西南国防医药
西南國防醫藥
서남국방의약
MEDICAL JOURNAL OF NATIONAL DEFENDING FORCES IN SOUTHWEST CHINA
2015年
2期
158-160
,共3页
米索前列醇%米非司酮%利凡诺%中孕引产
米索前列醇%米非司酮%利凡諾%中孕引產
미색전렬순%미비사동%리범낙%중잉인산
misoprostol%mifepristone%rivanol%induced labor of middle-stage pregnant woman
目的:探讨单用米索前列醇阴道给药对中孕引产的效果及可行性。方法168例中孕引产者分为单用组( n=48)、配伍组( n=86)与利凡诺组( n=34),单用组采用米索前列醇200μg置入阴道后穹窿,1次/4 h;配伍组在与单用组相同方法应用米索前列醇前,另给予米非司酮25 mg,2次/d,服用3 d;利凡诺组采用利凡诺100 mg羊膜腔内注射。对比分析各组胎儿娩出时间、引产效果、阴道出血量及药物副作用发生率。结果单用组引产成功率(75.0%),与配伍组(83.7%)及利凡诺组(70.6%)相比均无显著差异(p>0.05);引产不全率,单用组(18.7%)显著高于配伍组(5.8%)(p<0.05),与利凡诺组(17.7%)相比无显著差异(p>0.05);胎儿娩出时间和出血量,单用组与配伍组无显著差异(p>0.05),均比利凡诺组显著减少(p<0.05);单用组副作用发生率(12.5%)显著低于配伍组(32.6%)(p<0.05)。结论单用米索前列醇阴道给药的中孕引产效果与配伍米非司酮相似,但副作用少,用药简单经济,适合临床应用。
目的:探討單用米索前列醇陰道給藥對中孕引產的效果及可行性。方法168例中孕引產者分為單用組( n=48)、配伍組( n=86)與利凡諾組( n=34),單用組採用米索前列醇200μg置入陰道後穹窿,1次/4 h;配伍組在與單用組相同方法應用米索前列醇前,另給予米非司酮25 mg,2次/d,服用3 d;利凡諾組採用利凡諾100 mg羊膜腔內註射。對比分析各組胎兒娩齣時間、引產效果、陰道齣血量及藥物副作用髮生率。結果單用組引產成功率(75.0%),與配伍組(83.7%)及利凡諾組(70.6%)相比均無顯著差異(p>0.05);引產不全率,單用組(18.7%)顯著高于配伍組(5.8%)(p<0.05),與利凡諾組(17.7%)相比無顯著差異(p>0.05);胎兒娩齣時間和齣血量,單用組與配伍組無顯著差異(p>0.05),均比利凡諾組顯著減少(p<0.05);單用組副作用髮生率(12.5%)顯著低于配伍組(32.6%)(p<0.05)。結論單用米索前列醇陰道給藥的中孕引產效果與配伍米非司酮相似,但副作用少,用藥簡單經濟,適閤臨床應用。
목적:탐토단용미색전렬순음도급약대중잉인산적효과급가행성。방법168례중잉인산자분위단용조( n=48)、배오조( n=86)여리범낙조( n=34),단용조채용미색전렬순200μg치입음도후궁륭,1차/4 h;배오조재여단용조상동방법응용미색전렬순전,령급여미비사동25 mg,2차/d,복용3 d;리범낙조채용리범낙100 mg양막강내주사。대비분석각조태인면출시간、인산효과、음도출혈량급약물부작용발생솔。결과단용조인산성공솔(75.0%),여배오조(83.7%)급리범낙조(70.6%)상비균무현저차이(p>0.05);인산불전솔,단용조(18.7%)현저고우배오조(5.8%)(p<0.05),여리범낙조(17.7%)상비무현저차이(p>0.05);태인면출시간화출혈량,단용조여배오조무현저차이(p>0.05),균비리범낙조현저감소(p<0.05);단용조부작용발생솔(12.5%)현저저우배오조(32.6%)(p<0.05)。결론단용미색전렬순음도급약적중잉인산효과여배오미비사동상사,단부작용소,용약간단경제,괄합림상응용。
Objective To explore the effect and feasibility of simple use of vaginal misoprostol on induced labor of middle-stage pregnant women. Methods Total 168 pregnant women for induced labor were divided into simple group(n=48),compatibility group(n=86)and rivanol group(n=34). In the simple group,misoprostol of 200 μg was put into the posterior vaginal fornix,one time per four hours;in the compatibility group,before misoprostol was administered as the above method,mifepristone of 25 mg was administered,twice per day;in the rivanol group,rivanol of 100 mg was used for intra-amniotic injection. The childbirth time,effect of induced labor,vaginal bleeding volume and the incidence of side effects of drugs were compared and analyzed. Resuits The success rate in simple group(75. 0%)had no significant difference in comparison with those in the compatibility group(83. 7%)and rivanol group(70. 6%)(p>0. 05);the incompleteness of induced labor of the simple group(18. 7%)was significantly higher than that of the compatibilitygroup(5.8%)(p<0.05),buthadnosignificantdifferencefromthatoftherivanolgroup(17.7%)(p>0.05).The childbirth time and bleeding volume of the simple group had no significant difference from those in the compatibility group(p>0. 05), and those of both groups were significantly lower than that in the rivanol group(p<0. 05);the incidence of side effect in the simple group(12. 5%)was significantly lower than that in the compatibility group(32. 6%)(p<0. 05). Conciusion The effect of simple use of vaginal misoprostol on induced labor of middle-stage pregnant women is similar to the effect of mifepristone,with fewer side effects, and the administration is simple and economical,so it is suitable for clinical application.