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Controlled-release dinoprostone insert versus Foley catheter for labor induction: a meta-analysis
Hongye Wang1, Shukun Hong2, Yuanyuan Liu1
1a Department of Obstetrics and Gynecology and.
Summary
Controlled-release dinoprostone insert appears more effective for labor induction than Foley catheter, shortening delivery time. However, it increases excessive uterine contractions, necessitating careful monitoring during cervical ripening.
Area of Science:
- Obstetrics and Gynecology
- Reproductive Medicine
- Clinical Pharmacology
Background:
- Cervical ripening and labor induction are critical in managing pregnancy complications.
- Controlled-release dinoprostone insert and Foley catheter balloon are common methods for cervical ripening.
- Evidence comparing their effectiveness and safety is crucial for clinical decision-making.
Purpose of the Study:
- To compare the effectiveness and safety of controlled-release dinoprostone insert versus Foley catheter balloon for cervical ripening and labor induction.
- To analyze key outcomes including time to delivery, delivery rates, and adverse events.
Main Methods:
- A systematic review and meta-analysis of randomized controlled trials (RCTs).
- Searches conducted in PubMed, Cochrane, Web of Science, and China Knowledge Resource Integrated Database.
- Data synthesized using risk ratios (RR) and mean differences (MD) with 95% confidence intervals (CI).
Main Results:
- Six RCTs involving 731 women (dinoprostone) and 722 women (Foley catheter) were analyzed.
- Dinoprostone insert significantly shortened the time from induction to delivery (MD 5.73 h).
- No significant differences were observed in vaginal delivery within 24 hours or cesarean section rates. Dinoprostone was associated with increased excessive uterine contractions but less oxytocin use.
Conclusions:
- Controlled-release dinoprostone insert demonstrates greater effectiveness in labor induction compared to the Foley catheter.
- The use of dinoprostone insert is linked to a higher incidence of excessive uterine contractions.
- Further research may be warranted to optimize safety profiles and patient selection for each method.
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