开发宫内节育器自取出指南:一项混合方法定性和小型试点研究。

Francesca Collins, Kelly Gilmore, Kelsey A Petrie, Lyndsey S Benson
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引用次数: 1

摘要

背景:宫内节育器(IUD)是一种高效的长效可逆避孕(LARC),禁忌症少。然而,用户在进行所需的删除时经常遇到障碍。宫内节育器的自行移除可能会减轻这些障碍。我们试图开发一个指南的宫内节育器自我清除的目的是增加用户控制的方法。方法:这是一项两期混合方法的定性小型试点研究,目的是开发一种宫内节育器自取出指南。我们对宫内节育器自行取出的建议进行了在线内容分析,并对专家关键线人进行了访谈,以制定宫内节育器自行取出指南。接下来,我们招募了之前曾尝试自行摘除的宫内节育器使用者参加焦点小组讨论和个人访谈,以进一步完善指南。在研究的第二阶段,我们在8名有兴趣自行摘除的宫内节育器使用者中试用了该指南。结果:专家重点举报人一致认为宫内节育器自拔出安全、低风险。成功取出宫内节育器的主要组成部分是感觉和抓住绳子的能力,蹲下的姿势,多次尝试。强调了将宫内节育器自行取出作为安全的首选方法。在第二阶段,临床试验的参与者建议为不可触摸的字符串提供更多信息,但他们喜欢所提供的风格和信息。一名参与者成功取出了宫内节育器。结论:宫内节育器使用者对我们的指南表示满意。在我们的小型试验中,大多数人无法取出自己的宫内节育器。需要一个更大的研究来评估可接受性、可行性和提高成功自我清除的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Developing an intrauterine device self-removal guide: a mixed methods qualitative and small pilot study.

Background: The intrauterine device (IUD) is a highly effective form of long-acting reversible contraception (LARC) with few contraindications. Users, however, often encounter barriers to desired removal. IUD self-removal may mitigate these obstacles. We sought to develop a guide for IUD self-removal with the aim of increasing user control over the method.

Methods: This was a two-phase mixed-methods qualitative and small pilot study with the aim of developing an IUD self-removal guide. We conducted an online content analysis of advice for IUD self-removal as well as interviews with expert key informants to develop an IUD self-removal guide. We next recruited IUD-users who had previously attempted self-removal to participate in focus group discussion and individual interviews to further refine the guide. In the second phase of the study, we piloted the guide among eight IUD-users seeking removal interested in attempting self-removal.

Results: Expert key informants agreed that IUD self-removal was safe and low risk. The primary components of successful IUD self-removal elicited were ability to feel and grasp the strings, a crouched down position, and multiple attempts. A preference for presenting IUD self-removal as safe was emphasized. In the second phase, participants in the clinical pilot suggested more information for non-palpable strings, but liked the style and information provided. One participant successfully removed their IUD.

Conclusions: IUD-users reported satisfaction with our guide. In our small pilot, the majority were unable to remove their own IUD. A larger study is needed to assess acceptability, feasibility, and efficacy in increasing successful self-removal.

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