9. Causes of Preterm Labour
Major focus of O & G research.
80% spontaneous onset
50% PTL
30% PPROM
20% due to to intervention for maternal
or fetal indications
10. Four Major Categories
Activation of hypothalamic/pituitary/adrenal
maternal or fetal
Inflammation
Decidual hemorrhage
Uterine over-distention
axis:
11. Activation of HPA Axis
Maternal physical/emotional stress
Placental vasculopathy
Increased
Increased
Increased
secretion
secretion
secretion
of CRH – fetal ACTH
placental estrogen
of placental PG's
Activation of myometrium
12. Inflammation
Both systemic and genital tract infections
Chorioamnionitis in 50% of preterm labours
before 30 weeks' gestation
Can occur with intact membranes
Raised cytokines (interleukins, TNF, GSF)
Enhanced prostaglandin production
13. Bacteria
Some organisms have a direct role in PTL
independent of inflammatory mediators
Psudomonas, staph, strep, bacteroides,
enterobacter produce proteases that can break
down fetal membranes
Can also produce phospholipaseA2 and
endotoxins, stimulating uterine contractions
14. Bacteria
Increased rates of PTL noted in women
GBS, chlamydia and syphilis
with
Risk of PTL reduced by treating:
Asymptomatic bacteriuria
Gonorrhea
BV in high risk patients for PTL
15. Oral Bacteria
Increased rates of PTL noted in women with
periodontal disease
? intrauterine infection following “descent”
from
Case
from
oral cavity
report: Bergeyella bacterium isolated
both the mouth and amniotic fluid of
patient with intact membranes having PTL at
24 weeks
16. Decidual hemorrhage
Vaginal bleeding in more than one trimester
increases risk of PTL 7-fold
Placental histopathology: occult decidual
hemorrhage noted in 36-38% of cases of PTB
PPROM may be related to high concentrations
tissue factor
of
17. Decidual hemorrhage
Decidual TF combines with FVIIa to activate
FX, to generate thrombin
Thrombin is a potent inducer of IL8, causing
localised inflammatory reactions.
Leads to degradation of fetal membrane
extracellular matrix, PPROM
20. Cervical Incompetence
In most cases a secondary
Cervical cone biopsy
LLETZ, laser cone
Increased risk of PTL -
< 37 weeks: OR 3.4
<32 weeks: OR 4.6
<28 weeks: OR 12.4
effect
22. Potentially effective interventions
Progesterone supplements
Smoking cessation
Avoidance of drugs & alcohol
Reduce rate of multiple pregnancy
Cervical cerclage
Reduce occupational stress
Nutrition
Early diagnosis & treatment of infection
23. Progesterone supplements
Most trials use 17-alpha-hydroxyprogesterone
caproate, weekly IMI
Reduction in PTL rates by 15-70%
Most effective in women with previous PTL at
<34 weeks
Increased risk of GDM (OR 2.9)
ACOG recommends use in women with previous
PTL only
No reduction in perinatal mortality
More research needed
24. Stop smoking
Cigarette smoking has a dose-dependent
relationship with preterm labour
Partially due to smoking-related complications
Cessation of smoking likely to be beneficial, but
not proven in RCT’s
26. Reduction in multiple pregnancies
Multiple pregnancies six times more likely to
deliver preterm
Risk increases with increasing no. of fetuses
Valid indication before starting ART
Limit no. of embryos transferrred
27. Cervical Cerclage
Cervical incompetence based on history
ultrasound findings
RCOG study of 1292 women
or
Significant reduction in preterm births<33
weeks
NNT = 25 cerclages
Increased risk of puerperal infection
Increased risk of PTL in twins
28. Reduction of Work Fatigue
Excessive physical demands
increased risk (OR 1.63)
Working > 42 hrs/week
Standing > 6 hrs/day
Low job satisfaction
No RCT’s available
related to
29. Nutritional interventions
No fish consumption linked to excess risk of
PTL
Fish
high
(OR 19.6)
oil supplements: one multi-centre RCT in
risk women showed a significant
reduction in PTL (OR 0.54)
Trial with docosahexanoic acid supplements:
significant prolongation of pregnancy
CARRDIP trial: marked reduction in risk of
preterm labour (1/141 vs 11/149)
30. Early detection and treatment of
infection
Asymptomatic bacteriuria: treatment significantly
reduces risk of PTL or LBW infants (OR 0.60)
Chlamydia, gonorrhea, BV: routine screening not
indicated
Women with previous PTL and +ve for BV may
benefit from treatment
Trichomonas: treatment of asymptomatic women may
increase risk of PTL
31. Case Scenario 1
19 yo G3P1M1 late booking at 22 weeks
Previous preterm delivery at 29 weeks
Heavy smoker, nil alcohol
Works in supermarket as check-out
assistant, prolonged standing
Offensive vaginal discharge
32. Case Scenario 2
35 yo G5P1M3 booking at 9 weeks
Previous preterm delivery at 27 weeks
to placental abruption
Three first trimester miscarriages
Family history of thromboembolism
due
33. Diagnosis of Preterm Labor
No universally accepted definition
Regular uterine contractions and
Cervical dilatation or effacement
35. Treatment of Preterm Labor
No generally accepted criteria for
starting tocolysis
About 30-50% of threatened preterm
labours spontaneously resolve
Treat the underlying cause if possible
37. Objectives of Tocolysis
Delay delivery so that steroids may be
given
Allow safe transport of the mother if
possible
Prolong pregnancy when there are self-
limiting causes of labour e.g. sepsis
38. Contraindications to Tocolysis
APH with hemodynamic instability
Severe pre-eclampsia/eclampsia
Chorioamnionitis
Severe IUGR
Evidence of fetal compromise
Lethal fetal anomaly
Fetal demise
39. Benefits of Antenatal
Reduce risk of:
RDS (RR 0.66)
NEC (RR 0.46)
IVH (RR 0.54)
Severe bruising
Steroids
Systemic infection
(RR 0.56)
in the first 48 hr of life
Admission to NICU (RR 0.80)
Neonatal mortality (RR 0.69)
40. Antenatal Steroids
Effective in women with SROM
Maximum effect at 48 hrs
and PET
Betamethasone 11.4 mg IM 12 hrs apart
Beneficial effects wear off after 2 weeks
No significant maternal side effects
43. BETA-ADRENERGIC RECEPTOR AGONISTS
Mechanism of action:
Cause myometrial relaxation by binding
with beta-2 receptors and increasing
intracellular adenyl cyclase.
Drop in intracellular calcium
Target cells eventually become desensitized
to the effect of beta-adrenergic agonists
(tachyphylaxis).
48. CALCIUM CHANNEL BLOCKERS
Block the influx of Ca+ through the
cell membrane
Reduction of intracellular free calcium
Inhibition of myosin light chain kinase
phosphorylation
Relaxation of uterine muscle
49. EFFICACY OF NIFEDIPINE
Meta-analysis of 12 RCT’s:
Reduction in no. of births within 7 days (RR 0.76)
Reduction in no. of births before 34 weeks (RR 0.83)
Lower risk of RDS (RR 0.63), NEC (RR 0.23), IVH
(RR 0.59), jaundice (RR 0.73)
Fewer maternal side effects (RR 0.14)
50. NIFEDIPINE :
MATERNAL SIDE EFFECTS
Peripheral vasodilator:
Nausea, flushing, headache
Palpitations
Reduction in MAP, reflex tachycardia
Rarely severe hypotension
51. NIFEDIPINE :
FETAL SIDE EFFECTS
Animal studies: reduced uterine
umbilical blood flow
and
No evidence of toxicity in humans
53. NIFEDIPINE
DOSAGE
:
Half-life 2-3 hrs, single dose
20 mg po stat
lasts up to 6 hrs
Repeat 30 mins later if still contracting
Maintenance 20-40 mg qid
Max dose 160 mg in 24 hrs
54. ROUTINE ANTIBIOTICS IN PRETERM
LABOUR WITH INTACT MEMBRANES
Results of ORACLE and meta-analysis:
No improvement in neonatal outcomes
Reduction in maternal infection (RR 0.74)
Uncertainty about optimal antibiotics and
regime
56. MANAGEMENT FOLLOWING TOCOLYSIS:
SEXUALACTIVITY
Observational data only
Higher mortality amongst infected
associated with recent coitus: 11%
infants
vs 2.4%
Increased rates or RDS, jaundice, low Apgar
scores (x 2)
Effect stronger among preterm births
Prudent to suggest avoidance of coitus after
successful tocolysis
57. MANAGEMENT FOLLOWING TOCOLYSIS:
MAINTENANCE TOCOLYSIS
Most RCT’s are small
Endogenous prostaglandins may increase
oxytocin receptor density
Cochrane review of maintenance oral beta-
agonists: no significant benefits
May be useful for temporary relief of painful
contractions
58. MANAGEMENT FOLLOWING TOCOLYSIS:
REPEATED COURSES OF ANTENATAL
STEROIDS
Repeat courses of steroids improve neonatal
pulmonary outcomes, especially in earlier
gestational ages
Evidence of delayed neuronal maturation and
increased risk of IUGR in animal studies
Humans: reduced birth weight only with 4 or
more courses
Catch-up growth by time of discharge from
hospital
59. MANAGEMENT FOLLOWING TOCOLYSIS:
REPEATED COURSES OF ANTENATAL
STEROIDS
Long-term neuro-developmental data not
available
Optimal number of courses of steroids
unknown
Two courses probably safe
60. MANAGEMENT FOLLOWING TOCOLYSIS:
RISK OF IUGR
Threatened PTL may be an indication of fetal
stress arising from unfavourable intrauterine
environment.
Placental pathology: increased incidence of
fetal or maternal vascular lesions without
inflammation
Risk of giving birth to SGA infant (OR 2.2)
Need closer surveillance with USS for growth
and Doppler studies
61. CASE SCENARIO 3
33 y.o
weeks
G1P0 presents to rural hospital at 31
Strong, painful contractions for 3 hours
Slight brownish PV loss
Normal recordings; cephlic presentation
CTG “irritable uterus” pattern
Cervix 2 cm long os closed
How would you manage?
62. CASE SCENARIO 4
21 y.o G2P1 at 29 weeks recently discharged
from hospital following TPL successfully
stopped with nifedipine
Completed course of steroids
Single mother, smokes 20/day
How would you manage her?