What are the methods to induce labour?

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Methods to Induce Labour

For labour induction with a favourable cervix, use oxytocin with artificial rupture of membranes; for an unfavourable cervix, use oral misoprostol solution 20-25 µg every 2-6 hours as the preferred pharmacological method, or mechanical methods (Foley catheter) in high-risk cardiac or cyanotic patients. 1, 2

Cervical Assessment First

  • Assess the Bishop score (cervical dilatation, effacement, consistency, position, and fetal station) to determine cervical favourability before selecting an induction method 1
  • A favourable Bishop score indicates readiness for oxytocin and membrane rupture, while an unfavourable cervix requires cervical ripening first 1

Primary Induction Methods

For Favourable Cervix

  • Oxytocin infusion with artificial rupture of membranes is the standard approach when the cervix is favourable 1, 3
  • Oxytocin dosing: Start at 1-2 mU/min IV, increase gradually by 1-2 mU/min increments until achieving a contraction pattern similar to normal labour 3
  • Prepare by combining 10 units oxytocin in 1000 mL non-hydrating physiologic electrolyte solution (10 mU/mL concentration) 3
  • Requires continuous fetal heart rate and uterine contraction monitoring with accurate infusion pump control 3

For Unfavourable Cervix: Pharmacological Options

Oral Misoprostol (Preferred)

  • Use 20-25 µg oral misoprostol solution every 2-6 hours as the optimal regimen, which results in fewer cesarean sections and lower uterine hyperstimulation rates compared to higher doses 2
  • Oral route is superior to vaginal administration, with lower hyperstimulation rates (RR 0.69) and fewer cesarean sections compared to vaginal dinoprostone (RR 0.84) 2
  • Requires continuous fetal heart rate and uterine activity monitoring from 30 minutes to 2 hours after each dose 2
  • Major cost advantage: $0.36-$1.20 per 100 µg tablet versus $65-$75 for dinoprostone gel or $165 for dinoprostone insert 2
  • Stable at room temperature, eliminating refrigeration requirements 2

Dinoprostone (Prostaglandin E2)

  • Dinoprostone vaginal insert (10 mg) or gel can be used for cervical ripening 4, 5
  • The vaginal insert can be safely used for up to 24 hours, though most tachysystole cases (68%) occur within 12 hours 5
  • In low-risk pregnancies, dinoprostone achieves 67.6% vaginal delivery rates 4
  • Vaginal misoprostol appears more effective than dinoprostone insert for premature rupture of membranes, with shorter time to active labour (7 vs 11 hours) and delivery within 24 hours (88.4% vs 58.0%) 6

For Unfavourable Cervix: Mechanical Methods

  • Foley catheter is preferable to pharmacological agents in patients with cyanosis, active cardiovascular disease, or conditions where drops in systemic vascular resistance or blood pressure would be detrimental 1
  • Mechanical methods avoid the hemodynamic effects of prostaglandins 1

Critical Contraindications and Safety Considerations

Absolute Contraindications

  • Misoprostol is absolutely contraindicated in women with previous cesarean delivery due to 13% uterine rupture risk, substantially higher than oxytocin (1.1%) or prostaglandin E2 (2%) 2, 7
  • The American College of Obstetricians and Gynecologists advises avoiding misoprostol entirely in this population 2
  • Dinoprostone is contraindicated in active cardiovascular disease due to profound blood pressure effects 1

Special Population Considerations

  • In women with advanced liver failure, misoprostol may be less suitable as it requires hepatic metabolism to convert from E1 to active E2 prostaglandin; consider alternative methods 2
  • In cardiac patients or those with cyanosis, mechanical methods (Foley catheter) are preferred over prostaglandins to avoid systemic vascular resistance drops 1
  • Prostaglandin E2 carries theoretical risk of coronary vasospasm and low risk of arrhythmias 1

Uterine Rupture Risk Stratification

  • Oxytocin in prior cesarean: 1.1% rupture risk 7
  • Prostaglandin E2 in prior cesarean: 2% rupture risk 1
  • Misoprostol in prior cesarean: 13% rupture risk 2
  • Induction decreases likelihood of successful vaginal birth after cesarean compared to spontaneous labour 7

Monitoring Requirements

  • Continuous fetal heart rate and uterine activity monitoring is mandatory during all pharmacological induction methods 2, 3
  • For oxytocin: Monitor fetal heart rate, resting uterine tone, and frequency/duration/force of contractions 3
  • Discontinue infusion immediately if uterine hyperactivity or fetal distress occurs; administer oxygen to mother 3

Common Pitfalls to Avoid

  • Avoid prolonged induction time when cervix is unfavourable - consider mechanical methods or cesarean delivery if cervical ripening fails 1
  • Do not use misoprostol in women with prior cesarean - the rupture risk is unacceptably high 2
  • Avoid dinoprostone in active cardiovascular disease due to blood pressure effects 1
  • Do not use general anesthesia if possible, particularly in respiratory disease patients 1

Adjunctive Considerations

  • Prostaglandin E2 for induction or oxytocin for augmentation has not been associated with worsening lung function or asthma exacerbation 1
  • Early epidural analgesia is preferred for pain relief and can be extended for emergency cesarean if needed 1
  • Active management of third stage with oxytocin is preferred over ergotamine (which may cause bronchospasm) 1

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Oral Misoprostol Solution for Labor Induction

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Dinoprostone vaginal pessary for induction of labour: safety of use for up to 24 h.

The Australian & New Zealand journal of obstetrics & gynaecology, 2012

Guideline

Pitocin Dosing for Labor Induction in Special Populations

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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