Department of Cardiology, Odense University Hospital, Sdr. Boulevard 29, DK-5000 Odense, Denmark.
Int J Cardiol. 2011 Jan 7;146(1):64-7. doi: 10.1016/j.ijcard.2010.01.006. Epub 2010 Feb 26.
This study was designed to assess whether pharmacologically treated depression was associated with increased mortality risk in systolic heart failure (SHF) patients.
Patients (n=3346) with SHF (left ventricular ejection fraction ≤ 0.45) and primarily New York Heart Association (NYHA) classes II-III (78%) were recruited from a clinical database used in 20 heart failure clinics in Denmark. The association between pharmacologically treated depression identified by at least one prescription of an antidepressant and mortality risk was evaluated.
Follow-up time was 540 days (range: 30-1600 days). 539 patients died. For 243 patients (7%) an antidepressant had been prescribed at least once. In a Cox Proportional Hazard Model, pharmacologically treated depression was associated with a 49% increased mortality risk (Hazard ratio: 1.49, 95% confidence interval: 1.03-2.16) after adjustment for traditional confounders. Three months after the baseline visit in the heart failure clinic, these patients received lower doses of beta-blockers than patients without antidepressant therapy (p=0.006). Female sex (p<0.001) and NYHA classes III-IV (p=0.007) were associated with the prescription of an antidepressant.
Our analyses suggest that pharmacologically treated depression is associated with a 49% increased mortality risk, and that these high-risk patients receive lower doses of beta-blockers than patients with no antidepressant therapy.
本研究旨在评估在射血分数降低的心力衰竭(SHF)患者中,经药物治疗的抑郁症是否与死亡率风险增加相关。
从丹麦 20 家心力衰竭诊所使用的临床数据库中招募了 3346 名 SHF(左心室射血分数≤0.45)且主要为纽约心脏协会(NYHA)II-III 级(78%)的患者。通过至少开一种抗抑郁药来确定药物治疗的抑郁症与死亡率风险之间的关联。
随访时间为 540 天(范围:30-1600 天)。有 539 名患者死亡。有 243 名患者(7%)至少开了一次抗抑郁药。在 Cox 比例风险模型中,在校正了传统混杂因素后,药物治疗的抑郁症与死亡率风险增加 49%相关(危险比:1.49,95%置信区间:1.03-2.16)。在心力衰竭诊所基线就诊后的 3 个月,这些患者接受的β受体阻滞剂剂量低于未接受抗抑郁治疗的患者(p=0.006)。女性(p<0.001)和 NYHA 分级 III-IV(p=0.007)与抗抑郁药的处方相关。
我们的分析表明,药物治疗的抑郁症与死亡率风险增加 49%相关,这些高风险患者接受的β受体阻滞剂剂量低于未接受抗抑郁治疗的患者。