中国医学装备
中國醫學裝備
중국의학장비
CHINA MEDICAL EQUIPMENT
2015年
9期
110-111,112
,共3页
温烯%刘彤%谢峰%迟心左
溫烯%劉彤%謝峰%遲心左
온희%류동%사봉%지심좌
米非司酮%米索前列醇%终止妊娠%利凡诺
米非司酮%米索前列醇%終止妊娠%利凡諾
미비사동%미색전렬순%종지임신%리범낙
Termination of pregnancy%Mifepristone%Misoprostol%Rivanol
目的:研究探讨利凡诺羊膜腔注射与米非司酮配伍米索前列醇阴道放药用于孕中期妊娠引产的临床有效性和安全性。方法:选取孕周在14~20周自愿要求终止妊娠的80名孕妇,随机分为观察组和对照组,每组40例,两组均给予米非司酮150 mg分3次口服,间隔12 h。观察组第3日晨7点阴道内放置米索前列醇200μg;对照组使用利凡诺引产,比较两组从用药到胎儿排出的时间、出血量及引产并发症等情况。结果:两组孕妇在年龄、引产前孕周及孕次等相比无差异。两组孕妇从用药到胎儿排出的时间、分娩出血量方面比较,差异有统计学意义(t=16.03,t=-8.0, P<0.05)。与利凡诺羊膜腔内注射相比,米非司酮配伍米索前列醇阴道上药引产成功率高,组织残留率和清宫率低,产程短,出血量亦较对照组少,差异均具有统计学意义。副反应方面,观察组恶心、呕吐发生率均较对照组高。结论:米非司酮联合米索前列醇阴道上药是终止中期妊娠的一种安全、有效方法。
目的:研究探討利凡諾羊膜腔註射與米非司酮配伍米索前列醇陰道放藥用于孕中期妊娠引產的臨床有效性和安全性。方法:選取孕週在14~20週自願要求終止妊娠的80名孕婦,隨機分為觀察組和對照組,每組40例,兩組均給予米非司酮150 mg分3次口服,間隔12 h。觀察組第3日晨7點陰道內放置米索前列醇200μg;對照組使用利凡諾引產,比較兩組從用藥到胎兒排齣的時間、齣血量及引產併髮癥等情況。結果:兩組孕婦在年齡、引產前孕週及孕次等相比無差異。兩組孕婦從用藥到胎兒排齣的時間、分娩齣血量方麵比較,差異有統計學意義(t=16.03,t=-8.0, P<0.05)。與利凡諾羊膜腔內註射相比,米非司酮配伍米索前列醇陰道上藥引產成功率高,組織殘留率和清宮率低,產程短,齣血量亦較對照組少,差異均具有統計學意義。副反應方麵,觀察組噁心、嘔吐髮生率均較對照組高。結論:米非司酮聯閤米索前列醇陰道上藥是終止中期妊娠的一種安全、有效方法。
목적:연구탐토리범낙양막강주사여미비사동배오미색전렬순음도방약용우잉중기임신인산적림상유효성화안전성。방법:선취잉주재14~20주자원요구종지임신적80명잉부,수궤분위관찰조화대조조,매조40례,량조균급여미비사동150 mg분3차구복,간격12 h。관찰조제3일신7점음도내방치미색전렬순200μg;대조조사용리범낙인산,비교량조종용약도태인배출적시간、출혈량급인산병발증등정황。결과:량조잉부재년령、인산전잉주급잉차등상비무차이。량조잉부종용약도태인배출적시간、분면출혈량방면비교,차이유통계학의의(t=16.03,t=-8.0, P<0.05)。여리범낙양막강내주사상비,미비사동배오미색전렬순음도상약인산성공솔고,조직잔류솔화청궁솔저,산정단,출혈량역교대조조소,차이균구유통계학의의。부반응방면,관찰조악심、구토발생솔균교대조조고。결론:미비사동연합미색전렬순음도상약시종지중기임신적일충안전、유효방법。
Objective:To access the effectiveness and safety of intravaginal misoprostol following mifepristone administration to terminate 14-20weeks gestation.Methods: Eighty patients requesting legal termination of pregnancy at gestational between 14 to 20 weeks were from the Xuan Wu Hospital of capital University of medical of science between January 2012 and December 2012. They were divided randomly into two groups. Both 40 women (experimental group) and 40 women (control group) received 50mg of oral mifepristone every 12h for three times. Then, the experimental group was given 200μg misoprostol intravaginal at 7am on the third day and the control group received intra-amniotic injection of rivanol.Results: Comparing with intra-amniotic injection of rivanol, the combination of mifepristone and misoprostol intravaginally has higher success rate, lower tissue residue rate and curettage of uterus, shorter labor and less hemorrhage, the difference were statistically significant. As to the side effects, nausea, vomiting are statistically significant.Conclusion: It is a safe and effective method for mifepristone and vaginal misoprostol to termination of mid-pregnancy.