Division of Obstetrics and Gynaecology, The University of Western Australia, Perth, Western Australia, Australia.
Division of Obstetrics and Gynaecology, The University of Western Australia, Perth, Western Australia, Australia; Biostatistics and Study Design, Women and Infants Research Foundation, King Edward Memorial Hospital, Perth, Western Australia, Australia.
Contraception. 2023 Sep;125:110080. doi: 10.1016/j.contraception.2023.110080. Epub 2023 May 26.
To assess the frequency of maternal adverse events associated with second trimester medical abortion using sequential mifepristone and misoprostol.
Retrospective analysis of medical abortions 13 to 28 weeks gestation using sequential mifepristone and misoprostol in a single center from January 2008 to December 2018. The main outcomes evaluated were the nature and incidence of adverse procedural events and the impact of gestation upon these outcomes.
During the study period, 1393 people underwent a medical abortion with sequential mifepristone and misoprostol. The median maternal age was 31 years (IQR 27-36 years) and 21.8% had at least one prior cesarean delivery. The median gestational age at abortion commencement was 19 weeks (IQR 17-21). The main adverse maternal events were complete or partial placental retention greater than 60 minutes triggering removal in the operating room (19%), maternal hemorrhage>1000 cc (4.3%), blood transfusion (1.7%), hospital readmission (1.4%), uterine rupture (0.29%) and hysterectomy (0.07%). There were significant reductions in placental retention rates with increasing gestational age (23.3% at 13-16 weeks gestation declining to 10.1% at>23 weeks gestation, p < 0.001).
Serious adverse maternal events associated with second trimester medical abortion with sequential mifepristone-misoprostol are uncommon.
Second trimester medical abortion with mifepristone and misoprostol is generally safe, however, on occasions serious complications may occur. All health care units providing a medical abortion service require the facilities and expertise to deal with these adverse events in a timely manner.
评估使用序贯米非司酮和米索前列醇进行妊娠中期药物流产相关的母体不良事件的发生频率。
回顾性分析 2008 年 1 月至 2018 年 12 月在单中心使用序贯米非司酮和米索前列醇进行的 13 至 28 周妊娠的药物流产。主要评估的结局是不良程序事件的性质和发生率,以及妊娠对这些结局的影响。
在研究期间,1393 人接受了序贯米非司酮和米索前列醇药物流产。产妇年龄中位数为 31 岁(IQR 27-36 岁),21.8%有至少一次剖宫产史。流产开始时的中位妊娠龄为 19 周(IQR 17-21)。主要的母体不良事件是完全或部分胎盘滞留超过 60 分钟,需在手术室取出(19%)、产妇出血>1000cc(4.3%)、输血(1.7%)、住院再入院(1.4%)、子宫破裂(0.29%)和子宫切除术(0.07%)。随着妊娠年龄的增加,胎盘滞留率显著降低(13-16 周妊娠时为 23.3%,降至>23 周妊娠时的 10.1%,p<0.001)。
与序贯米非司酮-米索前列醇妊娠中期药物流产相关的严重母体不良事件并不常见。
米非司酮和米索前列醇联合进行妊娠中期药物流产通常是安全的,但有时可能会出现严重并发症。所有提供药物流产服务的医疗单位都需要有及时处理这些不良事件的设施和专业知识。