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孕早期人工流产术前口服米索前列醇与安慰剂用于宫颈扩张的比较

Oral misoprostol versus placebo for cervical dilatation before vacuum aspiration in first trimester pregnancy.

作者信息

Ngai S W, Tang O S, Lao T, Ho P C, Ma H K

机构信息

Department of Obstetrics and Gynaecology, University of Hong Kong, Tsan Yuk Hospital.

出版信息

Hum Reprod. 1995 May;10(5):1220-2. doi: 10.1093/oxfordjournals.humrep.a136122.

Abstract

Intravaginal misoprostol has been shown to be effective for cervical priming before a surgically induced abortion. The objective was to investigate the effectiveness of oral misoprostol in cervical dilatation prior to vacuum aspiration between the 6th and 12th weeks of pregnancy. The results showed that in nulliparous patients, the median cervical dilatation in the treatment group (7.8 mm) was significantly greater than that in the placebo group (3.7 mm). In multiparous patients, the difference was also statistically significant (9.8 versus 6.0 mm). The ease of dilatation, assessed subjectively by the operating surgeons, was significantly improved in the treatment group. There was also a significant reduction in the duration of the operation and in the mean blood loss in the treatment group. The side-effects encountered in the treatment group were mild and well accepted by the women. Oral misoprostol is an effective and safe method for cervical dilatation prior to vacuum aspiration in first trimester pregnancy.

摘要

阴道内使用米索前列醇已被证明在手术诱导流产前用于宫颈预处理是有效的。目的是研究口服米索前列醇在妊娠第6至12周行真空吸引术前宫颈扩张中的有效性。结果显示,在未生育患者中,治疗组宫颈扩张的中位数(7.8毫米)显著大于安慰剂组(3.7毫米)。在经产妇中,差异也具有统计学意义(9.8对6.0毫米)。手术医生主观评估的扩张难易程度在治疗组有显著改善。治疗组的手术时间和平均失血量也显著减少。治疗组出现的副作用轻微,女性患者易于接受。口服米索前列醇是孕早期行真空吸引术前宫颈扩张的一种有效且安全的方法。

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