Barriers and facilitators to medical care retention for pediatric systemic lupus erythematosus in South Africa: a qualitative study.

IF 2.8 3区 医学 Q1 PEDIATRICS Pediatric Rheumatology Pub Date : 2024-05-28 DOI:10.1186/s12969-024-00994-0
Naira Ikram, Laura B Lewandowski, Melissa H Watt, Christiaan Scott
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Abstract

Background: Systemic lupus erythematosus (SLE) is a life-threatening, chronic, autoimmune disease requiring long term subspecialty care due to its complex and chronic nature. Childhood-onset SLE (cSLE) is more severe than adult-onset, and the cSLE population in South Africa has been reported to have an even higher risk than patients elsewhere. Therefore, it is critical to promptly diagnose, treat, and manage cSLE. In this paper, we aim to describe and evaluate barriers and enablers of appropriate long-term care of cSLE South Africa from the perspective of caregivers (parents or family members).

Methods: Caregivers (n = 22) were recruited through pediatric and adult rheumatology clinics. Individuals were eligible if they cared for youth (≤ 19 years) who were diagnosed with cSLE and satisfied at least four of the eleven ACR SLE classification criteria. Individual in-depth, semi-structured interviews were conducted between January 2014 and December 2014, and explored barriers to and facilitators of ongoing chronic care for cSLE. Data were analyzed using applied thematic analysis.

Results: Four barriers to chronic care engagement and retention were identified: knowledge gap, financial burdens, social stigma of SLE, and complexity of the South African medical system. Additionally, we found three facilitators: patient and caregiver education, robust support system for the caregiver, and financial support for the caregiver and patient.

Conclusion: These findings highlight multiple, intersecting barriers to routine longitudinal care for cSLE in South Africa and suggest there might be a group of diagnosed children who don't receive follow-up care and are subject to loss to follow-up. cSLE requires ongoing treatment and care; thus, the different barriers may interact and compound over time with each follow-up visit. South African cSLE patients are at high risk for poor outcomes. South African care teams should work to overcome these barriers and place attention on the facilitators to improve care retention for these patients and create a model for other less resourced settings.

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南非小儿系统性红斑狼疮保留医疗护理的障碍和促进因素:一项定性研究。
背景:系统性红斑狼疮(SLE)是一种危及生命的慢性自身免疫性疾病,由于其复杂性和慢性性,需要长期的亚专科治疗。儿童期发病的系统性红斑狼疮(cSLE)比成人期发病的系统性红斑狼疮更为严重,据报道,南非儿童期发病的系统性红斑狼疮患者比其他地方的患者风险更高。因此,及时诊断、治疗和管理 cSLE 至关重要。本文旨在从护理者(父母或家庭成员)的角度出发,描述和评估南非系统性红斑狼疮患者在接受适当的长期护理时遇到的障碍和遇到的有利因素:护理人员(n = 22)是通过儿科和成人风湿病诊所招募的。只要他们照顾的青少年(≤ 19 岁)被诊断患有系统性红斑狼疮,并符合 ACR 系统性红斑狼疮 11 项分类标准中的至少 4 项标准,就有资格成为照顾者。在 2014 年 1 月至 2014 年 12 月期间进行了个人深度半结构式访谈,探讨了持续慢性系统性红斑狼疮护理的障碍和促进因素。采用应用主题分析法对数据进行了分析:结果:我们发现了阻碍参与和保留慢性病治疗的四个障碍:知识差距、经济负担、系统性红斑狼疮的社会耻辱感以及南非医疗系统的复杂性。此外,我们还发现了三个促进因素:患者和护理者教育、为护理者提供强大的支持系统以及为护理者和患者提供经济支持:这些研究结果突显了在南非对慢性系统性红斑狼疮进行常规纵向护理时所面临的多重、交叉障碍,并表明可能有一部分确诊的儿童没有接受随访护理,从而失去了随访机会。慢性系统性红斑狼疮需要持续的治疗和护理;因此,不同的障碍可能会相互作用,并随着每次随访的时间而加剧。南非的系统性红斑狼疮患者面临着不良后果的高风险。南非的护理团队应努力克服这些障碍,并重视促进因素,以改善这些患者的护理保留率,并为其他资源较少的环境树立典范。
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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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