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首页> 外文期刊>The Lancet >Use of oral prednisolone or naproxen for the treatment of gout arthritis: a double-blind, randomised equivalence trial.
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Use of oral prednisolone or naproxen for the treatment of gout arthritis: a double-blind, randomised equivalence trial.

机译:口服泼尼松龙或萘普生治疗痛风性关节炎的用途:一项双盲,随机等效试验。

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BACKGROUND: 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. METHODS: 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. FINDINGS: 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. INTERPRETATION: Oral prednisolone and naproxen are equally effective in the initial treatment of gout arthritis over 4 days.
机译:背景:用于治疗痛风性关节炎的非甾体类抗炎药和秋水仙碱具有胃肠道,肾脏和心血管疾病的不良反应。全身性皮质类固醇可能是有益的选择。我们调查了萘普生和泼尼松龙在初级保健中的等效性。方法:我们进行了一项随机临床试验,以测试泼尼松龙和萘普生在治疗单关节痛风中的等效性。通过尿酸一钠晶体证实存在痛风的初级保健患者符合条件。将120例患者随机分配至计算机生成的随机分组中,以接受泼尼松龙(每天一次35 mg; n = 60)或萘普生(每天两次500 mg; n = 60),持续5天。对患者和医生而言,治疗都被掩盖了。主要结局是用100毫米视觉模拟量表测量疼痛,等效先验余量定为10%。根据方案并按意向进行分析。该研究已注册为国际标准随机对照试验,编号为ISRCTN14648181。结果:每个治疗组中一位患者的数据不完整,因此按方案分析包括了每组59位患者。 90小时后,泼尼松龙和萘普生的疼痛评分分别降低了44.7 mm和46.0 mm(差异1.3 mm; 95%CI -9.8至7.1),表明等效。疼痛变化的大小差异为1.57毫米(95%CI -8.65至11.78)。各组之间的不良反应相似,轻微,并在3周的随访中得到缓解。解释:口服泼尼松龙和萘普生对痛风性关节炎的初始治疗在4天内同样有效。

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