From RAND Corporation, Santa Monica, and Veterans Affairs Greater Los Angeles Healthcare System and David Geffen School of Medicine at the University of California, Los Angeles, Los Angeles, California.
Ann Intern Med. 2017 Jan 3;166(1):37-51. doi: 10.7326/M16-0461. Epub 2016 Nov 1.
Gout is a common type of inflammatory arthritis in patients seen by primary care physicians.
To review evidence about treatment of acute gout attacks, management of hyperuricemia to prevent attacks, and discontinuation of medications for chronic gout in adults.
Multiple electronic databases from January 2010 to March 2016, reference mining, and pharmaceutical manufacturers.
Studies of drugs approved by the U.S. Food and Drug Administration and commonly prescribed by primary care physicians, randomized trials for effectiveness, and trials and observational studies for adverse events.
Data extraction was performed by one reviewer and checked by a second reviewer. Study quality was assessed by 2 independent reviewers. Strength-of-evidence assessment was done by group discussion.
High-strength evidence from 28 trials (only 3 of which were placebo-controlled) shows that colchicine, nonsteroidal anti-inflammatory drugs (NSAIDs), and corticosteroids reduce pain in patients with acute gout. Moderate-strength evidence suggests that low-dose colchicine is as effective as high-dose colchicine and causes fewer gastrointestinal adverse events. Moderate-strength evidence suggests that urate-lowering therapy (allopurinol or febuxostat) reduces long-term risk for acute gout attacks after 1 year or more. High-strength evidence shows that prophylaxis with daily colchicine or NSAIDs reduces the risk for acute gout attacks by at least half in patients starting urate-lowering therapy, and moderate-strength evidence indicates that duration of prophylaxis should be longer than 8 weeks. Although lower urate levels reduce risk for recurrent acute attacks, treatment to a specific target level has not been tested.
Few studies of acute gout treatments, no placebo-controlled trials of management of hyperuricemia lasting longer than 6 months, and few studies in primary care populations.
Colchicine, NSAIDs, and corticosteroids relieve pain in adults with acute gout. Urate-lowering therapy decreases serum urate levels and reduces risk for acute gout attacks.
Agency for Healthcare Research and Quality. (Protocol registration: http://effectivehealth-care.ahrq.gov/ehc/products/564/1992/Gout-managment-protocol-141103.pdf).
痛风是初级保健医生所诊治的常见炎性关节炎。
综述治疗急性痛风发作、高尿酸血症管理以预防发作,以及成人慢性痛风药物停药的相关证据。
2010 年 1 月至 2016 年 3 月的多个电子数据库、参考文献挖掘和制药商。
美国食品和药物管理局批准的药物和初级保健医生常开处方的药物的研究、有效性的随机试验,以及不良事件的试验和观察性研究。
一名评审员进行数据提取,另一名评审员复核。两名独立评审员评估研究质量。通过小组讨论进行证据强度评估。
28 项试验(仅有 3 项为安慰剂对照)的高强度证据表明,秋水仙碱、非甾体抗炎药(NSAIDs)和皮质类固醇可减轻急性痛风患者的疼痛。中等强度证据表明,小剂量秋水仙碱与大剂量秋水仙碱同样有效,且胃肠道不良事件更少。中等强度证据表明,尿酸降低治疗(别嘌醇或非布司他)可降低 1 年或更久后急性痛风发作的长期风险。高强度证据表明,开始降尿酸治疗时每日秋水仙碱或 NSAIDs 预防可使急性痛风发作风险至少降低一半,而中等强度证据表明预防应持续 8 周以上。虽然降低尿酸水平可降低复发性急性发作的风险,但针对特定目标水平的治疗尚未得到检验。
急性痛风治疗的研究较少,高尿酸血症管理超过 6 个月的安慰剂对照试验较少,初级保健人群的研究较少。
秋水仙碱、NSAIDs 和皮质类固醇可缓解成人急性痛风患者的疼痛。降尿酸治疗可降低血清尿酸水平,降低急性痛风发作风险。
美国医疗保健研究与质量署。(方案注册:http://effectivehealth-care.ahrq.gov/ehc/products/564/1992/Gout-managment-protocol-141103.pdf)。