Dollinger J, Neville C, Pineau C A, Vinet E, Hazel E, Lee J L F, Bernatsky S
Centre for Outcome Research and Evaluation, Research Institute of the McGill University Health Centre, 5252 boul. de Maisonneuve Ouest, (3F.51), Montreal, QC, H4A 3S5, Canada.
Division of Rheumatology, McGill University Health Centre, Montreal, QC, Canada.
Clin Rheumatol. 2020 Oct;39(10):3083-3090. doi: 10.1007/s10067-020-05091-7. Epub 2020 Apr 25.
To assess challenges to optimal rheumatology care from the perspective of patients served by our institution's rheumatology division.
Focus group study of adult rheumatic disease patients who attend clinics at a university teaching hospital in Montreal, Canada.
Individuals participated in 1-h focus group discussions concerning their experiences and beliefs regarding rheumatology care. Sessions were recorded and transcripts generated. A thematic analysis approach was used by two individual analyzers.
Eighteen patients participated in three focus groups (group one = 8 patients; group two = 5; group three = 5). Eleven patients had systemic lupus erythematosus, 6 had rheumatoid arthritis, and 1 patient had psoriatic arthritis. The average age (standard deviation) was 51.2 (14.0) years, disease duration 23.5 (14.5) years, and in the majority had at least a high school education. All participants were female and 72.2% were Caucasian. Three main themes emerged: theme 1 identified patients' needs for information and support, at diagnosis and throughout the disease trajectory; theme 2 identified barriers to accessing health care: theme 3 identified patients' beliefs regarding improvements needed to optimize their experiences throughout the disease course.
Our focus group study not only clarified the needs of rheumatology patients with chronic inflammatory disease, and identified barriers to optimal rheumatology care, but also was a source of recommendations that might improve patient experiences in seeking health care in a rheumatology setting. Limitations include the fact that our participants were all female, and mostly were middle aged, Caucasian and well educated. Regardless, the findings can help inform efforts to improve rheumatology care. Key Points • Our focus group study clarified the needs of chronic inflammatory rheumatic disease, and identified barriers to optimal rheumatology care. • Despite some potential limitations, our work provides recommendations that could improve patient experiences when seeking health care in a rheumatology setting.
从我院风湿病科服务的患者角度评估优化风湿病护理所面临的挑战。
设计、地点和参与者:对在加拿大蒙特利尔一家大学教学医院门诊就诊的成年风湿性疾病患者进行焦点小组研究。
参与者参加了为期1小时的焦点小组讨论,内容涉及他们对风湿病护理的经历和看法。会议进行了录音并生成了文字记录。两名独立分析人员采用了主题分析方法。
18名患者参加了3个焦点小组(第一组=8名患者;第二组=5名;第三组=5名)。11名患者患有系统性红斑狼疮,6名患有类风湿性关节炎,1名患者患有银屑病关节炎。平均年龄(标准差)为51.2(14.0)岁,病程23.5(14.5)年,大多数患者至少接受过高中教育。所有参与者均为女性,72.2%为白种人。出现了三个主要主题:主题1确定了患者在诊断时及整个疾病过程中对信息和支持的需求;主题2确定了获得医疗保健的障碍;主题3确定了患者对在整个疾病过程中优化体验所需改进的看法。
我们的焦点小组研究不仅明确了慢性炎症性疾病风湿病患者的需求,确定了优化风湿病护理的障碍,还提供了一些建议,可能会改善患者在风湿病环境中寻求医疗保健的体验。局限性包括我们的参与者均为女性,且大多为中年、白种人和受过良好教育的人。尽管如此,研究结果有助于为改善风湿病护理的努力提供参考。要点:• 我们的焦点小组研究明确了慢性炎症性风湿病的需求,并确定了优化风湿病护理的障碍。• 尽管存在一些潜在局限性,但我们的研究提供了一些建议,可改善患者在风湿病环境中寻求医疗保健时的体验。