How effective are second-generation antipsychotic drugs? A meta-analysis of placebo-controlled trials

被引:349
作者
Leucht, S. [1 ]
Arbter, D. [1 ]
Engel, R. R. [2 ]
Kissling, W. [1 ]
Davis, J. M. [3 ]
机构
[1] Tech Univ Munich, Klin Psychiat & Psychotherapie TU Munchen, Klinikum Rechts Isar, Dept Psychiat & Psychotherapy, D-81675 Munich, Germany
[2] Univ Munich, Dept Psychiat & Psychotherapy, Psychiat Klin, Munich, Germany
[3] Univ Illinois, Dept Psychiat, Chicago, IL 60612 USA
关键词
meta-analysis; schizophrenia; antipsychotic agents; treatment outcome; bias; methodology; PRIMARY NEGATIVE SYMPTOMS; DOUBLE-BLIND; ACUTE EXACERBATION; SCHIZOPHRENIC-PATIENTS; SCHIZOAFFECTIVE DISORDER; ZIPRASIDONE; 40; 160; MG/DAY; EFFICACY; RISPERIDONE; OLANZAPINE;
D O I
10.1038/sj.mp.4002136
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We conducted a systematic review and meta-analysis of randomized controlled trials that compared second-generation antipsychotic (SGA) drugs with placebo in schizophrenic patients and which considered 13 different outcome measures. Thirty-eight randomized controlled trials with 7323 participants were included. All SGA drugs were more effective than placebo, but the pooled effect size (ES) for overall symptoms (primary outcome) was moderate (-0.51). The absolute difference (RD) in responder rates was at 18% (41% responded to drug compared with 24% to placebo, number needed to treat = 6). Similar ESs were found for the other efficacy parameters: negative symptoms (ES = -0.39), positive symptoms (ES = -0.48), depression (ES = -0.26), relapse (RD 20%) and discontinuation due to inefficacy (RD 17%). Curiously, the efficacy of haloperidol for negative and depressive symptoms was similar to that of the SGA drugs. In contrast to haloperidol, there was no difference in terms of EPS between any SGA drugs and placebo, and there was also no difference in terms of dropouts due to adverse events. Meta-regression showed a decline in treatment response over time, and a funnel plot suggested the possibility of publication bias. We conclude that the drug versus placebo difference of SGA drugs and haloperidol in recent trials was moderate, and that there is much room for more efficacious compounds. Whether methodological issues account in part for the relatively low efficacy ESs and the scarcity of adverse event differences compared with placebo needs to be established.
引用
收藏
页码:429 / 447
页数:19
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