Birth and Delivery · Birth Outcomes

Systematic review of the incidence and consequences of uterine rupture in women with previous caesarean section

Guise JM, McDonagh MS, Osterweil P, Nygren P, Chan BK, Helfand M

BMJ (Clinical research ed.), 2004
DOI 10.1136/bmj.329.7456.19 PMID 15231616

Abstract

Objective

To evaluate the incidence and consequences of uterine rupture in women who have had a delivery by caesarean section.

Design

Systematic review.

Data Sources

Medline, HealthSTAR, Cochrane Database of Systematic Reviews, Cochrane Controlled Trials Register, National Centre for Reviews and Dissemination, reference lists, and national experts. Studies in all languages were eligible if published in full.

Review Methods

Methodological quality was evaluated for each study by using criteria from the United States Preventive Services Task Force and the National Health Service Centre for Reviews and Dissemination. Uterine rupture was categorised as asymptomatic or symptomatic.

Results

We reviewed 568 full text articles to identify 71 potentially eligible studies, 21 of which were rated at least fair in quality. Compared with elective repeat caesarean delivery, trial of labour increased the risk of uterine rupture by 2.7 (95% confidence interval 0.73 to 4.73) per 1000 cases. No maternal deaths were related to rupture. For women attempting vaginal delivery, the additional risk of perinatal death from rupture of a uterine scar was 1.4 (0 to 9.8) per 10,000 and the additional risk of hysterectomy was 3.4 (0 to 12.6) per 10 000. The rates of asymptomatic uterine rupture in trial of labour and elective repeat caesarean did not differ significantly.

Conclusions

Although the literature on uterine rupture is imprecise and inconsistent, existing studies indicate that 370 (213 to 1370) elective caesarean deliveries would need to be performed to prevent one symptomatic uterine rupture.

Topics

By this author

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Marian S McDonagh, Patricia Osterweil, Benjamin K S Chan, Mark Helfand
M McDonagh, Pat Osterweil, Trish Osterweil, P Osterweil, Ben Chan, B Chan, M Helfand
PMID 15231616 15231616 DOI 10.1136/bmj.329.7456.19 10.1136/bmj.329.7456.19 Guise JM; McDonagh MS; Osterweil P; Nygren P; Chan BK; Helfand et al. 2004, Guise JM; McDonagh MS; Osterweil P; Nygren P; Chan BK; Helfand 2004