Misoprostol for Cervical Ripening in Non-pregnant Women: A Randomized Double-blind Controlled Trial of Oral versus Vaginal Regimens
C. Choksuchat, S. Cheewadhanaraks, C. Getpook, V. Wootipoom, K.Dhanavoravibul
Department of Obstetrics and Gynecology, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand. E-mail: [email protected]
บทคัดย่อ
Background: The objective was to compare the efficacy of oral versus vaginal misoprostol for cervical ripening in non-pregnant women. Methods: Sixty non-pregnant women scheduled for diagnostic hysteroscopy were randomized by computerized randomization schedule to 400 µg of misoprostol orally (n = 30) or 200 µg vaginally (n = 30) administered 12 h prior to surgery. The diameter of the cervical canal measured with a Hegar dilator, adverse events and any complications were recorded and compared between the two groups. Rresults: The mean pre- and postmedication cervical canal diameter and cervical diameter difference were 2.00 ± 1.93 versus 2.37 ±1.83 mm (P = 0.453), 5.10 ± 1.75 versus 5.60 ± 1.69 mm (P = 0.265) and 3.10 ± 1.79 versus 3.23 ±1.74 mm (P = 0.771) in the oral and vaginal group, respectively. Seven patients in the oral group and one patient in the vaginal group experienced diarrhoea within 24 h of administration of the misoprostol. Cconclusion: Oral misoprostol 400 µg had similar efficacy in cervical ripening to 200 µg of vaginal misoprostol.
ที่มา
ปี 2549, August ปีที่: 21 ฉบับที่ 8 หน้า 2167-2170
คำสำคัญ
Misoprostol, Oral, vaginal, Cervical ripening, Hysteroscopy