病人参与与初级保健服务相结合的生物心理社会护理模式:刚果民主共和国南基伍三个卫生区的经验

Bertin Mutabesha Kasongo, Christian Eboma Ndjangulu Molima, Gérard Jacques Mparanyi, Samuel Lwamushi Makali, Pacifique Lyabayungu Mwene-Batu, Albert Mwembo Tambwe, Hermès Karemere, Ghislain Balaluka Bisimwa, Abdon Mukalay wa Mukalay
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导言:在提供优质医疗服务的过程中,让人们参与到医疗服务的提供和有关其健康的决策中,是取得成功和改善服务提供的关键之一。在刚果民主共和国(DRC),患者参与生物-心理-社会护理模式的记录很少。本研究旨在描述患者参与选择医疗政策的情况、他们在整体护理中的责任以及他们支持生物心理社会模式的能力:这项定性研究在刚果民主共和国南基伍省的三个卫生区进行。受国际患者组织联盟《以患者为中心的医疗保健宣言》的启发,我们在 2024 年 2 月至 4 月期间使用一种工具进行了 27 次个人访谈。这些访谈涉及研究覆盖的六个卫生领域中情况复杂、在医疗中心就诊以及属于患者俱乐部的人群。我们对各种访谈中的话语进行了内容分析:结果:病人参与生物心理社会护理模式取决于多种因素,包括关系方面(医疗服务提供者与病人之间的伙伴关系、治疗可能性的讨论和选择指导)、教育方面(从护理人员那里获得的建议和教导、技能的发展)、赋权(护理责任)、组织方面(包容性和参与性规划、获得不同医疗服务的途径)和社区方面(随行人员和病人俱乐部的作用):在制定政策和整合生物心理社会护理的过程中,应考虑到影响患者参与 BPS 模式的各种因素。为支持该模式而提出的一些战略,如提高对护理人性化的认识、改善资源的可用性和加强财务自主权,将有助于提高护理质量和优质医疗服务的可及性。
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Patient involvement in the biopsychosocial model of care integrated with primary health services: Experience from three health districts in South Kivu, Democratic Republic of Congo
Introduction: Involving people in the provision of care and in decision-making about their health is one of the keys to success and to improving service delivery in the provision of quality health care. Patient involvement in the biopsychosocial model of care is poorly documented in the Democratic Republic of Congo (DRC). The aim of this study is to describe patients' involvement in the choice of their health policy, their responsibility in holistic care and their capacity to support the biopsychosocial model. Methods: This qualitative research was conducted in three health districts in the province of South Kivu, DRC. Using a tool inspired by the International Alliance of Patients' Organizations' Declaration of Patient-Centered Healthcare, we conducted 27 individual interviews between February and April 2024. These interviews concerned people in complex situations, attending health centers and belonging to patient clubs in six health areas covered by the study. A content analysis of the discourse from the various interviews was carried out. Results: Patient involvement in the biopsychosocial model of care depended on multiple factors, including relational aspects (partnership between providers and patients, discussion of therapeutic possibilities and guidance for choice), educational aspects (advice and teaching received from caregivers, development of skills), empowerment (responsibility for care), organizational aspects (inclusive and participatory planning, access to different health services) and community aspects (role of entourage and patient clubs). Conclusions: The various factors influencing patient involvement in the BPS model should be taken into account in the definition of policies and the process of integrating biopsychosocial care. Some of the strategies suggested to support the model, such as raising awareness of the humanization of care, improving the availability of resources and strengthening financial autonomy, will help to improve the quality of care and accessibility to quality health services.
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