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Contraception Lecture

The document discusses various methods of contraception, including oral contraceptives, injectables, intrauterine devices, and barrier methods, along with their mechanisms of action, efficacy, and contraindications. It highlights factors influencing the choice of contraceptive methods and provides detailed information on specific types such as combined oral contraceptives and progestin-only pills. Additionally, it addresses the importance of proper usage and management of missed doses for effective contraception.

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0% found this document useful (0 votes)
24 views76 pages

Contraception Lecture

The document discusses various methods of contraception, including oral contraceptives, injectables, intrauterine devices, and barrier methods, along with their mechanisms of action, efficacy, and contraindications. It highlights factors influencing the choice of contraceptive methods and provides detailed information on specific types such as combined oral contraceptives and progestin-only pills. Additionally, it addresses the importance of proper usage and management of missed doses for effective contraception.

Uploaded by

kansabwaroyd02
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPT, PDF, TXT or read online on Scribd

Contraception

Dr Bellington Vwalika
Obstetrician and
Gynaecologist-UTH
Honorary Lecturer -UNZA
Definition

 Theprevention of an unwanted pregnancy


using a contraceptive which acts by
preventing fertilization of the ovum by
spermatozoa

2
Measurement of Contraception

 Pearl Index

 Life table Analysis

3
Methods available

 Oral contraception  Withdrawal


 Injectables  Natural
 Intrauterine devices  Sterilization
 Implants
 Barrier

4
Factors affecting choice of method

Whether or not a  is easy to obtain


method:  is easy to use and
 is permanent or discontinue
reversible  has frequent or
 is effective undesirable side effects
 is inexpensive
 is perceived to be safe

5
Factors affecting choice cont’d

 can be used while  requires partner


b/feeding cooperation
 must be used each time
 protects against STIs the couple have sexual
intercourse

6
‘Contraceptive Method Mix’

 Refersto the variety of contraceptives


available to clients through a family planning
programme

7
Combined oral contraceptives
(COCs)

 Consists of oestrogen (E) and progestin (P)


 Monophasic pills - same dose of E/P all through the
course
 Biphasic pills - fixed dose or E/P & more P in the last
14/7
 Triphasic pills - variable dose of E/P
 Sequential pills - fixed dose of E, No P for first 7/7
then P for 14/7

8
Mechanism of action
- COCs

 Prevents ovulation by inhibiting


gonadotrophin secretion via an effect on both
pituitary and hypothalamic centres
 The progestin suppresses LH secretion (&
thus prevents ovulation, while the
oestrogenic agent suppresses FSH secretion
(& thus prevents the selection and
emergence of a dominant follicle

9
Efficacy of COC

 Typical usage is associated with a 3.0%


failure rate during the first year of use

 Efficacydecreases significantly when the


oestrogen component is removed

10
Absolute contraindications to COC
use

 thrombophlebitis,  undiagnosed abnormal


thromboembolic vaginal bleeding
disorders, CVA,  known or suspected
coronary occlusion pregnancy
 markedly impaired liver  smokers over the age
function of 35 years
 known or suspected
breast cancer

11
Relative contraindications to COC
use

 Migraine headaches  H/O obstructive


 Hypertension jaundice in pregn
  Sickle cell disease or
H/O gestational
diabetes sickle C disease
  Diabetes mellitus
Elective surgery
  Gall bladder disease
Epilepsy

12
Clinical problems associated with
COCs

 Breakthrough bleeding  Ovarian cysts


 Amenorrhoea  Drugs that affect
 weight gain efficacy
  Migraine headaches
Acne

13
Non-Contraceptive Benefits of
OCs

These can broadly be grouped into two main


categories:
 Benefits that incidentally accrue when OC is
specifically utilized for contraception &;
 Benefits that result from the use of OCs to
treat problems or disorders

14
Non contraceptive incidental
benefits of OCs

 less PID
 effective contraception  less rheumatoid arthritis
 less endometrial cancer  increased bone density
 less ovarian cancer  ~ less endometriosis
 fewer ectopic pregns.  ~ less benign breast disease
 more regular menses  ~ fewer ovarian cysts

15
OC as treatment

 DUB  hormone therapy for


 dysmenorrhoea hypothalamic
 amenorrhoea
mittelschmerz
 control of bleeding
 endometriosis
 ~ functional ovarian
prophylaxis
 cysts
acne & hirsutism
 ~ premenstrual
syndrome

16
Pill taking

 Effective contraception is present during the


first cycle of pill use, provided the pills are
started no later than the 5th day of the cycle
and no pills are missed

17
Missed Pills

 If a woman misses 1 pill, she should take that


pill as soon as she remembers and take the
next pill as usual. No back-up is needed.
 If she misses 2 pills in the first two weeks,
she should take two pills on each of the next
two days, and back-up for the next 7 days

18
Missed pills cont’d

 If2 pills are missed in the third week, or if


more than 2 active pills are missed at any
time, another form of contraception should
be used as back-up immediately and for 7
days or start a new pack with back-up for 7
days

19
The Progestin-Only Pill (POP)
Minipill

 Theminipill contains a small dose of


progestational agent (25% of that in COC)
and must be taken daily, in a continuous
fashion

20
Mechanism of Action - POP

The contraceptive effect is more dependent


upon endometrial and cervical mucus effects,
since the gonadotrophins are not consistently
suppressed
 The endometrium involutes and becomes
hostile to implantation and the cervical
mucus becomes thick and impermeable

21
POP cont’d

 There are no significant metabolic effects


(lipid levels, CHO metabolism and
coagulation factors remain unchanged)
 There is an immediate return to fertility upon
discontinuation
 Failure rates range form 1.1 to 9.6% per 100
women in the first year of use

22
POP cont’d

Pill taking
 The minipill should be started on the first day
of menses and a back-up method must be
used for the first 7 days
 The pill should be taken at the same time of
the day
 If more than 3 hours late in taking a pill, a
back-up method should be used for 48 hours
23
Problems associated with POP

POP have unpredictable  20% total lack of cycles


effect on ovulation ranging from irregular
 40% of patients can bleeding to spotting and
expect to have normal amenorrhoea
ovulatory cycles  development of
 40% short irregular functional cysts
cycles  levonorgestrel minipill
may be associated with
acne

24
POP

There are two situations where excellent


efficacy is achieved:
 In lactating women, the contribution of the
minipill is combined with prolactin-induced
suppression of ovulation adding up to very
effective protection
 In women over age 40, reduced fecundity
adds to the minipill’s effects.
25
Implant contraception -
NORPLANT

 Progestin circulating at levels 1/4 to 1/10 th of


those in COC, prevents conception by
suppressing ovulation and thickening cervical
mucus to inhibit sperm penetration
 Side effects include changes in menstrual
patter, weight gain, headache, and effects on
mood

26
NORPLANT

 consists of 6 capsules  the capsules release ~


34mm in length, 2.4 80 micro grams of
mm outer diameter, levonorgestrel per 24
containing 36 mm hours during the first 6-
crystalline 12 months of use
levonorgestrel.  once inserted have an
 the 6 capsules contain effective life of 5 years
a total of 216 mg of
levonorgestrel which is
very stable
27
The mechanism of action

 Suppression at both the hypothalamic and


pituiatry LH surge necessary for ovulation
 The constant level of progestin has a marked
effect on the cervical mucus
 Suppression of the estradiol-induced cyclic
maturation of the endometrium and
eventually causes atrophy

28
Disadvantages of NORPLANT

 disruption of bleeding  implants can be visible


patterns in up to 80% of under the naked eye
users  does not protect
 implants must be against STI/HIV
inserted and removed  acne
in a surgical procedure  30% of pregnancies are
by trained personnel
ectopic

29
Absolute contraindications

 active thrombophlebitis  benign or malignant


or thromboemboilc liver tumours
phenomena  known or suspected
 undiagnosed genital breast cancer
bleeding
 acute liver disease

30
IMPLANON

A single implant 4 cm long contains 60 mg of


3-keto desogestrel
 The hormone is released at a rate of about
60 micro grams per day
 Is designed to be provide contraception for 2-
3 years
 Efficacy and side effects are similar to those
or NORPLANT
31
Jadelle

 Two rods containing 75mg LNG crystals embedded


in a coplolymer and encased in silastic tubing
 Rods are 43mm long and 2.5mm wide
 Lasts for 5 years
 Rods are easier and more convenient to insert and
remove
 Norplant and Jadelle are bioequivalent over 5 years
of use

32
Injectable Contraception:
Depo-Provera

 Comes as microcrystals, suspended in an


aqueous solution
 Correct dose is150 mg IM (gluteal or deltoid)
every 3 months
 Relies on higher peaks of progestin to inhibit
ovulation and thicken cervical mucus. The
progestin level is high enough to block the
LH surge
33
Depo-Provera
cont’d

 The injection should be given within the first


5 days of the current menstrual cycle,
otherwise a back-up method is necessary for
2 weeks
 The injection must be given deeply in muscle
by the Z-track technique and not massaged

34
Depo-Provera
Advantages

 easy to use, no daily or  free from eostrogen


coital acton required related problems
 safe no serious health  private use not
effects detectable
 effective as sterilization,  enhances lactation
IUCD & implant  has noncontraceptive
contraception benefits

35
Depo-Provera
Disadvantages

 irregular menstrual  can’t be removed


bleeding  return to fertility is
 breast tenderness delayed
 weight gain  regular injections
 depression required
 no STI/HIV protection

36
Depo-Provera
Absolute contraindications

 Pregnancy

 Unexplained genital bleeding

37
Intrauterine Contraception

Types of IUDS

 Unmedicated IUDs -Lippes Loop


 Copper IUDs - TCu-380A, Tcu-220C, Nova
T, Mulitload-375
 Hormone-releasing IUDs - Progestasert

38
IUDS
Mechanism of Action

 The mechanism of action is the production of


an intrauterine environment that is
spermicidal

 Ovulation is not affected nor is the IUD an


abortifacient

39
Efficacy of IUDS

 The actual failure rate in the first year is


approximately 3%, with a 10% expulsion
rate, and a 15% rate of removal, mainly for
bleeding and pain.
 The non medicated IUDs never have to be
replaced

40
Timing of IUD insertion

 An IUD can be safely inserted at any time


after delivery, abortion or during the
menstrual cycle

 The IUD can also be inserted at Caesarean


section

41
IUD Use
and Medical conditions

 a woman with a H/O  women at risk of


ectopic pregn can use a bacterial endocarditis
copper IUD or the should receive
Levonorgestrel IUD prophylactic antibiotics
 a progestin releasing at insertion & removal
IUD should be  current, recent, or
considered for women recurrent PID is a
with bleeding disorder contraindication for IUD
use

42
Pregnancy with IUD in situ

 Spontaneous abortion - 40-50%, IUDs should


be removed if pregnancy is diagnosed and the
strings are visible
 Septic abortion - there is no evidence that there
is an increased risk of septic abortion if pregn
occurs, other than with the Dalkon Shield
 Pre-term labour and birth - incidence is
increased 4-fold

43
Barrier methods

Have been the most widely used contraceptive


technique throughout recorded history.
 Spermicides - 21% failure rate
 Cervical cap - 18-28%
 Sponge - 18%
 Diaphragm - 18%
 Condom - 12%

44
Periodic abstinence

 Is keyed to the observation of naturally


occurring signs and symptoms of the fertile
phase of the menstrual cycle.
 It takes into account the viability of sperm in
the female reproductive tract and the life
span of the ovum

45
Methods of Periodic abstinence

 Rhythm of Calender method

 Cervical Mucus method

 Symptothermal method

46
Periodic abstinence

Periodic abstinence is associated with good


efficacy when used correctly and consistently
and the following rules are observed:
 No intercourse during mucus days
 No intercourse within 3days after peak
fecundity
 No intercourse during times of stress

47
Withdrawal

 Involves removal of the penis from the


vagina before ejaculation takes place
 1st year failure rate - 18%
 Some sperm may be released before
ejaculation
 Is a better method than using no method at
all

48
Lactational Amennorrhoea Method
(LAM)

 High concentrations of prolactin work at both


central and ovarian sites to produce
lactational amenorrhoea and anovulation

 Elevated levels of prolactin inhibit the


pulsatile secretion of GnRH

49
LAM

 Onlyamenorrhoeic women who


exclusively breastfeed at regular intervals,
including at nighttime, during the first 6
months have the contraceptive protection
equivalent to the provided by oral
contraception

50
LAM

 With menstruation or after 6 months, the risk


of ovulation increases
 Supplemental feeding increases the risk of
ovulation (and pregnancy) even in
amenorrheic women
 Total protection against pregnancy is
achieved by exclusively b/feeding for 10
weeks
51
B/feeding and Contraception

The rule of 3s
 In the presence of FULL b/feeding, a
contraceptive method should be used
beginning in the 3rd postpartum month
 With PARTIAL b/feeding or NO b/feeding, a
contraceptive method should begin during
the 3rd postpartum week

52
B/feeding and Contraception

 Oral contraception even in low doses


diminishes the quantity and quality of breast
milk

 Depo-provera does not affect breast feeding

53
B/feeding and Contraception
cont’d

 Periodic abstinence cannot be used with a


great deal of confidence
 Barrier methods are an excellent choice for
motivated couples
 IUDs can be inserted after vaginal or C/S

54
Female Sterilization

 Unipolar coagulation
 Postpartum tubal excision
 Silastic (Falope or Yoon) ring
 Interval tubal excision
 Bipolar coagulation
 Hulka-Clemens clip/Filshie clip

55
Advantages of female sterilization

 Very effective-failure one in 200


 Permanent
 Nothing to remember
 No interference with sex
 Increased enjoyment-no worries
 No effect on milk
 No health risks
 Can be done soon after birth

56
Disadvantages

 Painful for few days


 Uncommon complications of surgery
– Infection
– Internal infection and bleeding
– anaesthetic risks
– Death
– Ectopic
– Requires trained staff
– Reversal difficult and expensive
– No protection against STI
– No method of proving effectiveness

57
Male Sterilization

 Standard vasectomy

 “No scalpel” technique

58
Advantages of vasectomy

 Very effective-failure 1/700


 Permanent
 Nothing to remember after 20 ejaculations or
3 months
 No interference with sex
 Increased enjoyment
 No apparent longterm health risks

59
 Easier to perform,less expensive
 Able to test for efectiveness at any time

60
disadvantages

 Complications of surgery
– Discomfort for 2-3 days
– Pain in scrotum
– Brief feeling of faintness
– Bleeding
– Blood clots in scrotum
 Requires someone trained
 Not immediately effective-unless after 20
ejaculations or 3/12

61
 Reversal expensive
 No STI protection

62
Reversal of Sterilization

 Pregnancy rates correlate with the length of


remaining tube, a length of 4 cm or more is
optimal
 Pregnancy rates are lowest with
electrocoagulation, and reach 70-80% with clips,
rings and surgical methods such as the
Pomeroy
 About 2 per 1000 women will eventually
undergo tubal anastomosis
63
counselling

 Consider reason for request


 Age
 Permanet
 Irreversible
 Explain procedure
 Failure rate

64
Medical methods for the Male

 Hormonal contraception is inherently a


difficult physiological problem, because
unlike cyclic ovulation in the female,
spermatogenesis is continuous

65
Medical methods for the Male

 Sex steroids reduce testosterone synthesis


which leads to loss of libido and development
of female 2o sexual characteristics. Sperm
counts are not reduced adequately
 GnRH analogues also decrease endogenous
synthesis of testosterone, and supplemental
testosterone must be provided

66
Medical methods for the Male

 Gossypol a derivative of cotton seed oil,


effectively decreases sperm counts to
contraceptive levels, by incapacitating the sperm
producing cells
 The pills are taken daily for 2 months until sperm
are no longer observed in the ejaculate, and then
weekly
 Fertility returns to normal 3 months after
discontinuation
67
Emergency Contraception

 Emergency contraception methods can


prevent pregnancy after unprotected
intercourse, method failure or incorrect
method use
 Can help reduce unplanned pregnancies,
many of which result in unsafe abortion

68
Emergency contraception
methods

 Combined oral contraceptive pills

 Progestin only pills

 Intra uterine contraceptive device

69
Oral contraceptive pills

 Emergency contraceptive pills use the same


ingredients as regular contraceptives
 Should be initiated ideally within 3 days (72
hours) of unprotected intercourse
 Should be taken in two doses 12 hours apart

70
COC

 Eachof the two doses of COC should


contain at least 100 ug (0.10 mg) Ethinyl
Estradiol (EE) and 500 ug (0.50 mg)
Levonorgestrel

71
COC

PC-4, Eugoynon 50, Neogynon, Noral, Nordiol,


Ovidon, Ovral, Ovran

 Two tablets per dose: each tablet contains


50 ug EE & either 0.25mg or 0.50 mg
levonorgestrel

72
COC

LoFemenal, Microgynon 30, Nordette, Ovral L,


Rigevidon

 Four tablets per dose: each tablet contains


30 ug EE & either 0.15 mg or 0.30 mg
Levonorgestrel

73
POP

 Eachof the two doses of POP contraceptives


should contain at least 0.75 mg
Levonorgestrel

74
POP

 Ovrette - 20 tablets per dose, each tablet


contains 0.0375 mg Levonorgestrel
 Microlut, Microval, Norgestron - 25 tablets
per dose, each tablet contains 0.03mg
Levonorgestrel

75
IUCDs

 Copper T and others

 Insertionwithin 120 hours (five days) of


unprotected intercourse

76

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