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首页> 外文期刊>Health expectations: an international journal of public participation in health care and health policy >Empowerment and pathologization: A case study in Norwegian mental health and substance abuse services
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Empowerment and pathologization: A case study in Norwegian mental health and substance abuse services

机译:赋予权力和病理化:挪威心理健康和药物滥用服务的案例研究

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Abstract Context Service user involvement in service development and research is an international goal. However, research illuminating the patient stakeholder role is limited. Objective The aim was to explore what may hinder patients’ voices being heard when collaborating with staff and leaders to improve services. Design This action research project targeted Norwegian public mental health and substance abuse services, utilizing co‐operative inquiry principles. Data were collected and member‐checked collaboratively by the researcher and coresearchers. Results Results centre on patient involvement in services, service development and research. The patient voice was regarded as important but not necessarily decisive, as patients’ change needs could be perceived as pathology‐based. Patients provided feedback about fellow patients and medication—opioid maintenance treatment, in particular. Barriers to patient involvement included patients not being permitted to influence other patients’ individual treatment and a leader's difficulty accepting patients’ medication advice. Additionally, an apparent hierarchy among the professionals may have disempowered some staff members. Discussion Results point to an organizational diagnostic culture, where stigmatizing and risk pathologization may limit patient input. Empowerment appeared to be perceived as something allowed by the staff and leaders, at their discretion. Although all parties may have agreed that patient involvement was valuable, acting as a united group about opioid maintenance treatment appeared difficult. Conclusion Barriers to patient involvement may hinder the availability and efficacy of patients’ perspectives in service development. Awareness about reciprocal empowerment might contribute to service users’ voices being heard, enabling a united voice from service users and providers regarding service development.
机译:摘要上下文服务用户参与服务开发和研究是一个国际目标。然而,研究患者利益相关者作用的研究有限。目标是探讨在与员工和领导人合作改善服务时会探讨可能妨碍患者的声音。设计此动作研究项目针对挪威公共心理健康和药物滥用服务,利用合作审查原则。通过研究人员和CoreSearchers收集数据和成员,由研究人员合作。结果患者参与服务,服务开发和研究方面的结果。患者声音被认为是重要的,但不一定决定性,因为患者的变化需求可以被认为是基于病理的。患者提供了关于同胞和药物 - 阿片类药物维持治疗的反馈。患者参与的障碍包括未被允许影响其他患者的个人治疗和领导者的困难接受患者的药物建议的障碍。此外,专业人员之间的表观等级可能会让一些工作人员丢弃。讨论结果指向组织诊断文化,其中耻辱和风险病理化可能限制患者输入。赋予权力似乎被认为是员工和领导人允许的东西。虽然各方可能已同意患者参与是有价值的,但作为阿片类药物维持治疗的联合团体似乎困难。结论患者受累的障碍可能会阻碍患者的服务发展前景的可用性和功效。对互惠赋权的认识可能有助于提供服务用户的声音,从服务用户和提供者提供有关服务开发的提供者。

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