Experiences of Black Women With Pelvic Floor Disorders-A Qualitative Analysis Study.

Pub Date : 2024-06-27 DOI:10.1097/SPV.0000000000001542
Jennifer Chyu, Oriyomi Alimi, Shreeya Popat, Gjanje Smith-Mathus, Una J Lee
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Abstract

Importance: Disparities research in Black women with pelvic floor disorders (PFDs) has primarily focused on epidemiology or surgical outcomes, but little is known about the patient perspective on seeking PFD care.

Objective: To provide quality and equitable care to Black women with PFDs, we conducted a qualitative study to hear their perspectives and lived health care experiences.

Study design: Black women seeking care for PFDs at a tertiary care institution were invited to participate in qualitative interviews. Open-ended questions explored participants' knowledge, attitudes, and health care experiences. Interviews were transcribed verbatim and coded line-by-line. Inductive content analysis was performed to identify key themes, and consensus was achieved among the research team.

Results: Eight Black women aged 21-83 years consented to participate. Patients noted a stigma surrounding PFDs, both among health care professionals and their community. They noted several barriers to care: financial, logistical, and racial bias. They cited difficulties in patient-health care professional communication, including not feeling heard or treated as an individual. They preferred gender and racial concordance with their physicians. These women expressed both a desire for more knowledge and to share this knowledge and advocate for other women.

Conclusions: Black women expressed distinct obstacles in their PFD health care. They reported not feeling heard or treated as a unique individual. The themes derived from this study identify complex patient-centered needs that can serve as the basis for future quality improvement work and/or hypothesis-driven research. By grounding health disparities research in patient perspectives, we can improve the health care experiences of Black women.

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患有盆底障碍的黑人妇女的经历--定性分析研究。
重要性:对患有盆底功能障碍(PFDs)的黑人妇女的差异研究主要集中在流行病学或手术结果方面,但对患者寻求 PFD 护理的角度却知之甚少:为了向患有 PFDs 的黑人妇女提供优质、公平的护理,我们开展了一项定性研究,以听取她们的观点和医疗保健生活经历:研究设计:我们邀请了在一家三级医疗机构寻求 PFD 护理的黑人妇女参加定性访谈。开放式问题探讨了参与者的知识、态度和医疗保健经验。访谈内容逐字转录并逐行编码。对访谈内容进行归纳分析,以确定关键主题,并在研究小组之间达成共识:八名年龄在 21-83 岁之间的黑人妇女同意参加访谈。患者指出,无论是在医护人员还是在她们所在的社区,PFD 都是一种耻辱。她们指出了接受治疗的几个障碍:经济、后勤和种族偏见。他们提到了患者与医护专业人员沟通时遇到的困难,包括感觉自己没有被倾听或被当作一个个体对待。她们希望与医生在性别和种族方面保持一致。这些妇女表示希望获得更多的知识,并分享这些知识,为其他妇女代言:黑人妇女在 PFD 医疗保健方面遇到了明显的障碍。她们表示没有被倾听,也没有被当作一个独特的个体对待。本研究得出的主题确定了以患者为中心的复杂需求,可作为未来质量改进工作和/或假设驱动型研究的基础。通过将健康差异研究建立在患者视角的基础上,我们可以改善黑人女性的医疗保健体验。
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