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Patient participation in mental healthcare: When is it difficult? A qualitative study of users and providers in a mental health hospital in Norway

机译:病人参与精神保健:什么时候困难?挪威一家精神卫生医院的使用者和提供者的定性研究

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Background: In western countries, patient participation is requested in policies on mental health services. Participation is built on ideas of democracy and individual responsibility. Mental illness has, however, been characterized by its irrational features. Aim: To investigate mental health service users and providers views on patient participation during episodes of mental illness. Methods: Qualitative interview study with 20 users and 25 staff from a mental health hospital in central Norway. Results: Both users and professionals saw poor illness phases as an obstacle to patient participation. Lack of insight, lack of verbal ability and difficulty cooperating made participation difficult. During such phases, patient participation was redefined. There was a shift in responsibility where professionals took charge through strategies of providing information, motivating patients and reducing choices. Respect and dignity were maintained and not redefined. Conclusions: In poor phases of mental illness, patient participation was redefined and weighed against what was perceived to be the patients best interest.
机译:背景:在西方国家,精神卫生服务政策要求患者参与。参与建立在民主和个人责任观念的基础上。然而,精神疾病的特征是其非理性特征。目的:调查精神卫生服务使用者和提供者对精神疾病发作期间患者参与的看法。方法:来自挪威中部一家精神卫生医院的20名用户和25名工作人员的定性访谈研究。结果:用户和专业人员都认为疾病的恶化阶段是患者参与的障碍。缺乏见识,缺乏口头表达能力和合作困难使参与变得困难。在这些阶段中,患者参与度被重新定义。责任转移了,专业人员通过提供信息,激励患者和减少选择的策略来负责。尊重和尊严得到维护,没有重新定义。结论:在精神疾病的较弱阶段,患者参与度被重新定义,并权衡被认为是患者最大利益的因素。

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