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Chlorhexidine is the preferred agent for vaginal antisepsis prior to cesarean delivery: a systematic review and network meta-analysis.

American journal of obstetrics and gynecology2026-01-05PubMed
Total: 82.5Innovation: 7Impact: 0Rigor: 0Citation: 0

Summary

Across 50 trials (n=14,515), vaginal antisepsis before cesarean delivery reduced postoperative infectious morbidity, with chlorhexidine consistently ranking as most effective. Concentration-stratified analyses identified 0.2% chlorhexidine as the top option for wound infection reduction, and results were robust across subgroups and sensitivity analyses.

Key Findings

  • Vaginal antisepsis reduced endometritis, wound infection, wound complications, and postpartum fever versus no preparation.
  • Chlorhexidine was most consistently effective; 0.2% chlorhexidine achieved the highest SUCRA for wound infection (0.995).
  • Compared to chlorhexidine, no preparation had higher odds of endometritis (OR 3.65), wound infection (OR 2.34), wound complications (OR 2.28), and fever (OR 3.60).
  • Findings were consistent across subgroup and sensitivity analyses, with integrity screening of trials.

Clinical Implications

Adopt chlorhexidine for pre-cesarean vaginal antisepsis, preferentially near 0.2% when available; standardize protocols and documentation of concentration. Incorporate into infection prevention bundles alongside antibiotics.

Why It Matters

Provides comparative effectiveness and ranking by concentration for a widely used perioperative intervention with immediate practice implications. Reverses prior rankings favoring povidone-iodine by leveraging a larger, integrity-screened evidence base.

Limitations

  • Heterogeneity in antiseptic concentrations and formulations across trials
  • Some agents (e.g., clindamycin, cetrimide) supported by few small trials; reliance on indirect comparisons for ranking

Future Directions

Head-to-head RCTs comparing chlorhexidine concentrations; standardization of outcome definitions and follow-up; assessment of safety and tolerance across concentrations.

Study Information

Study Type
Meta-analysis
Research Domain
Prevention
Evidence Level
I - Network meta-analysis pooling randomized trials provides the highest level of comparative efficacy evidence.
Study Design
OTHER