首页> 美国卫生研究院文献>Health Expectations : An International Journal of Public Participation in Health Care and Health Policy >Same description different values. How service users and providers define patient and public involvement in health care
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Same description different values. How service users and providers define patient and public involvement in health care

机译:相同的描述不同的值。服务使用者和提供者如何定义患者和公众参与医疗保健

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摘要

>Background  Patient and public involvement in health care is important, but the existing definitions of the concept do not integrate the stakeholders’ own perceptions. >Objective  To investigate and compare service users’ and service providers’ own definitions of patient and public involvement and their implications. >Design, setting and participants  Qualitative study with mainly individual in‐depth semi‐structured interviews conducted between June 2007 and June 2009. Data were analysed using a grounded theory approach. >Results  A total of 20 patients, 13 public representatives and 44 health service providers/managers in both somatic and mental health care were interviewed. A common definition of patient and public involvement emerged: It is founded on mutual respect, carried out through dialogue aiming at achieving shared decision making. Nevertheless, users and providers assigned different values to the core aspects: Respect was imperative for service users and implied for providers, dialogue was a way to gain respect for service users and to achieve good outcome for providers, and both worried that the other party wanted to make sole decisions. >Conclusions  Users and providers need to consider that although they have a common definition of involvement in health care, they assign different values to its aspects. Increasing and improving patient and public involvement therefore requires knowledge on and dialogue between the parties about these differences.
机译:>背景患者和公众参与医疗保健很重要,但是该概念的现有定义并未整合利益相关者的看法。 >目的:调查和比较服务用户和服务提供商对患者和公众参与及其含义的定义。 >设计,环境和参与者:定性研究,主要是在2007年6月至2009年6月之间进行的单独的深入半结构化访谈。使用扎根理论方法对数据进行了分析。 >结果总共接受了20位患者,13位公共代表和44位身体和精神卫生保健服务提供者/经理的采访。出现了患者和公众参与的通用定义:它是建立在相互尊重的基础上的,相互尊重是通过对话实现共同决策的目的。但是,用户和提供者在核心方面分配了不同的价值:尊重对于服务用户是必不可少的,并且对提供者是隐含的;对话是获得对服务用户的尊重并为提供者取得良好结果的一种方式,并且双方都担心对方想要做出唯一的决定。 >结论:用户和提供者需要考虑,尽管他们对医疗保健有共同的定义,但他们在医疗保健方面赋予了不同的价值观。因此,增加和改善患者和公众的参与需要各方了解这些差异并进行对话。

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