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A randomized stepped care intervention trial targeting posttraumatic stress disorder for surgically hospitalized injury survivors

机译:针对创伤后应激障碍患者的手术后创伤幸存者的随机分步护理干预试验

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Objective:: To test the effectiveness of a stepped care intervention model targeting posttraumatic stress disorder (PTSD) symptoms after injury. Background:: Few investigations have evaluated interventions for injured patients with PTSD and related impairments that can be feasibly implemented in trauma surgical settings. METHODS:: The investigation was a pragmatic effectiveness trial in which 207 acutely injured hospitalized trauma survivors were screened for high PTSD symptom levels and then randomized to a stepped combined care management, psychopharmacology, and cognitive behavioral psychotherapy intervention (n = 104) or usual care control (n = 103) conditions. The symptoms of PTSD and functional limitations were reassessed at 1, 3, 6, 9, and 12 months after the index injury admission. RESULTS:: Regression analyses demonstrated that over the course of the year after injury, intervention patients had significantly reduced PTSD symptoms when compared with controls [group by time effect, CAPS (Clinician-Administered PTSD Scale): F(2, 185) = 5.50, P < 0.01; PCL-C (PTSD Checklist Civilian Version): F(4, 185) = 5.45, P < 0.001]. Clinically and statistically significant PTSD treatment effects were observed at the 6-, 9-, and 12-month postinjury assessments. Over the course of the year after injury, intervention patients also demonstrated significant improvements in physical function [MOS SF-36 PCS (Medical Outcomes Study Short Form 36 Physical Component Summary) main effect: F(1, 172) = 9.87, P < 0.01]. CONCLUSIONS:: Stepped care interventions can reduce PTSD symptoms and improve functioning over the course of the year after surgical injury hospitalization. Orchestrated investigative and policy efforts could systematically introduce and evaluate screening and intervention procedures for PTSD at US trauma centers. (Trial Registration: clinicaltrials.gov identifier: NCT00270959) ? 2013 by Lippincott Williams & Wilkins.
机译:目的::测试针对创伤后应激障碍(PTSD)症状的分级护理干预模型的有效性。背景:很少有研究评估针对创伤后应激障碍(PTSD)及相关障碍的患者的干预措施,这些干预措施可在创伤外科手术环境中可行地实施。方法:该研究是一项实用性试验,其中筛选了207名严重创伤后住院的创伤幸存者,以寻找较高的PTSD症状水平,然后将其随机分为联合护理管理,心理药理学和认知行为心理治疗干预(n = 104)或常规护理控制(n = 103)条件。入院后1、3、6、9和12个月,对PTSD的症状和功能限制进行了重新评估。结果:回归分析表明,在受伤后的一年中,与对照组相比,干预组患者的PTSD症状明显减轻[按时间效应分组,CAPS(临床医生管理的PTSD量表):F(2,185)= 5.50 ,P <0.01; PCL-C(PTSD清单民用版):F(4,185)= 5.45,P <0.001]。在伤后6个月,9个月和12个月的评估中观察到具有临床和统计学意义的PTSD治疗效果。在受伤后的一年中,干预患者的身体机能也得到显着改善[MOS SF-36 PCS(医学成果研究简短形式36身体成分摘要),主要作用:F(1,172)= 9.87,P <0.01 ]。结论:在外科损伤住院后的一年中,分步护理干预措施可以减轻PTSD症状并改善功能。精心安排的调查和政策工作可以系统地引入和评估美国创伤中心对PTSD的筛查和干预程序。 (试用注册:clinicaltrials.gov标识符:NCT00270959)? Lippincott Williams&Wilkins,2013年。

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