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基于 PANSS 评估的非典型抗精神病药安慰剂对照随机临床试验的辍学率的荟萃分析。

Meta-analysis of Dropout Rates in Placebo-Controlled Randomized Clinical Trials of Atypical Antipsychotics Assessed by PANSS.

机构信息

Department of Clinical Medicine (Pharmaceutical Medicine), Graduate School of Pharmaceutical Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.

出版信息

Clin Drug Investig. 2019 Oct;39(10):917-926. doi: 10.1007/s40261-019-00813-5.

Abstract

BACKGROUND AND OBJECTIVES

Subject dropout rates in placebo-controlled randomized clinical trials (RCTs) of antipsychotics are high. The missing values due to dropout represent a potential source of bias in clinical trials. We aimed to identify the potential factors affecting subject dropout in atypical antipsychotics RCTs by conducting a meta-analysis.

METHODS

Placebo-controlled RCTs for atypical antipsychotics using positive and negative syndrome scale (PANSS) as a psychiatric assessment scale were selected by database search. The potential factors affecting subject dropout, such as publication year, study design, and operational factors, were analyzed by meta-regression.

RESULTS

Forty-seven placebo controlled RCTs of atypical antipsychotics of which results were published between 1993 and 2018 were identified through the database search. In the multivariate meta-regression analysis, earlier publication year, older age of subjects, and longer study duration were significantly associated with high subject dropout rates in placebo-controlled clinical trials of atypical antipsychotics.

CONCLUSION

Subject dropout rates in clinical trials of atypical antipsychotics published between 1993 and 2018 year decreased over time. Study duration should be taken into consideration when designing future studies, where short study periods yet appropriate for evaluating the efficacy of new atypical antipsychotics are preferable. Additionally, previous medications and the degree of subject satisfaction with antipsychotics might affect subject dropout rate.

摘要

背景与目的

抗精神病药安慰剂对照随机临床试验(RCT)中的受试者脱落率较高。由于脱落而导致的缺失值是临床试验中潜在的偏倚来源。我们旨在通过Meta 分析确定影响非典型抗精神病药 RCT 中受试者脱落的潜在因素。

方法

通过数据库检索,选择阳性和阴性症状量表(PANSS)作为精神科评估量表的非典型抗精神病药安慰剂对照 RCT。通过Meta 回归分析,分析了影响受试者脱落的潜在因素,如发表年份、研究设计和操作因素等。

结果

通过数据库检索,共确定了 47 项非典型抗精神病药的安慰剂对照 RCT,这些 RCT 的研究结果发表于 1993 年至 2018 年之间。在多变量 Meta 回归分析中,较早的发表年份、受试者年龄较大以及研究持续时间较长与非典型抗精神病药安慰剂对照临床试验中的高受试者脱落率显著相关。

结论

1993 年至 2018 年发表的非典型抗精神病药临床试验中,受试者脱落率随时间推移呈下降趋势。在设计未来研究时应考虑研究持续时间,对于评估新型非典型抗精神病药疗效的研究,较短的研究周期更为可取。此外,既往用药和受试者对抗精神病药的满意度可能会影响受试者脱落率。

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