首页> 外文期刊>Journal of clinical nursing >Comparing patient and professional views of expected treatment outcomes for chronic obstructive pulmonary disease: A Delphi study identifies possibilities for change in service delivery in England, UK
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Comparing patient and professional views of expected treatment outcomes for chronic obstructive pulmonary disease: A Delphi study identifies possibilities for change in service delivery in England, UK

机译:比较患者和专业人士对慢性阻塞性肺疾病预期治疗结果的看法:一项Delphi研究确定了英国英格兰改变服务方式的可能性

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Aims and objectives: To clarify by consensus the professional and patient views of expected treatment outcomes for chronic obstructive pulmonary disease and to compare the similarities and differences and identify the potential for adjusting service delivery. Background: Chronic obstructive pulmonary disease is an under-researched topic necessary to illuminate health planning, and patient partnership needs in the UK clinical screening is low priority for this condition. Government policy expects that service users are involved in planning services for their condition, but few opportunities exist for this process. Design: A feasibility study in two phases conducted three service user focus groups and one specialist professional group to provide statements of expected treatment outcomes from chronic obstructive pulmonary disease interventions. The statements then formed a further two-round Delphi structured survey to compare service users' and carers' views with those of specialist professionals to ascertain what differences could be developed in service delivery for people with chronic obstructive pulmonary disease. Methods: Three rounds of Delphi survey were administered. Round 1: Specialist professionals and patients with chronic obstructive pulmonary disease ranked statements using nominal group technique. A nine-point scale Delphi consensus study used the statements in two further rounds. Results: Twenty-four of 54 professionals contacted, and 52 of 152 patients and carers completed Delphi rounds 2 and 3. Consensus was found within and between both groups. The greatest difference was where professionals sought government targets and did not realise patient expectations, which were constrained by policy disincentives. The greatest agreement was for accurate record keeping and the need for revised chronic obstructive pulmonary disease services. Conclusions: Patients consider that services should support them to retain their independence and enable their adaptation to the condition. Relevance to clinical practice: Health professionals aim to provide patient focused care based on need. This helps improve outcomes of interventions. Patients are willing and able if supported to increase independence and maintain self-help.
机译:目的和目标:通过共识阐明专业人士和患者对慢性阻塞性肺疾病预期治疗结果的看法,比较异同,确定调整服务提供的潜力。背景:慢性阻塞性肺疾病是阐明健康计划所必需的研究不足的话题,在英国临床筛查中患者伙伴关系的需求对于这种情况而言并不重要。政府政策期望服务用户参与为其条件制定服务计划,但是这一过程几乎没有机会。设计:在两个阶段的可行性研究中,进行了三个服务用户焦点小组和一个专业专家小组的讨论,目的是对慢性阻塞性肺疾病干预措施的预期治疗结果进行陈述。声明随后形成了进一步的两轮Delphi结构化调查,以比较服务使用者和护理者的观点与专业人士的观点,以确定在慢性阻塞性肺疾病患者的服务提供方面会产生哪些差异。方法:进行三轮德尔菲调查。第1轮:专家组和慢性阻塞性肺疾病患者使用名义组技术对陈述进行排名。一项9分制的Delphi共识研究在另外两轮中使用了这些陈述。结果:54位专业人员中有24位与之联系,152位患者和护理人员中的52位完成了Delphi第2轮和第3轮。最大的不同之处在于,专业人员寻求政府的目标而没有实现患者的期望,这受到政策障碍的限制。达成的最大协议是准确记录并需要修订慢性阻塞性肺疾病服务。结论:患者认为服务应支持他们保持独立性并使其适应疾病。与临床实践的相关性:卫生专业人员旨在根据需要提供针对患者的护理。这有助于改善干预效果。如果得到支持,患者愿意并有能力增加独立性并保持自助。

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