Center for Behavioral Intervention Technologies, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Lupus. 2021 Jun;30(7):1058-1077. doi: 10.1177/09612033211005085. Epub 2021 Mar 28.
Patients with systemic lupus erythematous (SLE) experience psychological comorbidities and impaired quality of life (QOL). We conducted a systematic review to examine the efficacy of non-pharmacological interventions for improving psychological outcomes and/or QOL in patients with SLE. To expand on a previous systematic review in this area and enhance our understanding of efficacious interventions for this population, our search included quasi-experimental and experimental studies of interventions delivered or supported by remote methods (including digitally) or in person.
A comprehensive literature search was conducted with a research librarian using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and was registered before data extraction on the international prospective register of systematic reviews PROSPERO Web site (CRD42020154962). The search included controlled-vocabulary and title/abstract terms related to non-pharmacological interventions for SLE published through October 2019 in MEDLINE (Ovid), Cochrane Library databases (Wiley), Embase (Elsevier), CINAHL (EBSCO), PsycINFO (EBSCO), Web of Science (Clarivate), ACM Digital (Association of Computer Machinery), and IEEE Xplore. Studies were synthesized using a systematic narrative synthesis framework. Risk of bias was assessed.
Twenty-three studies were included: 21 randomized controlled trials and two quasi-experimental studies. Non-pharmacological diet, physical activity, psychological, and course-based interventions improved QOL and psychological outcomes, and were delivered in traditional settings (e.g., hospital) or remotely. No studies assessing digital non-pharmacological interventions were identified in our search. Quality assessments showed serious risk of bias for the two quasi-experimental studies, and high risk of bias in a subset of experimental studies.
Non-pharmacological interventions benefit patients with SLE. Future research should include more representative samples in rigorous evaluations and consider ways to incorporate digital technologies to increase accessibility.
系统性红斑狼疮(SLE)患者会出现心理合并症和生活质量(QOL)受损。我们进行了系统评价,以研究非药物干预措施对改善 SLE 患者心理结局和/或 QOL 的疗效。为了扩展该领域之前的系统评价,并增进我们对该人群有效干预措施的理解,我们的搜索包括通过远程方法(包括数字方法)或亲自提供或支持的干预措施的准实验和实验研究。
研究馆员使用系统评价和荟萃分析的首选报告项目(PRISMA)指南进行了全面的文献搜索,并在数据提取前在国际前瞻性系统评价注册处 PROSPERO 网站(CRD42020154962)上进行了注册。搜索包括与 SLE 的非药物干预相关的受控词汇和标题/摘要术语,这些术语通过 2019 年 10 月在 MEDLINE(Ovid)、Cochrane 图书馆数据库(Wiley)、Embase(Elsevier)、CINAHL(EBSCO)、PsycINFO(EBSCO)、Web of Science(Clarivate)、ACM Digital(Association of Computer Machinery)和 IEEE Xplore 发布。研究采用系统叙述性综合框架进行综合。评估了偏倚风险。
共纳入 23 项研究:21 项随机对照试验和 2 项准实验研究。非药物饮食、身体活动、心理和基于课程的干预措施改善了 QOL 和心理结局,并在传统环境(如医院)或远程环境中进行。我们的搜索未发现评估数字非药物干预的研究。质量评估显示,这两项准实验研究存在严重的偏倚风险,部分实验研究存在高偏倚风险。
非药物干预措施有益于 SLE 患者。未来的研究应在严格的评估中纳入更具代表性的样本,并考虑采用数字技术的方法来提高可及性。