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Misoprostol use in medical evacuation of spontaneous miscarriage: Pilot drug use evaluation study at the Womens Hospital in Qatar

机译:米索前列醇用于自发流产的医疗疏散:卡塔尔妇女医院的药物使用评估研究

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>Background: Misoprostol is a synthetic prostaglandin E1 that induces cervical effacement and uterine contractions at all gestational ages, thus facilitating uterine evacuation and pregnancy termination. Successful medical evacuation of spontaneous miscarriage with minimal adverse effects can be performed using misoprostol-only regimen if given as indicated and if the administered dose, frequency of the dosage, and number of total doses are appropriate. >Aim: To conduct a drug use evaluation by investigating indications, appropriateness of dosing, and clinical outcome of misoprostol-only regimen when used for medical evacuation of spontaneous miscarriage at the Women's Hospital in Doha, Qatar. >Materials and methods: A retrospective descriptive drug use evaluation was conducted on women with spontaneous miscarriage who received misoprostol for medical evacuation during August 2013. The current practice at the Women's Hospital was compared with the recommendation from the World Health Organization (WHO). Patients were stratified into three groups based on weeks of amenorrhea. >Results: A total of 107 patients received misoprostol during August 2013, of which 33 (31%) were included in the study. In these patients, the main indication for misoprostol use was missed miscarriage (54.5%). In the group of patients at ≤ 9 weeks of gestation, 80% received an initial dose of 800 μg, 80% received frequency within the WHO recommendation, and the majority had surgical evacuation (80%). In the group of patients at 10–12 weeks of gestation, more than 80% received an initial dose of 800 μg, 6% received frequency within the WHO recommendation, and more than 75% had successful medical evacuation. In the group of patients at 13–22 weeks of gestation, more than 80% received an initial dose of 400 μg, more than 80% received frequency within the WHO recommendation, and 54% had successful medical evacuation. Overall, more than 70% of the patients received ≤ 3 total doses of misoprostol and more than 60% had successful medical evacuation as a clinical outcome. >Conclusions: Despite the current practice at the Women's Hospital not always being in accordance with the WHO recommendation, successful medical evacuation was achieved in most patients.
机译:>背景:米索前列醇是一种合成的前列腺素E1,可在所有胎龄时引起宫颈癌变和子宫收缩,从而促进子宫排空和终止妊娠。如果按照说明使用米索前列醇,并且给药剂量,给药频率和总剂量合适,则可以使用仅使用米索前列醇的方案成功进行自然流产的医疗撤离,并将不良反应降至最低。 >目标:通过在卡塔尔多哈妇女医院用于对自然流产进行医疗后送的米索前列醇纯药方案的适应症,剂量的适当性和临床结果进行药物使用评估。 >材料和方法:对2013年8月间接受米索前列醇用于医疗后送的自发流产妇女进行了回顾性描述性药物使用评估。将妇女医院的现行做法与世界卫生组织的建议进行了比较组织(WHO)。根据闭经数周将患者分为三组。 >结果:2013年8月,共有107例患者接受米索前列醇治疗,其中33例(31%)被纳入研究。在这些患者中,米索前列醇使用的主要指征是流产漏诊(54.5%)。在妊娠≤9周的患者中,有80%的患者接受了800μg的初始剂量,其中80%的患者接受了WHO推荐的使用频率,而大多数患者接受了手术后撤离(80%)。在妊娠10–12周的患者组中,超过80%的患者接受了800μg的初始剂量,6%的患者接受了WHO推荐的使用频率,超过75%的患者成功进行了医疗后送。在妊娠13–22周的患者组中,超过80%的患者接受了400μg的初始剂量,超过80%的患者接受了WHO推荐的使用频率,而54%的患者成功进行了医疗后送。总体而言,超过70%的患者接受了≤3次总剂量的米索前列醇,超过60%的患者成功进行了医疗后送作为临床结果。 >结论:尽管妇女医院目前的做法并不总是符合WHO的建议,但大多数患者仍成功完成了医疗后送。

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