When is Induction of Labour Recommended?
Induction of labour is recommended for medical or obstetric indications where continuing pregnancy poses greater risks than delivery, including gestational hypertension/preeclampsia at ≥37 weeks, post-term pregnancy at ≥41 weeks, premature rupture of membranes, maternal diabetes with poor control, and Rh disease; additionally, elective induction at 39 weeks 0 days can be offered to low-risk nulliparous women to reduce cesarean delivery and hypertensive complications. 1, 2
Medical and Obstetric Indications for Induction
Hypertensive Disorders
- Induction should be advised for women with gestational hypertension or mild preeclampsia at 37 weeks' gestation to improve maternal outcomes 1
- Induction at 39 weeks in low-risk nulliparous women reduces hypertensive disorders from 14.1% to 9.1% (RR 0.64) 1
Post-Term Pregnancy
- Induction is recommended at 41 weeks of gestation or later in low-risk pregnancy due to stillbirth risk of 2-3 per 1000 deliveries 3
- Fetal mortality increases with advancing gestational age beyond 39 weeks 3
Maternal Diabetes
- Induction is indicated when delivery is in the best interest of mother and fetus, particularly with poor glycemic control 2
- Timing should be individualized based on glycemic control and fetal surveillance 4
Premature Rupture of Membranes
- Induction is indicated when membranes are prematurely ruptured and delivery is indicated 2
Other Medical Indications
- Rh problems requiring early delivery 2
- Intrahepatic cholestasis of pregnancy 4
- Intrauterine growth restriction (timing based on clinical features) 5
Elective Induction at 39 Weeks in Low-Risk Nulliparous Women
Key Benefits
- Cesarean delivery rate reduced from 22.2% to 18.6% (RR 0.84) - need to induce 28 women to prevent one cesarean 1
- Hypertensive disorders reduced from 14.1% to 9.1% (RR 0.64) 1
- No increase in adverse neonatal outcomes 1
Strict Eligibility Criteria (ARRIVE Trial)
You must ensure women meet ALL of the following criteria before offering elective induction at 39 weeks: 1
- Low-risk nulliparous women only (evidence does not extend to multiparous women) 1
- Gestational age ≥39 weeks 0 days (never before 39 weeks due to respiratory morbidity risk) 1
- Dating confirmed by early ultrasonography:
- No medical or obstetric complications 1
Critical Implementation Requirements
- Adequate facility capacity and staffing (nurses, anesthesiologists) must be available 1
- Shared decision-making is mandatory - discuss both options (induction vs expectant management) 1
- Medical/obstetric indications take priority for induction slots 1
Contraindications to Elective Induction
Absolute Contraindications
- Suspected fetal macrosomia is NOT an indication for induction - it doubles cesarean risk without reducing shoulder dystocia or neonatal morbidity 1
- Before 39 weeks 0 days gestation - associated with increased respiratory morbidity 1
- Previous cesarean delivery with misoprostol use - 13% uterine rupture risk 6
Relative Contraindications
- Unfavorable cervix without adequate time for cervical ripening 6
- Facilities lacking capacity for emergency cesarean delivery 1
Common Clinical Pitfalls to Avoid
Critical errors that worsen outcomes: 1, 6
Never induce before 39 weeks 0 days for elective reasons - early term neonates (37-38 weeks) have increased respiratory morbidity 1
Never use misoprostol in women with prior cesarean - rupture risk is 13% vs 1.1% with oxytocin 6
Never induce for suspected macrosomia alone - induction doubles cesarean risk without benefit 1
Never offer elective induction without confirmed dating by early ultrasound - risk of iatrogenic prematurity 1
Do not extrapolate ARRIVE findings to multiparous women - evidence is insufficient 1
Induction Methods Based on Indication
For Favorable Cervix
For Unfavorable Cervix
- Oral misoprostol solution 20-25 µg every 2-6 hours (preferred pharmacological method) 6
- Mechanical methods (Foley catheter) preferred in cardiac patients, cyanosis, or prior cesarean 6