Why do people with chronic disease not contact consumer health organisations? A survey of general practice patients

F. Boyle, Julie H. Dean, Charlotte E. Young, Allyson Mutch
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引用次数: 3

Abstract

Aim Consumer health organisations (CHOs) are non-profit or voluntary sector organisations that promote and represent the interests of patients and carers affected by particular conditions. The purpose of this study was to examine, among patients with chronic disease, what differentiates those who contact CHOs from those who do not and what stops people from making contact. Background CHOs can enhance people’s capacity to manage chronic disease by providing information, education and psychosocial support, but are under-utilised. Little is known about barriers to access. Methods Data were from a baseline telephone survey conducted as part of a randomised trial of an intervention to improve access to CHOs. Participants constituted a consecutive sample of 276 adults with diagnosed chronic disease recruited via 18 general practitioners in Brisbane, Australia. Quantitative survey items examined participants’ use and perceptions of CHOs and a single open-ended question explored barriers to CHO use. Multiple logistic regression and thematic analysis were used. Findings Overall, 39% of participants had ever contacted a CHO for their health and 28% had contacted a CHO specifically focussed on their diagnosed chronic condition. Diabetes, poorer self-reported physical health and greater health system contact were significantly associated with CHO contact. The view that ‘my doctor does it all’ was prevalent and, together with a belief that their health problems were ‘not serious enough’, was the primary reason patients did not make contact. Conclusion Attitudinal and system-related barriers limit use of CHOs by those for whom they are designed. Developing referral pathways to CHOs and promoting awareness about what they offer is needed to improve access.
为什么慢性病患者不与消费者健康组织联系?对全科病人的调查
目的消费者健康组织是促进和代表受特殊疾病影响的患者和护理人员利益的非营利性或自愿部门组织。这项研究的目的是在患有慢性疾病的患者中,研究是什么区别了那些接触慢性阻塞性肺疾病的人,以及是什么阻止了人们接触慢性阻塞性肺疾病。社区卫生组织可以通过提供信息、教育和社会心理支持来提高人们管理慢性病的能力,但没有得到充分利用。人们对进入的障碍知之甚少。方法数据来自一项基线电话调查,该调查是一项改善获得CHOs的干预措施的随机试验的一部分。参与者由澳大利亚布里斯班18名全科医生招募的276名诊断为慢性疾病的成年人组成连续样本。定量调查项目检查了参与者对CHO的使用和看法,一个开放式问题探讨了CHO使用的障碍。采用多元逻辑回归和专题分析。总体而言,39%的参与者曾就健康问题联系过CHO, 28%的参与者曾联系过专门针对其诊断出的慢性疾病的CHO。糖尿病、较差的自我报告身体健康状况和更多的卫生系统接触与CHO接触显著相关。“我的医生包办一切”的观点很普遍,再加上认为自己的健康问题“不够严重”,这是病人不愿与医生联系的主要原因。结论态度障碍和制度障碍限制了cho的使用。需要发展转介到卫生组织的途径,并提高对其所提供服务的认识,以改善获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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