小型铜质宫内节育器的避孕效果及副作用比较。

NEJM evidence Pub Date : 2025-08-01 Epub Date: 2025-07-22 DOI:10.1056/EVIDoa2400480
Courtney A Schreiber, Kavita Nanda, David Hubacher, David K Turok, Jeffrey T Jensen, Mitchell D Creinin, Katharine O White, Ila Dayananda, Stephanie B Teal, Pai-Lien Chen, Beatrice A Chen, Alisa B Goldberg, Jennifer L Kerns, Clint Dart, Anita L Nelson, Michael A Thomas, David F Archer, Jill E Brown, Paula M Castaño, Anne E Burke, Bliss Kaneshiro, Diana L Blithe
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引用次数: 0

摘要

背景:宫内节育器(iud)是非常有效的,但可接受性和连续性因使用者和节育器的特点而异。我们评估了欧洲和加拿大可买到的380毫米铜宫内节育器NTCu380 Mini的疗效,并与美国可买到的380毫米铜宫内节育器TCu380A的安全性和连续性进行了比较。方法:我们将16至40岁的参与者以4:1的比例随机分配给NTCu380 Mini或TCu380A,并进行37个月的评估。主要终点是35岁及以下参与者的NTCu380 Mini疗效,通过Pearl指数(定义为每100名妇女年的怀孕次数)来衡量。其他结果包括通过生存分析NTCu380 Mini到妊娠的时间,以及NTCu380 Mini与TCu380A的不良事件(ae)和延续率的比较。结果:我们将887名受试者随机分配到NTCu380 Mini组(744名[83.9%]nulliparous)和218名受试者到TCu380A组(183名[83.9%]nulliparous),其中875名(98.6%)和213名(97.7%)受试者放置成功。NTCu380迷你宫内节育器3年累计珍珠指数为1.86(95%可信区间[CI], 1.20 ~ 2.74) / 100名妇女年;第3年的累计妊娠率为4.8% (95% CI, 2.8 ~ 6.9%)。ntcu380mini用户发生严重不良事件31例(3.5%),TCu380A用户发生严重不良事件4例(1.9%)(P=0.28)。有449名(51.3%)NTCu380 Mini用户和122名(57.3%)TCu380A用户停药(P=0.07)。NTCu380 Mini患者(152例[20.8%])的ae导致停药的频率低于TCu380A患者(57例[33.2%])(P=0.001),特别是出血或盆腔疼痛ae(103例[14.5%]比46例[27.3%];结论:在这个主要为未生育的人群中,NTCu380迷你宫内节育器在3年内的妊娠率约为5%,与TCu380A使用者相比,其导致停药的副作用更少。(由比尔及梅琳达·盖茨基金会等资助;ClinicalTrials.gov号码:NCT03124160。)这篇文章的发现和结论是作者的,并不一定反映美国计划生育联合会的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contraceptive Efficacy and Comparative Side Effects of a Mini Copper Intrauterine Device.

Background: Intrauterine devices (IUDs) are highly effective, yet acceptability and continuation differ by user and device characteristics. We evaluated the efficacy of the NTCu380 Mini, a 380-mm2 copper IUD available in Europe and Canada, and compared safety and continuation with the TCu380A IUD, the 380-mm2 copper IUD available in the United States.

Methods: We randomly assigned participants between 16 and 40 years of age in a 4:1 ratio to the NTCu380 Mini or TCu380A and assessed over 37 months. The primary outcome was NTCu380 Mini efficacy measured by the Pearl Index (defined as the number of pregnancies per 100 woman-years) in participants 35 years of age and under. Additional outcomes included NTCu380 Mini time to pregnancy by survival analysis, and comparative adverse events (AEs) and continuation rates of NTCu380 Mini versus TCu380A.

Results: We randomly assigned 887 participants to NTCu380 Mini (744 [83.9%] nulliparous) and 218 to TCu380A (183 [83.9%] nulliparous), of whom 875 (98.6%) and 213 (97.7%), respectively, had successful placement. The NTCu380 Mini IUD 3-year cumulative Pearl Index was 1.86 (95% confidence interval [CI], 1.20 to 2.74) pregnancies per 100 women-years; the cumulative rate of pregnancy through year 3 was 4.8% (95% CI, 2.8 to 6.9%). Serious AEs occurred in 31 (3.5%) NTCu380 Mini and 4 (1.9%) TCu380A users (P=0.28). Discontinuation occurred in 449 (51.3%) NTCu380 Mini and 122 (57.3%) TCu380A users (P=0.07). AEs led to discontinuation less frequently among NTCu380 Mini (152 [20.8%]) than TCu380A users (57 [33.2%]) (P=0.001), particularly bleeding or pelvic pain AEs (103 [14.5%] vs. 46 [27.3%], respectively; P<0.001).

Conclusions: In this predominantly nulliparous population, the NTCu380 Mini IUD had an approximate 5% pregnancy rate over 3 years, with fewer side effects leading to discontinuation than observed among TCu380A users. (Funded by the Bill and Melinda Gates Foundation and others; ClinicalTrials.gov number, NCT03124160.) The findings and conclusions in this article are those of the authors and do not necessarily reflect the views of the Planned Parenthood Federation of America, Inc.

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