Department of Health Systems Management, School of Health Sciences, Ariel University, Science Park, P.O.B. 3, Ariel, 40700, Israel.
Ramat Gan Academic College, Pinchas Rotenberg 87, Ramat Gan, 52275, Israel.
Isr J Health Policy Res. 2024 Sep 16;13(1):47. doi: 10.1186/s13584-024-00635-7.
Patient Organizations (POs) are an important support factor in helping chronically ill patients cope with their illness. Patient involvement in the management of their disease helps to achieve the best possible care for the patient, streamline the work of healthcare providers, shape healthcare policy, and even influence the structures of healthcare systems. The perspective of chronically ill patients on the activities and services provided by patient organizations has not been evaluated yet. This study aimed to identify and map the services and activities of all types of non-profit patient organizations from the perspective of chronically ill patients so that they can be integrated as an integral part of the healthcare system.
Nineteen services and activities of patient organizations were sampled from Israeli patient organizations and scientific literature. These services and activities were evaluated by chronically ill patients in Israel. Patient-Oriented Questionnaires (POQ) were distributed among patients with chronic diseases (N = 1395) using snowball sampling.
Exploratory factor analysis (EFA) was performed, followed by confirmatory factor analysis (CFA) for convergent and discriminant validity. Findings showed that twelve services and activities suggested by patient organizations were found to represent chronically ill patients' needs and categorized into three groups: Interpersonal support (five items), patients' rights (four items), and medical information (three items). CFA showed a good fit for the observed data. CFI = 0.98, NFI = 0.97, TLI = 0.96, RMSEA = 0.058.
Well-organized patient organizations are an important pillar in reformed healthcare systems. They can serve as the social arm of the healthcare system and as an intermediary between patients and healthcare institutions. We narrowed down twelve services and activities given by patient organizations that were important to chronically ill patients in Israel. patient organizations can utilize patient needs or preferences into clinical practice and influence health policy planning, patient-caregiver relationships, research and even healthcare costs. patient organizations recognition by the healthcare system, and establishment of a national patient council will help to realize these processes.
患者组织(PO)是帮助慢性病患者应对疾病的重要支持因素。患者参与疾病管理有助于为患者提供尽可能好的护理,简化医疗保健提供者的工作,塑造医疗保健政策,甚至影响医疗保健系统的结构。慢性病患者对患者组织提供的活动和服务的看法尚未得到评估。本研究旨在从慢性病患者的角度确定和绘制各类非营利性患者组织的服务和活动,以便将其作为医疗保健系统的一个组成部分进行整合。
从以色列患者组织和科学文献中抽取了 19 项患者组织的服务和活动。这些服务和活动由以色列慢性病患者进行评估。采用雪球抽样法向慢性病患者发放患者导向问卷(POQ)(N=1395)。
进行了探索性因素分析(EFA),随后进行了收敛和判别有效性的验证性因素分析(CFA)。研究结果表明,患者组织提出的 12 项服务和活动被认为代表了慢性病患者的需求,并分为三组:人际支持(5 项)、患者权利(4 项)和医疗信息(3 项)。CFA 对观察数据拟合良好。CFI=0.98,NFI=0.97,TLI=0.96,RMSEA=0.058。
组织良好的患者组织是改革后的医疗保健系统的重要支柱。它们可以作为医疗保健系统的社会臂膀,以及患者和医疗机构之间的中介。我们缩小了以色列慢性病患者从患者组织获得的 12 项重要服务和活动范围。患者组织可以将患者的需求或偏好纳入临床实践,并影响卫生政策规划、医患关系、研究甚至医疗保健成本。患者组织在医疗保健系统中的认可,以及建立国家患者委员会,将有助于实现这些进程。