From the Department of Psychology and the Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle; and the Department of Psychiatry and the Department of Psychology, Case Western Reserve University, Cleveland.
Am J Psychiatry. 2019 Apr 1;176(4):287-296. doi: 10.1176/appi.ajp.2018.17090995. Epub 2018 Oct 19.
The authors examined the effect of patient treatment preference on the differential effectiveness of prolonged exposure and sertraline for the treatment of posttraumatic stress disorder (PTSD).
In a doubly randomized preference trial, 200 patients with PTSD viewed standardized treatment rationales prior to randomization. Patients were first randomized to choice of treatment or no choice. Those assigned to no choice were then randomized to prolonged exposure or sertraline. Acute treatment was 10 weeks, with 24-month follow-up. Interviewer-rated PTSD symptom severity was the main outcome measure, and depression, anxiety, and functioning were assessed as additional outcomes.
Patients preferred prolonged exposure over sertraline (number needed to benefit [NNTB]=4.5). Using intent-to-treat analyses (N=200), both prolonged exposure and sertraline showed large gains that were maintained over 24 months. Although no differential effect was observed on interviewer-rated PTSD severity, there was a significant benefit of prolonged exposure over sertraline on interview-rated loss of PTSD diagnosis (NNTB=7.0), responder status (NNTB=5.7), and self-reported PTSD, depression, and anxiety symptoms and functioning (effect sizes, 0.35-0.44). Patients who received their preferred treatment were more likely to be adherent, lose their PTSD diagnosis (NNTB=3.4), achieve responder status (NNTB=3.4), and have lower self-reported PTSD, depression, and anxiety symptoms (effect sizes, 0.40-0.72).
Prolonged exposure and sertraline confer significant benefits for PTSD, with some evidence of an advantage for prolonged exposure. Giving patients with PTSD their preferred treatment also confers important benefits, including enhancing adherence.
作者研究了患者治疗偏好对延长暴露疗法和舍曲林治疗创伤后应激障碍(PTSD)的差异疗效的影响。
在一项双重随机偏好试验中,200 名 PTSD 患者在随机分组前观看了标准化的治疗理由。患者首先随机选择治疗或不选择。那些被分配到没有选择的患者,然后随机分配到延长暴露或舍曲林。急性治疗为 10 周,随访 24 个月。访谈者评定的 PTSD 症状严重程度是主要结局指标,抑郁、焦虑和功能作为附加结局进行评估。
患者更喜欢延长暴露治疗而非舍曲林(需要治疗的人数[NNTB]=4.5)。使用意向治疗分析(N=200),延长暴露和舍曲林均显示出较大的获益,并在 24 个月时得以维持。尽管在访谈者评定的 PTSD 严重程度上未观察到差异效应,但在访谈者评定的 PTSD 诊断丧失(NNTB=7.0)、应答者状态(NNTB=5.7),以及自我报告的 PTSD、抑郁和焦虑症状和功能方面,延长暴露治疗显示出显著的获益(效应大小,0.35-0.44)。接受他们首选治疗的患者更有可能坚持治疗、失去 PTSD 诊断(NNTB=3.4)、达到应答者状态(NNTB=3.4),以及自我报告的 PTSD、抑郁和焦虑症状较低(效应大小,0.40-0.72)。
延长暴露治疗和舍曲林治疗 PTSD 均有显著获益,延长暴露治疗有一定优势。给予 PTSD 患者他们首选的治疗也有重要的获益,包括增强依从性。