妇女对子宫内膜异位症相关性交障碍的自我管理:定性研究。

IF 4 2区 医学 Q1 CLINICAL NEUROLOGY
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引用次数: 0

摘要

鉴于子宫内膜异位症的药物治疗存在局限性,自我管理是症状管理的重要组成部分,为患者提供信息和教育是对药物干预的必要补充。虽然 50-70% 的子宫内膜异位症患者会出现性生活疼痛,但针对性生活疼痛的自我管理知识却很有限。全面了解所使用的自我管理策略是制定支持性护理干预措施的基础,有助于缓解疼痛和相关的社会心理后遗症。我们的目的是描述人们在应对子宫内膜异位症相关性疼痛和制定自我管理策略方面的经验。我们在定性解释性描述方法的指导下,采用恒定比较和主题分析技术分析了 20 位女性的访谈数据。参与者(年龄在 18-44 岁之间)均为女性,主要是白种人(90%)和异性恋者(80%)。在她们的一生中,这些女性在经历痛苦的性经历时,似乎逐渐形成了自我管理的策略。这一复杂的历程包括四个阶段:i) 将痛苦的性行为视为正常;ii) 经历不断变化的想法和情绪;iii) 逐渐理解痛苦的性行为并寻求帮助;iv) 学习驾驭痛苦性行为的策略,其中包括为性行为做好心理和生理准备,以及与亲密伴侣沟通。本研究中的女性通过与了解她们所面临挑战的其他人接触,逐渐形成了自我管理的策略。未来有必要开展相关研究,以抵制性生活疼痛的正常化,开发和传播面向患者的信息,提供专门针对性生活疼痛的教育,改善获得多学科护理的途径,促进社会联系和支持,并加强与亲密伴侣的沟通。观点:在本文中,我们报告了患有子宫内膜异位症相关性疼痛的妇女的经历及其自我管理策略。临床医生可能会对子宫内膜异位症相关性疼痛的定性研究感兴趣,因为他们希望进一步了解患者的经历以及可以采取哪些策略来缓解性生活疼痛。数据提供:本研究中产生和/或分析的数据集不对外公开,因为参与者不同意公开其数据,但可向通讯作者提出合理要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Women’s Self-Management of Dyspareunia Associated With Endometriosis: A Qualitative Study

Given the limitations of medical treatment for endometriosis, self-management is a critical component of symptom management, and providing patients with information and education is a necessary complement to medical interventions. Though 50 to 70% of people with endometriosis experience dyspareunia (painful sex), there is limited knowledge of self-management specific to painful sex. A comprehensive understanding of the self-management strategies used is foundational to developing supportive care interventions that help ease pain and related psychosocial sequelae. The objective was to describe people's experiences of navigating endometriosis-associated painful sex and developing self-management strategies. We analyzed interview data from 20 women using constant comparative and thematic analysis techniques, guided by qualitative interpretive description methodology. Participants (age range 18–44 years) all identified as women and were predominately Caucasian (90%) and heterosexual (80%). Throughout their lives, the women appeared to gradually develop self-management strategies while navigating painful sexual experiences. This complex journey encompassed four phases: 1) viewing painful sex as normal, 2) experiencing evolving thoughts and emotions, 3) coming to understand painful sex and seeking help, and 4) learning strategies to navigate painful sex, these include preparing mentally and physically for sex and communicating with intimate partner(s). Women in this study developed self-management strategies over time through engagement with others who understood their challenges. Future research is warranted regarding initiatives to counter the normalization of painful sex, develop and disseminate patient-facing information, provide education specific to dyspareunia, improve access to multidisciplinary care, facilitate social connections and support, and enhance communication with intimate partners.

Perspective

In this paper, we report on the experiences of women with endometriosis-associated painful sex and their self-management strategies. Clinicians may be interested in a qualitative exploration of endometriosis-associated painful sex as they seek to further understand their patient’s experiences and what strategies can be implemented to alleviate dyspareunia.

Data Availability

The data sets generated during and/or analyzed during the current study are not publicly available as participants did not consent to making their data publicly available but are available from the corresponding author on reasonable request.

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来源期刊
Journal of Pain
Journal of Pain 医学-临床神经学
CiteScore
6.30
自引率
7.50%
发文量
441
审稿时长
42 days
期刊介绍: The Journal of Pain publishes original articles related to all aspects of pain, including clinical and basic research, patient care, education, and health policy. Articles selected for publication in the Journal are most commonly reports of original clinical research or reports of original basic research. In addition, invited critical reviews, including meta analyses of drugs for pain management, invited commentaries on reviews, and exceptional case studies are published in the Journal. The mission of the Journal is to improve the care of patients in pain by providing a forum for clinical researchers, basic scientists, clinicians, and other health professionals to publish original research.
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