Şık Aytek, Bilecan Sedat, Kumbasar Serkan, Akpak Yaşam Kemal, Aba Yilda Arzu
Istanbul Aydın University, Department of Obstetrics and Gynaecology, Istanbul, Turkey.
Süleymaniye Research and Education Hospital, Department of Obstetrics and Gynaecology, Istanbul, Turkey.
Afr Health Sci. 2019 Mar;19(1):1544-1553. doi: 10.4314/ahs.v19i1.28.
A retrospective (case-controlled) study was conducted with the aim of identifying the effect of the use of misoprostol on termination time in patients who did and did not undergo feticide procedures in second trimester pregnancy terminations.
The sampling of the study consisted of 144 pregnant women who were diagnosed as having major fetal anomalies incompatible with life, and were recommended for termination of pregnancy. The investigation showed that feticide procedures were performed for 99 women, and feticide procedures were not performed for 45 women. Misoprostol protocol was administered for 48 hours in the termination period; whether the feticide procedure directly affected the termination duration in patients who did and did not undergo feticide was evaluated.
Abortion/birth was achieved in 103 (71.5%) women during the first 48 hours. There was no significant difference between the termination duration of the misoprostol protocol among the women who did and did not undergo feticide. There was no significant difference between the termination durations and fetal biometric measurements (BPD, HC) except head diameters (p=0.020 and p=0.015).
The misoprostol protocol is shown to be effective and safe for the termination of pregnancies during the second trimester. Feticide has no affect on the duration of termination.
进行了一项回顾性(病例对照)研究,目的是确定米索前列醇的使用对中期妊娠终止时接受和未接受胎儿灭活程序的患者终止时间的影响。
该研究的样本包括144名被诊断患有与生命不相容的严重胎儿畸形并被建议终止妊娠的孕妇。调查显示,99名妇女进行了胎儿灭活程序,45名妇女未进行胎儿灭活程序。在终止期给予米索前列醇方案48小时;评估胎儿灭活程序是否直接影响接受和未接受胎儿灭活的患者的终止持续时间。
103名(71.5%)妇女在头48小时内实现了流产/分娩。接受和未接受胎儿灭活的妇女中,米索前列醇方案的终止持续时间之间没有显著差异。除头径外,终止持续时间与胎儿生物测量值(双顶径、头围)之间没有显著差异(p = 0.020和p = 0.015)。
米索前列醇方案被证明对中期妊娠终止有效且安全。胎儿灭活对终止持续时间没有影响。