艾滋病毒护理寻求途径和障碍的护理面临的艾滋病毒感染者在尼泊尔农村:一个定性研究。

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Amit Timilsina, Anisha Shrestha, Pabitra Neupane, Sudip Nepal, Bishow Kandel, Sudha Devkota, Subash Thapa
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引用次数: 0

摘要

背景:人类免疫缺陷病毒(HIV)对一个人的社会和个人生活产生重大影响,影响身体和心理健康。为了实现全球95-95-95目标,必须了解和应对改善对艾滋病毒感染者持续护理的多层次挑战。本研究深入研究了居住在尼泊尔农村地区的PLWH寻求护理的途径和遇到的障碍,揭示了获得和导航连续护理的复杂性。设计:本研究设计为定性专题研究,包括对尼泊尔Koshi省农村地区21个PLWH的深度访谈和对4个卫生服务提供者的关键信息提供者的访谈。采用半结构化访谈准则来确保数据收集过程的一致性,然后采用归纳编码来识别数据并将其分类为代码。随后,制定分主题和主题,并进行清单分析,对数据进行分析。本文以节选的形式介绍了研究结果。结果:艾滋病毒护理连续性的多层次障碍包括:(1)社会文化障碍,如耻辱、歧视、害怕披露和对传统治疗师的严重依赖;(二)社会经济障碍,如贫穷、获得医疗保险的机会有限、卫生知识普及程度低以及根据《社会保障法》将PLWH排除在外;(iii)以大量饮酒和抗逆转录病毒治疗依从性差为特征的宿命论生活方式;(iv)与卫生系统相关的障碍,如卫生保健提供者的虐待,以及距离抗逆转录病毒治疗中心很远。结论:有必要扩大治疗以外的服务,包括以社区为重点的认识和宣传、社区组织牵头的项目、经济赋权以及将农村地区艾滋病病毒持续护理纳入社会保障机制。患者和公众贡献:在研究设计阶段,咨询了两个PLWH和两个服务提供商,讨论研究差距,了解当前的做法,讨论数据收集工具及其内容。同样,四家服务提供商支持该研究的实施,并被咨询以解释数据的潜在含义。一个服务提供商也为手稿开发过程做出了贡献。PLWH和服务提供者也是研究的参与者。本研究的发现基于数据收集阶段提供的数据/信息,因此对本研究有意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HIV Care Seeking Pathways and Barriers to the Continuum of Care Faced by Persons Living With HIV in Rural Nepal: A Qualitative Study

Background

The Human Immunodeficiency Virus (HIV) has a major impact on a person's social and personal lives, affecting both physical and mental health. To meet the global 95-95-95 target, it is essential to understand and address the multi-level challenges to improve the continuum of care for persons living with HIV (PLWH). This study delves into the care-seeking pathways and barriers encountered by PLWH residing in rural areas of Nepal, shedding light on the complexities of accessing and navigating the continuum of care.

Design

This study was designed as a qualitative thematic study that consisted of in-depth interviews among 21 PLWH and key-informant interviews among four health service providers in rural districts of Koshi province in Nepal. Semi-structured interview guidelines were used to ensure consistency in the data collection process, followed by Inductive Coding to identify and categorize the data into codes. Subsequently, sub-themes and themes were developed, and manifest analysis was conducted to analyze the data. The findings of the study are presented in this paper in the form of excerpts.

Results

The multilevel barriers to HIV care continuum included (i) socio-cultural barriers such as stigma, discrimination, fear of disclosure, and heavy reliance on traditional healers; (ii) socio-economic barriers such as poverty, limited access to health insurance, low health literacy and the exclusion of PLWH under Social Security Act; (iii) fatalistic lifestyles characterized by heavy alcohol consumption, and poor adherence to antiretroviral therapy and (iv) health system-related barriers such as mistreatment by healthcare providers, and long distances to ART centers.

Conclusions

There is a need to expand services beyond treatment, including community-focused awareness and sensitization, programs led by community-based organization, economic empowerment and inclusion of PLWH under social security mechanisms in rural areas for HIV continuum of care.

Patient and Public Contribution

During the study design phase, two PLWH and two service providers were consulted to discuss the research gap, understand the current practices and discuss the data collection tools and their content. Similarly, four service providers supported implementation of the study and were also consulted to interpret the underlying meaning of the data. One service provider also contributed to the manuscript development process. PLWH and the service providers were also the study participants. The findings of the study are grounded in the data/information provided during the data collection phase, thus meaningfully contributing to this study.

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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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