Maasstad Hospital and Erasmus School of Health Policy and Management, Rotterdam, The Netherlands.
Erasmus Medical Center, Rotterdam, The Netherlands.
Arthritis Care Res (Hoboken). 2023 Aug;75(8):1659-1672. doi: 10.1002/acr.24965. Epub 2023 Feb 22.
Whereas in the treatment of rheumatoid arthritis much evidence exists on the effects of current pharmacologic treatment on clinical outcomes, little is known about the effects on patient-reported outcomes. This systematic review aims to evaluate the effects of disease-modifying antirheumatic drugs (DMARDs) on the patient-relevant domains of pain, fatigue, activity limitation, overall emotional and physical health impact, and work/school/housework ability and productivity.
A literature search was conducted to identify randomized controlled trials wherein registered DMARDs were compared with placebo or methotrexate and reported the effects on patient-reported outcomes included in the International Consortium of Health Outcomes Measurement standard set for inflammatory arthritis. Random effects meta-analyses using the standardized mean differences of change scores as the effect measure were performed for the domains of pain, fatigue, and activity limitation, comparing DMARDs with placebo and methotrexate. The other 2 domains were presented narratively.
Across the 5 domains, 69 records belonging to 52 studies were identified. All meta-analyses showed a decrease of burden when DMARDs were compared with placebo (standardized mean differences [95% confidence interval] in pain -0.80 [-0.99, -0.61], fatigue -0.48 [-0.64, -0.32], and activity limitation -0.56 [- 0.63, -0.49]) and when compared with methotrexate (-0.55 [-0.70, -0.41), -0.44 [-0.55, -0.33], and - 0.37 [-0.44, -0.30], respectively).
DMARDs decrease the burden in all the domains that are relevant to patients. Effect sizes may be influenced by DMARD type. Therefore, in the decision for rheumatoid arthritis treatment, patient-reported outcomes should be taken into account.
虽然在类风湿关节炎的治疗中,有大量证据表明当前药物治疗对临床结局的影响,但对于这些治疗对患者报告结局的影响知之甚少。本系统评价旨在评估改善病情抗风湿药物(DMARDs)对疼痛、疲劳、活动受限、整体情绪和身体健康影响、工作/上学/家务能力和生产力等与患者相关的领域的影响。
进行文献检索,以确定将注册的 DMARDs 与安慰剂或甲氨蝶呤进行比较并报告纳入国际健康结局测量联合会炎症性关节炎标准集的患者报告结局的随机对照试验。使用变化评分的标准化均数差作为效应量,对 DMARDs 与安慰剂和甲氨蝶呤进行了疼痛、疲劳和活动受限领域的随机效应荟萃分析。其他 2 个领域以叙述性方式呈现。
在 5 个领域中,共确定了 69 项记录,涉及 52 项研究。所有荟萃分析均表明,与安慰剂相比(疼痛的标准化均数差异[95%置信区间]为-0.80[-0.99,-0.61],疲劳为-0.48[-0.64,-0.32],活动受限为-0.56[-0.63,-0.49]),与甲氨蝶呤相比(-0.55[-0.70,-0.41],-0.44[-0.55,-0.33],-0.37[-0.44,-0.30]),DMARDs 减轻了所有与患者相关的领域的负担。效应大小可能受到 DMARD 类型的影响。因此,在类风湿关节炎治疗的决策中,应考虑患者报告的结局。