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Volume 195, Issue 4, Pages 1143-1147 (October 2006)


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Is vaginal birth after cesarean (VBAC) or elective repeat cesarean safer in women with a prior vaginal delivery?

Alison G. Cahill, MDa, David M. Stamilio, MD, MSCEbc, Anthony O. Odibo, MDa, Jeffrey F. Peipert, MD, MPHa, Sarah J. Ratcliffe, PhDc, Erika J. Stevens, MAa, Mary D. Sammel, ScDc, George A. Macones, MD, MSCEa

Received 10 March 2006; received in revised form 17 May 2006; accepted 10 June 2006. published online 16 July 2006.

Objective

This study was undertaken to determine whether vaginal birth after cesarean (VBAC) or elective repeat cesarean delivery is safer overall for a woman with a prior vaginal delivery.

Study design

This retrospective cohort study of pregnant women from 1996 to 2000 who had a prior cesarean delivery, was conducted in 17 centers. Trained nurses extracted historical and maternal outcome data on subjects by using standardized tools. This planned secondary analysis examined the subcohort that had also previously undergone a vaginal delivery, comparing those who underwent a VBAC trial with those who elected to have a repeat cesarean delivery. Outcomes included uterine rupture, bladder injury, fever, transfusion and a composite (uterine rupture, bladder injury, and artery laceration). We performed bivariate and multivariable analyses.

Results

Of 6619 patients with a prior cesarean delivery who had also had a prior vaginal delivery, 5041 patients attempted a VBAC delivery and 1578 had an elective cesarean delivery. Although there was no significant difference in uterine rupture or bladder injury between the two groups, women who underwent a VBAC attempt were less likely to experience the composite adverse maternal outcome, have a fever, or require a transfusion.

Conclusion

Among VBAC candidates who have had a prior vaginal delivery, those who attempt a VBAC trial have decreased risk for overall major maternal morbidities, as well as maternal fever and transfusion requirement compared with women who elect repeat cesarean delivery. Physicians should make this more favorable benefit-risk ratio explicit when counseling this patient subpopulation on a trial of labor.

a Department of Obstetrics and Gynecology, Washington University in St. Louis, MO

b Departments of Obstetrics and Gynecology

c Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia PA

 Supported by a grant from NICHD (RO1 HD 35631; to GAM). G. A. M. is a recipient of a K24 grant from NICHD (K24 HD01289), which partially supports this work. J. F. P. is a recipient of a K24 grant from NICHD (K24 HD01298), which partially supports this work.

Presented at the 26th Annual Meeting of the Society for Maternal Fetal Medicine, January 30-February 4, 2006, Miami, FL.

Reprints not available from the authors.

PII: S0002-9378(06)00769-1

doi:10.1016/j.ajog.2006.06.045


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