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类风湿关节炎中短期低剂量泼尼松龙与安慰剂及非甾体抗炎药的荟萃分析。

Meta-analysis of short-term low dose prednisolone versus placebo and non-steroidal anti-inflammatory drugs in rheumatoid arthritis.

作者信息

Gøtzsche P C, Johansen H K

机构信息

Nordic Cochrane Centre, Rigshospitalet, Department 7112, Copenhagen, Denmark.

出版信息

BMJ. 1998 Mar 14;316(7134):811-8. doi: 10.1136/bmj.316.7134.811.

Abstract

OBJECTIVE

To determine whether short-term, oral low dose prednisolone (< or = 15 mg daily) is superior to placebo and non-steroidal anti-inflammatory drugs in patients with rheumatoid arthritis.

DESIGN

Meta-analysis of randomised trials of oral corticosteroids compared with placebo or a non-steroidal anti-inflammatory drug.

SETTING

Trials conducted anywhere in the world.

SUBJECTS

Patients with rheumatoid arthritis.

MAIN OUTCOME MEASURES

Joint tenderness, pain, and grip strength. Outcomes measured on different scales were combined by using the standardised effect size (difference in effect divided by SD of the measurements).

RESULTS

Ten studies were included in the meta-analysis. Prednisolone had a marked effect over placebo on joint tenderness (standardised effect size 1.31; 95% confidence interval 0.78 to 1.83), pain (1.75; 0.87 to 2.64), and grip strength (0.41; 0.13 to 0.69). Measured in the original units the differences were 12 (6 to 18) tender joints and 22 mm Hg (5 mm Hg to 40 mm Hg) for grip strength. Prednisolone also had a greater effect than non-steroidal anti-inflammatory drugs on joint tenderness (0.63; 0.11 to 1.16) and pain (1.25; 0.26 to 2.24), whereas the difference in grip strength was not significant (0.31; -0.02 to 0.64). Measured in the original units the differences were 9 (5 to 12) tender joints and 12 mm Hg (-6 mm Hg to 31 mm Hg). The risk of adverse effects during moderate and long term use seemed acceptable.

CONCLUSION

Prednisolone in low doses (< or = 15 mg daily) may be used intermittently in patients with rheumatoid arthritis, particularly if the disease cannot be controlled by other means.

摘要

目的

确定短期口服低剂量泼尼松龙(每日≤15毫克)在类风湿关节炎患者中是否优于安慰剂和非甾体抗炎药。

设计

口服皮质类固醇与安慰剂或非甾体抗炎药的随机试验的荟萃分析。

地点

在世界任何地方进行的试验。

受试者

类风湿关节炎患者。

主要观察指标

关节压痛、疼痛和握力。通过使用标准化效应量(效应差异除以测量的标准差)将不同量表测量的结果合并。

结果

荟萃分析纳入了10项研究。泼尼松龙在关节压痛(标准化效应量1.31;95%置信区间0.78至1.83)、疼痛(1.75;0.87至2.64)和握力(0.41;0.13至0.69)方面对安慰剂有显著效果。以原始单位测量,差异为压痛关节数12个(6至18个),握力为22毫米汞柱(5毫米汞柱至40毫米汞柱)。泼尼松龙在关节压痛(0.63;0.11至1.16)和疼痛(1.25;0.26至2.24)方面也比非甾体抗炎药有更大效果,而握力差异不显著(0.31;-0.02至0.64)。以原始单位测量,差异为压痛关节数9个(5至12个),握力为12毫米汞柱(-6毫米汞柱至31毫米汞柱)。中、长期使用期间的不良反应风险似乎可以接受。

结论

低剂量(每日≤15毫克)泼尼松龙可间歇用于类风湿关节炎患者,尤其是在疾病无法通过其他方法控制时。

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