黎巴嫩社区获得初级保健中心的经验:老年人、家庭成员和服务提供者的观点。

IF 3.2 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Saydeh Dableh, Kate Frazer, Mathilde Azar, Thilo Kroll
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引用次数: 0

摘要

引言:中低收入国家忽视了老年人获得初级卫生保健的经历,导致以人为本的护理的不公平获取和有限提供。在黎巴嫩,经济危机增加了老年人的脆弱性和对初级保健中心提供的服务的依赖。本研究探讨了(1)影响使用phcc决策的因素;(2)老年人从自身、家庭成员和服务提供者三个角度访问初级保健中心的体验;(3)家庭成员使用初级保健中心的经历;(4)服务提供者在黎巴嫩北部地区初级保健中心内为老年人提供护理的经验。方法:本研究采用定性描述性设计和归纳性内容分析法。通过7次焦点小组讨论和15次个人访谈(n = 57名老年人、家庭成员和服务提供者)收集数据。结果:决定使用初级保健中心服务的因素包括社会经济地位、服务知识、家庭成员的影响、感知到的服务质量和距离、与年龄相关的变化以及提供者的态度和行为。老年人报告了受个人、组织、社区、政府和全球各级因素影响的不同获取经验。积极体验包括自主性增强、对接受所需服务的感激、感知到的护理质量和社交机会。然而,负面体验包括羞辱和不适、焦虑、依赖、感知到的地位倒退、感知到的质量差和成为负担的感觉。虽然一些家庭成员报告说,获得负担得起的医疗服务让他们感到宽慰,但其他人报告说,他们感到不适,感到地位下降,被指责忽视,以及在多个提供者之间协调医疗服务面临挑战。服务提供者的经历包括为支持老年人感到自豪,但也有因报酬不公平而产生的怨恨。结论:研究结果揭示了老年人和家庭成员所欣赏的护理方面以及导致负面体验的其他方面。老年人、家庭成员和服务提供者的经验是相互关联的。质量改进需要全面的方法来解决他们的需求。调查结果为从业人员和政策制定者提供了信息,以设计多维度和以人为本的方法,最大限度地提高医疗保健的可及性。患者和公众贡献:本研究或分析中未应用PPI介入方法。然而,研究结果为与老年人的讨论提供了信息,并促进了合作伙伴关系,共同设计了一项侧重于制定解决方案的后续研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Experience of Accessing Primary Healthcare Centres in a Lebanese Community: Perspectives of Older People, Family Members and Service Providers

The Experience of Accessing Primary Healthcare Centres in a Lebanese Community: Perspectives of Older People, Family Members and Service Providers

Introduction

Older people's experiences with access to primary healthcare are overlooked in LMICs, leading to inequitable access and limited delivery of person-centred care. In Lebanon, the economic crisis has increased older people's vulnerabilities and reliance on services provided through primary healthcare centres (PHCCs). This study explores (1) factors shaping decisions of using PHCCs; (2) experiences of older people accessing PHCCs from three perspectives: the older people themselves, family members and service providers; (3) family members' experiences with accessing PHCCs; and (4) service providers' experiences with providing care for older people within PHCCs in a Northern Lebanese district.

Methods

This study adopts a qualitative descriptive design with an inductive content analysis approach. Data were collected through seven focus group discussions and 15 individual interviews (n = 57 older people, family members, and service providers).

Results

Factors shaping decisions of using PHCCs' services include socio-economic status, knowledge of services, influences of family members, perceived service quality and proximity, age-related changes, and providers' attitudes and behaviours. Older people reported varied access experiences shaped by factors at individual, organisational, communal, governmental and global levels. Positive experiences included enhanced autonomy, gratitude for receiving needed services, perceived care quality and socialising opportunities. However, negative experiences included humiliation and discomfort, anxiety, dependency, perceived status regression, perceived poor quality and a sense of being a burden. While some family members reported relief from getting affordable care, others reported discomfort, perceived status regression, blame for neglect and challenges with coordinating care across multiple providers. Service providers' experiences included pride in supporting older people, but resentment due to unfair remuneration.

Conclusion

Findings reveal aspects of care that older people and family members appreciate and others that contribute to negative experiences. Experiences of older people, family members and service providers are interconnected. Quality improvement requires comprehensive approaches addressing their needs. Findings inform practitioners and policymakers to design multidimensional and people-centred approaches to maximise healthcare access.

Patient and Pubic Contribution

No PPI engagement methods were applied in this study or analysis. However, the findings informed discussions with older people and facilitated partnerships to co-design a follow-up study focused on developing solutions.

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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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