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针对所有临床病症的安慰剂干预措施。

Placebo interventions for all clinical conditions.

作者信息

Hróbjartsson A, Gøtzsche P C

机构信息

Nordic Cochrane Centre, Rigshospitalet, Department 7112, Blegdamsvej 9, Copenhagen Ø, Denmark, DK-2100.

出版信息

Cochrane Database Syst Rev. 2004(3):CD003974. doi: 10.1002/14651858.CD003974.pub2.

Abstract

BACKGROUND

Placebo interventions are often claimed to improve patient-reported and observer-reported outcomes, but this belief is not based on evidence from randomised trials that compare placebo with no treatment.

OBJECTIVES

To assess the effect of placebo interventions.

SEARCH STRATEGY

We searched the Cochrane Central Register of Controlled Trials (CENTRAL) (The Cochrane Library Issue 4, 2002), MEDLINE (1966 to 2002), EMBASE (1980 to 2002), Biological Abstracts (1986 to 2002), and PsycLIT (1887 to 2002). We contacted experts on placebo research, and read references in the included trials.

SELECTION CRITERIA

We included randomised placebo trials with a no-treatment control group investigating any health problem.

DATA COLLECTION AND ANALYSIS

Two reviewers independently assessed trial quality and extracted data. We contacted study authors for additional information.

MAIN RESULTS

Outcome data were available in 156 out of 182 included trials, investigating 46 clinical conditions. We found no statistically significant pooled effect of placebo in 38 studies with binary outcomes (4284 patients), relative risk 0.95 (95% confidence interval (CI) 0.89 to 1.01). The pooled relative risk for patient-reported outcomes was 0.95 (95% CI 0.88 to 1.03) and for observer-reported outcomes 0.91 (95% CI 0.81 to 1.03). There was heterogeneity (P=0.01) but the funnel plot was symmetrical. There was no statistically significant effect of placebo interventions in the four clinical conditions investigated in three trials or more: pain, nausea, smoking, and depression, but confidence intervals were wide. We found an overall effect of placebo treatments in 118 trials with continuous outcomes (7453 patients), standardised mean difference (SMD) -0.24 (95% CI -0.31 to -0.17). The SMD for patient-reported outcomes was -0.30 (95% CI -0.38 to -0.21), whereas no statistically significant effect was found for observer-reported outcomes, SMD -0.10 (95% CI -0.20 to -0.01). There was heterogeneity (P<0.001) and large variability in funnel plot results even for big trials. There was an apparent effect of placebo interventions on pain (SMD -0.25 (95% CI -0.35 to-0.16)), and phobia (SMD -0.63 (95% CI -1.17 to -0.08)); but also a substantial risk of bias. There was no statistically significant effect of placebo interventions in eight other clinical conditions investigated in three trials or more: nausea, smoking, depression, overweight, asthma, hypertension, insomnia and anxiety, but confidence intervals were wide.

REVIEWERS' CONCLUSIONS: There was no evidence that placebo interventions in general have clinically important effects. A possible small effect on continuous patient-reported outcomes, especially pain, could not be clearly distinguished from bias.

摘要

背景

安慰剂干预措施常被宣称能改善患者报告和观察者报告的结果,但这种观点并非基于将安慰剂与不治疗进行比较的随机试验证据。

目的

评估安慰剂干预措施的效果。

检索策略

我们检索了Cochrane对照试验中心注册库(CENTRAL)(《Cochrane图书馆》2002年第4期)、MEDLINE(1966年至2002年)、EMBASE(1980年至2002年)、生物学文摘数据库(1986年至2002年)和心理学文摘数据库(1887年至2002年)。我们联系了安慰剂研究方面的专家,并查阅了纳入试验中的参考文献。

入选标准

我们纳入了设有不治疗对照组的随机安慰剂试验,这些试验研究任何健康问题。

数据收集与分析

两名评价员独立评估试验质量并提取数据。我们联系研究作者以获取更多信息。

主要结果

在纳入的182项试验中的156项试验里有结果数据,这些试验研究了46种临床病症。在38项有二元结局的研究(4284例患者)中,我们未发现安慰剂有统计学显著的合并效应,相对危险度为0.95(95%置信区间(CI)0.89至1.01)。患者报告结局的合并相对危险度为0.95(95%CI 0.88至1.03),观察者报告结局的合并相对危险度为0.91(95%CI 0.81至1.03)。存在异质性(P = 0.01),但漏斗图是对称的。在三项或更多试验中研究的四种临床病症(疼痛、恶心、吸烟和抑郁)中,安慰剂干预措施没有统计学显著效应,但置信区间较宽。在118项有连续结局的试验(7453例患者)中,我们发现安慰剂治疗有总体效应,标准化均数差(SMD)为 -0.24(95%CI -0.31至 -0.17)。患者报告结局的SMD为 -0.30(95%CI -0.38至 -0.21),而观察者报告结局未发现统计学显著效应,SMD为 -0.10(95%CI -0.20至 -0.01)。存在异质性(P < 0.001),即使对于大型试验,漏斗图结果的变异性也很大。安慰剂干预措施对疼痛(SMD -0.25(95%CI -0.35至 -0.16))和恐惧症(SMD -0.63(95%CI -1.17至 -0.08))有明显效应;但也存在很大的偏倚风险。在三项或更多试验中研究的其他八种临床病症(恶心、吸烟、抑郁、超重、哮喘、高血压、失眠和焦虑)中,安慰剂干预措施没有统计学显著效应,但置信区间较宽。

评价员结论

没有证据表明安慰剂干预措施总体上具有临床重要效应。对连续的患者报告结局,尤其是疼痛,可能存在的微小效应无法与偏倚明确区分。

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