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Prelabor Rupture of Membranes (PROM) : DR Yonas G

This document summarizes prelabor rupture of membranes (PROM), also known as premature rupture of membranes. PROM occurs in about 10% of pregnancies and is defined as the spontaneous rupture of membranes before the onset of labor, after 28 weeks of gestation. It discusses the risk factors, diagnosis, differential diagnosis, investigations, complications, and management of term and preterm PROM. Management depends on factors like gestational age, fetal presentation, likelihood of lung maturity, and presence of infection. Conservative management of preterm PROM includes bed rest, monitoring, antibiotics, and corticosteroids if between 23-34 weeks. Chorioamnionitis is treated with antibiotics and may require early delivery.

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0% found this document useful (0 votes)
176 views19 pages

Prelabor Rupture of Membranes (PROM) : DR Yonas G

This document summarizes prelabor rupture of membranes (PROM), also known as premature rupture of membranes. PROM occurs in about 10% of pregnancies and is defined as the spontaneous rupture of membranes before the onset of labor, after 28 weeks of gestation. It discusses the risk factors, diagnosis, differential diagnosis, investigations, complications, and management of term and preterm PROM. Management depends on factors like gestational age, fetal presentation, likelihood of lung maturity, and presence of infection. Conservative management of preterm PROM includes bed rest, monitoring, antibiotics, and corticosteroids if between 23-34 weeks. Chorioamnionitis is treated with antibiotics and may require early delivery.

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© © All Rights Reserved
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Dr yonas G

Prelabor rupture of membranes


(PROM)
PROM
 Definition:
 Previously known as premature rupture of membranes
PROM is the Spontaneous premature rupture of membranes
after 28 weeks of gestation and before the onset of labor.(at
least one hr)
 Occurs in ~ 10% of pregnancies
Term PROM: after 37 weeks
Preterm PROM: Before 37 weeks
Latency period: time between rupture of membranes to
onset of labor.
Prolonged PROM: latency longer than 12 hrs.
RISK FACTORS 
Incidence: average around 10%, ranges 3-19 %.
The pathogenesis of PPROM is not completely
understood.
It shows association with
A history of PPROM in a previous pregnancy,
Genital tract infection,
APH
Cigarette smoking
Low socioeconomic status
Polyhydramnios
Cervical incompetence
Multiple pregnancy
Emergency circlage
PROM- Dx
Diagnosis is generally clinical
History:
 a sudden "gush" of clear or pale yellow fluid from the vagina.
 Intermittent or constant leaking of small amounts of fluid or
 just a sensation of wetness within the vagina or on the perineum
Physical findings:
 Negative uterine size discrepancy
 Meconium or vernix on the vulva
 Sterile speculum examination with or without valsalva
maneuver( leakage or pooling)
 direct observation of amniotic fluid coming out of the cervical canal or
pooling in the vaginal fornix
NB
 Digital examination should be avoided unless induction is
planned or the woman is in labor because it may decrease the
latency period (i.e., time from rupture of membranes to
delivery) and increase the risk of intrauterine infection
Diagnosis-cont’d
• Nitrazine paper test:….
– Testing the pH of the vaginal fluid (color change to blue
– Amniotic Fluid- alkaline (PH~7.3)
– False positive result alkaline fluids in the vagina Eg blood, semen,
bacterial vaginosis, and trichomoniasis
 Ferning Test :arborization (ferning).
– Fluid from the posterior vaginal fornix is swabbed onto a glass slide and
allowed to dry for at least 10 minutes.
– Amniotic fluid produces a delicate ferning pattern ( High Na+ and
protein contents)
 Pad Test Perineal pad wetting
 Dye test -a definitive dx  in equivocal cases,
-1 mL of indigo carmine dye in 9 mL of sterile saline
– Tampoon placed in the vagina inspected after 30 min for blue staining
 Ultrasonography- decreased AF volume
PAMG-1 (AmniSure) Rapid slide test that uses
immunochromatography methods to detect trace amounts of
placental alpha microglobulin-1 protein in vaginal fluid.
- not affected by semen or trace amounts of blood
Ferning Pattern
PROM- Differential diagnosis
Stress Urinary incontinence
Vaginal discharge (Leucorrhea gravidarum or
pathological)
Perspiration
PROM- investigations
CBC
U/A, Culture & Sensitivity
High vaginal swab for culture
Phosphatidylglycerol from vaginal pool (for fetal lung
maturity)
Complications of PROM
 Preterm Labor
In Preterm PROM, labor starts in 70-80% of cases in one week
time
 Ascending infection: one third
 Increased incidence of cord prolapse
 Fetal pulmonary hypoplasia
 Prematurity
 Operative delivery
 Abruption
 facial deformation, and orthopedic abnormalities esp at early GA
PROM- Management
Management of pregnancies complicated by PROM
depends on
Fetal conditions
 Gestational age
 Fetal presentation (breech and transverse lies are unstable and may
increase the risk for cord prolapse)
 Likelihood of fetal lung maturity
 Availability of neonatal intensive care
 Fetal heart rate (FHR) tracing pattern
Cervical condition
 Cervical status (by visual, not digital, inspection unless induction is
planned or the woman is in labor)
Presence or absence of maternal/fetal infection
Presence or absence of labor
Indications for pregnancy termination in
PROM
 Cessation of fluid leakage is rare, except in women with
PPROM related to amniocentesis
Term PROM
Labor
Presence of infection (chorio amnionitis)
IUFD
Congenital anomalies of fetus incompatible to life
Abnormal fetal surveillance
Preterm PROM
GA > 34 weeks either conservative management or
termination
GA< 34 weeks, conservative management
Components of conservative management:
– Avoid digital vaginal examination
– Bed rest
– Monitor maternal PR, Temp., FHR every 4 hours
– CBC, U/A, ESR/CRP twice per week
– BPP/NST twice per week
– Administer antibiotics: ampicillin (iv)+ erythromycin X 48hrs
followed by amoxicillin (po) & erythromycin to complete a
total of seven days.

Drug regimen
A regimen with reasonable activity against the major
pelvic pathogens should be used for prophylaxis, but the
optimal regimen is unclea
Up todate preference:
●Azithromycin one gram orally upon admission, PLUS
Ureaplasmas, Chlamydia trachomatis
●Ampicillin 2 g intravenously every 6 hours for 48 hours,
FOLLOWED BY Amoxicillin 500 mg orally three times
daily or 875 mg orally twice daily for an additional five days
-group B Streptococcus (GBS),
-many aerobic gram-negative bacilli, and some anaerobes
Corticosteroids
if 23 and 34 weeks of gestation
duration of neonatal respiratory support were significantly
reduced by antenatal glucocorticoid treatment
Neonatal death,
 respiratory distress syndrome,
intraventricular hemorrhage (IVH),
necrotizing enterocolitis (NEC), and
Does not increase either maternal or neonatal infection
Mean risk reduction for these adverse events ranged from 30
to 60 percent
 TIMING BEFORE DELIVERY — 2-7 days after
administration of the first dose of antenatal corticosteroids.
 Efficacy is incomplete <24 hours from administration and appears to
decline after 7 days
Chorioamnionitis
 Clinical or subclinical
 Criteria for clinical chorioamnionitis:
- Maternal temperature > 38o C
- Maternal &/ or fetal tachycardia
- Uterine tenderness
- Foul smelling amniotic fluid
- High WBC count
Sub clinical chorioamnionitis
 Amniocentesis: intramniotic infection is present if:
1. Culture: bacterial colony count > 102 / ml fluid
2. Presence of bacteria on gram stain
3. Glucose level<15 mg/dl
4. WBC> 100/ml
Management of chorioamnionitis
 Antibiotics:
1. Ampicillin+ Gentamycin+
clindamycin/metronidazole/chloramphenicol
2. Ceftriaxone +/- metronidazole
 Terminate pregnancy: Vaginal route is preferred
PROM
( uncomplicated)

GA< 34 weeks
GA 34-37 weeks GA> 37 weeks
Conservative
Deliver/conservative Deliver
management
Thank you !!!

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