Marshall Martin N, Hiscock Julia, Sibbald Bonnie
National Primary Care Research and Development Centre, University of Manchester, Manchester M13 9PL, UK.
BMJ. 2002 Nov 30;325(7375):1278. doi: 10.1136/bmj.325.7375.1278.
To examine the attitudes of service users, general practitioners, and clinical governance leads based in primary care trusts to the public dissemination of comparative reports on quality of care in general practice, to guide the policy and practice of public disclosure of information in primary care.
Qualitative focus group study using mock quality report cards as prompts for discussion.
12 focus groups held in an urban area in north west England and a semirural area in the south of England.
35 service users, 24 general practitioners, and 18 clinical governance leads.
There was general support for the principle of publishing comparative information, but all three stakeholder groups expressed concerns about the practical implications. Attitudes were strongly influenced by experience of comparative reports from other sectors-for example, school league tables. Service users distrusted what they saw as the political motivation driving the initiative, expressed a desire to "protect" their practices from political and managerial interference, and were uneasy about practices being encouraged to compete against each other. General practitioners focused on the unfairness of drawing comparisons from current data and the risks of "gaming" the results. Clinical governance leads thought that public disclosure would damage their developmental approach to implementing clinical governance. The initial negative response to the quality reports seemed to diminish on reflection.
Despite support for the principle of greater openness, the planned publication of information about quality of care in general practice is likely to face considerable opposition, not only from professional groups but also from the public. A greater understanding of the practical implications of public reporting is required before the potential benefits can be realised.
调查服务使用者、全科医生以及初级保健信托机构的临床治理负责人对在全科医疗中公开医疗质量比较报告的态度,以指导初级保健中信息公开的政策与实践。
采用模拟质量报告卡作为讨论提示的定性焦点小组研究。
在英格兰西北部的一个市区和英格兰南部的一个半农村地区举行了12个焦点小组会议。
35名服务使用者、24名全科医生和18名临床治理负责人。
对于发布比较信息的原则普遍表示支持,但所有三个利益相关者群体都对实际影响表示担忧。态度受到其他领域比较报告经验的强烈影响,例如学校排行榜。服务使用者不信任他们所认为的推动该倡议的政治动机,表达了“保护”其医疗机构免受政治和管理干预的愿望,并对鼓励医疗机构相互竞争感到不安。全科医生关注从当前数据进行比较的不公平性以及“操纵”结果的风险。临床治理负责人认为公开披露会损害他们实施临床治理的发展方式。对质量报告的最初负面反应经反思后似乎有所减弱。
尽管支持更大程度公开的原则,但计划在全科医疗中发布医疗质量信息可能会面临相当大的反对,不仅来自专业团体,也来自公众。在实现潜在益处之前,需要对公开报告的实际影响有更深入的理解。