Department of Psychology, Emory University.
Department of Psychiatry and Behavioral Sciences, Emory University.
J Consult Clin Psychol. 2018 Feb;86(2):189-199. doi: 10.1037/ccp0000279.
This study followed remitted patients from a randomized controlled trial of adults with major depressive disorder (MDD). The aims were to describe rates of recurrence and to evaluate 3 clinical predictor domains.
Ninety-four treatment-naïve patients (50% female; Mage = 38.1 years; 48.9% White; 30.9% Hispanic) with MDD who had remitted to 12-week monotherapy (escitalopram, duloxetine, or cognitive behavior therapy [CBT]) participated in a 21-month maintenance phase (i.e., continued medication or 3 possible CBT booster sessions per year). Recurrence was assessed quarterly, and the clinical predictors were the following: 2 measures of residual depressive symptoms, 1 measure of lifetime depressive episodes, and 2 measures of baseline anxiety. Survival analysis models evaluated recurrence rates, and regression models evaluated the predictors.
Among all patients, 15.5% experienced a recurrence, and the survival distributions did not statistically differ among treatments. Residual depressive symptoms on the Hamilton Depression Rating Scale at the end of monotherapy were associated with increased risk for recurrence (hazard ratio = 1.31, 95% confidence interval [CI: 1.02, 1.67], Wald χ2 = 4.41, p = .036), and not having a comorbid anxiety disorder diagnosis at study baseline reduced the risk of recurrence (hazard ratio = .31, 95% CI [.10, .94], Wald χ2 = 4.28, p = .039).
The study supported the benefits of maintenance treatment for treatment-naïve patients who remitted to initial monotherapy; nevertheless, remitted patients with a comorbid anxiety disorder diagnosis at the beginning of treatment or residual depressive symptoms after initial treatment were at risk for poorer long-term outcomes. (PsycINFO Database Record
本研究随访了一项成人重度抑郁症(MDD)随机对照试验中缓解的患者。目的是描述复发率,并评估 3 个临床预测因素领域。
94 名首次接受治疗的 MDD 患者(50%为女性;平均年龄=38.1 岁;48.9%为白人;30.9%为西班牙裔)在 12 周的单药治疗(艾司西酞普兰、度洛西汀或认知行为疗法[CBT])中缓解后,参加了 21 个月的维持治疗阶段(即继续用药或每年进行 3 次可能的 CBT 强化治疗)。每季度评估复发情况,临床预测因素包括以下 2 项残留抑郁症状指标、1 项终生抑郁发作指标和 2 项基线焦虑指标。生存分析模型评估复发率,回归模型评估预测因素。
在所有患者中,有 15.5%经历了复发,治疗之间的生存分布没有统计学差异。单药治疗结束时汉密尔顿抑郁评定量表上的残留抑郁症状与复发风险增加相关(风险比=1.31,95%置信区间[CI:1.02,1.67],Wald χ2=4.41,p=.036),而研究基线时没有共病焦虑障碍诊断则降低了复发风险(风险比=0.31,95%CI [0.10,0.94],Wald χ2=4.28,p=.039)。
该研究支持了对初始单药治疗缓解的首次接受治疗的患者进行维持治疗的益处;然而,治疗开始时患有共病焦虑障碍诊断或初始治疗后残留抑郁症状的缓解患者存在长期预后较差的风险。