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Volume 81, Issue 2, Pages 161-164 (February 2010)


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Buccal misoprostol for cervical ripening prior to first trimester abortion

Hemang B. Panchala, Emily M. GodfreyabCorresponding Author Informationemail address, Ashlesha Patela

Received 4 January 2009; received in revised form 23 September 2009; accepted 6 October 2009. published online 13 November 2009.

Abstract 

Background

Cervical priming prior to uterine suction evacuation softens the cervix and lessens the force needed for dilation, thereby potentially reducing the probability of procedural complications. The use of buccal misoprostol has been shown to be an adequate cervical primer in second trimester surgical procedures, but its use in first trimester aspiration procedures is not well documented. Our objective was to assess the necessity of manual dilation of the cervix when buccal misoprostol is used for cervical priming prior to first trimester uterine aspiration procedures.

Study Design

Retrospective case review of 685 patients who underwent a first trimester aspiration abortion with buccal misoprostol cervical priming from August 24, 2006, to February 23, 2007. All procedures were performed by three experienced physicians.

Results

Adequate dilatation of the cervix was achieved in 44.2% patients. The proportion of patients with adequate dilation decreased with increasing gestational age. Patients requiring additional mechanical dilatation differed significantly between those who were parous (51.0%) and those who were nulliparous (72.4%) (p<.001).

Conclusion

Buccal misoprostol appeared to decrease our need for manual dilation prior to first trimester aspiration abortion. Earlier gestations and parous patients showed less need for manual dilitation than later gestations or nulliparous women. A larger study with a control group is needed to confirm the benefit of the use of buccal misoprostol in first trimester aspiration abortion.

a Department of Obstetrics and Gynecology, John H. Stroger Jr. Hospital of Cook County, Chicago, IL 60612, USA

b Departments of Family Medicine and Community Health Sciences, University of Illinois-Chicago, Chicago, IL 60612, USA

Corresponding Author InformationCorresponding author. Tel.: +1 312 4133213.

 This research study was not funded. The authors report no conflict of interest.

PII: S0010-7824(09)00448-X

doi:10.1016/j.contraception.2009.10.002


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