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Empowerment in people with COPD

机译:向COPD患者赋权

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Background: Patient empowerment is recognized as an important aspect of chronic disease management. There is an increasing expectation that health providers engage patients as active participants in their own self-management. This engagement is crucial to the chronic care model as patients with COPD and their families manage the majority of the care in the community. Understanding what influences empowerment will help health care professionals to better engage in collaborative care planning and decision making that meet the needs of this new generation of health consumers. Aim: The aim of the present study was to identify interventions or approaches that empower patients in the management of COPD. Methods: An integrative review was undertaken following the preferred reporting items for systematic reviews and meta-analyses approach. Papers were included if they 1) provided a definition or conceptualization of empowerment, and 2) reported interventions or approaches fostering empowerment in patients with COPD. Thematic analysis was used to develop conceptual themes on patient empowerment in COPD. These conceptual themes were validated by a panel of specialists in COPD, chronic disease management, self-management, and patient education. Results: Literature searching revealed 183 papers of which 15 studies conceptualized or defined empowerment interventions or approaches to support COPD management. These were grouped into the following five categories: pulmonary rehabilitation, social support, web-based interventions, approaches that support knowledge development, and the approach taken by the health care professional. Conclusion: Pulmonary rehabilitation, knowledge acquisition, social support, telehealth and web-based interfaces, and collaboration with health care professionals empower patients to recognize their own strengths and to manage the impact of the condition. Patients' abilities to direct their own care are additionally influenced by physical debilitation, treatment complexity, economic status, and health literacy. Health care professional–patient relationships must shift to a more collaborative approach that recognizes the patient as an expert in their own condition and facilitates patients to determine their own plan of care and life goals.
机译:背景:赋予患者权力是慢性疾病管理的重要方面。人们越来越期望卫生服务提供者将患者作为积极的参与者进行自我管理。这种参与对于慢性病护理模式至关重要,因为COPD患者及其家人管理着社区中的大部分护理。了解增强赋权的影响将有助于医疗保健专业人员更好地参与可满足新一代医疗消费者需求的协作式医疗计划和决策。目的:本研究的目的是确定能使患者有能力进行COPD治疗的干预措施或方法。方法:按照首选报告项目进行综合审查,以进行系统审查和荟萃分析。如果论文1)提供了赋权的定义或概念,2)报告了促进COPD患者赋权的干预措施或方法,则将其包括在内。主题分析被用来制定有关COPD患者赋权的概念性主题。这些概念性主题已由COPD,慢性病管理,自我管理和患者教育方面的专家小组验证。结果:文献检索显示183篇论文,其中15篇研究概念化或定义了支持COPD管理的赋权干预措施或方法。这些分为以下五类:肺康复,社会支持,基于网络的干预措施,支持知识发展的方法以及卫生保健专业人员采取的方法。结论:肺康复,知识获取,社会支持,远程医疗和基于Web的界面以及与医疗保健专业人员的协作使患者能够认识到自己的长处并管理疾病的影响。病人身体状况,治疗的复杂性,经济状况和健康素养也会影响其指导自己护理的能力。医护专业人员与患者之间的关系必须转向更具协作性的方法,该方法应将患者视为自身情况的专家,并帮助患者确定自己的护理计划和生活目标。

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