will tell where the future of microkeratomes lies, but one can be assured that micro-
keratome advances will continue (3638).
REFERENCES
1. SG Farah, DT Azar, C Gurdal, J Wong. Laser in situ keratomileusis: literature review of a de-
veloping technique. J Cataract and Refract Surg 1998;24(7):9891006.
2. O Gris, JL Guell, A Muller. Keratomileusis update. J Cataract Refract Surg 1996;22:620623.
3. CA Swinger, J Krumeich, D Cassiday. Planar lamellar refractive keratoplasty. J Refract Surg
1996;2:1724.
4. SF Brint, DM Ostrick, C Fisher, SG Slade, RK Maloney, R Epstein, RD Stulting, KP Thomp-
son. Six-month results of the Multicenter Phase I Study of Excimer Laser Myopic Ker-
atomileusis. J Cataract Refract Surg 1994;20:610615.
5. L Buratto, M Ferrari. Indications, techniques, results, limits, and complications of laser in situ
keratomileusis. Curr Opin Ophthalmol 1997;8(4):5966.
6. SL Trokel, R Srinivasan, B Braren. Excimer laser surgery of the cornea. Am J Ophthalmol
1983;96:710715.
7. L Buratto, M Ferrari, C Genisi. Myopic keratomileusis with the excimer laser: one year follow-
up. Refract Corneal Surg 1993;9:1219.
8. IG Pallikaris, ME Papatzanaki, DS Siganos, MK Tsilimbaris. A corneal flap technique for laser
in situ keratomileusis; human studies. Arch Ophthalmol 1991;109:16991702.
9. M Duplessie. Surgical technique for laser-assisted in situ keratomileusis. International Oph-
thalmology Clinics 1996;36(4):4551.
10. DT Azar. Refractive Surgery. In: SW Chang, L Ruiz, M Gomez, eds. Lamellar Refractive
Surgery Instruments. New Jersey: Appleton and Lange, 1997, pp 239251.
11. American Academy of Ophthalmology. Automated lamellar keratoplasty. Ophthalmology
1996;103(5):852861.
12. EJ Velasco-Martinelli, FA Tarcha. Superior hinge laser in situ keratomileusis. J Refract Surg
1999;15(2S):S209S211.
13. BJ Jacobs, TA Deutsch, JB Rubenstein. Reproducibility of corneal flap thickness in LASIK.
Ophthalmic Surgery and Lasers 1999;30(5):350353.
14. R Pineda. Comparative analysis of microkeratome flap thickness in LASIK. 21st Biennial
Cornea Research Conference, Boston, 1999;21:45.
15. AM Bas, R Onnis. Excimer laser in situ keratomileusis for myopia. J Refract Surg 1995;
11S:S229S233.
16. L Buratto, M Ferrari, P Rama. Excimer laser surgery of the cornea. Am J Ophthalmol 1992;
113:291295.
17. PI Condon, M Mulhern, T Fulcher, A Foley-Nolan, M Okeefe. Laser intrastromal ker-
atomileusis for high myopia and myopic astigmatism. Br J Ophthalmol 1997;81:199206.
18. DD Dulaney, RW Barnet, SA Perkins, GM Kezirian. Laser in situ keratomileusis for myopia
and astigmatism: 6 month results. J Cataract Refract Surg 1998;24(6):758764.
19. A El-Maghraby, T Salah, GO Waring III, S Klyce, O Ibrahim. Randomized bilateral compari-
son of excimer laser in situ keratomileusis and photorefractive keratectomy for 2.50 to 8.00
diopters of myopia. Ophthalmology 1999;106(3):447457.
20. DC Fiander, F Tayfour. Excimer laser in situ keratomileusis in 124 myopic eyes. J Refract Surg
1995;11S:S234S238.
21. PS Hersh, SF Brint, RK Maloney, DS Durrie, M Gordon, MA Michelson, VM Thompson, RB
Berkeley, OD Schein, RF Steinert. Photorefractive keratectomy versus laser in situ ker-
atomileusis for moderate to high myopia. A randomized prospective study. Ophthalmology
1998;105(8):15121523.
22. HV Gimbel, EE Penno, JA van Westenbrugge, M Ferensowicz, MT Furlong. Incidence and
70 Kakaria et al.
ROBERT T. ANG
Massachusetts Eye and Ear Infirmary and Harvard Medical School,
Boston, Massachusetts, U.S.A., and Asian Eye Institute, Makati, The Philippines
DIMITRI T. AZAR
Massachusetts Eye and Ear Infirmary, Schepens Eye Research Institute,
and Harvard Medical School, Boston, Massachusetts, U.S.A.
The measurement of visual acuity (VA) is an essential part of the ophthalmological exam-
ination, and it represents the most common useful test for assessing visual function. In clin-
ical practice, the primary need is to document the occurrence or evolution of pathology; and
in clinical trials or research projects, the need is to perform a reliable and reproducible base-
line and evaluation of outcome. In refractive surgery, it is relevant to measure the best-cor-
rected VA before and after surgery, to rule out any pathology other than refractive error,
and to analyze differences and changes over time.
Charts with a regular progression of optotype size and spacing, with the same number
of letters per row of approximately equal recognition difficulty (Landolt C or Sloan letters),
are more useful for the standardization requirements. The Landolt ring has been consistently
advocated as a standard test object since 1909 and was eventually adopted as the primary
standard optotype by the National Academy of SciencesNational Research Council (NAS-
NRC) Committee on Vision in 1980 (1). The Sloan and British Standard Institution optotype
sets are substantially equivalent to the Landolt rings in terms of recognition difficulty (1).
Optotype sizes must be reduced in a constant way in order to obtain an equal variation all
over the scale extension. A logarithmic progression in steps of 0.1 logUnits corresponds to a
geometric progression in which each row contains optotypes about 1.26 times smaller than
the preceding one. Optotypes must also be quite far apart to avoid the crowding effect. The
71
72 Ang and Azar
NAS-NRC recommended ten optotypes divided into two rows of five; eight letters per row
is the minimum accepted. The same number of letters at each size level is required (1).
In individuals with normal vision, visual acuity (VA) increases as a function of the
background luminance from mesopic to high photopic conditions until glare is experienced
and VA subsequently decreases. VA increases from a luminance of 0.025 cd/m2 to 60
cd/m2, but above 80 cd/m2 the variation is very slight, and above 500 cd/m2 it becomes
negligible (1, 2). Maximal VA is achieved under photopic conditions. It is advisable to
avoid VA measurement in a dark room, but ambient background lighting should not exceed
one half of the chart background luminance. The ability to identify an optotype is related
not only to its angular width but also to the test target contrast. VA is reduced as the con-
trast between the test target and the background decreases. The maximal VA is achieved
when the contrast between optotypes and background is above 80%. The standard chart
testing distance should be 4 meters. With this distance, there is easy approximation to in-
finity by adding algebraically 0.25 D to the refractive correction; easy conversion of the
Snellen ratio between 4 meters and 20 feet; and maximal acuity and minimal dispersion of
acuity scores at distances close to 4 meters.
1. Distance Charts
The Snellen chart is the most widely used chart for VA testing in all English-speaking coun-
tries. It is based on the assumption that a subject with normal recognition acuity can resolve
an optotype with a visual angle of 5 and a resolution angle (stroke) of 1 (minute of arc). The
VA level is expressed as the ratio between the reading distance and the distance in meters at
which the stroke width of the equivalent Landolt ring subtends 1 minute of arc. It has sev-
eral limitations including a different number of optotypes per row, irregular progression in
letter size, differences in the recognition difficulty of the optotypes, and difference in back-
ground luminance related to different chart manufacturers. The back-illuminated Snellen vi-
sual acuity chart routinely used in a clinic has a luminance of approximately 550 cd/m2.
Snellen is generally credited with inventing letter-chart acuity testing, and although many
variants of his original test exist, the Snellen chart has gained universal clinical acceptance.
The basic principle of measuring visual acuity with letter test charts is that the small-
est level of letters that can be read satisfactorily provides the index of visual acuity. It is
therefore reasonable that each level on the test chart should have an equal degree of diffi-
culty. In 1976, Bailey and Lovie described a chart with the following features: the same
number of symbols used on each line; the between-symbol spacing is proportionally the
same on each line; the vertical spacing between one line and the next is a constant propor-
tion of symbol size; and the ratio of symbol size on a given line to that on the next line is
constant (approximately 1.25) (2,3). The British Standards Institution adopted a series of
ten nonserif letters of equal legibility, based on the findings of Coates and Woodruff as re-
ported by Bennett (2). This was the basis for the optotypes selected by Bailey and Lovie to
give standard legibility to each row of their acuity chart. Ten 55 Sloan letters (S, D, K,
H, N, O, C, V, R, and Z) were subsequently adopted by the NAS-NRC Committee. The
55 format designates that each optotype is constructed on a square framework 5 units
wide by 5 units high and having a stroke width equal to 1 unit (4).
The BaileyLovie distance visual acuity chart was developed to overcome the inac-
curacies of the Snellen chart and has been widely accepted as an accurate and efficient mea-
sure of visual acuity, particularly for assessing patients with low vision (2,5,6). The chart
has approximately equally legible letters (British Standards Institution, 1968) on each row,
Adjunctive Instrumentation in LASIK 73
and the separation of letters within rows and between rows is uniform, so that contour in-
teraction is controlled. The visual task at each level of the chart is therefore the same irre-
spective of acuity or test distance. The BaileyLovie chart employs a logarithmic progres-
sion of sizes and the logMAR visual acuity notation, which has been shown to represent a
good approximation to an equal discriminability scale and has been recognized by many in-
vestigators as the most logical measure of visual acuity (4,5,7). LogMAR charts are theo-
retically superior because interpatient differences and follow-up measurements over time
are objectively and consistently evaluated and measured. The LogMAR design also mini-
mizes the crowding phenomenon because of logical spacing of the optotypes. The Bai-
leyLovie chart or adaptations of it have been used in notable research projects including
the Early Treatment of Diabetic Retinopathy Study, the Macular Photocoagulation Study,
and the Prospective Evaluation of Radial Keratotomy Study (79), among others.
The Early Treatment Diabetic Retinopathy Study (ETDRS) chart, also known as the
Lighthouse Distance Visual Acuity Chart, uses lines of letter combinations determined to be
of equal confusability and not containing words or acronyms (7,10). The chart was intro-
duced by Ferris and is a modification of the Bailey and Lovie chart. It utilizes five Sloan op-
totypes per row with a regular progression of the type size and spacing, following a loga-
rithmic scale in steps of 0.1 logUnits. The reduced number of optotypes may increase the
probability of guessing brought about by easier memorization of the few optotypes. The
background luminance is about 150 cd/m2 without any possibility of regulation. (Fig. 5.1.)
2. Near Charts
The near test chart is a 1:10 scaled-down chart that uses a test distance of 40 cm. The range
of sizes on these charts extends from 80 point to 2 point print, and the progression of size
is essentially logarithmic. The Times Roman font was chosen because it is similar in ap-
pearance and legibility to the styles of typefaces customarily used in newspapers and books
and because it has already been adopted by the British as the standard typeface for near-vi-
sion charts (11).
The Snellen near chart is expressed as the ratio between the test distance in centime-
ters and the distance in centimeters at which the stroke of the equivalent Landolt ring sub-
Figure 5.1 ETDRS visual acuity chart. This chart is valuable for LASIK studies, although it may
be less convenient than the Snellen chart for routine measurements of visual acuity.
74 Ang and Azar
tends 1 minute of arc. With the Sloan M system, a 1-M letter is defined as an optotype
whose height subtends a visual angle of 5 at a distance of one meter.
One of the main reasons why near acuity in the consulting room can be misleadingly
good is due to the high luminance of the chart and the high contrast of the print.
Furthermore, standardization in near vision tests has not been established with regard
to using text-reading or optotypes recognition. Test cards using the Jaeger system and the
point system also vary across different manufacturers, making standardization difficult.
The practical near acuity chart (PNAC) offers a quick but accurate way to measure
near acuity and shows a high degree of correlation with distance acuity, contrast sensitiv-
ity, and ability to read newsprint (12). The PNAC encompasses print sizes from large (N80,
such as newspaper headlines) to small (N5, such as telephone directory entries). It has a
regular increasing progression of print size and line spacing (0.1 logMAR). Three words
were used on each line; one three letter word, one four letter word, and one five letter word.
Thus each line has an equivalent task demand having 12 letters split into 3 words. The
words are easy to recognize by children and those with poor language and cognitive skills.
The PNAC uses the Times Roman font, as it is a print type commonly used in newspapers
and books. Paragraphs of the most commonly used print sizes are located on the reverse
side of the chart, so reading a set size of print can be practiced once the near acuity thresh-
old has been established. Although the PNAC only uses three words on each line, it was
shown to be as accurate as the BaileyLovie near chart. Near acuity threshold was mea-
sured in half the time using the PNAC than with the BaileyLovie chart. It was found that
most people can read newspaper headlines with a near acuity of N48 (1.4 logMAR), large
text (such as childrens books) with N20 (1.0 logMAR), and normal newspaper text with
N6 (0.5 logMAR) or better at 25 cm.
B. AUTOREFRACTORS
It is almost half a century since Collins reported the design and construction of the first ob-
jective infrared optometer. However, the first fully automated optometer, the Ophthal-
motron, did not appear until 1970 (13). Automated objective refractors that do not require
any operator or patient judgment have been available since then. These instruments are
easy to use and are much quicker than manual refraction.
An ideal objective refraction technique should be able to determine the actual
ametropia without dilating with cycloplegic agents. To achieve this, modern autorefractors
use fogging techniques to relax accommodation (Fig. 5.2). In most autorefractors, accom-
modation is relaxed only once prior to the start of the measurement (14).
Ghose believed that the automatic fogging system of some autorefractors cannot suf-
ficiently control accommodation (15). It is therefore still necessary to check and refine the
displayed readings by subjective refraction or retinoscopy. Autorefractors can be used as a
preliminary refraction or screening method because they provide a starting point for
retinoscopy or subjective refraction, but they cannot serve as a substitute for it.
During the 1970s and 1980s, several subjective autorefractors were introduced but
were not widely accepted because they were not quick and easy to operate and they did not
provide binocular or near point testing. Among the early models were the Humphrey Vi-
sion Analyzer and the American Optical SR III Subjective Refraction System (16). The
more recent autorefractors are quicker, easier to use, have good reliability and accuracy but
still do not provide for binocular balance or nearpoint testing and therefore could not serve
as substitutes for conventional refraction. Autorefractors have become an integral part of
Adjunctive Instrumentation in LASIK 75
Figure 5.2 Automated refractors are helpful in obtaining a rough idea of the patients refractive
error. They should not be used as the sole basis of LASIK treatments.
ophthalmological practice. They are simple enough to be used by technicians with a mod-
erate degree of training, they save time, and they serve as a complement to subjective re-
fraction.
The indications for measuring corneal curvature and evaluating corneal topography include
contact lens fitting, biometry for determining the power of an intraocular lens, screening for
refractive surgery, evaluation of pathologies such as keratoconus, irregular astigmatism,
and contact lens warpage, identification of postlaser decentrations, central islands, regres-
sions, and postoperative assessment of astigmatism after penetrating keratoplasty and
cataract surgery. Currently, the corneal curvature can be quantified and assessed using the
manual keratometer, the automated keratometer, and videokeratoscopes such as the
Placido-based topography unit, the rasterphotogrammetry unit, and the scanning slit beam
system.
The anterior corneal surface behaves like a convex mirror and reflects light. This
property allows the keratometer to measure the size of the reflected image and to determine
the radius of curvature of the corneal surface (17,18).
The manual keratometer measures the dimensions of a virtual image from the corneal
reflection in two orthogonal meridians simultaneously. Dials indicating the principal cur-
vatures of a toric surface are adjusted with the end result of focusing and aligning reflective
mires thereby producing a virtual image with the same dimensions (19). The keratometer
has been used as the gold standard to which autokeratometers and corneal topography units
have been compared (20). Examples of manual keratometers are the Haag-Streit/Javal
Schiotz, the Bausch & Lomb (Fig. 5.3), the Carl Zeiss, and the Marco keratometer.
The limitations of the manual keratometer are that it assumes a spherocylindrical
cornea with a major and minor axis separated by 90 degrees; it does not provide informa-
tion about the cornea outside of a circle 2.8 to 4 mm in diameter where the measurements
76 Ang and Azar
are taken, and corneal irregularities can distort the mires making measurements difficult or
impossible (17,18).
Autokeratometers utilize the same principles as the manual keratometer but use soft-
ware that electronically projects light onto the cornea and captures the reflections to pro-
duce keratometry readings. The Humphrey automated keratometer (Humphrey Instru-
ments, San Leandro, CA) uses three near-infrared light rays that are reflected off the
cornea. Three photodiode receptors receive the images and utilize vector algebra equations
to analyze and calculate the keratometry parameters. The Canon automated keratometer
projects a single keratoscope ring onto the cornea and analyzes the data in a similar man-
ner.
Several reports have compared the manual and automated keratometer. Tate et al.
found no statistical difference in the accuracy of the manual (Haag-Streit) and the auto-
mated (Humphrey, Canon) keratometers (21). Lusby et al. concluded that both keratome-
ters have been shown to give reproducible results on repeated measurements of the same
eye (22). Binder demonstrated that the Humphrey automated keratometer and the Bausch
& Lomb keratometer are comparable in their ability to measure abnormal corneal surfaces
following radial keratotomy and corneal transplantation (23). Because it is quick and easy
to operate, Nakada et al. recommended that the automated keratometer should be widely
used, especially when examining children (24). Automated keratometers have become
more popular than manual keratometers because they are accurate and reliable; they can
measure a larger range of curvatures and astigmatism, eliminate observer bias, produce a
hard copy of the results, and require less skill and less time to operate (25).
In 1993, Sanders et al. stated that videokeratoscopes were becoming invaluable tools
and predicted that they will replace keratometers in standard clinical practice (26). Their
prediction was based on experience in using keratometers and obtaining misleading ker-
atometric measurements from corneas that had asymmetric astigmatism, asymmetry after
radial keratotomy, and unusual variants of keratoconus. With the growing demand for re-
fractive surgery and increased applications in assessment of pathologies and postoperative
care, corneal topography units have indeed become indispensable diagnostic tools in oph-
thalmological practice. Videokeratoscopes offer several advantages over keratometers;
Adjunctive Instrumentation in LASIK 77
they do not assume that the cornea is spherocylindrical, they allow the assessment of the
peripheral cornea, and the images from the systems are digitized, analyzed quantitatively
with various softwares, and printed in color-coded images for easy interpretation.
Placido-based topography systems use a transilluminated Placido cone, an imaging
system that consists of a lens, a camera, a video grabber, and a computer system (17,18).
Illuminated concentric rings are centered and projected radially from the corneal apex. A
camera focuses on the image plane of the cornea and captures the image of the rings. Anal-
ysis of the size and displacement of the ring segments is used to calculate the slope of the
corneal surface. The accuracy of Placido-based units may be affected by intraobserver vari-
ability, interobserver variability, centration, alignment, calibration, and software errors.
Furthermore, a limitation of Placido systems is that elevation data is generated by fitting
the slope to a predefined mathematical model such as spheric, aspheric, or conic, which
may not be right for abnormal corneas. Systems currently in use may differ in the number,
thickness, and position of the rings, the cone design, the illumination, and the software that
they used. Examples of systems using Placido-based topography are the EyeSys, Tech-
nomed C-Scan, Topography Modeling System, Alcon EyeMap, and Humphrey Atlas (Fig.
5.4).
Rasterphotogrammetry defines elevation points by projecting a grid of known geom-
etry onto the corneal surface and analyzing the distortion from this pattern (17,18,20,27,28).
The PAR Corneal Topography System (CTS, PAR Vision Systems Corp., New Hartford,
NY) uses a stereotriangulation technique by utilizing flourescein on the tear film, project-
ing a grid pattern composed of horizontal and vertical lines spaced about 0.22 mm apart, and
viewing the light pattern from an offset angle. A CCD camera collects the reflected images
and the x, y, and z coordinates are determined from the geometry of the measured grid posi-
tion and instrument optics. The PAR CTS determines surface elevation without using the
shape assumptions necessary in Placido-based systems. It relies on projection on the floures-
cein film and therefore does not require a smooth reflective surface nor precise spatial align-
ment for accurate imaging, making it useful in corneas with scars, epithelial defects, or ir-
regular surfaces.
Figure 5.5 An elevation-based topographical unit is useful in detecting substantial changes in the
posterior corneal surface and in measuring corneal pachymetry.
The scanning slit beam system is used by the Orbscan (Bausch and Lomb, Rochester,
NY; Fig. 5.5) to measure corneal surface elevation using stereotriangulation techniques
similar to the PAR CTS system (17,18,20). The examination takes 1.5 seconds wherein two
scanning slit lamps project 20 slit beams from the left and 20 slit beams from the right at
an angle of 45 degrees covering the whole cornea form limbus to limbus. A tracking sys-
tem locks on to the eye to minimize errors from involuntary eye movements during the ex-
amination. The software analyzes up to 240 data points per slit, enabling it to calculate and
produce more data. The Orbscan can provide information on the axial curvature of the an-
terior and posterior cornea, the elevation of the anterior and posterior corneal surface rela-
tive to the best fit sphere, and the corneal thickness on the entire cornea. The system yields
more information than Placido or rasterphotogrammetric systems because it takes mea-
surement of the posterior corneal surface as well (29). The Orbscan and the PAR CTS di-
rectly measure surface elevation and measure topography regardless of the orientation of
the eye, unlike the Placido-based systems.
Previous studies have attempted to determine the most reliable system to use in eval-
uating corneal curvature by comparing keratometers with corneal topography units and
corneal topography units among themselves.
In evaluating normal corneal power measurements, Hannush et al. reported that the
manual keratometer was more reproducible than the Corneal Modeling System and the
Corneascope (30). Moura et al. compared three computerized videokeratoscopy systems
with a manual keratometer and found that the most reproducible was the EyeSys, followed
by the manual keratometer, the PAR CTS, and the C-Scan Technomed (31). Jeandervin and
Barr, on the other hand, found no statistical differences in repeatability when comparing the
Alcon EyeMap, the EyeSys 2000, the Humphrey Mastervue, the Humphrey Atlas, and the
Marco manual keratometer (32). However, they observed that the EyeSys had the highest
repeatability and that the Humphrey Atlas was the most accurate system tested (32). Wil-
son et al. reported that the TMS was statistically more accurate in determining the power
of calibrated spheres at 1 mm from the apex, while the Corneal Analysis System (CAS,
EyeSys Laboratories, Houston, TX) was more accurate at 3 mm from the apex (33). These
Adjunctive Instrumentation in LASIK 79
small differences in accuracy between the EyeSys and the TMS were unlikely to be of clin-
ical significance. Tennen et al. did same-day measurements of the steepest and flattest pow-
ers of the central 3 mm of 200 eyes and found no statistical difference in reliability between
the Haag Streit, the Marco, the Alcon handheld keratometer, and the Corneal Analysis Sys-
tem (EyeSys Laboratories, Houston, TX) (34). With regard to elevation data, Priest and
Munger showed that the PAR CTS presented elevation measurements more accurately than
the TMS-1 (Topography Modeling System, Tomey Corp.). Unlike the PAR CTS, which
provides a direct measurement of elevation, errors made by the TMS-1 are the result of as-
sumptions made regarding the corneal shape and position (28). Schultze made a similar ob-
servation that the PAR CTS accurately provides peripheral elevation data on a model rep-
resenting an eye after PRK (35).
Numerous studies have presented data on the accuracy and reliability of different sys-
tems in evaluating corneal curvature. Perhaps the most significant observation was made
by Moura et al. They stated that whenever a particular system is used, it should be used con-
tinually for that patient, otherwise errors may be seen when interchanging and interpreting
data from one system to another (31).
D. PUPILLOMETRY
Sophisticated pupillometry video equipment, which can determine diameters to hundredths
of a millimeter, have been used in neuro-ophthalmic evaluation (36). In refractive surgery,
assessment of pupil diameters is important because despite excellent visual acuity, a well-
centered ablation zone, a good-looking postoperative topographical map, and the absence
of significant corneal haze, widely dilating pupils at low levels of illumination are prone to
halos, glare, and reduced night vision when the pupil dilates to a size larger than the abla-
tion zone. These symptoms should be anticipated, considered, and explained to the patient
before deciding to proceed with refractive surgery if the pupil size measurements in dim il-
lumination reveal that it can dilate to a size larger than the zone of treatment. Careful mea-
surement of scotopic pupil dilation is therefore an integral part of the preoperative evalua-
tion of the refractive patient.
Comparison pupillometry has been performed using the Rosenbaum card (Cleveland,
OH). It contains a series of increasing half-circle diameters denoted by 1.0 mm intervals
printed on one edge of the card. The examiner held the card temporal to the patients eye
in the corneal plane and matched the horizontal pupil diameter with the appropriate half-
circle. Pupil measurements were made in 1.0 mm steps unless the pupil appeared between
two half-circles on the card, and a 0.5 mm measurement interval was then made (37). The
Rosenbaum method was found to overestimate consistently the pupil diameter by 0.5 mm,
with a standard deviation of 0.6 mm. A conversion factor of subtracting 0.5 mm from the
measurement was found to be sufficient to adjust for this overestimation.
Because of the subjective nature of the measurements using the Rosenbaum card, in-
frared pupillometry is presumed to be more accurate in measuring the pupil, especially in
dark conditions. Hippus of the iris and the emotional state of the patient may sometimes af-
fect the pupil diameter and prevent obtaining the largest natural pupil diameter. But the in-
frared device allows a more objective assessment between examiners.
Infrared pupillometry was previously performed with the Iowa Pupillometer (Henry
Louis, Inc., Iowa City, IA) (37). The device consisted of a charged coupling device (CCD)
camera tuned for infrared detection and two infrared side lamps for pupil illumination. Us-
ing two vertical lines on the video monitor, calibration of the pupillometer was performed
80 Ang and Azar
for each subject before pupil measurements were made. The center of the monitor was used
for measurement because distortions in the peripheral monitor may induce measurement er-
ror. This device measured the horizontal pupils to 0.01 mm increments, and analysis was
performed rounding to the nearest 0.1 mm.
The Colvard pupillometer (Oasis Medical) is a handheld pupillometer that uses light
amplification technology (Fig. 5.6) (38). Low levels of light energy entering the device
stimulate a photocathode, which results in electron excitation. The electrons strike a phos-
phor screen, which intensifies the image. A lens system in the instrument brings the ante-
rior segment into focus, and a bright phosphorescent image of the anterior segment is vi-
sualized through the examiners ocular. A reticle in the device superimposes a millimeter
ruler over the enhanced image of the iris and the pupil to measure pupil diameter in a sco-
topic environment. Using the Colvard pupillometer, pupil dilation at the level of light typ-
ically encountered while driving on a suburban street at night, can be reproduced by turn-
ing off all the lights in a windowless examining room and opening the door 1 to 2 inches.
It was found that mean pupil size at 15 lumens was 5.1 mm (range 2.5 to 8.0 mm) and at 3
lumens was 6.2 mm (range 3.0 to 9.0 mm).
The Video Vision Analyzer (VIVA) pupillometer allows binocular measurement of
the dark adapted pupil (39). The subject sits 1 meter in front of and beneath the device and
fixates on a red light. Both eyes are focused on a rectangular field on the pupillometer dis-
play. Then a button is pressed, and the device automatically takes three images by infrared
light. By digital processing, the pupil diameter under scotopic light conditions is calculated.
Precise measurements within 0.3 mm at 1 meter are possible.
Several studies using the above-mentioned instruments have measured pupil diame-
ters under scotopic light conditions. Evaluation of the pupil size with the Rosenbaum card
detected a mean pupil size of 5.4 1.1 mm, with the IOWA infrared pupillometer 4.95
1.08 mm, and with the Colvard pupillometer 6.2 mm (range 3.0 to 9.0 mm) (37,38). In a
recent study by Schnitzler, the mean scotopic pupil diameter was reported to be 6.08 1.16
mm with the Colvard pupillometer and 6.24 1.28 mm with the VIVA pupillometer. She
concluded that measurements with the VIVA pupillometer seem slightly overestimated,
Figure 5.6 Colvard pupillometer. Measurement can be optimized by controlling ambient illumi-
nation during pupil measurements.
Adjunctive Instrumentation in LASIK 81
whereas measurements with the Colvard delivered more similar data on scotopic pupil size,
indicating that measurements with the Colvard are more reliable and precise (39).
Pupil diameters have also been measured using topography devices including the
Technomed C-Scan, the Humphrey Masterview, and the Alcon EyeMap. The measure-
ments obtained were 3.35 mm (C-Scan), 2.96 mm (Masterview), 2.34 m (EyeMap), and
5.94 mm (mesopic condition). It was concluded that topography devices gave significantly
smaller pupil measurements than mesopic conditions because of the bright luminance of
the Placido rings. These instruments are not recommended in the determination of pupil di-
ameters prior to refractive surgery (37).
E. PACHYMETRY
Pachymetry is the measure of corneal thickness. It is essential to measure central corneal
thickness in myopic eyes before scheduling for LASIK surgery to ensure that the central
thickness is sufficient to prevent leaving the corneal bed too thin after treatment and prone
to ectasia. The residual bed depth is dependent on both the thickness of the flap and the
depth of laser ablation. The U.S. Food and Drug Administration (FDA) has recommended
that the residual thickness in the bed not be less than 250 m to avoid corneal ectasia (40).
Because of the variability of resection depths of different microkeratomes, calculations by
the surgeon should consider leaving a generous residual bed after resection and planned ab-
lation.
The electronic digital optical pachymeter used a depth measuring attachment for the
900 Haag Streit slit lamp and the 6090 package by Diagnostic Concept. It was calibrated
on PMMA lenses according to the method described by Mandell and Polse (4143). The
angle between the measuring eyepiece (right) and the illumination system of the optical pa-
chometer was set at 47.5. The Haag Streit optical pachymeter emphasized keeping the slit
beam of light perpendicular to the surface of the central cornea. Care was taken to ensure
that the slit of light that passed through the cornea bisected the pupil, both vertically and
horizontally, as seen by the split image during alignment. Ideally, the pupillary axis should
coincide with the pachometric one. Fluorescein was instilled in the eye and the measure-
ment done in darkness to increase contrast and facilitate alignment. Appropriate alignment
was attained when the internal boundary of the endothelium was continuous with the ep-
ithelium seen in the lower field of the pachometer (touch criterion). Alignment was
achieved when the reflecting images of the centration lights were aligned at the projected
slit and in front of the pupil center; 10 readings were then recorded on each eye (44,45).
The MishimaHedbys attachment could be utilized to improve the accuracy of the optical
method (46). The disadvantages of the optical pachymeter with the Haag Streit device are
that it is a subjective measurement wherein the examiner must make sure the slit of light is
perpendicular to the cornea when making the reading and that it requires the cooperation of
the patient in holding fixation during the duration of the measurement.
Ultrasonic pachymetry eliminates the disadvantages of the optical pachymeter since
it can take rapid measurements without asking the patient to hold still for a long time (Fig.
5.7). There is no examiner variability since the machine takes readings upon contact with
the cornea. It is easy to use and allows mapping of corneal thickness. In addition, the ul-
trasonic units are portable with small probe tips making possible intraoperative measure-
ments before proceeding with laser ablation.
The Humphrey ultrasonic pachometer model 8050 uses pulsed ultrasound to evalu-
ate corneal thickness. Although the location of the measurement is arbitrary, it is possible
82 Ang and Azar
Figure 5.7 Ultrasonic pachymetry. To be able to measure intraoperative corneal pachymetry, the
machine may require standardization in the range of 200 m.
to take peripheral measurements by direct touch of the probe to the cornea. The instrument
has automatic alignment properties so that the probe has to be within 3 from normal to the
posterior corneal surface for a thickness to be recorded. Other models (DGH Technology,
Inc., Exton, PA) have since been manufactured with variable features. The probe diameters
range from 1.6 to 3.0 mm. The probes emit and receive pulses with frequencies of 1220
MHz. Most instruments use a calibration speed of 1640 m/s. Some manufacturers sug-
gested 1550 as the correct sound velocity, although it has been reported that 1639 is the ve-
locity of sound through the human cornea at 37C (47). The probe has to be aligned as per-
pendicularly as possible to the cornea. Some pachymeters provide a tone or beep when
proper alignment or a measurement is obtained.
In a study by Salz et al., it was found that the optical pachymeter had two to three
times as much intrasession variation as that of the ultrasound pachymeters, significant in-
terobserver variation (P 0.015), and significant differences between left and right eye
thickness determinations (P 0.005). On the other hand, ultrasonic pachymeters showed
superiority by demonstrating high reproducibility, no interobserver variation, and no
left/right variation, in addition to its user- and patient-friendly features (45).
The Obscan Topography System (Orbtek, Inc.) is an optical scanning slit instrument
that provides both topographic analysis and pachymetric measurements in the same exami-
nation (Fig. 5.5) (48). This instrument is capable of measuring corneal thickness at any point
on the cornea with one procedure. Its sampling method takes into account a broader area of
the cornea than does the ultrasonic pachymeter. A calibrated video and scanning slit beam
system measures the position of several thousand points throughout the thickness of the
cornea. Computer analysis then converts these data into a topographic map of the corneal
surface and provides measurements of corneal thickness over the entire corneal surface, as
well as keratometric measurements and corneal power and elevation maps.
The Orbscan system is noninvasive, requiring no contact for data acquisition, but it
does require the patient to be able to sit at a chin rest while fixating for 1 to 3 seconds. Ul-
trasonic pachymetry, on the other hand, is associated with problems and limitations that the
Adjunctive Instrumentation in LASIK 83
Figure 5.8 A pneumatonometer is used to check the intraocular pressure after application of the
suction ring.
Orbscan system avoids. The ultrasonic pachymeter lacks fixation lights for precise control
of patient gaze during repeated measurements, so probe placement in a reproducible manner
is difficult and is markedly affected by the person performing the evaluation. Also, the speed
of sound may vary in edematous tissue compared with that in normally hydrated tissue.
In a study by Yaylali, it was found that the two devices were quite comparable in their
measurements in the same subjects, with the difference in corneal thickness between the
two devices ranging from 23 to 28 m (48).
Corneal pachymetry can also influence Goldmann tonometry. Use of a pneu-
matonometer (Fig. 5.8) may yield more accurate IOP measurements. See Chapter 27 for
more details.
F. INSTRUMENTATION
1. Eyelid Drape
Plastic disposable eyelid drapes are used to maintain sterility of the surgical field during
LASIK (Fig. 5.9A). The drape is applied after sterilizing the periocular area with a betadine
solution. Aside from sterility, the eyelashes can be moved out of the way and secured when
applying the adhesive on the eyelid. Retracting the adhesive along with the eyelid can aid
the speculum in providing adequate exposure to the globe. Patient comfort is not compro-
mised when breathing under the disposable drape. We have had good experience in using
the 15 inch 15 inch Steri-Drape (3M Healthcare, St. Paul, MN).
2. Speculum
Stable retraction of the eyelids and adequate exposure of the cornea are necessary in refrac-
tive surgery. This is even more critical in laser in situ keratomileusis (LASIK) because a pneu-
matic suction ring is applied on the globe during construction of the corneal flap. The ideal
speculum should provide maximal access to the globe, accommodate the pneumatic suction
84
Figure 5.9 Intraoperative adjunctive instrumentation. (A) An eyelid drape is applied to ensure sterility and move the eye-
lashes out of the surgical field. (B) A wire speculum is used to provide maximal exposure of the globe for accommodating
Ang and Azar
the suction ring. (C) An RK marker may be used to place asymmetric peripheral corneal marks. The Chayet ring (D) is help-
ful in minimizing deposition of debris into the flap interface.
Adjunctive Instrumentation in LASIK 85
ring within the palpebral opening, allow for temporal and superior surgical approaches, and
provide maximum comfort when fully opened (49). Wire speculums are preferred over solid
blade speculums because they provide more space for applying the suction ring.
After applying the wire speculum, a few minutes are allowed to pass for the eyelids
to adjust to the pressure of the speculum. We have found it helpful to instill one or two ad-
ditional drops of topical anesthesia before completely opening the speculum. These ma-
neuvers minimize patient discomfort and enable the surgeon to maximize the capability of
the speculum in providing adequate exposure. If exposure is still inadequate, the globe can
be proptosed by exerting downward pressure on the arms of the speculum while applying
the suction ring.
Innovations in speculum design have been made to aid in providing better exposure
and added comfort to the patient. Among these are increased angulations in the arms of
the speculum to maximize globe exposure, heavy duty wire bases strong enough to resist
powerful eyelid squeezing, and suction attachments to remove tears and debris from
the surgical area. Popular designs available are the Barraquer wire speculum, the Lieber-
mann Adjustable wire speculum (Fig. 9B), the Machat adjustable speculum (ASICO, West-
mont, IL), the Slade speculum (ASICO), and the Lindstrom-Chu Aspirating speculum
(Rhein).
Figure 5.10 (A) A Merocel sponge is used to wipe off any blood from the exposed stromal bed
and to sweep the flap during repositioning. (B) A nontoothed forceps is used to lift the flap. (C) A
Machat retreatment spatula and a jewelers forceps are used to locate the interface plane and dissect
the flap edge. (D) A Fechtner conjunctival ring forcep is used to grasp the flap edge and lift the flap.
The same nontoothed forceps can be used to reposition the flap. (E) An irrigating cannula is used to
hydrate the stroma after ablation and to float the flap and avoid wrinkles. Illustrated is a straight dis-
posable cannula. Several surgeons prefer curved cannulae (to conform to the curvature of the corneal
stromal bed). (F) A Pineda iron is helpful to iron flap wrinkles especially during LASIK retreatment
procedures.
Adjunctive Instrumentation in LASIK 87
(Devon Skin Markers, Graphic Controls, Buffalo, NY). The marking pen is also useful when
placing marks on the flap edge prior to lifting during retreatments.
6. Irrigating Cannulae
An irrigating cannula is used to irrigate under the flap, wash out any interface debris, and
float the flap into the correct position. The diameter of the cannula can range from gauge
26 to 30 and the length and angulation can be variable depending on the designer and man-
ufacturer (Fig. 5.10E). Some cannulas have spatulated or flattened tips to allow for easy in-
sertion underneath the LASIK flap. Other innovations are side ports or multiple openings
for diffuse irrigation and effective floating of the flap. Examples of specialized cannulas are
the 26 gauge Slade cannula (ASICO) with a spatulated tip, the 25 gauge Buratto cannula
(ASICO), and the Kritzinger needle (Storz). Our preference is a 22 mm 30 gauge Rycroft
anterior chamber cannula (Becton Dickinson and Co., Franklin Lakes, NJ), which provides
easy insertion into the flap interface and gentle controlled irrigation (Fig. 5.10E). Excessive
irrigation should be avoided because it can cause delayed flap adherence and stromal
hydration.
planated area is larger than the mire, reflecting an intraocular pressure of less than 65
mmHg, the suction should be discontinued, the tonometer checked to ensure dryness to
avoid false readings, and the ring reapplied. If the readings are still inadequate, the proce-
dure should be aborted and all the instruments checked.
The pneumatonometer (Model 30 Classic, Medtronic, Jacksonville, FL) is an alter-
native, easy-to-use instrument with tonometry functions (Fig. 5.8; also see Fig 12.3.C). It
utilizes a pneumatic sensor, consisting of a piston floating on an air bearing, that is touched
to the anesthetized cornea. A precisely regulated flow of filtered air from an internal pump
enters the piston. A small 5 mm fenestrated membrane (soft silicone tip) at the end of the
piston reacts both to the force of the air blowing through it and to the force represented by
the pressure behind the cornea, against which it is pressed. The balance between these two
forces represents the intraocular pressure, and it is displayed on the screen. The system
records pressures in the range of 5 to 80 mmHg. The pneumatonometer allows us to eval-
uate the adequacy of suction by displaying real-time readings of the progressive rise in in-
traocular pressure. Should the steady rise of pressure falter, the suction can be discontinued
and reapplied right away. There is also no added variable of maintaining a dry cornea,
which could give false readings.
In order to avoid excessive laser ablation and subsequent corneal ectasia, the use of
intraoperative ultrasound or optical pachymetry is increasing in patients with high myopia
or thin corneas (Fig. 5.7). See chapter 10 for details.
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90 Ang and Azar
A. INTRODUCTION
Corneal refractive procedures are currently widely applied to correct ametropia. A suc-
cessful refractive procedure is gauged by many criteria: safety, efficacy, predictability, and
long-term stability. Laser-assisted in-situ keratomileusis (LASIK) is presently the most
widely performed refractive procedure, but it is not appropriate for all patients. Optimal re-
sults are achieved through proper patient selection, education, examination, and consent. A
complete understanding of the risks of the procedure and the effects of pre-existing ocular
conditions are critical in selecting patients for surgery. The ability to recognize subtle ocu-
lar conditions through careful patient examination will reduce the likelihood of complica-
tions. Finally, helping patients have realistic expectations and the ability to say no to pa-
tients who clearly are poor surgical candidates are the keys to building a successful LASIK
practice. This chapter will outline the present refractive indications for LASIK with special
attention given to the preoperative evaluation and patient preparation prior to refractive
surgery. Clinical tips for maximizing refractive outcomes and contraindications to LASIK
will be discussed.
91
92 Braunstein et al.
B. INDICATIONS
Laser in situ keratomilieusis may be considered for patients who are dependent on optical
correction of various refractive errors who desire to reduce or eliminate their dependence
on glasses or contact lenses. In the United States, FDA approval for LASIK is a confusing
issue for surgeons and patients alike. The FDA does not approve procedures, it only ap-
proves drugs and devices. How those drugs and devices are used after approval is up to
physicians under a provision known as the practice of medicine. The FDA labels the de-
vices and drugs according to the information provided by the developers and serves as a
guide for their use. The specific approval guidelines for LASIK are different for each ex-
cimer laser manufacturer based on data from FDA clinical trials. The approval range of re-
fractive errors is only one criterion of judging a prospective candidate, as patients who fall
within the guidelines may not qualify for surgery owing to other conditions (e.g., thin
cornea or flat cornea).
The excimer laser is currently approved for a wide range of myopia, myopic astig-
matism, and hyperopia. Many studies indicate that the predictability of LASIK decreases
with increasing preoperative myopia and astigmatism (1). Hyperopia ranging up to 6
diopters is correctible, but at higher levels of attempted correction, predictability is again
reduced (2). For hyperopia greater than 6 diopters, loss of spectacle-corrected visual acu-
ity occurred in a significant number of eyes in some studies, and accuracy was sufficiently
poor to advise against LASIK in these eyes (3). Approval for treatment of hyperopic astig-
matism and mixed astigmatism is expected in the near future.
C. CONTRAINDICATIONS
Contraindications for LASIK include patients with systemic collagen vascular disease, im-
munodeficiency, autoimmune disease, severe atopy, and diabetes mellitus, diseases all
likely to affect corneal wound healing. Patients who have unstable refractive errors or sig-
nificant pre-existing ocular pathology of the cornea or anterior segment including but not
limited to scarring, severe dry eye syndrome, uncontrolled blepharitis, uveitis, or early
cataract should also not have laser vision correction. Surgery should not be performed on
women who are pregnant or nursing or on patients taking Amiodarone or Acutane. LASIK
is contraindicated in eyes with a history of herpes simplex keratitis or herpes zoster oph-
thalmicus. Special concern should be given to eyes with corneal neovascularization within
1 mm of the ablation zone and those patients with difficult anatomy including small orbital
aperture, narrow interpalpebral fissure or deep-set eyes. Patients with keratoconus or kera-
toconus suspects should not have LASIK surgery. Finally, patients with signs of anterior
basement membrane dystrophy may be better served with photorefractive keratectomy
(surface ablation) rather than LASIK, as the likelihood of an intraoperative epithelial de-
fect may create numerous postoperative management difficulties.
The cornea should not be flattened to less than 33 D or steepened to greater than 52
D, as refractive outcomes in this range are less predictable (4). To determine the postoper-
ative corneal curvature, the preoperative keratometry is reduced or increased by the amount
of desired correction at the corneal plane. All candidates for LASIK procedures should
have a stable refraction for at least 12 months prior to the procedure differing by no more
than 0.50 diopter in manifest sphere or manifest cylinder. For hyperopic patients, manifest
and cycloplegic refraction should not differ more than 0.75 diopter.
LASIK Indications, Contraindications and Preoperative Evaluation 93
D. IATROGENIC KERATECTASIA
LASIK alters both the shape and the structural integrity of the cornea. Preoperative evalu-
ation involves determining what the resultant corneal curvature and residual stromal thick-
ness will be, prior to proceeding with surgery. Preoperative corneal thickness is of particu-
lar concern in preventing iatrogenic keratectasia. Post LASIK keratectasia results in a
progressive central corneal steepening and myopic shift causing irreversible damage by one
year. It occurs in approximately 1 in 1000 eyes (5). Preoperative assessment of corneal
thickness, flap and resultant stromal bed thickness, and amount of desired ablation are es-
sential to prevent such ectasias. The average thickness of the human cornea is 520 microns,
and an average flap created by a microkeratome is from 130 to 160 microns. The keratec-
tomy depth of the excimer laser ablation on average must not exceed 45 to 120 microns
with 325 (conservative case) to 250 microns, respectively, left in the stromal bed (6). This
sparks questions regarding the minimal thickness of residual stroma, which needs to be
maintained to prevent keratectasia. Many LASIK surgeons currently employ a 250 micron
limit to the residual stromal bed following LASIK, but this is only an average value, and
the biomechanical constants of the human cornea vary over a wide range, so that the range
of residual corneal thickness that would prevent keratectasia is unknown. Some advocate
using a percentage of the corneal thickness as a minimal residual stromal thickness rather
than an absolute number, given ultrasound pachymetry measurement errors and biome-
chanical considerations, such as the deeper stroma having less tensile strength compared to
the anterior layers (6). This dilemma can ultimately be resolved when we are better
equipped to measure the biomechanical constants of the cornea in vivo. Promising ap-
proaches such as mechanical spectroscopy and measurement of birefringence of the cornea
can assist in future determination of preoperative stromal bed thickness, which would be
necessary to avoid iatrogenic keratectasia. The residual stromal bed following a LASIK
procedure should be calculated prior to surgery based on a nonnomogram adjusted treat-
ment of the refractive error to be corrected.
Preoperatively, each patient must have a complete evaluation including a medical, surgical,
and ocular history as well as an ocular examination. A general medical history with em-
phasis on the above-mentioned systemic diseases should be discussed and a medication list
obtained. Past ocular surgery and any previous or existing ophthalmic conditions, such as
glaucoma, dry eye, amblyopia, and past contact lens use, should be reviewed.
An initial preoperative evaluation for LASIK in contact lens wearers should be per-
formed at least two weeks after discontinuation of soft contact lenses or at least three weeks
after discontinuation of soft toric, hard, or rigid gas permeable lenses. Patients wearing
rigid lenses must demonstrate keratometric and refractive stability prior to treatment. It
may be necessary to discontinue contact lenses in these patients at least one month for ev-
ery decade of contact lens use. Previous glasses and contact lens prescriptions should be
compared to the manifest refraction.
cable to different refractive errors. When refracting the myope, a resolution-based refrac-
tion should be performed to avoid overcorrections. A resolution-based end point involves
using the least minus lens to visualize the most letters. The refraction is not terminated at
20/20 if an additional 0.25 diopters yields several letters on the 20/15 line. The Jackson
Cross cylinder is used to determine the maximal amount of cylinder. The correct axis of the
cylinder is easier to determine in eyes with higher degrees of astigmatism. Occasionally,
autorefraction may be helpful in finding the astigmatic axis. Care should be taken to ensure
that the trial lens frame or phoropter is appropriately positioned and level to define the axis
most accurately.
Hyperopic manifest refraction should emphasize a push plus technique. Patients
are encouraged to accept the most plus sphere to see the most letters. Cycloplegic refrac-
tion with 1% cyclopentolate should be performed on all patients because it eliminates ac-
commodation. This is essential to identify the overminused myope and to uncover latent
hyperopia. For patients with hyperopia, manifest and cycloplegic examination should dif-
fer by 0.75 diopter or less. If a large amount of latent hyperopia is identified or if there is a
significant discrepancy between the manifest and cycloplegic refraction in a myope, a post
cycloplegic manifest refraction should be performed with an emphasis on pushing addi-
tional plus power. Occasionally, glasses may be prescribed temporarily to help the patient
accept the additional plus power prior to performing surgical correction.
A clinical workup should include manual keratometry, a pupillary examination, and
a slit lamp examination with emphasis on any lid margin inflammation, corneal epithelial
disease, basement membrane dystrophy, or stromal scars consistent with prior keratitis.
Tonometry should be performed on all patients and gonioscopic examination on all hyper-
opes. Central corneal pachymetry readings should be performed on all patients. A careful,
dilated fundus examination is performed to analyze the optic nerve and retina for any
pathology with careful attention to the peripheral retina in highly myopic eyes that may be
at risk for lattice degeneration. Identified retinal tears or large areas of lattice may require
laser photocoagulation prior to performing LASIK (7).
Special attention should be given to the pupillary examination in myopic and partic-
ularly astigmatic patients. Pupil size should be measured in dim and in bright lighting con-
ditions and recorded. Measurement can be made with a pupil gauge or with an infrared
pupillometer. Patients with higher degrees of refractive error and larger pupils may be at
greater risk for postoperative night vision disturbances, although this remains a subject of
great controversy (3).
G. CORNEAL TOPOGRAPHY
Corneal topography is essential in all patients prior to refractive surgery. Topography is used
to identify patients with corneal curvature abnormalities that are not apparent on slit lamp
examination. True keratoconus is often easy to detect by clinical history and examination,
but subclinical cases may only be apparent by corneal topography. Corneal topography is
necessary to determine whether patients have contact lens related warpage and to help de-
termine when a cornea is stable following contact lens discontinuation. We recommend that
any patient who wears contact lenses have corneal topography repeated 1 week apart to as-
certain stability prior to surgery. Topography is also used to verify postoperative results and
complications such as decentrations, central islands, and irregular astigmatism.
LASIK Indications, Contraindications and Preoperative Evaluation 95
those who are likely keratoconus suspects are not candidates for LASIK using present al-
gorithms and treatment profiles and should be considered to have a progressive corneal dis-
ease. Patients with asymmetric bow tie astigmatism and inferior steepening who do not ap-
pear to have keratoconus may be treated surgically with appropriate informed consent.
suction ring during LASIK will further decrease optic nerve head perfusion pressure and
can cause additional damage to an already susceptible glaucomatous optic nerve.
5. The Presbyope
Many LASIK patients are presbyopes. Patients who already wear some reading correction
are easier to counsel than patients who simply remove their glasses to read. Patients need
to be informed that the procedure will not correct distance and near vision completely. An
informed patient can help determine what would be best for them. Patients should be of-
fered various options including distance vision in both eyes, monovision, or slight under-
correction of both eyes. If the patient is a successful contact lens wearer with monovision,
this is likely to be the best route. If the patient does not wear lenses, a preoperative mono-
vision contact lens trial can be used to demonstrate the effects of monovision to the candi-
date for refractive surgery (14). The add power and selection of the distance and near eye
can also be determined with a contact lens trial.
8. The Hyperope
LASIK, at present, shows great promise for effective and stable correction for mild to mod-
erate hyperopia. A gonioscopic examination should be performed prior to LASIK in all hy-
peropic patients and a prophylactic peripheral iridotomy may be indicated for an occlud-
able angle. Although there is no cause and effect relation between hyperopic LASIK and
acute angle closure glaucoma, patients with hyperopia and narrow angles should be fol-
lowed for the possibility of angle closure at a later time (15). The ablation profile for hy-
peropia extends out to 9 mm requiring a large corneal flap. Patients with a history of con-
tact lens wear and corneal neovascularization may have significant bleeding with LASIK
surgery, and potential complications of bleeding should be discussed and included in the
consent prior to surgery.
98 Braunstein et al.
9. The Astigmat
A preoperative evaluation of the astigmat is essential for successful refractive surgery.
Astigmatism has a directional component and a magnitude, and sources of astigmatism can
be corneal or lenticular. As the magnitude of cylinder decreases, the ability to measure pre-
cisely the cylinder axis also decreases. Refractive, keratometric, and topographic cylinder
occasionally do not match in axis or magnitude, but treatment is based on refractive cylin-
der. When disparity occurs, proceed cautiously and ascertain stability by repeating mea-
surements over time.
I. PATIENT SELECTION
Selecting the appropriate candidate for refractive surgery requires an understanding of the
patients expectations, desires, and disposition in addition to a clinical ocular examination.
A candidate must have the ability to understand the risks and benefits of LASIK and be able
to give informed consent. The patient must be able to tolerate the procedure and have the
ability to lie flat without difficulty, to tolerate topical anesthesia, and to fixate steadily and
accurately for the duration of the procedure. Patients must be targeted toward their differing
visual needs. A myope prior to laser vision correction enjoyed close and clear visual space
and will be disappointed if overcorrected postoperatively. Some presbyopes desire mono-
vision, while others would rather wear spectacle correction. Patients who demand spectacle
independence all the time and have unrealistic expectations of laser vision correction should
be avoided in addition to all patients with the above-mentioned systemic diseases or ocular
pathology that otherwise jeopardize the efficacy, safety, and stability of LASIK.
J. LASIK CONSENT
A patients understanding of the possible postoperative complications and adverse symp-
tomatology is an essential component of an informed consent. Patients should be given a
copy of the FDA brochure provided from the excimer laser manufacturer citing the results
of clinical trials using the specific laser. Additional statistics may be provided regarding the
doctors own data and experience.
A detailed informed consent document is often helpful in highlighting many of the
known side effects and complications of LASIK surgery. Undercorrection, overcorrection,
and induced astigmatism and the possibility of additional surgery should be discussed.
Complications that could lead to a loss of best corrected visual acuity include but are not
limited to irregular flaps, irregular astigmatism, haze, scarring, infection, central islands,
striae, and epithelial ingrowth; these must be explained to the patient in a manner that they
can understand. Many patients do not appreciate that they do risk a loss in best corrected
visual acuity and possibly blindness due to an infection or retinal vascular event. Patients
who require excellent night vision (e.g., truck drivers) should be cautioned prior to LASIK
surgery regarding their risk of night vision impairment. Night vision impairment has been
reported by Guell and Muller in 23% of patients at 6 months postoperatively, and other re-
ports of night halos occurred in up to 30% of eyes at 6 months (16). Halos around lights and
night vision impairment appear to decrease with larger ablation zones and smaller pupil
size and often improve with time (17). Finally, patients should be advised of the possibil-
ity of dry eye symptoms, which may affect vision following laser vision correction. Prior
to surgery, the patient should be given an opportunity to read all of the materials provided
and to have all of their questions answered by their surgeon.
LASIK Indications, Contraindications and Preoperative Evaluation 99
REFERENCES
1. T Salah, GO Waring III, A El-Maghraby, K Moadel, SB Grimm. Excimer laser in situ ker-
atomileusis under a corneal flap for myopia of 2 to 20 diopters. Am J Ophthalmol 1996;121:
143155.
2. S Esquenazi, A Mendoza. Two year follow-up of laser in situ keratomileusis for hyperopia. J
Refract Surg 1999;15:648652.
3. MC Arbelaez, MC Knorz. Laser in situ keratomileusis for hyperopia and hyperopic astigma-
tism. J Refract Surg 1999;15:406414.
4. DJ Salchow, ME Zirm, C Stieldorf, A Parisi. Comparison of objective and subjective refraction
before and after laser in situ keratomileusis. J Cataract Refract Surg 1999;25:827835.
5. T Seiler. Iatrogenic keratectasia: academic anxiety or serious risk? J Cataract Refract Surg
1999;25:13071308.
6. T Seiler, K Koufala, G Richter. Iatrogenic keratectasia after laser in situ keratomileusis. J Re-
fract Surg 1998;14:312317.
7. TP Werblin. Barraquer Lecture 1998. Why should refractive surgeons be looking beyond the
cornea? J Refract Surg 1999;15:357376.
8. YS Rabinowitz, K Rasheed, H Yang, J Elashoff. Accuracy of ultrasonic pachymetry and
videokeratography in detecting keratoconus. J Cataract Refract Surg 1998;24:196201.
9. YS Rabinowitz. Keratoconus. Surv Ophthalmol 1998;42:297319.
10. N Maeda, SD Klyce, MK Smolek. Comparison of methods for detecting keratoconus using
videokeratography. Arch Ophthalmol 1995;113(7):870874.
11. YS Rabinowitz, K Rasheed. KISA% index: a quantitative videokeratography algorithm em-
bodying minimal topographic criteria for diagnosing keratoconus. J Cataract Refract Surg
1999;25:13271335.
12. B Seitz, A Langenbucher. Intraocular lens calculations status after corneal refractive surgery.
Curr Opin Ophthalmol 2000;11:3546.
13. J Najman-Vainer, RJ Smith, RK Maloney. Interface fluid after LASIK: misleading tonometry
can lead to end-stage glaucoma. J Cataract Refract Surg 2000;26:471472.
14. MM Hom. Monovision and LASIK. J Am Optom Assoc 1999;70:117122.
15. M Paciuc, CF Velasco, R Naranjo. Acute angle closure glaucoma after hyperopic laser in situ
keratomileusis. J Cataract Refract Surg 2000;26:620623.
16. JL Guell, A Muller. Laser in situ keratomileusis (LASIK) for myopia from 7 to 18 diopters.
J Refract Surg 1996;12:222228.
17. SG Farah, DT Azar, C Gurdal, J Wong. Laser in situ keratomileusis: literature review of a de-
veloping technique. J Cataract Refract Surg 1998;24:9891006.
7
Preoperative Optical Considerations in
LASIK
Refractive Errors, Monovision, and Contrast
Sensitivity
BALAMURALI K. AMBATI
Massachusetts Eye and Ear Infirmary and Harvard Medical School,
Boston, Massachusetts, U.S.A.
LEON STRAUSS
The Wilmer Eye Institute, Johns Hopkins University School of Medicine,
Baltimore, Maryland, U.S.A.
DIMITRI T. AZAR
Massachusetts Eye and Ear Infirmary, Schepens Eye Research Institute,
and Harvard Medical School, Boston, Massachusetts, U.S.A.
Preoperative optical considerations in LASIK have gained increased importance, for they
allow interpretation and anticipation of postoperative aberrations and provide a basis for
patient education prior to surgery. This chapter will focus on refractive error evaluation,
monovision, and contrast sensitivity. Subsequent chapters will cover the topics of corneal
topography, wavefront analysis, and corneal biomechanics.
A. REFRACTIVE ERRORS
Emmetropic eyes focus parallel rays from an object point at optical infinity to a point on
the retina. The secondary focal point of such an eye is on the retina, and the far point plane
is at optical infinity. Myopic eyes focus parallel rays anterior to the retina. Thus the focal
point of the eye is in the vitreous, and the far point of the eye is located between the eye and
optical infinity (1). Hyperopic eyes have insufficient power without accommodation to fo-
cus parallel rays of light on the retina; accommodation may produce enough plus power to
bring parallel or even diverging rays to focus on the retina. Astigmatism is due to asym-
101
102 Ambati et al.
metry usually of the cornea and sometimes of the lens. Regular astigmatism is correctable
with a spherocylindrical lens, whereas irregular astigmatism is not correctable with such a
lens. Regular astigmatism is called with the rule when the steepest (most refracting) merid-
ian lies near 90 degrees. It is termed against the rule when the steepest meridian lies near
180 degrees. When regular astigmatism is neither with nor against the rule, it is termed
oblique.
1. Spectacle-Correction of Ametropias
Spectacle lenses placed in front of the eye must have their focal point coinciding with the
far point of the eye, so that parallel rays are focused onto the retina. Drawbacks of this sys-
tem include image distortion, prism effects, anisometropic effects, and field tilt. Minus
lenses minify images by approximately 2% per diopter, while plus lenses magnify the im-
age but create a peripheral scotoma between what is viewed inside and outside the specta-
cle frame. Astigmatic correction produces meridional minification or magnification, dis-
torting the image. Off-axis viewing and lens tilt alter the effective spherocylindrical power
of the lens, while viewing away from the center of the lens produces prism, leading to the
well-known pincushion and barrel distortions of hyperopic and myopic lenses, respec-
tively. Disparity between astigmatic correction of the two eyes produces a perceived tilt of
the object. This can be minimized by decreasing the cylinder power and/or rotating the axis
of the cylinder, albeit at the expense of clarity. All of these effects are heightened in higher
power lenses.
B. PREOPERATIVE CONSIDERATIONS
What should the refractive surgeon aim for in patients whose spectacle usage has entailed
such compromises? The surgeon should still aim for full correction of astigmatism, as cor-
rection at the cornea minimizes distortion effects. Further, surgery may relieve distortion
due to anisometropia. Indeed, patients who are undercorrected with surgery often report
double images not eliminated by monocular patching and other distortion effects not due to
meridional magnification. Some patients who have adapted to spectacle distortion and tilt
may take some time to readapt their binocular spatial sense and appreciate the lack of op-
tical distortion. Refractive surgery in the myope, by removing the minification of the spec-
tacle lens, produces a larger retinal image of objects, improving visual acuity even when
clarity, i.e., optic resolving power, is the same or decreased.
For the same reason that a presbyopic myope has a more remote near point when
wearing contact lenses than when wearing glasses, refractive surgery giving full correction
of myopia may make reading without reading glasses more difficult than it was with glasses
before surgery.
2. High Myopia
In patients with unilateral high myopia, placement of a corrective contact lens allows a pre-
operative prediction of the degree of aniseikonia they may experience after refractive
surgery. Patients with bilateral high myopia should be appraised of the possibility of dis-
turbing aniseikonia after one eye has undergone surgery before the other eye: the possibil-
ity of unequal photoreceptor spacing is considered in cases of high refractive errors, in
which case aniseikonia testing should be performed.
3. Cycloplegic Refraction
Cycloplegic refraction allows the examiner to discern the degree of myopia in the manifest
refraction due to accommodative tone; however, pupil dilation leads to a mild myopic shift
due to spherical aberration of the lens. Cycloplegic refractions of hyperopes enables the de-
termination of latent, manifest, and therefore total hyperopia; the surgeon must consider
that the latent portion will gradually become manifest as the patient ages.
4. Diabetes
Diabetic fluctuations in blood sugar can change lens size and curvature. Stability of refrac-
tive error is essential prior to refractive surgery. Further, diabetes is a relative contraindi-
cation to elective corneal surgery, as diabetic corneal epithelium is more prone to persis-
tent epithelial defects, duplication of basement membrane, and recurrent erosions.
5. Pupil Size
Larger pupils allow light rays peripheral to the optical zone to be transmitted to the fovea.
The StylesCrawford effect dampens this somewhat, as photoreceptors are oriented to-
wards reception of light passing through the central cornea.
6. Ocular Motility
Motility examination with measurements of convergence and divergence amplitudes is part
of the preoperative evaluation for refractive surgery, which can increase or decrease ac-
commodative requirements in various circumstances. As mentioned above, the myope pre-
viously corrected with spectacles will lose the near effectivity of distance-corrective minus
lenses. Undercorrection of myopia with surgery relieves the demand for accommodation at
near but increases the need for nonaccommodative convergence at near. Patients with low
reserves of fusional divergence may become symptomatic if surgery overcorrects myopia,
as the resultant hyperopia increases the demand for accomodation and attendant acco-
modative convergence. Thus measuring with prisms the amplitudes of convergence and di-
vergence (far and near, and with or without accomodation) helps predict whether a change
of accomodative demand may create problems of convergence or divergence insufficiency.
7. Accomodation
Accomodative amplitude with the correction mode at the cornea should be measured be-
fore surgery to plan targeting for near vision, i.e., equal correction vs. monovision, full cor-
rection vs. partial. The amplitude of accomodation can be measured several ways, e.g., the
difference in diopters between the least and most spheres accepted with clear vision while
gazing at a distant target. Low amplitudes may be due to medication, oculomotor nerve
104 Ambati et al.
paresis, trauma, lack of effort, incorrect distance refraction, or accomodative spasm. Mea-
surement of the near point while wearing myopic spectacles will overestimate the ampli-
tude of accomodation amplitude, because of the so-called near-effectivity of the myopic
spectacle lens. Correcting the same eye for emmetropia by contact lens or refractive
surgery will yield a more remote near point and smaller amplitude of accomodation.
Myopes who have been overminused with presbyopic symptoms may become less
symptomatic once the extra minus is eliminated. Determination that a patient is overmi-
nused can be performed with cycloplegia or possibly with prolonged fogging with plus
lenses. If the cycloplegic manifest refraction is accepted in new glasses, surgery should be
based on those values. However, it should be borne in mind that some patients who have
had overcorrected myopia for years will not be able to relax completely their accomodative
tone soon after surgery. The surgeon and patient must then be aware of the prospect of
blurred vision in either the short or the long term.
C. REFRACTIVE EVALUATION
Making the central cornea flatter and the peripheral cornea steeper with LASIK produces
blur, which is more pronounced when the pupil is large, as it is in dim light. When the pupil
dilates, the peripheral lens is also more exposed; this part of the lens has greater plus power.
The clinical relevance of peripheral corneal irregularity, scars, decentration, and central
corneal haze are topics of active investigation. The impact of postoperative irregular astig-
matism of the central cornea on uncorrected and spectacle-corrected vision is unclear. Pre-
dictive factors for good spectacle correction remain to be identified.
1. Astigmatism
An objective for surgical correction of astigmatism is a relatively spherical central corneal
zone. The outline of this region is oval, the narrower aspect being the meridian with the
maximum difference in curvature between central and peripheral cornea. When the pupil
dilates, the peripheral cornea becomes more relevant, resulting in blur or monocular
diplopia, especially noticeable when details vary with torsion of the eye or observed object.
As these patients have a clear image from the central zone, the blurred regions of an object
stand in contrast to the sharper portions: this can be more disturbing than preoperative dif-
fuse blur.
2. Retinoscopy
Streak retinoscopy is performed in the standard fashion with attention to the central reflex.
Retinoscopy after refractive surgery may be more easily performed using minus cylinder
techniques to neutralize against motion. The endpoint of retinoscopy is less influenced by
the steeper peripheral cornea if the target is neutralization of any part of the against motion,
generally seen first in the flattest central cornea. A novice depending on complete neutral-
ization of against motion or any part of with motion may overcorrect patients significantly.
Further, when against motion is observed, the patient is fogged and thus less likely to ac-
comodate during retinoscopy.
During retinoscopy, skew, break, and straddling are useful to refine the axis of cor-
rective cylinder. Skew is streak motion not paralleling the motion of the retinoscope and is
helpful in patients with postoperative irregular astigmatism, when break (when the streak
falls on iris, indicating imperfect alignment of the retinoscopic reflex) is not easily ob-
Preoperative Optical Considerations in LASIK 105
served. Straddling involves observing reflexes 45 degrees on either side of the presumed
axis. With motion should be observed with this technique and can be produced by adding
minus sphere or moving closer to the eye.
When using plus cylinders, the correct axis is approached turning towards the thin-
ner, brighter reflex. When using minus cylinders, the correct axis is approached by turning
away from the thinner, brighter reflex. Retinoscopy after dilation may be confused due to
scissoring of the reflex; this is commonly seen after refractive surgery. In this situation, one
should focus on the reflex of the central three millimeters. Further, it should be remembered
that off-axis retinoscopy will give a false measurement of astigmatism.
4. Anisometropia
During the preoperative evaluation, a discussion of the possibility of anisometropia en-
countered postoperatively is valuable. The management of these cases is similar to that of
anisometropes in general, depending on what sensorimotor adaptations the patient has de-
veloped, the presence of amblyopia, etc. A contact lens worn in the unoperated eye can al-
leviate aniseikonia and spectacle-induced vertical prism effects on up and downgaze. Par-
tial correction or a balance lens can be used in spectacle correction in cases where deep
amblyopia is present or symptoms of aniseikonia and anisophoria are severe. Spectacles
may be attempted in the postoperative period to protect a dominant eye when the other eye
is amblyopic.
Monovision (one eye targeted for distance, the other for near) may be given without
compromise when there is good vision but little stereopsis in both eyes. A preoperative trial
with contact lenses can be used to predict whether significant anisophoria or aniseikonia
106 Ambati et al.
would occur in patients after correction for monovision. In patients with high myopia, pre-
existing strabismus and suppression may be present. Surgical overcorrection may lead to
accommodative spasm and esodeviations. In this situation, contact lenses or enhancement
surgery may correct the consecutive hyperopia.
5. Spasm of Accommodation
Convergence and accommodation issues are also encountered postoperatively. Uncor-
rected hyperopes, astigmatics, and overcorrected myopes can develop spasm of accommo-
dation, causing asthenopia, headache, or blurred vision. Exophoria, stress, convergence in-
sufficiency, iridocyclitis, and certain medications (especially anticholinesterase agents) can
worsen this phenomenon. Accommodative spasm can be addressed with reading glasses,
adding plus to spectacles, bifocals, or chronic cycloplegia. Subclinical convergence insuf-
ficiency may be unmasked after refractive surgery for hyperopia, as accommodation-re-
lated convergence is lessened. Spectacle-induced hyperopia usually solves this problem.
of patients reported in 19 articles was 76% (434 out of 573 patients). Failure was due to
contact lens intolerance or poor visual adaptation. If previously contact-lens intolerant pa-
tients are excluded, monovision success rates are approximately 86% (2).
There are several factors determining monovision success: ocular dominance, sight-
ing preference, interocular blur suppression, stereo acuity, and phorias. When the dominant
eye was corrected for distance, overall monovision success rate was 75% (3). These pa-
tients performed better at visual locomotor tasks requiring directional prediction (walking,
driving) and also had lesser esophoric shifts at distance. Patients with alternating domi-
nance (no sighting preference) have interocular blur suppression, another factor predictive
of monovision success. Those with strong sighting preferences had reduced blur suppres-
sion, decreased binocular depth of focus (relative to others), and higher monovision failure
rates; they frequently reported ghosting at near or distance (secondary images that can be
distracting and sometimes affect balance) (4). After monovision correction, unsuccessful
monovision patients had a mean of 50 to 62 seconds of arc less in stereopsis than success-
ful patients (56). Postoperative esophoric shifts were less in successful monovision pa-
tients than in unsuccessful patients, but no differences in fusional vergence ranges have
been documented. Age has yet to be shown to be a factor affecting monovision success.
Monovision affects several visual functions (713). Monovision correction generally
produces a small reduction in high and low-contrast visual acuity, especially in conditions
of low lighting (11). The average visual acuity reduction was 0.05 0.02 logMAR units.
The decrease in high-contrast binocular visual acuity is quite variable and worsens with
larger pupils and greater astigmatic errors. Monovision has no significant effect on binoc-
ular peripheral visual acuity or visual field width (6). Contrast sensitivity is 42% less with
monovision than with binocular vision (12). Thus monovision is not preferable in those
whose occupations require fine, detailed work. Task performance is reduced by less than
6% in activities requiring moderate stereopsis, e.g., card-filing (13). In those with alternat-
ing dominance (no sighting preference), the binocular depth of focus is almost equal to the
sum of monocular depths of focus (9). In those with strong sighting preferences, the binoc-
ular image becomes blurred as the object moves from the dominant eyes clear range to the
nondominant eyes clear range, and thus the binocular depth of focus in these patients is
much less than the sum of the monocular depths of focus. After 3 weeks of monovision
adaptation, a significant recovery of stereo acuity occurs (8). Increasing the ocular blur in-
creases the stereoscopic threshold. In presbyopes, the stereo acuity decreased greatly when
the blur was more than 1.75 D. Monovision reduced secondary fusion in 10 to 20% of pa-
tients but did not affect simultaneous perception or gross stereopsis. The binocular visual
stress created by monovision is thought to cause esophoric shifts. These shifts are greater
when the nondominant eye is corrected for distance. Divergence and convergence ranges
at distance are reduced with monovision, but reductions in fusional vergence ranges are sig-
nificant only when the nondominant eye is corrected for distance. Monovision reduces the
typical exophoria seen in presbyopes at near by 2.5 to 5.2 prism diopters (6). The diver-
gence range is significantly less with monovision at near viewing, but not the convergence
range.
Monovision should be avoided in patients with strong sighting preference, significant
loss of stereoacuity with monocular correction, large esophoric shifts, minimal interocular
suppression, or occupations requiring fine work. Patients must be informed of the reduc-
tion in visual acuity and stereopsis. Spectacle lenses may need to be prescribed for tasks re-
quiring sharp distance vision (aniseikonia is generally acceptable in these circumstances).
Monovision is clearly not a panacea for presbyopia and should be used only in patients who
108 Ambati et al.
have been carefully screened and who are willing to tolerate its attendant visual compro-
mises. Preoperative use of monovision contact lenses may identify those who are likely to
do well with monovision refractive surgery; these should be conducted for at least 3 weeks.
If patients do not improve significantly in their adaptation to monovision over that time pe-
riod, they may not be good candidates. Lastly, it should be noted that there are presently no
published reports of LASIK being used to produce monovision.
single-zone vs. multizone LASIK (22). Multizone eyes were found to have a greater de-
crease in log contrast sensitivity at 12 cycles/degree under undilated conditions. Perez-San-
tonja et al. found that contrast sensitivity 1 month after LASIK decreased significantly only
at low and intermediate spatial frequencies (3 and 6 cycles/degree) (23). By 3 months, there
were no significant differences in contrast sensitivity at all spatial frequencies compared to
baseline. Wang et al. found that LASIK eyes recovered contrast sensitivity by 3 months as
well, a significant difference from their control group, PRK eyes, in whom recovery took
6 to 12 months (24).
F. CONCLUSION
Several preoperative optical considerations are important when evaluating a patient con-
sidering LASIK surgery. In addition to understanding the basics of refractive error evalua-
tion, anticipation of postoperative outcomes and of optical aberrations after surgery are es-
sential for patient education prior to surgery. The use of corneal topography and wavefront
analysis is valuable to achieve this goal. An understanding of certain fundamental princi-
ples of optics will facilitate and optimize clinical application of LASIK. Refractive sur-
geons must be aware of more than spherocylindrical thin-lens first-order optics in order to
make informed decisions. The following chapters will cover additional preoperative con-
siderations that are necessary to optimize LASIK outcomes and improve patient satisfac-
tion.
REFERENCES
1. American Academy of Ophthalmology. Ophthalmology, Optics, Refraction, and Contact
Lenses: Basic and Clinical Science Course. San Francisco, 1998.
2. S Jain, I Arora, DT Azar. Success of monovision in presbyopes: review of the literature and po-
tential applications to refractive surgery. Surv Ophthalmol 1996;40:491499.
3. EC McGill, P Erickson. Sighting dominance and monovision distance binocular fusional
ranges. J Am Optom Assoc 1991;62:738742.
4. C Schor, M Carson, G Peterson, J Suzuki, P Erickson. Effects of interocular blur suppression
ability on monovision task performance. J Am Optom Assoc 1989;60:188192.
5. P Erickson, EC McGill. Role of visual acuity, stereo acuity, and ocular dominance in monovi-
sion patient success. Optom Vis Sci 1992;69:761764.
6. MJ Collins, B Brown, SJ Verne, M Makras, KJ Bowman. Peripheral visual acuity with mono-
vision and other contact lens corrections for presbyopia. Optom Vis Sci 1989;66:370374.
7. JE Sheedy, MG Harris, L Busby, E Chan, I Koga. Monovision contact lens wear and occupa-
tional task performance. Am J Optom Physiol Opt 1988;65:1418.
8. JH McLendon, JL Burcham, CH Pheiffer. Presbyopic patterns and single vision contact lenes.
South J Optom 1968;10:710.
9. A Back, T Grant, N Hine. Comparative visual performance of three presbyopic contact lens cor-
rections. Optom Vis Sci 1992;69:474480.
10. M Collins, A Good, B Brown. Distance visual acuity and monovision. Optom Visc Sci 1989;
66:370374.
11. S Pradhan, J Gilchrist. The effect of monocular defocus on binocular contrast sensitivity. Oph-
thal Physiol Opt 1990;10:3336.
12. MJ Collins, B Brown, KJ Bowman. Contrast sensitivity with contact lens corrections for pres-
byopia. Ophthal Physiol Opt 1989;9:133138.
13. KA Lebow, JB Goldberg. Characteristics of binocular vision found for presbyopic patients
wearing single vision contact lenses. J Am Optom Assoc 1975;46:11161123.
110 Ambati et al.
14. GS Rubin. Contrast sensitivity and glare testing in keratorefractive surgery. In: D Azar, ed. Re-
fractive Surgery. Stamford, CT: Appleton & Lange, 1997, pp 143151.
15. JA Marron, IL Bailey. Visual factors and orientation-mobility performance. Am J Optom Phys-
iol Opt 1982;59:413426.
16. DG Pelli, JG Robson, AJ Wilkins. The design of a new letter chart for measuring contrast sen-
sitivity. Clin Vis Sci. 1988;2:169177.
17. GS Rubin, GE Legge. Psychophysics of readingthe role of contrast in low vision. Vis Res
1989;29:7991.
18. DB Elliott, MA Bullimore. Assessing the reliability, discriminative ability, and validity of dis-
ability glare tests. Inv Ophthalmol Vis Sci 1993;34:108119.
19. JT Holladay, TC Prager, J Trujillo, RS Ruis. Brightness acuity test and outdoor visual acuity in
cataract patients. J Cataract Refract Surg 1987;13:6769.
20. JT Holladay, DR Dudeja, J Chang. Functional vision and corneal changes after laser in situ ker-
atomileusis determined by contrast sensitivity, glare testing, and corneal topography. J Cataract
Refract Surg 1999;25:663669.
21. MA El Danasoury. Prospective bilateral study of night glare after laser in situ keratomileusis
with single zone and transition zone ablation. J Refract Surg 1998;14:512516.
22. JD Carr, RD Stulting, Y Sano, KP Thompson, W Wiley, GO Waring III. Prospective compari-
son of single zone and multizone laser in situ keratomileusis for the correction of low myopia.
Ophthalmology 1998;105:15041511.
23. JJ Perez-Santonja, HF Sakla, JL Alio. Contrast sensitivity after laser in situ keratomileusis. J
Cataract Refract Surg 1998;24:183189.
24. Z Wang, J Chen, B Yang. Comparison of laser in situ keratomileusis and photorefraactive ker-
atectomy to correct myopia from 1.25 to 6.00 diopters. J Refract Surg 1997;13:528534.
8
Corneal Topography and LASIK
Applications
The use of computerized videokeratography (CVK) for the evaluation of the corneal sur-
face has become widespread. CVK is an indispensable tool for refractive surgeons for pre-
operative screening, surgical planning, assessment of surgical outcomes, detection and
management of complications, and refinement and development of surgical techniques.
This chapter reviews the basic principles of CVK, the recognition of corneal topographic
patterns, and the role of corneal topography in refractive surgery.
111
112 Wang et al.
The tear film of the anterior corneal surface acts like a convex mirror to form a virtual, erect
image of reflected light. This image is called the corneal light reflex or the first Purkinje
image.
The line of sight is a line connecting a fixation point at optical infinity with the cen-
ter of the entrance pupil (1). The pupillary axis is a line normal to the corneal surface pass-
ing through the center of the entrance pupil, which is usually temporal to the line of sight,
and the angle between them is known as angle lambda and is in the range of 3 to 6.
The topography of the cornea can be arbitrarily broken down into four zones. The
central zone generally refers to the central 3 to 4 mm of the cornea. The paracentral zone is
an annulus with inner and outer diameters of 4 and 7 mm, respectively. The peripheral zone
is an annular region with inner and outer diameters of 7 and 11 mm, respectively. The lim-
bal zone is the border, about 0.5 mm wide, between the cornea and sclera.
A meridian is a line that spans the diameter of the cornea from one point on the lim-
bus to a point on the opposing limbus. Meridians are located by their angular position, in-
creasing counterclockwise from 0 at the 3 oclock position to 180 at the 9 oclock posi-
tion for both the right and left eyes (2). A semimeridian is a radial line on the corneal
surface from its center, and it is located by its angular position from 0 at the 3 oclock po-
sition, increasing counterclockwise around the full 360 for both the right and the left eyes.
In the literature, there is confusion over the terms apex and vertex as applied to the
cornea. Waring defined the apex as the high spot of the corneal (2). Maloney suggested de-
noting the high point of the cornea as the corneal vertex and the apex as the region of great-
est curvature (3). According to Webster, however, both terms refer to a point on a shape
furthest from its base (4). A vertex sometimes also refers to the point where the axis of a
curve intersects the curve itself. It is important to understand that the high point and the re-
gion of greatest curvature often do not coincide. In this chapter, we will use Maloneys def-
initions, referring to the vertex as the high point on the cornea relative to the imaging sys-
tem (and hence the center of the placido disk rings), apex referring to the region of steepest
curvature.
Figure 8.1 The principles of Placido disk technology. The larger the distances between the rings,
the flatter the cornea, and the less dioptric power it has. The reverse is true with a steeper cornea,
which shows smaller distances between the rings and a higher corneal power.
The placido target is projected onto the cornea and reflected off the tear film to form
a smaller upright image that is in focus near the iris plane. This two-dimensional digital im-
age is captured by a CCD camera and analyzed to reconstruct three-dimensional corneal
shapes, using the distances between rings or ring edges as the basis for calculating the ra-
dius of curvature or refractive power. A larger spacing between ring edges indicates a flat-
ter cornea with a greater radius of curvature (Fig. 8.1).
b. Data Processing and Map Display
Three basic formulas exist for calculating corneal power: axial radius of curvature, instan-
taneous (or tangential) radius of curvature, and refractive. Clinically significant differences
exist in the corneal power values calculated by the three formulas (6). The topographic data
may then be represented in a variety of ways. Clinically, the most useful representation to
the clinician is the color-coded map. The warm colors, red and orange, represent relatively
higher powers (steeper curvatures), green and yellow are used for powers associated with
normal corneas, and cool colors, hues of blue, denote relatively lower powers (flatter cur-
vatures). Types of topographic displays include
1. Axial radius of curvature maps. The axial radius of curvature maps are the orig-
inal and most commonly used CVK maps and are derived from the axial radius of curva-
ture. This formula is used by the keratometer and is based on the distance from the corneal
vertex to the center or edge of the ring. This distance is then used to calculate the length
of the radial line connecting this point to the optical (or sagittal) axis. This approach
simplifies the optical principles of the cornea by assuming that the rays of light striking
the cornea are paraxial, i.e., the angles of incidence are small. The simplified paraxial
formula is
n 1
Paxial
(1)
raxial
where n 1.3375 (standardized value for keratometric index of refraction) and raxial the
distance from the corneal surface to a point of intersection on the optical axis (Fig. 8.2A).
The standardized value for keratometric index of refraction, n, is not the true refractive in-
dex of the cornea but an approximated index to yield the total corneal power as a single re-
fracting surface by compensating for the negative power of the posterior surface. Axial
power tends to have a spherical bias because each curvature measured is referred to the op-
tical axis. For aspherical surfaces, this bias gives an accuracy of 0.25 D in the central
cornea, but errors of 3 D or more can be found in the periphery (7).
114 Wang et al.
Figure 8.2 Two approaches for the calculation of the corneal radius of the curvature: (A) axial ra-
dius, (B) instantaneous radius.
The axial radius of curvature map is the standard that may be used by most clinicians.
However, it is less accurate than instantaneous radius of curvature maps in providing detail
regarding corneal curvature, and it is less accurate than refractive maps in portraying the
refractive power of the anterior corneal surface. As a result, it may be less valid than these
other two maps, despite its popularity.
2. Instantaneous radius of curvature maps. The instantaneous radius of curvature
varies from the axial radius of curvature in that it calculates a true radius of curvature in-
dependent of the sagittal axis (Fig. 8.2B):
n 1
Pinst
(2)
rinst
where rinst is the radius of curvature for any given point on the cornea. The difference be-
tween axial radius of curvature and instantaneous radius of curvature maps can be dramatic.
Axial radius of curvature maps tend to appear more uniform because abrupt changes in lo-
cal curvature are underestimated because the calculated radius of curvature must terminate
at the sagittal axis. Instantaneous radius of curvature maps typically show more marked
changes in dioptric power over smaller regions and provide more accurate measurements
of corneal curvature and certainly better representation of local irregularity (7).
Corneal Topography and LASIK Applications 115
Both of these maps, however, have marked limitations in predicting corneal refrac-
tive power. For the central paraxial rays, these formulas can be used to estimate corneal re-
fractive power. Outside of the central region, however, the assumptions and their equations
are not necessarily valid, and in particular they ignore the incident angle of the incoming
light, thereby underestimating the refractive effect of peripheral rays (spherical aberration)
(8).
3. Refractive maps. The appropriate equation for the refractive power (secondary
focal point power) for the incoming parallel rays was first described by Gullstrand (9) and
modified by Klein (10) as
n n
P
(3)
x/tan (i r)
where is the focal length, defined as the distance from the corneal vertex to the intersec-
tion of the refracted ray with the optical axis, x the corneal zone, i the angle of incidence,
and r the angle of refraction. Maps calculated using this formula attempt to estimate the
refractive power of the anterior corneal surface.
This map best characterizes the image-forming properties of the anterior corneal sur-
face.
4. Elevation maps. Elevation data, which describe the difference between the
height of the cornea and a reference surface, are provided by many of the Placido-based
units. These elevation data are derived from the placido ring measurements, which is an ap-
proach that obviously differs from the projection principle used by elevation-based systems
to obtain direct height measurements (see below).
As will be described below, elevation maps have particular value in assessing post-
operative visual problems, such as central islands.
5. Difference maps. These are typically calculated using axial radius of curvature
maps. They are useful in characterizing the change that has occurred during any interval.
As with any color-coded map, it is important to note the scale for the difference map. In the
authors view, a 0.5 D and 0.25 D interval is often most useful.
6. Other comparative maps. Different devices have a number of color-coded maps
that compare corneal curvature or refractive power to some standard surface. An irregu-
larity map may compare local changes in curvature to an idealized spherical cylindrical sur-
face. A profile map may compare corneal curvature to a standard aspheric corneal surface
as a way of evaluating the asphericity of the cornea. Corneal acuity maps display the esti-
mated visual acuity potential for any given region of the cornea and for the cornea as a
whole.
In viewing a color-coded dioptric map, it is critical first to ascertain the dioptric scale.
A number of different dioptric intervals have been recommended for standardized scales,
but the authors prefer a 0.5 D scale. Scales with intervals greater than 0.5 D are useful for
corneas with large dioptric ranges, such as advanced keratoconus. However, for refractive
surgery, a 0.5 D scale is required to obtain sufficient detail regarding nuances that affect vi-
sual performance. Fortunately, most topographers now offer some type of standardized ab-
solute scale and adjustable scales that allow the clinician to customize the information for
maximal clinical value.
c. Indices
CVK devices provide a number of quantitative indices that can tremendously enhance anal-
ysis of topographic maps. Simulated Keratometry (Sim K), which is provided by all de-
116 Wang et al.
vices, is a value that attempts to mimic conventional keratometry readings. However, there
are differences between Sim K values and standard keratometry. Whereas Sim K values
represent orthogonal curvatures at the 3 mm zone, for the keratometer, the diameter of the
measured zone varies according to corneal curvature: the flatter the cornea the larger the di-
ameter of the zone that is measured (11). In addition, different devices presumably use dif-
ferent formulas for calculating Sim K, depending upon the number of points that are sam-
pled in order to make this calculation.
Many devices offer a number of specialized indices. The Tomey unit (Tomey Cor-
poration USA, Waltham, MA) provides several indices, including the surface regularity in-
dex (SRI) and the surface asymmetry index (SAI) (12). The SRI is a measure of the local
regularity of the corneal surface within the central 4.5 mm diameter. SRI values increase
with increasing irregular astigmatism and approach zero for a smooth corneal surface.
Studies have demonstrated that the SRI is highly correlated with best spectacle-corrected
visual acuity (1215). SAI measures the difference in corneal powers at each ring 180 de-
grees apart as a measure of symmetry. Theoretically, the SAI value would be zero for a per-
fect sphere, a surface with perfectly spherocylindrical regular astigmatism, and for any sur-
face with a power that is radially symmetrical. The potential visual acuity (PVA) is an
estimation of predicted visual acuity based on surface regularity index. Other Tomey in-
dices include those that can be used to estimate the likelihood of the presence of kerato-
conus (see below).
The EyeSys Corneal Analysis System (EyeSys Technologies, Houston, TX) also
provides several numeric indexes in its Holladay Diagnostic Summary Display (16). Ef-
fective refractive power (EffRP) is the calculated mean refractive power of the cornea
over the central 3 mm, including the role of the Stiles Crawford effect. Corneal unifor-
mity index (CUI) is a measure of the uniformity of the distortion of the corneal surface
within the 3 mm pupil, expressed as a percentage. A CUI of 100% indicates that the op-
tical quality of the cornea is perfectly uniform over the 3 mm pupil, and a CUI of 0% in-
dicates the nonuniform optical quality of the cornea. It is important to note that a CUI of
100% does not indicate that the cornea has good optical quality, simply that it is uniform;
it could be uniformly bad or good. Predicted corneal acuity (PCA) measures the extent
of corneal microirregularity by comparing the video-captured image with a best-fit ellipse
(17). It is the estimated range of visual acuity that could be expected if the cornea were
the only factor limiting vision. Weiss and Oplinger found that the PCA appears to be
most useful in predicting the BCVA in patients with normal corneas but is less precise in
patients with corneal abnormalities (18).
In the Humphrey Atlas, the irregularity map displays wavefront error to characterize
the irregularity of anterior corneal surface. Wavefront error is the difference between
the corneal surface and a best fitted toric surface. It describes the condition of the light
rays as they pass through the corneal surface and are refracted onto the retina through the
clear media of the eye. Wavefront error, which closely measures a toric surface, will be dis-
played as green, with red and blue representing positive and negative wavefront errors, re-
spectively.
Early Placido-based systems were susceptible to errors induced by focusing and align-
ment (centration) (19). To minimize these sources of errors, most current units use special
methods, such as correcting algorithms (Tomey, Humphrey, and TechnoMed) or employ-
ing three cameras to measure precisely the distance from the Placido surface to the cornea
(EyeSys). However, the Placido-based topography systems still have some limitations:
Corneal Topography and LASIK Applications 117
3. Elevation-Based Systems
Elevation-based systems utilize the principle of projection to measure directly corneal ele-
vation. Curvature values are derived from the elevation data.
a. Scanning Slit Imaging System
The Orbtek ORBSCAN (Bausch & Lomb) uses a scanning slit beam and direct stereotrian-
gulation to measure the anterior corneal surface, the posterior corneal surface, and the ante-
rior iris and anterior lens surfaces (Fig. 8.3). It employs a calibrated video and a forty scan-
ning slit beam system (20 from the left and 20 from the right) to measure independently the
x, y, and z locations of several thousand points on each surface with a resolution of 2 m.
Figure 8.4 illustrates the data acquisition by the slit beam system. The cornea is scanned lim-
bus to limbus, and the images are accessed by a calibrated video camera with 240 data points
per slit. These directly measured points are used to construct topographic maps.
Orbscan displays color maps as 3-D, profile, and traditional for elevation, curvature,
and pachymetry. The elevation map shows the difference between the best fit sphere (BFS)
Figure 8.3 Series of surface planes measured with the Orbscan system from anterior corneal sur-
face to anterior lens surface.
118 Wang et al.
Figure 8.4 Data acquisition by the slit beam system. Forty single images are captured by a cali-
brated video camera (240 data points/slit). Resolution and accuracy of the central area (35 mm) are
improved by the overlapped images.
and the eye surface in mm, expressed in distance radially from the center of the sphere (by
default) or sagittal height between the two surfaces. The BFS is used to match best the an-
terior or posterior corneal surfaces, and this match is determined using a least squares
method. Positive elevation measurements indicate that the corneal surface falls above the
BFS and are represented as warm colors, while negative values indicate that the corneal
surface falls below the BFS and are represented as cool colors on the elevation maps. It
should be noted, however, that the elevation display depends on reference surface size,
shape, alignment, fitting zone, and elevation direction (normal or axial) (2223).
Corneal pachymetry is calculated at more than 5000 points from the elevation differ-
ence of the anterior and posterior surfaces. The pachymetry map displays thickness at the
thinnest point and in an array from center to the limbus.
Advantages of the slit beam scanning technology include direct measurement of
corneal height, lack of spherical bias, entire corneal coverage, and information about all
surfaces of the anterior segment. The Orbscan measurement of anterior chamber depth
has been reported to be accurate and reliable in normal eyes, as well as in high myopic
and hyperopic eyes (2425). However, corneal pachymetry measured by Orbscan has
been found to exceed ultrasonic pachymetric measurements (2627). A recent study
found poor accuracy of Orbscan pachymetric readings in corneas that had undergone
LASIK (28).
Elevation data have been used for customized laser ablation to correct irregular astig-
matism due to different causes (2930). Results have been mixed, a relatively high per-
centage of patients do not achieve any improvement in spectacle-corrected visual acuity.
Causes for this may include inaccuracy of the corneal measurements, inaccurate laser al-
gorithms, or difficulty in correctly aligning the laser to the cornea.
A limitation of this device is the relatively long time (1.5 seconds) required for imag-
ing the 40 scanning slits, although the system employs a tracking system that attempts to
minimize the influence of involuntary eye movement. A more significant concern is that
clinical accuracy of this technology has not been fully established, particularly the accuracy
of posterior curvature measurements. One study has shown relative inaccuracy, and Mal-
oney has suggested that measuring the testretest variability is an appropriate method of
controlling the accuracy of posterior curvature measurements(31).
Corneal Topography and LASIK Applications 119
b. Rasterphotogrammetry
The PAR Corneal Topography System (PAR CTS, PAR Vision System Corp., New Hart-
ford, NY) was the first topography system to produce an elevation map of the corneal
surface. The system projects onto the corneal surface a grid composed of horizontal and
vertical lines spaced about 0.2 mm (200 microns) apart and computes elevation data
based on the distortion of the grid. The PAR system requires that a small amount of flu-
orescein be placed in the tear film, and the images are collected using standard fluores-
cence-based photography. Image acquisition is rapid and relatively insensitive to focus-
ing. From the known geometry of the grid projection and imaging system paths, rays can
be intersected in three-dimensional space to compute the x, y, and z coordinates of the
surface (32).
Studies showed that the PAR system was both accurate and reproducible and had the
ability to image irregular, deepithelialized, and keratectomized corneas (3336). On the
other hand, the use of fluorescein staining and limited measurement points (1400) are
among the major drawbacks of this system. Although this technology is intriguing, it is no
longer commercially available.
c. Interferometric System
The KeraMetrics Corneal Laser Analysis System 1000 (CLAS 1000; Kera Metrics Inc.,
Solana Beach, CA) utilizes laser holographic interferometry fringe patterns to depict devi-
ation of the corneal surface. Interferometry records the interference pattern generated on
the corneal surface by two coherent wave fronts (37). Although high accuracy is theoreti-
cally possible here, there have been no detailed studies on the accuracy of topographic mea-
surement using this technology or on specific clinical applications. This device is not com-
mercially available.
Moir interference occurs when two sets of parallel lines are superimposed at different ori-
entation (38). There are few peer-reviewed data available validating the system.
Although myopia is predominantly caused by increased length, a weak but statistically sig-
nificant relation has been shown to exist between the corneal power and refractive error,
i.e., corneal power increases (corneal radius decreases) with increasing myopia (3945).
Two studies have noted that the cornea flattens less rapidly in the periphery with increas-
ing myopia (more negative Q values, see below) (4546).
Using the EyeSys Corneal Analysis System, Budak and colleagues provided a
corneal topographic classification of myopic eyes based on axial, instantaneous, refractive,
and profile difference maps (47). They defined six types of patterns for axial, instanta-
neous, and refractive maps: circular, circular with central bow tie, circular with central ir-
regularity, symmetric bow tie, asymmetric bow tie, and irregular pattern (Fig. 8.5AF)
120 Wang et al.
B
Figure 8.5 Six types of myopic patterns for axial, instantaneous, and refractive maps: (A) circu-
lar, (B) circular with central bow tie, (C) circular with central irregularity, (D) symmetric bow tie, (E)
asymmetric bow tie, and (F) irregular pattern.
Corneal Topography and LASIK Applications 121
F
Figure 8.5 Continued
Corneal Topography and LASIK Applications 123
(Table 1). The circular with central irregularity and irregular patterns were associated with
lower values for Predicted Corneal Acuity and Corneal Uniformity Index.
2. Hyperopia
A study by Strang and coauthors found that hyperopia, like myopia, is predominantly axial
in nature, although in some hyperopes the cornea is abnormally flat and either contributes
to or accounts for the hyperopic refractive error (48). No study has yet been done to classify
the patterns on topographic maps using computerized videokeratography (CVK).
3. Astigmatism
In patients with regular astigmatism, the astigmatic patterns in curvature maps are often
represented as a bow tie or figure eight, with the steepest and flattest axes of curvature of
the cornea lying at right angles to one another (orthogonal) (Fig. 8.6A). On the elevation
map, the astigmatic cornea may appear as a regular, irregular, or incomplete ridge pattern,
with the elevated portion or ridge representing the flatter astigmatic cylinder of the cornea
(Fig. 8.6B).
In patients with irregular astigmatism, corneal topographic patterns include circular
with central irregularity, asymmetric bow tie (characterized by asymmetric powers in or-
thogonal steep and/or flat semimeridians or by nonorthogonal semi-meridians), and irreg-
ular pattern as defined by Budak et al. (47) (Fig. 8.5). In elevation maps, the pattern may
be an irregular ridge, an incomplete ridge, or an unclassified pattern.
C. CORNEAL ASPHERICITY
The anterior corneal surface is asymmetrically aspheric, as the radius of curvature changes
from the center to the limbus and does so at different rates along different semimeridians
(4950). Many authors have tried to describe the complex aspheric asymmetric shape of the
cornea, either mathematically or graphically (49, 5154).
The ellipse is perhaps the most useful shape for describing corneal curvature, and the
profile of the cornea along any meridian can be considered as part of an ellipse. The nor-
mal cornea has a prolate shape, which means that the central zone is steeper than the para-
central and peripheral zones; this is the shape of a section across the steep end of an ellipse
Auto-scale
Axial Instantaneous refractive
Pattern map (%) map (%) map (%)
B
Figure 8.6 Patient with regular astigmatism: (A) bow tie pattern on curvature map, (B) irregular
ridge pattern on elevation map.
Corneal Topography and LASIK Applications 125
(Fig. 8.7). The reverse shape is oblate, in which the central zone is flatter than the periph-
eral zone; this corresponds to the flat side of an ellipse and is often seen in corneas that have
undergone myopic refractive surgery.
Usually corneal asphericity is quantitatively described by the Q value. For a sphere,
Q 0. For prolate surfaces, Q 0, and for oblate surfaces, Q
0 (55). For example, a
corneal asphericity with Q 0.26 indicates that, at a distance of 5 mm from the center,
the cornea flattens by about 7% as radius of curvature compared to a sphere. Mean reported
Q values have ranged from 0.15 to 0.30 (5660). Related parameters include eccen-
tricity of the equivalent conic section (e) and shape factor (P), where Q e2, and P Q
1, respectively.
CVK plays a critical role in the ongoing evaluation of potential and in all phases of the care
of the refractive surgical patient, including preoperative screening, postoperative monitor-
ing of results, and postoperative planning for retreatment procedures.
1. Preoperative Screening
CVK plays several roles in the preoperative evaluation of refractive surgical patients.
a. Determining Topographic Stabilization Following Discontinuation of
Contact Lens Wear
Contact lens wear can alter the shape of the cornea by a process termed warpage, which re-
sults from direct mechanical pressure of the lens and possibly from metabolic factors, such
as low oxygen tension. Corneal topographic patterns of warpage are characterized by the
presence of central irregular astigmatism, loss of radial symmetry, and frequent reversal of
the normal topographic pattern of progressive flattening of corneal contour from the center
to the periphery (61). Superior-riding lenses produced flattening superiorly and result in a
relatively steeper contour inferiorly that simulates the topography of early keratoconus. Us-
ing the Orbscan topography system, Liu and Pflugfelder found that long-term contact lens
126
Figure 8.8 Contact lensinduced corneal warpage reversed in 1 month after discontinuation of contact lens wear.
Wang et al.
Corneal Topography and LASIK Applications 127
wear ( 5 years) appeared to decrease the entire corneal thickness and increase the corneal
curvature and surface irregularity (62).
Following discontinuation of contact lens wear, it is important to monitor corneal to-
pographic changes and defer obtaining final refractive measurements until corneal topog-
raphy stabilizes (Fig. 8.8). Using the CVK (EyeSys Corneal Analysis System), Budak and
colleagues evaluated corneal stability after discontinuation of contact lens wear in preop-
erative refractive surgery candidates (63). They found that, if the manifest refraction and
CVK maps were within 0.5 diopters of values obtained 2 weeks earlier, topographic indices
were normal, suggesting return of the cornea to its baseline topographic state. In their study
this was noted after discontinuation of soft contact lenses wear for 2 weeks and of rigid gas-
permeable contact lenses wear for 5 weeks.
b. Detecting Ectatic Corneal Disorders or Other Topographic
Abnormalities
Keratoconus
The detection of keratoconus and keratoconus suspects has assumed greater significance in
light of the development and expansion of refractive surgery over recent years. Patients
with keratoconus do not achieve high-quality vision with either glasses or contact lenses,
and they tend to seek out refractive surgery. The percentage of candidates who were found
to have keratoconus or subclinical keratoconus during the preoperative screening for re-
fractive surgery has been reported to be as high as 33% (64).
Patients with moderate to advanced keratoconus are readily recognizable on the to-
pographic maps and easily diagnosed clinically (Fig. 8.9). The difficulty is to detect the
keratoconus in its early stages before obvious topographic and clinical signs are present.
These corneas are sometimes referred to as forme fruste keratoconus or keratoconus sus-
pects, because of the subtle topographic abnormalities that are present. Several quantitative
specific corneal indices and detection programs designed to aid the topographic diagnosis
of keratoconus have been developed.
1. RABINOWITZMCDONNELL INDICES. These investigators described two criteria
for detected keratoconus. The first is the inferiorsuperior value (IS), which is defined as
an average refractive power difference between five inferior points and five superior points
3 mm from the center at 30 intervals (65); it is designed to detect clinically significant in-
ferior corneal steepening. When used alone, an IS value greater than 1.4 D is suggestive of
keratoconus. A disadvantage of the I-S value is that the steepening in keratoconus is not al-
ways limited to the inferior periphery (6667). The second criterion, which is designed to
detect central cones, is central corneal power
47.2 D. Because of the variability of the lo-
cation of the cone, these two diagnostic features should be used in concert, and subjective
interpretation is necessary (68).
2. KERATOCONUS PREDICTABILITY INDEX (KPI). Maeda and colleagues devel-
oped the KPI, which is a single value derived by linear discriminant analysis of eight quan-
titative topographic indices (69). A KPI value greater than 0.23 is indicative of kerato-
conus.
3. KERATOCONUS INDEX (KCI). In addition to the discriminant analysis classi-
fier, the authors (69) developed an expert system classifier. An expert system is a form
of artificial intelligence that comprises an extensive set of decision rules. Decisions by
the expert system are made deductively with step-by-step logical operation. In addition
to the KPI, four indices were used in the binary decision tree. The degree of the kerato-
conus-like pattern is determined and expressed as a percentage, KCI%. A value of zero
is normal, with greater values describing an increasing likelihood of the presence of ker-
atoconus. In their study, the expert classifier system was found to be superior to dis-
criminate analysis in sensitivity and overall accuracy. In a subsequent study, three kera-
toconus detection schemes were compared: keratometry (average simulated keratometry
[SimK] readings
45.7 diopters [D]); the modified RabinowitzMcDonnell test (central
corneal power
47.2 D and/or inferosuperior asymmetry [IS] value
1.4 D); and the
expert system classifier (70). Results showed that for screening candidates for refractive
surgery, where high sensitivity is needed, either the modified RabinowitzMcDonnell test
or the expert system classifier is suitable. For diagnosing keratoconus, where high speci-
ficity is more useful, the expert system classifier is more appropriate than the other two
methods.
4. KERATOCONUS SEVERITY INDEX (KSI). Neural networks can interpolate or pre-
dict complicated data through learning, by simulating human neurological processing
abilities, and have been attracting considerable attention in science, economics, and indus-
try, as well as in many areas of medicine. The first application of a neural network model
to classify corneal topography was reported and tested in 183 topographic maps (71). The
correct classification was achieved by a trained neural network for all 108 maps in the train-
ing set. In the test set, the neural network correctly classified 60 of 75 maps (80%). For ev-
ery category, accuracy and specificity were greater than 90%, whereas sensitivity ranged
from 44% to 100%. The model has subsequently been improved (72) and KSI was pro-
posed, which is a combination of neural network models and decision tree analysis. Kera-
toconus suspicion is interpreted when KSI reaches 0.15. A KSI of 0.30 or higher indicates
clinical keratoconus.
Corneal Topography and LASIK Applications 129
5. KISA% INDEX. The KISA% index is derived from the product of four indices:
K value, IS value, AST index, and skewed radial axis (SRAX) index (73). At a cutoff point
for KISA% of 100, 280 of 281 participants (99.6%) were correctly classified. The KISA%
index set at 100 is highly sensitive and specific for diagnosing keratoconus, and a range of
60% to 100% can be used to designate or label patients as keratoconus suspects with min-
imal fear of significant overlap with the normal population (0.5%).
6. OTHER INDICES. The highest rate of steepening (HRS) is the highest rate
of corneal power changes (in diopters per millimeter) away from the apex (the point of max-
imum curvature) to the periphery measured along its semimeridian (74). The authors found
that a cutoff value of HRS of 1.40 D/mm has a sensitivity of 95.7% (67/70), a specificity of
96.4% (16 false positive cases), and an accuracy of 96.3% for detection of keratoconus.
Langenbucher and colleagues developed a keratoconus detection scheme with
wavefront parameters based on topography height data (75). A decomposition of corneal
topography height data into orthogonal Zernike polynomials was performed using
the corneal topographer TMS-1. This index was found to perform at least as well (sensi-
tivity in mild/severe keratoconus 93.4%/100%, with a specificity of 100%) as keratoconus
detection schemes based on the KlyceMaeda and the RabinowitzMcDonnell indices.
Clinical approach. The authors use two approaches to screen patients for kerato-
conus. First, patients are graded according to the keratoconus-screening chart proposed by
Azar, which accounts for both topographic features and slit lamp findings (for details see
Chap. 10). As a second step, corneas are measured using the Tomey topographer, and val-
ues for the KCI and KSI are obtained; any patient with any likelihood of the presence of
keratoconus by either index is rejected for LASIK surgery.
Corneal Scarring
The topographic pattern produced by corneal scars depends on the site and size of the scar.
Typically, there is corneal flattening overlying the scar with adjacent corneal steepening.
With larger scars, particularly if they are located in the anterior cornea, the videokerato-
scopic rings may merge into one another and cannot be distinguished well enough for the
topography to be reconstructed accurately, resulting in misleading or absent data (Fig.
8.11A, B).
gue that patients with any form of topographic irregularity should be excluded from un-
dergoing corneal refractive surgery. However, there is growing evidence that patients with
asymmetric inferior steepening may be at risk for developing keratectasia following
LASIK (84), whereas PRK may be a safe option in these instances. Another option in these
patients might be Intacs, assuming that the refractive error is low and there is little pre-ex-
isting refractive astigmatism. Finally, detection of forme fruste keratoconus or other sight-
threatening disorders may not preclude patients from undergoing a noncorneal procedure,
such as implantation of a phakic intraocular lens.
d. Topographically Driven Corneal Ablation
Several studies have addressed the potential role of CVK in determining the ablation pattern
to be employed. Tamayo and Serrano reported promising results performing customized ex-
cimer laser ablation based on the Contoured Ablation Patterns (CAP) software (VISX, Inc.),
which enables the surgeon to control the size, pattern, depth, and location of the ablation
based on the elevation data (85). Alessio and colleagues reported promising results in cor-
recting irregular astigmatism using Corneal Interactive Programmed Topographic Ablation
(CIPTA) (LIGI, Taranto, Italy), which provides customized laser ablation by transferring
programmed ablation from the corneal topography to a flying-spot excimer laser (30).
eyes that have undergone laser refractive surgery. Unfortunately, there is no strict correla-
tion between postoperative symptoms and topographic findings.
In evaluating postoperative CVK, the authors find it useful to examine several dif-
ferent kinds of maps, depending upon the circumstances. The axial radius of curvature
map is useful because the patterns are familiar and abnormal patterns are therefore read-
ily detected. To evaluate more precisely local irregularities, the instantaneous radius of
curvature map provides the requisite detail. Refractive maps best correlate with quality of
vision and are therefore useful to supplement the curvature data. Finally, elevation maps
can sometimes provide detail that is not as obvious in examining the other maps. In
B
Figure 8.11 Corneal scarring: (A) power map, (B) ring image.
132 Wang et al.
Figure 8.12 Elevation map on an eye 3 months postoperatively showing decentered ablation. Pa-
tient has lost two lines of spectacle-corrected visual acuity.
elevation maps, the authors look for local variations in height that may suggest asymme-
try that can contribute to loss of quality of vision (Fig. 8.12).
Several types of topographic patterns can be indicative of the sources of postoperative
visual problems. A central island is a region in the central corneal that receives relatively
less ablation. Multiple causes have been implicated for central islands, but these are found
only in diaphragm-based broad-beam lasers and are most likely produced by fluid that col-
lects as a result of the shock wave produced by the laser pulses (87). Central islands are de-
fined by their diameter and height in millimeters or power in diopters. In the authors expe-
rience, central islands tend to be symptomatic if they measure 1 mm or more in diameter and
are greater than 1 diopter in power. Whereas central islands following PRK tend to regress
over time, central islands of LASIK eyes tend to be more stable and therefore may require
treatment (88).
Decentration of the ablation is usually best seen with the instantaneous radius of cur-
vature, elevation, and difference maps. Decentration can produce regular and irregular
astigmatism with loss of best-correct acuity, glare, and halos. Treatment requires topo-
graphically driven or wavefront-guided ablation.
Other types of topographic abnormalities that can be seen include a variety of un-
classifiable irregular patterns that can have multiple etiologies, including epithelial irregu-
larity, irregular ablation, and postoperative wound healing problems. Examples of wound
healing problems would include visually significant haze or scarring following PRK and
Grade 4 diffuse lamellar keratitis, particularly the variant that has alsobeen called central
toxic keratopathy (Robert K. Maloney, personal communication). In central toxic ker-
atopathy, there is a pronounced stromal melting with marked irregular astigmatism, corneal
thinning, and striae (Fig. 8.13). Spectacle-corrected acuity can be reduced to as low as
20/200 and may require corneal transplantation.
Corneal Topography and LASIK Applications
Figure 8.13 An example of central toxic keratopathy (both eyes), with pronounced stromal melting, corneal thinning, and striae.
Spectacle-corrected visual acuity reducted to 20/32 (right eye) and 20/25 (left eye), respectively.
133
134
Figure 8.14 Patient with apparent central island 4 months following LASIK (upper left). Elevation (lower left) shows higher ele-
vation inferiorly in shape of a peninsula. A 7 m PTK measuring 2.2 mm optical zone with 0.5 mm transition zone was performed de-
centered 0.4 mm inferiorly; this was calculated using VISX CAP software. Note marked improvement in curvature (upper right) and
elevation (lower right) maps.
Wang et al.
Corneal Topography and LASIK Applications 135
CVK is important for determining when the cornea has stabilized following the initial re-
fractive surgical procedure. CVK can also be used to assist in planning the next surgical
procedure. This is particularly relevant if there is a topographic abnormality such as a cen-
tral island or decentration. Certainly, topographic data are essential in planning treatment
of central islands, and outcomes may be enhanced if the ablation can be customized using
special software such as CAP (Fig. 8.14). In the near future, software and hardware devel-
opments, including wavefront-guided ablation, will permit more precise planning and treat-
ment of a range of pre-existing and surgically induced topographic abnormalities.
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138 Wang et al.
NAOYUKI MAEDA
Osaka University Medical School, Osaka, Japan
A. INTRODUCTION
Spherical and cylinder corrections with spectacles for the refractive errors of the eyes have
been performed since the thirteenth and nineteenth centuries. From the latter time, refrac-
tive errors have been measured for sphere and cylinder components in the general oph-
thalmic practice. Although corneal topographic analysis can be performed to evaluate the
corneal irregular astigmatism, and rigid contact lenses can be used to correct corneal irreg-
ular astigmatism, it is still difficult to evaluate the irregular astigmatism components in re-
fraction and to correct for irregular astigmatism with any optical device until recently.
Nevertheless, we will eventually have the means of determining the complete refrac-
tive status including higher-order irregular astigmatism by wavefront sensing and to obtain
supernormal vision (1) with refractive surgery by applying the principle of adaptive op-
tics. In this chapter, the concepts of wavefront analysis and adaptive optics, (2) and the ap-
plication of these to the LASIK procedure, will be presented from an ophthalmologists
point of view.
Similarly, light coming from infinity is considered to be linear bundles of rays in ge-
ometrical optics. In physical optics, the wave from infinity has a plane wavefront, and the
plane of the wavefront is always perpendicular to the direction of the rays.
Although an optical system or lens is usually defined as one that refracts light rays,
it can also be defined as one that transforms the shape of wavefront (Fig. 9.2). If we think
of light emitted from the fovea passing through the lens and cornea towards the outside, the
refractive status, such as myopia, hyperopia, supernormal eyes, and eyes with higher-order
aberrations (irregular astigmatism), can be displayed using wavefronts as shown in Fig. 9.3.
The wavefront of the supernormal eye, that is, an emmetropic eye without any aberrations,
is shown as a perfect plane that is perpendicular to the line of sight. In myopic eyes, the
wavefront has a bowllike shape with the peripheral wavefront more advanced than the cen-
tral wavefront. As the wavefront is perpendicular to the ray, it is easy to imagine that the
peripheral rays go to the primary line of sight and bundles of ray converge on the axis.
The wavefront exiting the hyperopic eye, on the other hand, has a hill shape with the
central wavefront more advanced than the peripheral wavefront. Therefore the rays of a hill
shaped wavefront will diverge. If the measured eye has irregular astigmatism or higher-or-
der aberrations, the wavefront of the eye will have an irregular shape.
2. Wavefront Analysis
The purpose of wavefront analysis is to evaluate the optical quality of the eye by evaluat-
ing the shape of its wavefront. The optical quality of a wavefront is usually expressed as
wavefront aberrations, where wavefront aberration is defined as the deviation between the
wavefront that comes from an ideal optic system and the wavefront that originates from an
actual optical system. The unit used for wavefront analysis is not diopters but microns or
fractions of wavelength, because wavefront expresses the deformity of wavefront shape in
three-dimensional space. It is usually expressed as the root mean square or RMS.
The instruments used for wavefront analysis are called wavefront sensors, and these
instruments are classified into two categories based on their method of measurement, the
ray tracing method and the laser interferometry method. Examples of wavefront sensors
that use ray tracing are the Tscherning aberroscope, the HartmannShack sensor, the cross
cylinder aberroscope, optical path difference, and subjective ray tracing.
Higher-order aberrations in the human eye were measured first by Smirnov (3) in
1961 by a psychophysical method, and he predicted that custom lenses will be made to
compensate for the higher-order aberrations of individual eyes. A modified aberroscope
technique was developed by Howland (4), and Liang and Bille (5) measured the wavefront
aberration of the human eye objectively using the HartmannShack sensor in 1994.
The principle of the HartmannShack sensor is shown in Fig. 9.4. A very narrow
beam of light is projected onto the retina, and the light reflected from the fovea passes
through the lens and cornea and exits from the eye. The HartmannShack sensor has an ar-
ray of lenslets that consist of a matrix of small lenses (2,6). The light emerging from the
eye is focused on a CCD camera by each lenslet to form a spot pattern. The spot pattern of
an ideal subject with a perfect wavefront will be exactly the same pattern as the reference
grid. The spot pattern of a subject with a distorted wavefront will create an irregular spot
pattern. Displacements of lenslet images from their reference position are used to calculate
the shape of the wavefront.
Figures 9.5 and 9.6 show examples of spot patterns from a normal and a keratoconic
subject with the Topcon HartmannShack sensor. Although the spot pattern in the normal
subject is regular, the spot pattern in the patient with keratoconus is markedly distorted. As
the wavefront of each lenslet is perpendicular to the direction of the ray, i.e., displacement
of their focusing spots, the wavefront of the measured subjects can be reconstructed from
these spot patterns.
Wavefront aberrations, the quantitative measure of wavefront distortions, are usually
calculated using Zernike polynomials. The wavefront is expanded into sets of Zernike poly-
nomials to extract the characteristic components of the wavefront. The Zernike polynomi-
als are the combination of trigonometric functions and radial functions, and the terms of the
Zernike polynomials, represented as Z (Fig. 9.7), are useful to show the wavefront aberra-
tions because of their orthogonality (2).
Examples of Zernike polynomials up to the fourth order are shown in Fig. 9.8. The
zero order has one term that represents a constant. The first order represents tilt (two
terms, one for the X axis and another for the Y axis). The second order includes three
terms that represent defocus and astigmatism in the two directions. The third order has
four terms that represent coma and trefoil aberrations. The polynomials can be expanded
up to any arbitrary order unless there are enough numbers of measurements of points for
calculations. Spectacles can correct only second-order aberrations, not the third and
higher orders that represent irregular astigmatism. Using the Zernike coefficients of each
term, monochromatic aberrations can be evaluated quantitatively (7).
The wavefront can also be displayed as color-coded maps as shown in Figs. 9.5 and
9.6. The advancing part of a wavefront is shown by warmer colors and the trailing part of
the wavefront is shown by cooler colors.
3. Adaptive Optics
In general, optical systems, such as cameras, telescopes, fundus cameras, or spectacles,
with lower aberrations have better optical properties. However, even if we minimize the
aberrations in an optical system such as an astronomical telescope or a fundus camera,
the aberrations induced by the atmosphere or the aberrations of normal human eyes are
usually larger than the aberrations in the optic devices, and thus the final resolution of the
images is reduced, i.e., the optical quality is limited by the higher-order aberrations of the
subjects.
Adaptive optics is the concept of intentionally designing the optics of the observatory
system to compensate for the measured aberrations of the subject. As a result, the total aber-
rations of the subject and observatory system are reduced, and one can observe with mini-
mal aberrations.
An example of an adaptive optical system is shown in Fig. 9.9. The wavefront sen-
sor measures the aberrations of the subject, and this information is processed and sent to
actuators. The shape of the deformable mirror is controlled by actuators to reshape the sur-
face of the thin mirror to compensate for the aberration of the subject.
144
Babcock (8) arrived at the concept of adaptive optics in 1953, and this technology
was used for military purposes for a long time. In 1991, much of the United States mili-
tary work in adaptive optics was declassified, and the astronomical community applied this
technology to their field (9). In 1997, Liang and Williams corrected the monochromatic
aberrations of normal human eyes with adaptive optics and showed that this improved the
contrast sensitivity of the eye, and the imaging of cone cells in the living human retina.
With adaptive optics, images of the cone mosaic (short-, medium-, and long-wavelength-
sensitive cones) in living human eyes were observed (10).
If we use an excimer laser in place of the deformable mirror, we have the potential of
correcting irregular astigmatism and obtaining supernormal vision by eliminating the in-
herent optical aberrations of normal human eyes. Although this might not be classified as
adaptive optics by the strictest definition, this concept has become one of the most dis-
cussed topics in refractive surgery.
The question arises whether the current LASIK procedures are satisfactory. For correcting
refractive changes, current LASIK procedures have reasonably good predictability for mild
to moderate myopia and low hyperopia. As a result, most patients are satisfied with the out-
come. This is the one of the major reasons why LASIK has been accepted by the public in
such a short period. However, we have also noticed that the optical quality of the eye fol-
lowing LASIK is not optimal, and LASIK patients sometimes complain about problems
such as halo, glare, or difficulty with night driving. It is also very difficult to treat irregular
astigmatism with conventional LASIK procedures. Thus we must realize that current tech-
niques, while quite satisfactory, still have room to be improved.
The effect of corneal shape on the optical quality of the eye can be calculated as
corneal wavefront aberrations using corneal topography. It is possible to estimate the sur-
gically induced higher-order aberrations of the eye from the measurement of corneal wave-
front aberrations, because wavefront aberrations of the lens should be stable despite the re-
fractive corneal surgeries. The measurement of corneal aberrations showed that
higher-order aberrations of the cornea increased following PRK (11,12,13) and LASIK
146 Maeda
(12). This trend was more prominent for night vision (large pupil) than for day vision (small
pupil). Also, there is a significant correlation between the surgically induced higher-order
aberrations of the cornea and the attempted correction of the surgery (11,13). With the de-
velopment of wavefront sensors, the increase of higher-order aberrations of the eye fol-
lowing a conventional PRK procedure was confirmed (14).
These results suggest that custom ablation methods that can correct irregular astig-
matism or that can reduce surgically induced higher-order aberrations might reduce some
of the problems of the current LASIK procedures.
2. Wavefront-Guided LASIK
When wavefront-guided refractive surgery is performed, the following requirements
should be satisfied for the wavefront sensing and the photo ablation. For the measurement
of wavefront aberrations, wavefront sensors and softwares that can calculate the aberration
are essential. Since 1999, many prototype wavefront sensor instruments have been intro-
duced (Table 1). Figures 9.10, 9.11, and 9.12 show examples of wavefront sensors and
their outputs. Although all of these instruments are prototypes, they should soon be com-
mercially available.
Based on the measured wavefront aberrations, not only spherical and cylindrical er-
rors but also irregular astigmatism (higher-order wavefront aberrations) should be cor-
rectable with the excimer laser. For that purpose, very fine processing of the corneal shape
is required including asymmetrical or local ablations. Therefore laser instruments should
be equipped with a flying spot scanning system or an equivalent mechanism, and an active
eye tracking system is essential for precise ablation (Table 2). In addition, an algorithm that
can perform aberration correction (15) should be provided. The speed of light in the air is
faster than that in the corneal stroma. Therefore the corneal stroma where the wavefront is
delayed should be ablated in order to correct aberrations. The areas that are displayed with
cooler colors in the wavefront map should be cut to reduce the wavefront aberrations in-
cluding sphere, cylinder, and higher-order aberrations.
On June 12, 1999, Seiler and his coworkers reported the first application of wave-
front-guided LASIK. The early results in three eyes (16) were published by his group us-
ing the Wavelight Allegretto excimer laser. The results of this report were promising, as all
148 Maeda
three eyes gained up to two lines of visual acuity, and the wavefront deviations were re-
duced by 27% on the average. In the United States, McDonald started the first wavefront-
guided LASIK with the Autonomous system on October 1999. She has been performing a
comparative study by doing conventional LASIK in one eye and the wavefront-guided
LASIK in the other eye for myopia and hyperopia. Although wavefront-guided LASIK pro-
duced similar uncorrected visual acuity compared to conventional LASIK, a reduction of
higher-order aberrations by wavefront-guided LASIK was found in some cases. Also,
VISX and other laser companies have started clinical trials that evaluate the wavefront-
guided ablations. The safety and the efficacy of this procedure should be reported soon.
Wavefront Technology and LASIK Applications 149
LadarVision 4000 Alcon/Summit/ Flying spot (0.80.9 mm) Laser radar tracker
Autonomous (4000 Hz)
Star S3 VISX Broad beam followed by Infrared tracker (60 Hz)
scanning spot
EC-5000CX Nidek Scanning slit followed Infrared tracker (60 Hz)
by scanning spot
MEL 70 G-Scan Asclepion-Meditec 1.5 mm flying spot Infrared tracker (50 Hz)
Technolas 217Z B&L Dual-diameter flying Infrared tracker (120 Hz)
spot (2 and 1 mm)
Allegretto Wavelight 1 mm flying spot Infrared tracker (250 Hz)
ESIRIS Schwind 1 mm flying spot Infrared tracker (300 Hz)
LaserScan LSX Lasersight Flying spot (0.81 mm) Infrared tracker (60 Hz)
150 Maeda
D. SUMMARY
It is reasonable for refractive surgeons to remove pathological irregular astigmatism or sur-
gically induced aberrations that correlate with pupil diameter or attempt correction by re-
fractive surgeries. On the other hand, we will need to know the clinical significance of su-
pernormal vision, and also when we should correct for higher-order aberrations because
aberrations of refractive surgery candidates do change with age (17,18).
Wavefront-guided refractive surgery has just begun. Many aspects must be improved
to obtain better results than the conventional techniques, as many newly developed surgi-
cal procedures have problems for the first time. We need to know that conventional refrac-
tive surgeries induce higher-order aberrations, and custom ablation appears to be the only
solution.
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10
Preoperative Considerations
Diagnosis, Classification, and Avoidance of
Keratoconus Complications
PAUL CHUNG-SHIEN LU
Chang Gung Memorial Hospital, Taipei, Taiwan, and Harvard Medical School,
Boston, Massachusetts, U.S.A.
DIMITRI T. AZAR
Massachusetts Eye and Ear Infirmary, Schepens Eye Research Institute,
and Harvard Medical School, Boston, Massachusetts, U.S.A.
A. INTRODUCTION
Keratoconus patients have problems with contact lenses and poor visual acuity with
glasses, which contributes to the patients natural tendency to consider refractive surgery.
Keratoconus is a progressive, bilateral, and noninflammatory corneal disease associated
with central and paracentral stromal thinning; it is characterized by anterior and posterior
corneal protrusion, irregular astigmatism, stromal scarring, and decreased visual acuity,
which may reduce the patients ability to achieve 20/20 corrected visual acuity with spec-
tacles (1). Keratoconus may be associated with systemic diseases (Downs syndrome,
Lebers congenital amaurosis, connective tissue disease), trauma (2) (contact lens wear,
eye rubbing), and positive family history (35). Stromal thinning, epithelial iron ring
(Fleischer ring), Vogts striae, and scarring (6) are often noted on slit lamp examination.
Hydrops (Fig. 10.1) is generally associated with advanced keratoconus. Due to the patho-
logic conditions surgical trauma may exacerbate the disease. The corneas may be weakened
by a lamellar cut and cause further corneal instability.
Controversy of diagnosis of keratoconus exists especially in contact lenses wearers
(warpage or molding effects) and in other eye conditions simulating keratoconus, such as
pellucid marginal degeneration, and keratoglobus.
153
154 Lu and Azar
Figure 10.1 The advanced keratoconus with a hydrop in the central cornea. Th