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Use of quality information in decision-making about health and social care services - a systematic review

机译:在有关卫生和社会护理服务的决策中使用质量信息-系统审查

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User choice and personalisation have been at the centre of health and social care policies in many countries. Exercising choice can be especially challenging for people with long-term conditions (LTC) or disabilities. Information about the quality, cost and availability of services is central to user choice. This study used systematic review methods to synthesise evidence in three main areas: (i) how people with LTC or disabilities and their family carers find and access information about the quality of services; (ii) how quality information is used in decision-making; and (iii) what type of quality information is most useful. Quality information was defined broadly and could include formal quality reports (e.g. inspection reports, report cards, etc.), information about the characteristics of a service or provider (e.g. number and qualifications of staff, facilities, etc.) and informal reports about quality (e.g. personal experience, etc.). Literature searches were carried out using electronic databases in January 2012. Thirteen papers reporting findings from empirical studies published between 2001 and 2012 were included in the review. The majority of papers (n=9) had a qualitative design. The analysis highlighted the use of multiple sources of information in decision-making about services and in particular the importance of informal sources and extended social networks in accessing information. There is limited awareness and use of official' and online information sources. Service users or family carers place greater emphasis on general information and structural indicators. Clinical or quality-of-life outcomes are often difficult to interpret and apply. Trust emerged a key issue in relation to quality information. Experiential and subjective information is highly valued and trusted. Various barriers to the effective use of quality information in making choices about services are identified. Implications for policy and future research are discussed.
机译:用户选择和个性化已成为许多国家卫生和社会护理政策的中心。对于患有长期疾病(LTC)或残障人士而言,行使选择可能尤其具有挑战性。有关服务质量,成本和可用性的信息对于用户选择至关重要。这项研究使用了系统的审查方法来综合三个主要方面的证据:(i)长期护理或残障人士及其家庭照顾者如何找到并获取有关服务质量的信息; (ii)如何在决策中使用质量信息; (iii)哪种类型的质量信息最有用。质量信息定义广泛,可以包括正式的质量报告(例如检查报告,报告卡等),有关服务或提供者特征的信息(例如工作人员,设施的数量和资格等)以及有关质量的非正式报告(例如个人经验等)。文献检索是在2012年1月使用电子数据库进行的。该评价包括13篇论文,这些论文报告了2001年至2012年间发表的实证研究结果。大多数论文(n = 9)具有定性设计。分析强调了在服务决策中使用多种信息来源,尤其是非正式来源和扩展的社交网络在获取信息中的重要性。对官方和在线信息源的了解和使用有限。服务使用者或家庭照顾者更加重视一般信息和结构指标。临床或生活质量结果通常难以解释和应用。信任成为与质量信息相关的关键问题。经验和主观信息受到高度重视和信任。确定了在选择服务时有效使用质量信息的各种障碍。讨论了对政策和未来研究的影响。

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