Janssens Hein J E M, Janssen Matthijs, van de Lisdonk Eloy H, van Riel Piet L C M, van Weel Chris
Department of General Practice, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands.
Lancet. 2008 May 31;371(9627):1854-60. doi: 10.1016/S0140-6736(08)60799-0.
Non-steroidal anti-inflammatory drugs and colchicine used to treat gout arthritis have gastrointestinal, renal, and cardiovascular adverse effects. Systemic corticosteroids might be a beneficial alternative. We investigated equivalence of naproxen and prednisolone in primary care.
We did a randomised clinical trial to test equivalence of prednisolone and naproxen for the treatment of monoarticular gout. Primary-care patients with gout confirmed by presence of monosodium urate crystals were eligible. 120 patients were randomly assigned with computer-generated randomisation to receive either prednisolone (35 mg once a day; n=60) or naproxen (500 mg twice a day; n=60), for 5 days. Treatment was masked for both patients and physicians. The primary outcome was pain measured on a 100 mm visual analogue scale and the a priori margin for equivalence set at 10%. Analyses were done per protocol and by intention to treat. This study is registered as an International Standard Randomised Controlled Trial, number ISRCTN14648181.
Data were incomplete for one patient in each treatment group, so per-protocol analyses included 59 patients in each group. After 90 h the reduction in the pain score was 44.7 mm and 46.0 mm for prednisolone and naproxen, respectively (difference 1.3 mm; 95% CI -9.8 to 7.1), suggesting equivalence. The difference in the size of change in pain was 1.57 mm (95% CI -8.65 to 11.78). Adverse effects were similar between groups, minor, and resolved by 3 week follow-up.
Oral prednisolone and naproxen are equally effective in the initial treatment of gout arthritis over 4 days.
用于治疗痛风性关节炎的非甾体抗炎药和秋水仙碱具有胃肠道、肾脏和心血管方面的不良反应。全身用糖皮质激素可能是一种有益的替代药物。我们在初级保健中研究了萘普生和泼尼松龙的等效性。
我们进行了一项随机临床试验,以测试泼尼松龙和萘普生治疗单关节痛风的等效性。经尿酸钠晶体证实患有痛风的初级保健患者符合条件。120名患者通过计算机生成的随机分组被随机分配接受泼尼松龙(每日一次35毫克;n = 60)或萘普生(每日两次500毫克;n = 60),为期5天。患者和医生均对治疗进行了盲法处理。主要结局是用100毫米视觉模拟量表测量的疼痛,等效性的先验界值设定为10%。分析按方案和意向性分析进行。本研究注册为国际标准随机对照试验,编号为ISRCTN14648181。
每个治疗组各有1例患者数据不完整,因此按方案分析每组包括59例患者。90小时后,泼尼松龙和萘普生的疼痛评分降低分别为44.7毫米和46.0毫米(差异1.3毫米;95%CI -9.8至7.1),表明具有等效性。疼痛变化大小的差异为1.57毫米(95%CI -8.65至11.78)。两组间不良反应相似,程度较轻,在3周随访时消失。
口服泼尼松龙和萘普生在痛风性关节炎的初始4天治疗中同样有效。