Timing of Induction for Healthy Term Pregnancy at 40 Weeks
For a healthy term pregnancy that has reached 40 weeks, you should offer elective induction of labor at 39 weeks (39+0 to 39+4 days) rather than waiting until 40 weeks, as this reduces cesarean delivery rates and hypertensive disorders without increasing neonatal complications. 1
Evidence-Based Recommendation at 40 Weeks
Since the pregnancy has already reached 40 weeks, the management decision now shifts to timing of induction versus continued expectant management:
Immediate Action at 40 Weeks
- Recommend induction now rather than further expectant management, as the optimal window for elective induction (39 weeks) has passed and risks increase with advancing gestational age. 2
- At 41 weeks specifically, cesarean delivery risk becomes significantly elevated with expectant management compared to induction. 2
- Induction should be strongly recommended by 41+0 weeks at the latest for all low-risk pregnancies. 2, 3
Key Evidence Supporting Earlier Induction
Benefits of Induction at 39 Weeks (ARRIVE Trial)
The landmark ARRIVE trial demonstrated clear maternal benefits for nulliparous women:
- Cesarean delivery rate reduced from 22.2% to 18.6% (RR 0.84,95% CI 0.76-0.93), with number needed to treat of 28 to prevent one cesarean. 1, 4
- Hypertensive disorders reduced from 14.1% to 9.1% (RR 0.64,95% CI 0.56-0.74). 1, 4
- No statistically significant difference in perinatal death or severe neonatal morbidity (4.3% vs 5.4%). 1
Risks of Expectant Management Beyond 40 Weeks
- Stillbirth risk increases from 39 weeks onward with sharp rise after 40 weeks. 5
- At 41 weeks, stillbirth risk is 2-3 per 1000 deliveries. 6
- Perinatal mortality between 41-42 weeks: 0% with induction versus 0.16% with expectant management (NNT 613). 7
Clinical Algorithm for 40-Week Pregnancy
Step 1: Confirm Eligibility
- Singleton pregnancy with cephalic presentation 4
- Reliable dating 4
- No medical or obstetric contraindications 1
Step 2: Counsel Patient on Options
Option A: Immediate Induction (Recommended)
- Lower cesarean risk compared to waiting 1
- Lower risk of developing hypertensive disorders 1
- Prevents progression to higher-risk 41+ week timeframe 2
Option B: Expectant Management Until 41 Weeks
- Must include close surveillance 2
- Mandatory induction by 41+0 weeks 2, 3
- Higher cesarean risk if induction delayed 2
- 45.6% chance of spontaneous labor before 41 weeks in nulliparous women 8
Step 3: Induction Protocol
- Assess cervical favorability using modified Bishop score. 2
- If unfavorable cervix (Bishop <5): Use cervical ripening agents (avoid misoprostol if prior uterine surgery). 2
- Allow at least 12 hours after cervical ripening, membrane rupture, and oxytocin before considering cesarean for "failed induction" in latent phase. 1
- Cesarean should be reserved for obstetric indications only, not performed electively. 2
Important Caveats
Parity Considerations
- The ARRIVE trial data applies specifically to nulliparous women. 1, 4
- It is unknown whether findings extrapolate to multiparous women. 1, 4
- However, induction at 41 weeks is recommended for all low-risk pregnancies regardless of parity. 3
Shared Decision-Making
- Both immediate induction and expectant management until 41 weeks are reasonable options with similar neonatal outcomes. 1, 4
- Some women will prefer the lower cesarean risk and hypertensive disorder risk with induction. 1
- Others may prefer expectant management with possibility of spontaneous labor. 1
- Strong counseling about risks of declining induction is necessary while respecting patient autonomy. 2
What NOT to Do
- Do not wait beyond 41+0 weeks for induction in uncomplicated pregnancy. 2, 3
- Do not perform elective cesarean at 42 weeks; vaginal delivery with induction is the recommended approach. 2
- Do not induce before 39+0 weeks without medical indication due to increased respiratory morbidity. 3
Evidence Quality Note
The recommendation prioritizes the 2019 SMFM statement on the ARRIVE trial 1, which represents the highest quality evidence from a large multicenter randomized controlled trial (n=6,106) specifically addressing this clinical question. This is augmented by 2025 guideline summaries 2, 3, 4 that incorporate ACOG recommendations and recent evidence on management at 41 weeks.