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A Meta-Analysis of Bilateral Essure® Procedural Placement Success Rates on First Attempt

机译:首次尝试双边Essure®程序放置成功率的荟萃分析

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摘要

>Background: The Essure>® (Bayer HealthCare Pharmaceuticals, Leverkusen, Germany) female sterilization procedure entails using a hysteroscope to guide a microinsert into the Fallopian tube openings. Failed placement can lead to patient dissatisfaction, repeat procedures, unintended or ectopic pregnancy, perforation of internal organs, or need for subsequent medical interventions. Additional interventions increase women's health risks, and costs for patients and the health care industry. Demonstrated successful placement rates are 63%–100%. To date, there have not been any systematic analyses of variables associated with placement rates. >Objectives: The aims of this review were: (1) to estimate the average rate of successful bilateral Essure microinsert placement on first attempt; and (2) to identify variables associated with successful placement. >Materials and Methods: A meta-analysis was conducted on 64 published studies and 19 variables. Following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines, all published studies between November 2001 and February 2015 were reviewed. The studies were taken from from PubMed and Google Scholar, and by using the the “snowball” method that reported variables associated with successful bilateral Essure placement rates. >Results: The weighted average rate of successful bilateral microinsert placement on first attempt was 92% (0.92 [95% confidence interval: 0.904–0.931]). Variables associated with successful placements were: (1) newer device models; (2) higher body mass index; and (3) a higher percent of patients who received local anesthesia. >Conclusions: The data gathered for this review indicate that the highest bilateral success rates may be obtained by utilizing the newest Essure device model with local anesthesia in heavier patients. More standardized data reporting in published Essure studies is recommended. (J GYNECOL SURG 31:308)
机译:>背景:Essure >®(德国勒沃库森的拜耳医药保健制药公司)进行女性绝育手术时,需要使用宫腔镜将微型插入物导入输卵管开口。放置失败会导致患者不满意,重复操作,意外或异位妊娠,内脏器官穿孔或需要后续医疗干预。额外的干预措施会增加妇女的健康风险,并增加患者和医疗行业的成本。展示的成功安置率为63%–100%。迄今为止,还没有对与安置率相关的变量进行任何系统的分析。 >目的:此次审查的目的是:(1)估算首次尝试双边Essure微插入成功的平均率; (2)确定与成功放置相关的变量。 >材料和方法:对64项已发表的研究和19项变量进行了荟萃分析。遵循系统评价和荟萃分析的首选报告项目(PRISMA)指南,对2001年11月至2015年2月之间的所有已发表研究进行了审查。这些研究来自PubMed和Google Scholar,并使用“雪球”方法进行了报道,该方法报告了与成功的双边Essure安置率相关的变量。 >结果:首次尝试成功完成双边微插入的加权平均率为92%(0.92 [95%置信区间:0.904-0.931])。与成功放置相关的变量为:(1)较新的设备型号; (2)体重指数较高; (3)接受局部麻醉的患者比例更高。 >结论:本次审查收集的数据表明,在较重的患者中,采用局部麻醉的最新Essure装置模型可以获得最高的双侧成功率。建议在已发布的Essure研究中使用更标准化的数据报告。 (妇科医学杂志31:308)

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