Eminaga Fatma, La-Crette Jonathan, Jones Adrian, Abhishek A
Department of Medicine, Nottingham University Hospitals NHS Trust, Nottingham, NG7 2UH, UK.
Academic Rheumatology, Clinical Sciences Building, University of Nottingham, Nottingham, NG5 1PB, UK.
Rheumatol Int. 2016 Dec;36(12):1747-1752. doi: 10.1007/s00296-016-3579-z. Epub 2016 Oct 19.
The aim of this study was to systematically review the literature on effect of initiating urate-lowering treatment (ULT) during an acute attack of gout on duration of index attack and persistence on ULT. OVID (Medline), EMBASE and AMED were searched to identify randomized controlled trials (RCTs) of ULT initiation during acute gout attack published in English language. Two reviewers appraised the study quality and extracted data independently. Standardized mean difference (SMD) and relative risk (RR) were used to pool continuous and categorical data. Meta-analysis was carried out using STATA version 14. A total of 537 studies were selected. A total of 487 titles and abstracts were reviewed after removing duplicates. Three RCTs were identified. There was evidence from two high-quality studies that early initiation of allopurinol did not increase pain severity at days 10-15 [SMD (95 % CI) 0.18 (-0.58, 0.93)]. Data from three studies suggested that initiation of ULT during an acute attack of gout did not associate with dropouts [RR (95 % CI) 1.16 (0.58, 2.31)]. There is moderate-quality evidence that the initiation of ULT during an acute attack of gout does not increase pain severity and risk of ULT discontinuation. Larger studies are required to confirm these findings so that patients with acute gout can be initiated on ULT with confidence.
本研究的目的是系统回顾关于痛风急性发作期间开始降尿酸治疗(ULT)对首次发作持续时间及ULT持续治疗率影响的文献。检索了OVID(医学期刊数据库)、EMBASE和AMED,以确定用英文发表的关于痛风急性发作期间开始ULT的随机对照试验(RCT)。两名评价者独立评估研究质量并提取数据。采用标准化均数差(SMD)和相对危险度(RR)汇总连续性数据和分类数据。使用STATA 14版进行荟萃分析。共筛选出537项研究。去除重复项后,共审查了487篇标题和摘要。确定了3项RCT。两项高质量研究的证据表明,早期开始使用别嘌醇在第10至15天不会增加疼痛严重程度[SMD(95%CI)0.18(-0.58,0.93)]。三项研究的数据表明,痛风急性发作期间开始ULT与退出治疗无关[RR(95%CI)1.16(0.58,2.31)]。有中等质量的证据表明,痛风急性发作期间开始ULT不会增加疼痛严重程度和ULT停药风险。需要更大规模的研究来证实这些发现,以便痛风急性发作患者能够放心地开始ULT治疗。