1. A randomized controlled trial of methylergonovine prophylaxis after dilation and evacuation abortion
- Author
-
Rebecca A. Jackson, Kristin Harter, Biftu Mengesha, Eleanor A. Drey, Geffan Pearlson, and Jennifer L. Kerns
- Subjects
Excessive Bleeding ,medicine.medical_treatment ,Uterotonic ,Placebo ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,Methylergonovine ,Uterine artery embolization ,Randomized controlled trial ,Pregnancy ,law ,Humans ,Medicine ,030212 general & internal medicine ,Dilation and evacuation ,Methylergonovine Maleate ,030219 obstetrics & reproductive medicine ,business.industry ,Obstetrics and Gynecology ,Abortion, Induced ,Dilatation ,Abortion, Spontaneous ,Reproductive Medicine ,Anesthesia ,Female ,Uterine Hemorrhage ,business - Abstract
Objective To evaluate the efficacy of intramuscular methylergonovine maleate as prophylaxis against excessive bleeding when given after dilation and evacuation (D&E) at 20–24 weeks. Study design We performed a randomized, double-blinded, placebo-controlled trial in patients without excessive bleeding requiring intervention after D&E completion. We administered study treatment within one minute of the end of the procedure. We primarily compared outcomes using a composite of indicators of excessive post-procedure blood loss (post-procedure measured blood loss exceeding 125 mL, uterine massage or compression for at least two minutes, administration of additional uterotonic medication, intrauterine balloon tamponade, uterine re-aspiration, blood transfusion, uterine artery embolization, hospital admission for bleeding, or major surgery). Secondary outcomes included individual indicator occurrences, satisfaction, and side effects. Results From March 3, 2015 to March 31, 2017, we randomized 284 participants (n = 140 methylergonovine, n = 144 placebo), five before we registered the trial with clinicaltrials.gov. Baseline characteristics were similar between groups. The composite outcome occurred in 78 (56%) methylergonovine and 75 (52%) placebo participants (p = 0.5). Methylergonovine recipients required more intrauterine balloon use (n = 20 [14%]) versus placebo (n = 10 [7%]), p = 0.04. We also observed a non-significant trend towards more uterotonic administration (n = 56 [40%] versus n = 43 [30%], p = 0.07) and hospital admissions for bleeding (n = 4 [3%] versus n = 0, p = 0.06) in the methylergonovine group compared to placebo. Conclusion We observed no improvement in the composite outcome for excessive bleeding with prophylactic post-procedure methylergonovine. In addition, individual excessive bleeding outcomes occurred more frequently in the methylergonovine group, potentially indicating harm with its prophylactic use after D&E. Implications When administered prophylactically immediately after dilation and evacuation abortion at 20–24 weeks, methylergonovine increases uterine bleeding. Given the lack of data for effectiveness as a prophylactic agent and our findings indicating harm, we do not recommend its use for post-operative prophylaxis.
- Published
- 2021
- Full Text
- View/download PDF