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米索前列醇在不孕患者无麻醉下门诊宫腔镜检查中的有效性。

Effectiveness of misoprostol for office hysteroscopy without anesthesia in infertile patients.

机构信息

Department of Obstetrics and Gynecology, University Center of Reproductive Medicine, Hospital Universitario Dr Jose E Gonzalez, Universidad Autonoma de Nuevo Leon, Monterrey, Nuevo Leon, Mexico.

出版信息

Fertil Steril. 2011 Feb;95(2):759-61. doi: 10.1016/j.fertnstert.2010.07.1066. Epub 2010 Aug 21.

Abstract

OBJECTIVE

To evaluate and compare the effectiveness of oral and vaginal misoprostol versus placebo to facilitate office hysteroscopy without anesthesia during infertile diagnostic evaluation.

DESIGN

Randomized, prospective trial.

SETTING

Patients scheduled for diagnostic office hysteroscopy at a university hospital.

PATIENT(S): Seventy-five infertile patients scheduled for diagnostic office hysteroscopy.

INTERVENTION(S): Patients were divided into three groups: group A received oral misoprostol 600 μg; group B, vaginal misoprostol 400 μg; and group C, oral placebo.

MAIN OUTCOME MEASURE(S): Pain, evaluated by visual analogue scale, and surgical time were recorded and compared. Statistical analysis was done using Student's t-test.

RESULT(S): Pain was low in the vaginal misoprostol group. Mean visual analogue scale in the oral misoprostol group was 6.04 ± 1.5; in the vaginal misoprostol group 2.85 ± 1.2; and in the placebo group 7.50 ± 1.5. Procedural time for office hysteroscopy was shorter in the vaginal misoprostol group (2.7 ± 1.0 minutes) compared with group A (5.5 ± 1.1 minutes) and group C (6.3 ± 3.8 minutes).

CONCLUSION(S): Vaginal misoprostol, 400 μg, administered the day before office hysteroscopy considerably reduces pain and the time needed for hysteroscopy. This simple strategy may facilitate office hysteroscopy during an infertility work-up.

摘要

目的

评估和比较口服及阴道给予米索前列醇与安慰剂在不孕诊断评估中用于无麻醉门诊宫腔镜检查的效果。

设计

随机、前瞻性试验。

地点

一家大学医院门诊宫腔镜检查的患者。

患者

75 名计划行诊断性门诊宫腔镜检查的不孕患者。

干预

患者分为三组:A 组口服米索前列醇 600μg;B 组阴道给予米索前列醇 400μg;C 组口服安慰剂。

主要观察指标

疼痛程度采用视觉模拟评分法评估,并记录和比较手术时间。统计学分析采用 Student's t 检验。

结果

阴道给予米索前列醇组疼痛程度低。口服米索前列醇组平均视觉模拟评分 6.04±1.5;阴道给予米索前列醇组 2.85±1.2;安慰剂组 7.50±1.5。阴道给予米索前列醇组门诊宫腔镜检查时间更短(2.7±1.0 分钟),与 A 组(5.5±1.1 分钟)和 C 组(6.3±3.8 分钟)比较差异有统计学意义。

结论

阴道给予米索前列醇 400μg,于门诊宫腔镜检查前一天给药可显著减轻疼痛和宫腔镜检查所需时间。这种简单的策略可能有助于在不孕检查中进行门诊宫腔镜检查。

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