David L. Eisenberg, Courtney A. Schreiber, Paul D Blumenthal, D. Turok, Andrea I. Olariu, M. D. Creinin
{"title":"Feasibility study of a single‐handed inserter for levonorgestrel 52 mg intrauterine device placement","authors":"David L. Eisenberg, Courtney A. Schreiber, Paul D Blumenthal, D. Turok, Andrea I. Olariu, M. D. Creinin","doi":"10.1002/rfc2.68","DOIUrl":null,"url":null,"abstract":"To assess placement outcomes using a levonorgestrel 52 mg intrauterine device (IUD) inserter designed for single‐handed use.Investigators enroled participants 18–45 years to have the IUD inserted using a redesigned inserter with removal 5–15 min after placement. Physicians and participants provided feedback on their insertion experience.Successful placement occurred in 48 of 50 (96.0%) enroled participants. Investigators rated insertion device loading “easy” in 49 (98.0%) and placement “easy” in 44 (88.0%) cases. Cramping pain was reported at insertion by 47 (94.0%) participants, mostly mild (32 [64.0%]) or moderate (11 [22.0%]).The single‐handed inserter is easy to use and results in high rates of insertion success.","PeriodicalId":74669,"journal":{"name":"Reproductive, female and child health","volume":"76 7","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reproductive, female and child health","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/rfc2.68","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
To assess placement outcomes using a levonorgestrel 52 mg intrauterine device (IUD) inserter designed for single‐handed use.Investigators enroled participants 18–45 years to have the IUD inserted using a redesigned inserter with removal 5–15 min after placement. Physicians and participants provided feedback on their insertion experience.Successful placement occurred in 48 of 50 (96.0%) enroled participants. Investigators rated insertion device loading “easy” in 49 (98.0%) and placement “easy” in 44 (88.0%) cases. Cramping pain was reported at insertion by 47 (94.0%) participants, mostly mild (32 [64.0%]) or moderate (11 [22.0%]).The single‐handed inserter is easy to use and results in high rates of insertion success.