Institute of Health Informatics, University College London, London, United Kingdom.
School of Primary Care, Population Sciences and Medical Education, University of Southampton, Southampton, United Kingdom.
PLoS One. 2022 Aug 15;17(8):e0271978. doi: 10.1371/journal.pone.0271978. eCollection 2022.
Individuals with Long Covid represent a new and growing patient population. In England, fewer than 90 Long Covid clinics deliver assessment and treatment informed by NICE guidelines. However, a paucity of clinical trials or longitudinal cohort studies means that the epidemiology, clinical trajectory, healthcare utilisation and effectiveness of current Long Covid care are poorly documented, and that neither evidence-based treatments nor rehabilitation strategies exist. In addition, and in part due to pre-pandemic health inequalities, access to referral and care varies, and patient experience of the Long Covid care pathways can be poor. In a mixed methods study, we therefore aim to: (1) describe the usual healthcare, outcomes and resource utilisation of individuals with Long Covid; (2) assess the extent of inequalities in access to Long Covid care, and specifically to understand Long Covid patients' experiences of stigma and discrimination.
A mixed methods study will address our aims. Qualitative data collection from patients and health professionals will be achieved through surveys, interviews and focus group discussions, to understand their experience and document the function of clinics. A patient cohort study will provide an understanding of outcomes and costs of care. Accessible data will be further analysed to understand the nature of Long Covid, and the care received.
Ethical approval was obtained from South Central-Berkshire Research Ethics Committee (reference 303958). The dissemination plan will be decided by the patient and public involvement and engagement (PPIE) group members and study Co-Is, but will target 1) policy makers, and those responsible for commissioning and delivering Long Covid services, 2) patients and the public, and 3) academics.
长新冠患者代表了一个新的、不断增长的患者群体。在英国,不到 90 家长新冠诊所根据 NICE 指南提供评估和治疗。然而,由于缺乏临床试验或纵向队列研究,目前长新冠护理的流行病学、临床轨迹、医疗保健利用和效果记录不佳,也没有基于证据的治疗方法或康复策略。此外,部分由于大流行前的健康不平等,转诊和护理的机会存在差异,而且患者对长新冠护理途径的体验可能较差。因此,在一项混合方法研究中,我们旨在:(1)描述长新冠患者的常规医疗保健、结局和资源利用情况;(2)评估获得长新冠护理的不平等程度,并特别了解长新冠患者的耻辱感和歧视经历。
一项混合方法研究将解决我们的目标。通过调查、访谈和焦点小组讨论从患者和卫生专业人员收集定性数据,以了解他们的经历并记录诊所的功能。患者队列研究将提供对护理结局和成本的理解。将进一步分析可访问数据,以了解长新冠的性质和所接受的护理。
已从南中英格兰伯克郡研究伦理委员会获得伦理批准(参考 303958)。传播计划将由患者和公众参与和参与(PPIE)小组成员和研究共同负责人决定,但将针对 1)政策制定者,以及负责委托和提供长新冠服务的人员,2)患者和公众,以及 3)学者。