Health and Social Care Institute, Teesside University, Middlesbrough, UK.
BMJ Open. 2013 Sep 26;3(9):e003452. doi: 10.1136/bmjopen-2013-003452.
To elucidate the experiences and perceptions of people living with primary frozen shoulder and their priorities for treatment.
Qualitative study design using semistructured interviews.
General practitioner (GP) and musculoskeletal clinics in primary and secondary care in one National Health Service Trust in England.
12 patients diagnosed with primary frozen shoulder were purposively recruited from a GP's surgery, community clinics and hospital clinics. Recruitment targeted the phases of frozen shoulder: pain predominant (n=5), stiffness predominant (n=4) and residual stiffness predominant following hospital treatment (n=2). One participant dropped out.
adult, male and female patients of any age, attending the clinics, who had been diagnosed with primary frozen shoulder.
The most important experiential themes identified by participants were: pain which was severe as well as inexplicable; inconvenience/disability arising from increasing restriction of movement (due to pain initially, gradually giving way to stiffness); confusion/anxiety associated with delay in diagnosis and uncertainty about the implications for the future; and treatment-related aspects. Participants not directly referred to a specialist (whether physiotherapist, physician or surgeon) wanted a faster, better-defined care pathway. Specialist consultation brought more definitive diagnosis, relief from anxiety and usually self-rated improvement. The main treatment priority was improved function, though there was recognition that this might be facilitated by relief of pain or stiffness. There was a general lack of information from clinicians about the condition with over-reliance on verbal communication and very little written information.
Awareness of frozen shoulder should be increased among non-specialists and the best available information made accessible for patients. Our results also highlight the importance of patient participation in frozen shoulder research.
阐明原发性冻结肩患者的经历和感受,以及他们对治疗的优先需求。
采用半结构式访谈的定性研究设计。
英格兰一家国民保健制度信托的初级和二级保健中的全科医生(GP)和肌肉骨骼诊所。
从 GP 手术、社区诊所和医院诊所有针对性地招募了 12 名被诊断为原发性冻结肩的患者。招募的目标是冻结肩的各个阶段:疼痛占主导地位(n=5)、僵硬占主导地位(n=4)和医院治疗后残留僵硬占主导地位(n=2)。一名参与者退出。
任何年龄的成年男女患者,在诊所就诊,被诊断为原发性冻结肩。
参与者确定的最重要体验主题是:疼痛既严重又无法解释;由于运动受限逐渐增加(最初是由于疼痛,逐渐发展为僵硬)而引起的不便/残疾;与延迟诊断相关的困惑/焦虑以及对未来影响的不确定性;以及与治疗相关的方面。未直接转诊给专家(无论是物理治疗师、医生还是外科医生)的患者希望有一个更快、更明确的护理途径。专家咨询带来了更明确的诊断、减轻焦虑,通常还能自我评估改善。主要的治疗重点是改善功能,但人们认识到,这可能通过缓解疼痛或僵硬来实现。临床医生对病情的了解不足,过度依赖口头沟通,几乎没有书面信息。
应提高非专家对冻结肩的认识,并为患者提供最好的可用信息。我们的研究结果还强调了患者参与冻结肩研究的重要性。