The effects of prazosin on sleep disturbances in post-traumatic stress disorder: a systematic review and meta-analysis

被引:34
|
作者
Zhang, Ye [1 ]
Ren, Rong [1 ]
Sanford, Larry D. [2 ]
Yang, Linghui [1 ]
Ni, Yuenan [1 ]
Zhou, Junying [1 ]
Zhang, Jihui [3 ]
Wing, Yun-Kwok [3 ]
Shi, Jie [4 ]
Lu, Lin [4 ]
Tang, Xiangdong [1 ]
机构
[1] Sichuan Univ, Dept Resp & Crit Care Med, State Key Lab Biotherapy,West China Hosp, Mental Hlth Ctr,Translat Neurosci Ctr,Sleep Med C, Chengdu, Peoples R China
[2] Eastern Virginia Med Sch, Dept Pathol & Anat, Sleep Res Lab, POB 1980, Norfolk, VA 23507 USA
[3] Chinese Univ Hong Kong, Fac Med, Dept Psychiat, Shatin, Hong Kong, Peoples R China
[4] Peking Univ, Hosp 6, Natl Inst Drug Dependence, Beijing, Peoples R China
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
Prazosin; Nightmare; Post-traumatic stress disorder; Meta-analysis; COMORBID ALCOHOL DEPENDENCE; VIETNAM COMBAT VETERANS; AIRWAY PRESSURE THERAPY; NIGHTMARE DISORDER; OBJECTIVE SLEEP; PLACEBO; SYMPTOMS; ADULTS; TRIAL; SUICIDALITY;
D O I
10.1016/j.sleep.2019.06.010
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Nightmares are a highly prevalent and distressing feature of post-traumatic stress disorder (PTSD). Previous studies have reached mixed conclusions regarding the effects of prazosin on nightmares, sleep quality, and overall PTSD symptoms in patients with PTSD. Methods: MEDLINE, EMBASE, all EBM databases, PsycIFNO, and CINAHL were systematically searched from inception date to October 2018 for randomized clinical trials that included reporting of nightmares, sleep quality or overall PTSD symptoms. The analysis included data from eight trials involving 286 PTSD patients in the prazosin group and 289 PTSD patients in the placebo group. Results: In our meta-analysis, prazosin resulted in a statistically significant improvement in nightmares (standardized mean difference (SMD) = -1.13, 95% confidence interval (CI) = -1.91 to -0.36), but was not more beneficial than placebo for overall PTSD symptoms (SMD = -0.45, 95% CI = 0.95 to 0.05) and sleep quality (SMD = -0.44, 95% CI = -1.44 to 0.55). In terms of acceptability, there was no significant difference between the prazosin group and the placebo group with respect to discontinuation for all causes (odds ratio (OR) = 1.00, 95% CI = 0.62-1.62). In conclusion, the use of prazosin was associated with an improvement of nightmare symptoms. Conclusion: Our findings indicate that additional studies are needed before considering downgrading the use of prazosin in the treatment of nightmares in patients with PTSD. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:225 / 231
页数:7
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