Pharmacological and psychotherapeutic interventions for management of poststroke depression A Bayesian network meta-analysis of randomized controlled trials

被引:2
|
作者
Sun, Xuejun [1 ]
Deng, Linghui [2 ]
Qiu, Shi [3 ]
Tu, Xiang [3 ]
Wang, Deren [2 ]
Liu, Ming [2 ]
机构
[1] Kangning Hosp, Dept Psychiat 2, Anshan, Liaoning, Peoples R China
[2] Sichuan Univ, Dept Neurol, Stroke Clin Res Unit, Chengdu, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Inst Urol, Dept Urol, Chengdu, Sichuan, Peoples R China
关键词
Bayesian network meta-analysis; Hamilton depression scale; pharmacological; poststroke depression; psychotherapeutic; STROKE; MORTALITY; RISK;
D O I
10.1097/MD.0000000000006100
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Poststroke depression (PSD) constitutes an important complication of stroke, leading to great disability as well as increased mortality. Since which treatment for PSD should be preferred are still matters of controversy, we are aiming to compare and rank these pharmacological and nonpharmacological interventions. Methods and analysis: We will employ a network meta-analysis to incorporate both direct and indirect evidence from relevant trials. We will search PubMed, the Cochrane Library Central Register of Controlled Trials, Embase, and the reference lists of relevant articles for randomized controlled trials (RCT) of different PSD treatment strategies. The characteristics of each RCT will be summarized, including the study characteristics, the participant characteristics, the outcome measurements, and adverse events. The risk of bias will be assessed by means of the Cochrane Collaboration's risk of bias tool. The primary outcome was change in Hamilton Depression Scale (HAMD) score. Secondary outcomes involve patient response rate (defined as at least a 50% score reduction on HAMD), and remission rate (defined as no longer meeting baseline criteria for depression). Moreover, we will assess the acceptability of treatments according to treatment discontinuation. We will perform pairwise meta-analyses by random effects model and network meta-analysis by Bayesian random effects model. Conclusion: Formal ethical approval is not required as primary data will not be collected. Our results will help to reduce the uncertainty about the effectiveness and safety of PSD management, which will encourage further research for other therapeutic options. The review will be disseminated in peer-reviewed publications and conference presentations.
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页数:5
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