Neuroethics Research Unit, Institut de recherches cliniques de Montréal, Montreal, QC, Canada.
Division of Experimental Medicine and Biomedical Ethics Unit, McGill University, Montreal, QC, Canada.
Health Expect. 2017 Aug;20(4):655-664. doi: 10.1111/hex.12497. Epub 2016 Sep 14.
Patient-centred care is a recommended model of care for Parkinson's disease (PD). It aims to provide care that is respectful and responsive to patient preferences, values and perspectives. Provision of patient-centred care should entail considering how patients want to be involved in their care.
To understand the participation preferences of patients with PD from a patient-centred care clinic in health-care decision-making processes.
DESIGN, SETTING AND PARTICIPANTS: Mixed-methods study with early-stage Parkinson's disease patients from a patient-centred care clinic. Study involved a modified Autonomy Preference Index survey (N=65) and qualitative, semi-structured in-depth interviews, analysed using thematic qualitative content analysis (N=20, purposefully selected from survey participants). Interviews examined (i) the patient preferences for involvement in health-care decision making; (ii) patient perspectives on the patient-physician relationship; and (iii) patient preferences for communication of information relevant to decision making.
Preferences for participation in decision making varied between individuals and also within individuals depending on decision type, relational and contextual factors. Patients had high preferences for communication of information, but with acknowledged limits. The importance of communication in the patient-physician relationship was emphasized.
Patient preferences for involvement in decision making are dynamic and support shared decision making. Relational autonomy corresponds to how patients envision their participation in decision making. Clinicians may need to assess patient preferences on an on-going basis.
Our results highlight the complexities of decision-making processes. Improved understanding of individual preferences could enhance respect for persons and make for patient-centred care that is truly respectful of individual patients' wants, needs and values.
以患者为中心的护理是帕金森病(PD)推荐的护理模式。它旨在提供尊重和响应患者偏好、价值观和观点的护理。提供以患者为中心的护理应该考虑患者希望如何参与他们的护理。
了解来自以患者为中心的护理诊所的 PD 患者在医疗保健决策过程中参与的偏好。
设计、地点和参与者:采用混合方法研究,纳入来自以患者为中心的护理诊所的早期帕金森病患者。研究包括对 65 名患者进行修改后的自主性偏好指数调查,并进行定性、半结构化深入访谈,使用主题定性内容分析进行分析(从调查参与者中有意选择的 20 名患者)。访谈研究了(i)患者对参与医疗保健决策的偏好;(ii)患者对医患关系的看法;以及(iii)患者对与决策相关的信息沟通的偏好。
个人之间以及个人内部的决策类型、关系和背景因素决定了参与决策的偏好存在差异。患者对信息沟通有很高的偏好,但也有公认的限制。医患关系中的沟通至关重要。
患者参与决策的偏好是动态的,支持共同决策。关系自治与患者对参与决策的设想相对应。临床医生可能需要定期评估患者的偏好。
我们的研究结果强调了决策过程的复杂性。对个人偏好的更好理解可以增强对个人的尊重,并提供真正尊重个体患者的意愿、需求和价值观的以患者为中心的护理。