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Preterm Labour



     Max Mongelli
 Western Clinical School
  University of Sydney
     Nepean Hospital
Definitions


Threatened pre-term labour
Pre-term labour
Pre-term delivery
Incidence


Approx 5-6% in Australia
More than 10% in the USA
Second leading cause of mortality after
 congenital anomalies
Risk Factors (1)


Stress
Occupational fatigue
Smoking/substance abuse
Poor antenatal care
Risk Factors (2)

Excessive or impaired uterine distension:
  Multiple pregnancy
  Polyhydramnios
  Fibroids
  Uterine anomaly
Risk Factors (3)

Cervical factors:
  History of second trimester loss
  Cervical surgery
  Premature cervical dilatation or
  effacement
Risk Factors (4)

Infections:
   Systemic infections
   STD's
   Pyelonephritis
   Bacteriuria
   Periodontal disease
Risk Factors (5)
Fetal & placental factors:

 Congenital anomalies
 IUGR
 Abruption
 Vaginal bleeding
 Placenta previa
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
Four Major Categories


Activation of hypothalamic/pituitary/adrenal axis:
   maternal or fetal
Inflammation
Decidual hemorrhage
Uterine over-distention
Activation of HPA Axis


Maternal physical/emotional stress
Placental vasculopathy
Increased secretion of CRH – fetal ACTH
Increased secretion placental estrogen
Increased secretion of placental PG's
Activation of myometrium
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
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 phospholipase A2 and
endotoxins, stimulating uterine contractions
Bacteria

Increased rates of PTL noted in women with
GBS, chlamydia and syphilis

Risk of PTL reduced by treating:
  Asymptomatic bacteriuria
  Gonorrhea
  BV in high risk patients for PTL
Oral Bacteria

Increased rates of PTL noted in women with
periodontal disease
? intrauterine infection following “descent”
from oral cavity
Case report: Bergeyella bacterium isolated
from both the mouth and amniotic fluid of
patient with intact membranes having PTL at
24 weeks
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 of
tissue factor
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
Uterine Over-distention


Up-regulation of oxytocin receptors
Formation of gap junctions
PGE2 and PGF
Myosin light chain kinase
Uterine Over-distention


  Polyhydramnios
  Multiple pregnancy
Cervical Incompetence

In most cases a secondary effect
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
Prevention of Preterm
      Labour
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
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
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
Avoidance of drugs and alcohol


      Cocaine
      Alcohol
      ? Cannabis
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
Cervical Cerclage

Cervical incompetence based on history or
ultrasound findings
RCOG study of 1292 women
Significant reduction in preterm births<33
weeks
NNT = 25 cerclages
Increased risk of puerperal infection
Increased risk of PTL in twins
Reduction of Work Fatigue

Excessive physical demands related to
increased risk (OR 1.63)
Working > 42 hrs/week
Standing > 6 hrs/day
Low job satisfaction
No RCT’s available
Nutritional interventions

No fish consumption linked to excess risk of
PTL (OR 19.6)
Fish oil supplements: one multi-centre RCT in
high 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)
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
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
Case Scenario 2

35 yo G5P1M3 booking at 9 weeks
Previous preterm delivery at 27 weeks due
to placental abruption
Three first trimester miscarriages
Family history of thromboembolism
Diagnosis of Preterm Labor


No universally accepted definition
Regular uterine contractions and
Cervical dilatation or effacement
Tests for Prediction of Preterm
            Delivery
Cervico-vaginal
fibronectin
Ultrasound
measurement of
cervical length
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
General Measures


No proven benefits for:

 Bed rest
 Hydration
 Sedation
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
Contraindications to Tocolysis


  APH with hemodynamic instability
  Severe pre-eclampsia/eclampsia
  Chorioamnionitis
  Severe IUGR
  Evidence of fetal compromise
  Lethal fetal anomaly
  Fetal demise
Benefits of Antenatal Steroids
Reduce risk of:
  RDS (RR 0.66)
  NEC (RR 0.46)
  IVH (RR 0.54)
 Severe bruising
 Systemic infection in the first 48 hr of life
 (RR 0.56)
 Admission to NICU (RR 0.80)
 Neonatal mortality (RR 0.69)
Antenatal Steroids


Effective in women with SROM and PET
Maximum effect at 48 hrs
Betamethasone 11.4 mg IM 12 hrs apart
Beneficial effects wear off after 2 weeks
No significant maternal side effects
TOCOLYTIC AGENTS



Betamimetic agents
Nifedipine
NSAIDS
Atosiban
Magnesium sulphate
BETA-ADRENERGIC RECEPTOR AGONISTS
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).
BETA-ADRENERGIC RECEPTOR AGONISTS:
            EFFICACY


Meta-analyses:

 Reduction in no. of births within 48 hrs (RR
 0.63).
 No decrease in no. of births within 7 days
 No change in perinatal mortality
 Marginal decrease in RDS cases
BETA-ADRENERGIC RECEPTOR AGONISTS:
       MATERNAL SIDE EFFECTS



    Tachycardia
    Palpitations
    Lowered blood pressure
    SOB
    Myocardial ischemia
    Pulmonary oedema (0.3%)
    Hyperglycemia, hypokalemia
BETA-ADRENERGIC RECEPTOR AGONISTS:
        FETAL SIDE EFFECTS




     Tachycardia
     Neonatal hypoglycemia
TERBUTALINE:
           DOSAGE



Continuous iv infusion (2.5 mcg/min
increased to max. of 25 mcg/min)
S.C.I. 25 mg stat
Stop if HR>120 or symptomatic
Monitor K+ and BSL
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
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)
NIFEDIPINE :
        MATERNAL SIDE EFFECTS




Peripheral vasodilator:

  Nausea, flushing, headache
  Palpitations
  Reduction in MAP, reflex tachycardia
  Rarely severe hypotension
NIFEDIPINE :
       FETAL SIDE EFFECTS




Animal studies: reduced uterine and
umbilical blood flow
No evidence of toxicity in humans
NIFEDIPINE :
        CONTRAINDICATIONS



Known allergy
LV dysfunction or cardiac failure
Hepatic dysfunction
Concomitant use of magnesium:
       respiratory paralysis
NIFEDIPINE :
                 DOSAGE



Half-life 2-3 hrs, single dose lasts up to 6 hrs
20 mg po stat
Repeat 30 mins later if still contracting
Maintenance 20-40 mg qid
Max dose 160 mg in 24 hrs
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
MANAGEMENT FOLLOWING SUCCESSFUL
          TOCOLYSIS



Optimal approach unknown – limited data

  Prolonged hospitalisation probably of no value
  Bed rest not proven effective
  Avoid physically demanding work
MANAGEMENT FOLLOWING TOCOLYSIS:
        SEXUAL ACTIVITY


  Observational data only
  Higher mortality amongst infected infants
  associated with recent coitus: 11% 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
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
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
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
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
CASE SCENARIO 3



33 y.o G1P0 presents to rural hospital at 31
weeks
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?
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?

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Preterm labour

  • 1. Preterm Labour Max Mongelli Western Clinical School University of Sydney Nepean Hospital
  • 3. Incidence Approx 5-6% in Australia More than 10% in the USA Second leading cause of mortality after congenital anomalies
  • 4. Risk Factors (1) Stress Occupational fatigue Smoking/substance abuse Poor antenatal care
  • 5. Risk Factors (2) Excessive or impaired uterine distension: Multiple pregnancy Polyhydramnios Fibroids Uterine anomaly
  • 6. Risk Factors (3) Cervical factors: History of second trimester loss Cervical surgery Premature cervical dilatation or effacement
  • 7. Risk Factors (4) Infections: Systemic infections STD's Pyelonephritis Bacteriuria Periodontal disease
  • 8. Risk Factors (5) Fetal & placental factors: Congenital anomalies IUGR Abruption Vaginal bleeding Placenta previa
  • 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 axis: maternal or fetal Inflammation Decidual hemorrhage Uterine over-distention
  • 11. Activation of HPA Axis Maternal physical/emotional stress Placental vasculopathy Increased secretion of CRH – fetal ACTH Increased secretion placental estrogen Increased secretion 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 phospholipase A2 and endotoxins, stimulating uterine contractions
  • 14. Bacteria Increased rates of PTL noted in women with GBS, chlamydia and syphilis 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 oral cavity Case report: Bergeyella bacterium isolated from 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 of tissue factor
  • 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
  • 18. Uterine Over-distention Up-regulation of oxytocin receptors Formation of gap junctions PGE2 and PGF Myosin light chain kinase
  • 19. Uterine Over-distention Polyhydramnios Multiple pregnancy
  • 20. Cervical Incompetence In most cases a secondary effect 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
  • 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
  • 25. Avoidance of drugs and alcohol Cocaine Alcohol ? Cannabis
  • 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 or ultrasound findings RCOG study of 1292 women 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 related to increased risk (OR 1.63) Working > 42 hrs/week Standing > 6 hrs/day Low job satisfaction No RCT’s available
  • 29. Nutritional interventions No fish consumption linked to excess risk of PTL (OR 19.6) Fish oil supplements: one multi-centre RCT in high 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 due to placental abruption Three first trimester miscarriages Family history of thromboembolism
  • 33. Diagnosis of Preterm Labor No universally accepted definition Regular uterine contractions and Cervical dilatation or effacement
  • 34. Tests for Prediction of Preterm Delivery Cervico-vaginal fibronectin Ultrasound measurement of cervical length
  • 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
  • 36. General Measures No proven benefits for: Bed rest Hydration Sedation
  • 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 Steroids Reduce risk of: RDS (RR 0.66) NEC (RR 0.46) IVH (RR 0.54) Severe bruising Systemic infection in the first 48 hr of life (RR 0.56) Admission to NICU (RR 0.80) Neonatal mortality (RR 0.69)
  • 40. Antenatal Steroids Effective in women with SROM and PET Maximum effect at 48 hrs 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).
  • 44. BETA-ADRENERGIC RECEPTOR AGONISTS: EFFICACY Meta-analyses: Reduction in no. of births within 48 hrs (RR 0.63). No decrease in no. of births within 7 days No change in perinatal mortality Marginal decrease in RDS cases
  • 45. BETA-ADRENERGIC RECEPTOR AGONISTS: MATERNAL SIDE EFFECTS Tachycardia Palpitations Lowered blood pressure SOB Myocardial ischemia Pulmonary oedema (0.3%) Hyperglycemia, hypokalemia
  • 46. BETA-ADRENERGIC RECEPTOR AGONISTS: FETAL SIDE EFFECTS Tachycardia Neonatal hypoglycemia
  • 47. TERBUTALINE: DOSAGE Continuous iv infusion (2.5 mcg/min increased to max. of 25 mcg/min) S.C.I. 25 mg stat Stop if HR>120 or symptomatic Monitor K+ and BSL
  • 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 and umbilical blood flow No evidence of toxicity in humans
  • 52. NIFEDIPINE : CONTRAINDICATIONS Known allergy LV dysfunction or cardiac failure Hepatic dysfunction Concomitant use of magnesium: respiratory paralysis
  • 53. NIFEDIPINE : DOSAGE Half-life 2-3 hrs, single dose lasts up to 6 hrs 20 mg po stat 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
  • 55. MANAGEMENT FOLLOWING SUCCESSFUL TOCOLYSIS Optimal approach unknown – limited data Prolonged hospitalisation probably of no value Bed rest not proven effective Avoid physically demanding work
  • 56. MANAGEMENT FOLLOWING TOCOLYSIS: SEXUAL ACTIVITY Observational data only Higher mortality amongst infected infants associated with recent coitus: 11% 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 G1P0 presents to rural hospital at 31 weeks 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?