Department of Occupational Science and Occupational Therapy, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Department of Physical Therapy, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
Health Expect. 2020 Aug;23(4):813-824. doi: 10.1111/hex.13051. Epub 2020 Mar 17.
Therapeutic interventions for people with inflammatory arthritis (IA) increasingly involve multidisciplinary teams and strive to foster patient-centred care and shared decision making. Participation in health-care decisions requires patients to assert themselves and negotiate power in encounters with clinicians; however, clinical contexts often afford less authority for patients than clinicians. This disadvantage may inhibit patients' involvement in their own health care.
To identify communication attributes, IA patients use to influence and negotiate their treatment with members of their health-care network.
A qualitative social network approach was used to analyse data from a larger study that investigated IA patients' overall experiences of multidisciplinary care. Fourteen patients with IA attended individual semi-structured interviews. Researchers used thematic analysis to identify patterns of assertiveness and influence in the data.
Participants experienced loss of identity, control and agency in addition to the physical symptoms of IA. However, they had a sense of personal responsibility for managing their health care. Perceptions of health-care team support enhanced patients' influence in treatment negotiations. Notably, there appeared to be an underlying tension between being empowered or disempowered.
The findings have significant implications for treatment decision communication approaches to IA care. A social network perspective may provide a pathway for clinicians to better understand the complexities of communication with their patients. This approach may reduce unequal power dynamics that occur within clinician/patient interactions and afford people with IA agency, control and affirmation of identity within their health-care network.
治疗患有炎症性关节炎 (IA) 的患者的方法越来越多地涉及多学科团队,并努力培养以患者为中心的护理和共同决策。参与医疗决策需要患者维护自己的权益并与临床医生协商权力;然而,临床环境往往赋予患者的权力比临床医生少。这种劣势可能会抑制患者参与自己的医疗保健。
确定炎症性关节炎患者在与医疗保健网络成员协商治疗时使用的沟通属性。
采用定性社会网络方法分析了一项更大规模研究的数据,该研究调查了炎症性关节炎患者对多学科护理的整体体验。 14 名炎症性关节炎患者参加了个人半结构化访谈。研究人员使用主题分析来确定数据中自信和影响力的模式。
参与者除了患有 IA 的身体症状外,还经历了身份、控制和代理权的丧失。然而,他们对管理自己的医疗保健负有个人责任。对医疗团队支持的看法增强了患者在治疗谈判中的影响力。值得注意的是,似乎存在权力赋予或剥夺的潜在紧张关系。
这些发现对炎症性关节炎护理的治疗决策沟通方法具有重要意义。社会网络视角可能为临床医生提供一种更好地理解与患者沟通复杂性的途径。这种方法可以减少临床医生/患者互动中不平等的权力动态,并为患有 IA 的人提供代理权、控制权和对其医疗保健网络中身份的认可。