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INDUCTION OFINDUCTION OF
LABOURLABOUR
Dr Max MongelliDr Max Mongelli
Women & Childrens’ HealthWomen & Childrens’ Health
Nepean HospitalNepean Hospital
DefinitionsDefinitions
IOL: “Iatrogenic stimulation of uterineIOL: “Iatrogenic stimulation of uterine
contractions to accomplish delivery prior to thecontractions to accomplish delivery prior to the
spontaneous onset of labour”spontaneous onset of labour”
Cervical priming: Interventions designed toCervical priming: Interventions designed to
improve the Bishop score without necessarilyimprove the Bishop score without necessarily
inducing labourinducing labour
PrevalencePrevalence
 USA: frequency has increased from 9.5%USA: frequency has increased from 9.5%
to 22.5% over 16 yearsto 22.5% over 16 years
 Due to availability of better cervicalDue to availability of better cervical
ripening agents, more relaxed attitudesripening agents, more relaxed attitudes
towards marginal indications fortowards marginal indications for
inductioninduction
IndicationsIndications
 MaternalMaternal
 FetalFetal
Maternal IndicationsMaternal Indications
Maternal IndicationsMaternal Indications
 Pre-eclampsia/EclampsiaPre-eclampsia/Eclampsia
 Severe hypertensionSevere hypertension
 Gestational diabetesGestational diabetes
Pelvic arthropathyPelvic arthropathy
 Obstetric cholestasisObstetric cholestasis
 Severe cardio-respiratory diseaseSevere cardio-respiratory disease
 ““Social”Social”
 AnticoagulationAnticoagulation
Fetal IndicationsFetal Indications
Fetal IndicationsFetal Indications

Post-term pregnancyPost-term pregnancy
 IUGRIUGR
 Obstetric cholestasisObstetric cholestasis
 PROMPROM
AmnionitisAmnionitis
 Fetal demiseFetal demise
ContraindicationsContraindications
ContraindicationsContraindications
 Classical C/S scarClassical C/S scar
 Transmural myomectomy scarTransmural myomectomy scar
 Placenta or vasa previaPlacenta or vasa previa
 Active genital herpesActive genital herpes
 Large cervical fibroidsLarge cervical fibroids
 MalpresentationMalpresentation
 Cord presentation or prolapseCord presentation or prolapse
 Severe IUGRSevere IUGR
 Abnormal or non-reactive CTGAbnormal or non-reactive CTG
Pre-Induction AssessmentPre-Induction Assessment
 Confirm valid indicationConfirm valid indication
 Exclude contraindicationsExclude contraindications
 Patient information and consentPatient information and consent
 Bishop scoreBishop score
Pre-Induction Assessment:Pre-Induction Assessment:
Bishop ScoreBishop Score
Modified Bishop scoreModified Bishop score
Significance of Bishop scoreSignificance of Bishop score
If Bishop score >5 chance of vaginalIf Bishop score >5 chance of vaginal
delivery after IOL same as afterdelivery after IOL same as after
spontaneous onset of labourspontaneous onset of labour
Predictors of Successful IOLPredictors of Successful IOL
Other Predictors of Successful IOLOther Predictors of Successful IOL
 MultiparityMultiparity
 Tall stature ( > 5 ft 5” or 165 cm)Tall stature ( > 5 ft 5” or 165 cm)
 Normal BMINormal BMI
 Increasing GAIncreasing GA
 EFW < 3500 gEFW < 3500 g
Methods for Induction of LabourMethods for Induction of Labour
MethodsMethods
 Membrane strippingMembrane stripping
 Mechanical methodsMechanical methods
 AmniotomyAmniotomy
 OxytocinOxytocin
 ProstaglandinsProstaglandins
Membrane StrippingMembrane Stripping
 Finger through cervical os, to detach membranesFinger through cervical os, to detach membranes
from LUSfrom LUS
 Usually from 39 weeks onwardsUsually from 39 weeks onwards
 Can be repeated safelyCan be repeated safely
 Reduced risk of going beyond 41 (RR 0.59)Reduced risk of going beyond 41 (RR 0.59)
 Reduced frequency of formal IOL (NNT =8)Reduced frequency of formal IOL (NNT =8)
 May cause slight PV bleeding and crampsMay cause slight PV bleeding and cramps
Mechanical MethodsMechanical Methods
 Required for low Bishop scoresRequired for low Bishop scores
 Ideal when PG’s relatively contraindicatedIdeal when PG’s relatively contraindicated
 Foley’s catheterFoley’s catheter
 ATAD catheterATAD catheter
 LaminariaLaminaria
Induction of labour
Induction of labour
Induction of labour
Induction of labour
AmniotomyAmniotomy
 Usually when cx is partially dilatedUsually when cx is partially dilated
 Usually combined with oxytocinUsually combined with oxytocin
 Colour of amniotic fluid should beColour of amniotic fluid should be
notednoted
Induction of labour
Risks of AmniotomyRisks of Amniotomy
 Fetal hemorrhage if vasa previaFetal hemorrhage if vasa previa
 Cord prolapse, esp with high headCord prolapse, esp with high head
 InfectionInfection
Induction of labour
OxytocinOxytocin
 Almost always after amniotomyAlmost always after amniotomy
 Given i.v. by infusion pump because of short half-lifeGiven i.v. by infusion pump because of short half-life
 May take up to 40 mins to reach steady-stateMay take up to 40 mins to reach steady-state
concentrationsconcentrations
 May be stopped once active phase of labour establishedMay be stopped once active phase of labour established
 Continuous CTG monitoring requiredContinuous CTG monitoring required
Oxytocin regimesOxytocin regimes
 Low-dose: less likely to cause hyperstimulationLow-dose: less likely to cause hyperstimulation
 High dose: short incremental time intervals, noHigh dose: short incremental time intervals, no
more than 40 iu/minmore than 40 iu/min
 Pulsatile regime: boluses at 8-10 min intervals,Pulsatile regime: boluses at 8-10 min intervals,
reduced total overall dose of of oxytocinreduced total overall dose of of oxytocin
Risks of OxytocinRisks of Oxytocin
 Hyperstimulation / tachysystoleHyperstimulation / tachysystole
 Uterine ruptureUterine rupture
 High dose: water intoxicationHigh dose: water intoxication
 Increased risk of PPHIncreased risk of PPH
Induction of labour
Induction of labour
ProstaglandinsProstaglandins
 Required for low Bishop scoresRequired for low Bishop scores
 PGE2 gel or pessariesPGE2 gel or pessaries
 Slow-release systemsSlow-release systems
 MisoprostolMisoprostol
Prostanoids in Clinical UseProstanoids in Clinical Use
 Dinoprostone (PGE2)Dinoprostone (PGE2)
 Dinoprost (PGF2-alpha)Dinoprost (PGF2-alpha)
 Gemeprost: “cervagem”, analogue of PG E1,Gemeprost: “cervagem”, analogue of PG E1,
for TOPsfor TOPs
 Carboprost (analogue of PGF2-alpha)Carboprost (analogue of PGF2-alpha)
 Misoprostol (stable PGE2 analogue)Misoprostol (stable PGE2 analogue)
Induction of labour
Side Effects of ProstaglandinsSide Effects of Prostaglandins
SE’s of ProstaglandinsSE’s of Prostaglandins
 HyperstimulationHyperstimulation
 FeverFever
 Allergic reactionsAllergic reactions
 Exacerbation of asthmaExacerbation of asthma
Other Methods of IOLOther Methods of IOL
Other Methods of IOLOther Methods of IOL
 Nipple stimulationNipple stimulation
 Castor oilCastor oil
 Cervical vibratorsCervical vibrators
 AcupunctureAcupuncture
 SexSex
Prostaglandins in SemenProstaglandins in Semen
 PGE : 67.1 mg/LPGE : 67.1 mg/L
 PGF: 3.2 mg/LPGF: 3.2 mg/L
Patient’s consent for IOLPatient’s consent for IOL
 Indication to be explainedIndication to be explained
 Failure rate and need for C/SFailure rate and need for C/S
 Possible delay in starting IOLPossible delay in starting IOL
 Risks to be explained: cord prolapse, fetalRisks to be explained: cord prolapse, fetal
distress, PPHdistress, PPH
 Alternatives to inductionAlternatives to induction
 Patient info. sheetPatient info. sheet
Induction of labour
Induction of labour

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Induction of labour

  • 1. INDUCTION OFINDUCTION OF LABOURLABOUR Dr Max MongelliDr Max Mongelli Women & Childrens’ HealthWomen & Childrens’ Health Nepean HospitalNepean Hospital
  • 2. DefinitionsDefinitions IOL: “Iatrogenic stimulation of uterineIOL: “Iatrogenic stimulation of uterine contractions to accomplish delivery prior to thecontractions to accomplish delivery prior to the spontaneous onset of labour”spontaneous onset of labour” Cervical priming: Interventions designed toCervical priming: Interventions designed to improve the Bishop score without necessarilyimprove the Bishop score without necessarily inducing labourinducing labour
  • 3. PrevalencePrevalence  USA: frequency has increased from 9.5%USA: frequency has increased from 9.5% to 22.5% over 16 yearsto 22.5% over 16 years  Due to availability of better cervicalDue to availability of better cervical ripening agents, more relaxed attitudesripening agents, more relaxed attitudes towards marginal indications fortowards marginal indications for inductioninduction
  • 6. Maternal IndicationsMaternal Indications  Pre-eclampsia/EclampsiaPre-eclampsia/Eclampsia  Severe hypertensionSevere hypertension  Gestational diabetesGestational diabetes Pelvic arthropathyPelvic arthropathy  Obstetric cholestasisObstetric cholestasis  Severe cardio-respiratory diseaseSevere cardio-respiratory disease  ““Social”Social”  AnticoagulationAnticoagulation
  • 8. Fetal IndicationsFetal Indications  Post-term pregnancyPost-term pregnancy  IUGRIUGR  Obstetric cholestasisObstetric cholestasis  PROMPROM AmnionitisAmnionitis  Fetal demiseFetal demise
  • 10. ContraindicationsContraindications  Classical C/S scarClassical C/S scar  Transmural myomectomy scarTransmural myomectomy scar  Placenta or vasa previaPlacenta or vasa previa  Active genital herpesActive genital herpes  Large cervical fibroidsLarge cervical fibroids  MalpresentationMalpresentation  Cord presentation or prolapseCord presentation or prolapse  Severe IUGRSevere IUGR  Abnormal or non-reactive CTGAbnormal or non-reactive CTG
  • 11. Pre-Induction AssessmentPre-Induction Assessment  Confirm valid indicationConfirm valid indication  Exclude contraindicationsExclude contraindications  Patient information and consentPatient information and consent  Bishop scoreBishop score
  • 14. Significance of Bishop scoreSignificance of Bishop score If Bishop score >5 chance of vaginalIf Bishop score >5 chance of vaginal delivery after IOL same as afterdelivery after IOL same as after spontaneous onset of labourspontaneous onset of labour
  • 15. Predictors of Successful IOLPredictors of Successful IOL
  • 16. Other Predictors of Successful IOLOther Predictors of Successful IOL  MultiparityMultiparity  Tall stature ( > 5 ft 5” or 165 cm)Tall stature ( > 5 ft 5” or 165 cm)  Normal BMINormal BMI  Increasing GAIncreasing GA  EFW < 3500 gEFW < 3500 g
  • 17. Methods for Induction of LabourMethods for Induction of Labour
  • 18. MethodsMethods  Membrane strippingMembrane stripping  Mechanical methodsMechanical methods  AmniotomyAmniotomy  OxytocinOxytocin  ProstaglandinsProstaglandins
  • 19. Membrane StrippingMembrane Stripping  Finger through cervical os, to detach membranesFinger through cervical os, to detach membranes from LUSfrom LUS  Usually from 39 weeks onwardsUsually from 39 weeks onwards  Can be repeated safelyCan be repeated safely  Reduced risk of going beyond 41 (RR 0.59)Reduced risk of going beyond 41 (RR 0.59)  Reduced frequency of formal IOL (NNT =8)Reduced frequency of formal IOL (NNT =8)  May cause slight PV bleeding and crampsMay cause slight PV bleeding and cramps
  • 20. Mechanical MethodsMechanical Methods  Required for low Bishop scoresRequired for low Bishop scores  Ideal when PG’s relatively contraindicatedIdeal when PG’s relatively contraindicated  Foley’s catheterFoley’s catheter  ATAD catheterATAD catheter  LaminariaLaminaria
  • 25. AmniotomyAmniotomy  Usually when cx is partially dilatedUsually when cx is partially dilated  Usually combined with oxytocinUsually combined with oxytocin  Colour of amniotic fluid should beColour of amniotic fluid should be notednoted
  • 27. Risks of AmniotomyRisks of Amniotomy  Fetal hemorrhage if vasa previaFetal hemorrhage if vasa previa  Cord prolapse, esp with high headCord prolapse, esp with high head  InfectionInfection
  • 29. OxytocinOxytocin  Almost always after amniotomyAlmost always after amniotomy  Given i.v. by infusion pump because of short half-lifeGiven i.v. by infusion pump because of short half-life  May take up to 40 mins to reach steady-stateMay take up to 40 mins to reach steady-state concentrationsconcentrations  May be stopped once active phase of labour establishedMay be stopped once active phase of labour established  Continuous CTG monitoring requiredContinuous CTG monitoring required
  • 30. Oxytocin regimesOxytocin regimes  Low-dose: less likely to cause hyperstimulationLow-dose: less likely to cause hyperstimulation  High dose: short incremental time intervals, noHigh dose: short incremental time intervals, no more than 40 iu/minmore than 40 iu/min  Pulsatile regime: boluses at 8-10 min intervals,Pulsatile regime: boluses at 8-10 min intervals, reduced total overall dose of of oxytocinreduced total overall dose of of oxytocin
  • 31. Risks of OxytocinRisks of Oxytocin  Hyperstimulation / tachysystoleHyperstimulation / tachysystole  Uterine ruptureUterine rupture  High dose: water intoxicationHigh dose: water intoxication  Increased risk of PPHIncreased risk of PPH
  • 34. ProstaglandinsProstaglandins  Required for low Bishop scoresRequired for low Bishop scores  PGE2 gel or pessariesPGE2 gel or pessaries  Slow-release systemsSlow-release systems  MisoprostolMisoprostol
  • 35. Prostanoids in Clinical UseProstanoids in Clinical Use  Dinoprostone (PGE2)Dinoprostone (PGE2)  Dinoprost (PGF2-alpha)Dinoprost (PGF2-alpha)  Gemeprost: “cervagem”, analogue of PG E1,Gemeprost: “cervagem”, analogue of PG E1, for TOPsfor TOPs  Carboprost (analogue of PGF2-alpha)Carboprost (analogue of PGF2-alpha)  Misoprostol (stable PGE2 analogue)Misoprostol (stable PGE2 analogue)
  • 37. Side Effects of ProstaglandinsSide Effects of Prostaglandins
  • 38. SE’s of ProstaglandinsSE’s of Prostaglandins  HyperstimulationHyperstimulation  FeverFever  Allergic reactionsAllergic reactions  Exacerbation of asthmaExacerbation of asthma
  • 39. Other Methods of IOLOther Methods of IOL
  • 40. Other Methods of IOLOther Methods of IOL  Nipple stimulationNipple stimulation  Castor oilCastor oil  Cervical vibratorsCervical vibrators  AcupunctureAcupuncture  SexSex
  • 41. Prostaglandins in SemenProstaglandins in Semen  PGE : 67.1 mg/LPGE : 67.1 mg/L  PGF: 3.2 mg/LPGF: 3.2 mg/L
  • 42. Patient’s consent for IOLPatient’s consent for IOL  Indication to be explainedIndication to be explained  Failure rate and need for C/SFailure rate and need for C/S  Possible delay in starting IOLPossible delay in starting IOL  Risks to be explained: cord prolapse, fetalRisks to be explained: cord prolapse, fetal distress, PPHdistress, PPH  Alternatives to inductionAlternatives to induction  Patient info. sheetPatient info. sheet