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《与子宫内膜异位症共存:肯尼亚女性经历的叙事分析》。

Living with Endometriosis: A Narrative Analysis of the Experiences of Kenyan Women.

机构信息

Department of Sociomedical Sciences, Mailman School of Public Health, Columbia University, 722 W. 168th Street, New York, NY 10032, USA.

Endo Sisters East Africa Foundation, Laiboni Center, Off Lenana Rd., Nairobi P.O. Box 100798-00101, Kenya.

出版信息

Int J Environ Res Public Health. 2023 Feb 25;20(5):4125. doi: 10.3390/ijerph20054125.

Abstract

Despite the high global prevalence of endometriosis, little is known about the experiences of women living with the disease in low- and middle-income contexts, including in Kenya and other countries across sub-Saharan Africa. This study captures the perspectives and recommendations of Kenyan women living with endometriosis through written narratives about the impact of the disease on their daily lives and their journeys through diagnosis and treatment. Thirty-seven women between the ages of 22 and 48 were recruited from an endometriosis support group in Nairobi and Kiambu, Kenya (February-March of 2022) in partnership with the Endo Sisters East Africa Foundation. Narrative data (written anonymous stories submitted through Qualtrics) were analyzed using a deductive thematic analysis methodology. Their stories revealed three themes related to their shared experiences with endometriosis: (1) stigma and disruption to quality of life, (2) barriers to acceptable healthcare, and (3) reliance on self-efficacy and social support to cope with the disease. These findings demonstrate a clear need for improved social awareness of endometriosis in Kenya and the establishment of clear, effective, and supportive pathways, with trained, geographically and financially accessible health care providers, for endometriosis diagnosis and treatment.

摘要

尽管子宫内膜异位症在全球范围内的患病率很高,但对于生活在低收入和中等收入环境中的女性(包括肯尼亚和撒哈拉以南非洲其他国家)的患病经历,人们知之甚少。本研究通过记录肯尼亚子宫内膜异位症患者的生活经历和诊断治疗历程的书面叙述,捕捉了她们的观点和建议。本研究于 2022 年 2 月至 3 月,在肯尼亚内罗毕和基安布的子宫内膜异位症支持组织中,与东非 Endo Sisters 基金会合作,招募了 37 名年龄在 22 岁至 48 岁之间的女性。通过 Qualtrics 提交的匿名书面故事的叙述性数据,采用演绎主题分析方法进行分析。她们的故事揭示了与她们共同的子宫内膜异位症经历相关的三个主题:(1)耻辱感和生活质量的破坏,(2)获得可接受医疗保健的障碍,以及(3)依赖自我效能和社会支持来应对疾病。这些发现表明,肯尼亚明显需要提高对子宫内膜异位症的社会认识,并建立明确、有效和支持性的途径,由接受过培训、地理位置和经济上可及的医疗保健提供者来进行子宫内膜异位症的诊断和治疗。

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