Effects of antidepressant medication of morbidity and mortality in depressed patients after myocardial infarction

被引:385
作者
Taylor, CB
Youngblood, ME
Catellier, D
Veith, RC
Carney, RM
Burg, MM
Kaufmann, PG
Shuster, J
Mellman, T
Blumenthal, JA
Krishnan, R
Jaffe, AS
机构
[1] Stanford Univ, Med Ctr, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA
[2] Univ N Carolina, Dept Biostat, Chapel Hill, NC USA
[3] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[4] Washington Univ, Dept Psychiat & Behav Sci, St Louis, MO 63110 USA
[5] Yale Univ, Dept Psychiat, New Haven, CT 06520 USA
[6] NHLBI, Bethesda, MD 20892 USA
[7] Univ Alabama Birmingham, Dept Psychiat, Birmingham, AL USA
[8] Dartmouth Coll Sch Med, Dept Psychiat, Hanover, NH USA
[9] Duke Univ, Dept Psychiat, Durham, NC 27706 USA
[10] Mayo Clin & Mayo Fdn, Dept Cardiol & Internal Med, Rochester, MN 55905 USA
关键词
D O I
10.1001/archpsyc.62.7.792
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Depression after myocardial infarction (MI) is associated with higher morbidity and mortality. Although antidepressants are effective in reducing depression, their use in patients with cardiovascular disease remains controversial. Objective: To undertake a secondary analysis to determine the effects of using antidepressants on morbidity and mortality in post-MI patients who participated in the Enhancing Recovery in Coronary Heart Disease study. Design: Observational secondary analysis. Setting: Eight academic sites. Patients: The Enhancing Recovery in Coronary Heart Disease clinical trial randomized 2481 depressed and/or socially isolated patients from October 1, 1996, to October 31, 1999. Depression was diagnosed using a structured clinical interview. This analysis was conducted on the 1834 patients enrolled with depression (849 women and 985 men). Intervention: Use of antidepressant medication. Main Outcome Measures: Event-free survival was defined as the absence of death or recurrent MI. All-cause mortality was also examined. To relate exposure to antidepressants to subsequent morbidity and mortality, the data were analyzed using a time-dependent covariate model. Results. During a mean follow-up of 29 months, 457 fatal and nonfatal cardiovascular events occurred. The risk of death or recurrent MI was significantly lower in patients taking selective serotonin reuptake inhibitors (adjusted hazard ratio [HR], 0.57; 95% confidence interval [CI], 0.38-0.84), as were the risk of all-cause mortality (adjusted HR, 0.59; 95% CI, 0.37-0.96) and recurrent MI (adjusted HR, 0.53; 95% Cl, 0.32-0.90), compared with patients who did not use selective serotonin reuptake inhibitors. For patients taking non-selective serotonin reuptake inhibitor antidepressants, the comparable HRs (95% CIS) were 0.72 (0.44-1.18), 0.64 (0.34-1.22), and 0.73 (0.38-1.38) for risk of death or recurrent MI, all-cause mortality, or recurrent MI, respectively, compared with nonusers. Conclusions: Use of selective serotonin reuptake inhibitors in depressed patients who experience an acute MI might reduce subsequent cardiovascular morbidity and mortality. A controlled trial is needed to examine this important issue.
引用
收藏
页码:792 / 798
页数:7
相关论文
共 35 条
[1]   BIOBEHAVIORAL VARIABLES AND MORTALITY OR CARDIAC-ARREST IN THE CARDIAC-ARRHYTHMIA PILOT-STUDY (CAPS) [J].
AHERN, DK ;
GORKIN, L ;
ANDERSON, JL ;
TIERNEY, C ;
HALLSTROM, A ;
EWART, C ;
CAPONE, RJ ;
SCHRON, E ;
KORNFELD, D ;
HERD, JA ;
RICHARDSON, DW ;
FOLLICK, MJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1990, 66 (01) :59-62
[2]  
BALOGH S, 1993, PSYCHOPHARMACOL BULL, V29, P201
[3]  
Berkman L, 2001, PSYCHOSOM MED, V63, P747
[4]  
Berkman LF, 2003, JAMA-J AM MED ASSOC, V289, P3106
[5]  
Berkman LF, 2000, AM HEART J, V139, P1
[6]   Even minimal symptoms of depression increase mortality risk after acute myocardial infarction [J].
Bush, DE ;
Ziegelstein, RC ;
Tayback, M ;
Richter, D ;
Stevens, S ;
Zahalsky, H ;
Fauerbach, JA .
AMERICAN JOURNAL OF CARDIOLOGY, 2001, 88 (04) :337-341
[7]   Depression as a risk factor for cardiac mortality and morbidity - A review of potential mechanisms [J].
Carney, RM ;
Freedland, KE ;
Miller, GE ;
Jaffe, AS .
JOURNAL OF PSYCHOSOMATIC RESEARCH, 2002, 53 (04) :897-902
[8]   Depression, heart rate variability, and acute myocardial infarction [J].
Carney, RM ;
Blumenthal, JA ;
Stein, PK ;
Watkins, L ;
Catellier, D ;
Berkman, LF ;
Czajkowski, SM ;
O'Connor, C ;
Stone, PH ;
Freedland, KE .
CIRCULATION, 2001, 104 (17) :2024-2028
[9]   Change in heart rate and heart rate variability during treatment for depression in patients with coronary heart disease [J].
Carney, RM ;
Freedland, KE ;
Stein, PK ;
Skala, JA ;
Hoffman, P ;
Jaffe, AS .
PSYCHOSOMATIC MEDICINE, 2000, 62 (05) :639-647
[10]   Excess risk of myocardial infarction in patients treated with antidepressant medications: Association with use of tricyclic agents [J].
Cohen, HW ;
Gibson, G ;
Alderman, MH .
AMERICAN JOURNAL OF MEDICINE, 2000, 108 (01) :2-8