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医学管理稽留流产:来自前瞻性、单中心、澳大利亚队列的结果。

The medical management of missed miscarriage: outcomes from a prospective, single-centre, Australian cohort.

机构信息

Mater Mothers' Hospital, Brisbane, QLD, Australia.

出版信息

Med J Aust. 2013 Sep 2;199(5):341-6. doi: 10.5694/mja12.11813.

Abstract

OBJECTIVE

To report the prospective outcomes of medical management of missed miscarriage before 13 weeks' gestation from an Australian cohort.

DESIGN

Descriptive study of a cohort selected out of a randomised controlled trial.

SETTING

Outpatient management at a maternity hospital between 1 May 2007 and 28 July 2010.

PARTICIPANTS

264 women requesting medical management of missed miscarriage.

MAIN OUTCOME MEASURES

Number of doses of misoprostol required, unscheduled visits for care, findings at ultrasound follow-up, requirement for surgical management, number of cases of gestational trophoblastic disease (GTD), and self-reported patient experience.

RESULTS

107 women (40.5%) received a repeat dose of misoprostol, and 79 women (29.9%) made unscheduled visits for care. Among the 241 women with Day 7 ultrasound follow-up, a gestational sac was found in 32 women (13.3%), indicating failure of medical management. Complete miscarriage was induced without the need for surgery in 206 women (78.0%). Surgery was performed as an emergency in 13 women (4.9%). Twelve women (4.5%) had surgery for ongoing bleeding after medical management, and four of these did not have chorionic villi on histopathological examination. Five women (1.9%) had GTD, which was managed incidentally under the protocol. Among those who returned patient questionnaires, 73.0% participants (116/159) indicated that they would recommend medical management of miscarriage to other women, while 18.2% (29/159) indicated that they would undergo surgery next time.

CONCLUSION

The medical management of missed miscarriage on an outpatient basis is safe and effective.

TRIAL REGISTRATION

ACTRN12612000150842.

摘要

目的

报告澳大利亚队列中 13 周前妊娠丢失的药物治疗的前瞻性结局。

设计

从一项随机对照试验中选择的队列的描述性研究。

设置

2007 年 5 月 1 日至 2010 年 7 月 28 日在一家产科医院进行门诊管理。

参与者

264 名要求药物治疗妊娠丢失的女性。

主要观察指标

所需米索前列醇剂量、非计划就诊次数、超声随访结果、手术管理需求、妊娠滋养细胞疾病(GTD)病例数和患者自我报告的治疗体验。

结果

107 名女性(40.5%)接受了米索前列醇重复剂量,79 名女性(29.9%)进行了非计划就诊。在 241 名进行第 7 天超声随访的女性中,32 名女性(13.3%)发现有孕囊,表明药物治疗失败。206 名女性(78.0%)无需手术即诱导完全流产。13 名女性(4.9%)因药物治疗后持续出血而紧急手术,其中 4 名女性组织病理学检查未发现绒毛膜组织。12 名女性(4.5%)因药物治疗后持续出血而行手术治疗,其中 4 名女性组织病理学检查未发现绒毛膜组织。5 名女性(1.9%)患有 GTD,根据方案偶然发现并进行了处理。在返回患者问卷的女性中,73.0%(116/159)表示会向其他女性推荐药物治疗流产,18.2%(29/159)表示下次会选择手术。

结论

门诊药物治疗妊娠丢失是安全有效的。

试验注册

ACTRN12612000150842。

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