Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710, USA.
J Am Coll Cardiol. 2010 Aug 24;56(9):692-9. doi: 10.1016/j.jacc.2010.03.068.
The objective was to test the hypothesis that heart failure (HF) patients treated with sertraline will have lower depression scores and fewer cardiovascular events compared with placebo.
Depression is common among HF patients. It is associated with increased hospitalization and mortality.
The SADHART-CHF (Sertraline Against Depression and Heart Disease in Chronic Heart Failure) trial was a randomized, double-blind, placebo-controlled trial of sertraline 50 to 200 mg/day versus matching placebo for 12 weeks. All participants also received nurse-facilitated support. Eligible patients were age 45 years or older with HF (left ventricular ejection fraction < or =45%, New York Heart Association functional class II to IV) and clinical depression (Diagnostic and Statistical Manual of Mental Disorders-Fourth Edition criteria for current major depressive disorder). Those with significant cognitive impairment, psychosis, recent alcohol or drug dependence, bipolar or severe personality disorder, active suicidal ideation, and current antipsychotic or antidepressant medications were excluded. Primary end points were change in depression severity (Hamilton Depression Rating Scale total score) and composite cardiovascular status at 12 weeks.
A total of 469 patients were randomized (n = 234 sertraline, n = 235 placebo). The mean +/- SE change from baseline to 12 weeks in the Hamilton Depression Rating Scale total score was -7.1 +/- 0.5 (sertraline) and -6.8 +/- 0.5 (placebo) (p < 0.001 from baseline, p = 0.89 between groups, mean change between groups -0.4; 95% confidence interval: -1.7 to 0.92). The proportions whose composite cardiovascular score worsened, improved, or was unchanged were 29.9%, 40.6%, and 29.5%, respectively, in the sertraline group and 31.1%, 43.8%, and 25.1%, respectively, in the placebo group (p = 0.78).
Sertraline was safe in patients with significant HF. However, treatment with sertraline compared with placebo did not provide greater reduction in depression or improved cardiovascular status among patients with HF and depression. (Antidepressant Medication Treatment for Depression in Individuals With Chronic Heart Failure [SADHART-CHF]; NCT00078286).
本研究旨在验证假设,即与安慰剂相比,接受舍曲林治疗的心力衰竭(HF)患者的抑郁评分更低,心血管事件更少。
HF 患者中普遍存在抑郁。它与住院和死亡率增加有关。
SADHART-CHF(舍曲林治疗慢性心力衰竭伴抑郁)试验是一项随机、双盲、安慰剂对照试验,比较舍曲林 50 至 200mg/天与匹配安慰剂治疗 12 周。所有参与者还接受了护士协助的支持。合格的患者为年龄 45 岁或以上,有 HF(左心室射血分数<或=45%,纽约心脏协会功能 II 至 IV 级)和临床抑郁(精神疾病诊断和统计手册第四版当前重度抑郁障碍的标准)。排除有明显认知障碍、精神病、近期酒精或药物依赖、双相或严重人格障碍、有自杀意念、以及当前使用抗精神病药或抗抑郁药的患者。主要终点是 12 周时抑郁严重程度(汉密尔顿抑郁量表总分)和心血管综合状况的变化。
共随机分配了 469 名患者(n=234 舍曲林,n=235 安慰剂)。从基线到 12 周,汉密尔顿抑郁量表总分的平均变化为-7.1±0.5(舍曲林)和-6.8±0.5(安慰剂)(与基线相比,p<0.001,组间比较,p=0.89,组间平均变化-0.4;95%置信区间:-1.7 至 0.92)。舍曲林组恶化、改善和不变的复合心血管评分的比例分别为 29.9%、40.6%和 29.5%,安慰剂组分别为 31.1%、43.8%和 25.1%(p=0.78)。
舍曲林在有严重 HF 的患者中是安全的。然而,与安慰剂相比,舍曲林治疗并未为 HF 和抑郁患者提供更大程度的抑郁缓解或改善心血管状况。(抗抑郁药物治疗慢性心力衰竭患者的抑郁[ SADHART-CHF ];NCT00078286)。