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首页> 外文期刊>Journal of clinical psychopharmacology >Prazosin Versus Quetiapine for Nighttime Posttraumatic Stress Disorder Symptoms in Veterans An Assessment of Long-Term Comparative Effectiveness and Safety
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Prazosin Versus Quetiapine for Nighttime Posttraumatic Stress Disorder Symptoms in Veterans An Assessment of Long-Term Comparative Effectiveness and Safety

机译:Prazosin对古代夜间后颞损伤的古代植物症状,退伍军人的症状是长期比较效果和安全的评估

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Posttraumatic stress disorder (PTSD) is an anxiety disorder experienced by combat veterans. Nighttime symptoms are often unrelieved by selective serotonin reuptake inhibitor therapy, and increased use of prazosin or quetiapine for treatment is seen. The purpose of this study was to determine the short- and long-term effectiveness and safety of prazosin versus quetiapine for treating nighttime symptoms in veteran PTSD patients. This is a historical prospective cohort study using retrospective chart review. Three hundred twenty-four patients with a diagnosis of PTSD, based on International Classification of Diseases, Ninth Revision coding, who were initially prescribed prazosin or quetiapine for nighttime symptoms were screened for inclusion. Short-term effectiveness was determined by documentation of symptomatic improvement within 6 months, and long-term effectiveness if patients continued therapy to study end date. Safety was assessed by comparing incidence of adverse drug effects causing discontinuation of either study drug.This study included 237 patients: 62 received prazosin, and 175 received quetiapine. Short-term effectiveness was similar for prazosin (61.3%) and quetiapine (61.7%; P = 0.54). However, patients prescribed prazosin were significantly more likely to continue their therapy to study end date compared with quetiapine (48.4% vs 24%; P < 0.001; odds ratio, 3.0; 95% confidence interval, 1.62-5.45), thus achieving long-term effectiveness. Alternatively, patients in the quetiapine group were more likely to discontinue therapy because of adverse effects compared with the prazosin group (34.9% vs 17.7%; P = 0.008). Because of similar rate of short-term effectiveness, superior long-term effectiveness, and lower incidence of events leading to discontinuation, compared with quetiapine, prazosin should be used first-line for treating nighttime PTSD symptoms in a veteran population.
机译:术后应激障碍(PTSD)是战斗退伍军人经历的焦虑症。通过选择性血清素再摄取抑制剂治疗往往是不缓解的夜间症状,并且可以看到增加普罗唑辛或喹硫碱进行治疗的使用。本研究的目的是确定Prazosin的短期和长期有效性和安全性,用于治疗资深患者的夜间症状。这是一种使用回顾性图表审查的历史前瞻性队列研究。筛选基于国际疾病的疾病分类,第九次修订编码,初始规定的夜间症状的第九修订编码,第九次修订编码,第九次修订编码患者进行了三百二十四名患者。短期有效性是通过在6个月内对症状改善的文献进行的短期效果,以及如果患者继续治疗终止疗效,则长期有效性。通过比较不良药物效应的发生率来评估安全性,导致对任何研究药物停止的不良。研究包括237名患者:62名普拉索辛,175名血糖血症。普拉索辛(61.3%)和喹硫甙(61.7%; p = 0.54)相似。然而,与喹诗植物相比,普拉佐汀的患者显着更容易继续治疗终治日期(48.4%vs 24%; p <0.001;赔率比,3.0; 95%置信区间,1.62-5.45),从而实现长 - 术语有效性。或者,与普拉索辛基团相比,喹硫碱组中的患者更容易停止治疗(34.9%Vs 17.7%; p = 0.008)。由于短期有效性,卓越的长期效果率和导致停止的事件的发病率降低,与喹诗素相比,普拉索汀应使用一线以治疗退伍军人人群中的夜间可行的症状。

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