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
[11]   SERTRALINE SAFETY AND EFFICACY IN MAJOR DEPRESSION - A DOUBLE-BLIND FIXED-DOSE COMPARISON WITH PLACEBO [J].
FABRE, LF ;
ABUZZAHAB, FS ;
AMIN, M ;
CLAGHORN, JL ;
MENDELS, J ;
PETRIE, WM ;
DUBE, S ;
SMALL, JG .
BIOLOGICAL PSYCHIATRY, 1995, 38 (09) :592-602
[12]   Time-dependent covariates in the Cox proportional-hazards regression model [J].
Fisher, LD ;
Lin, DY .
ANNUAL REVIEW OF PUBLIC HEALTH, 1999, 20 :145-157
[13]   DEPRESSION FOLLOWING MYOCARDIAL-INFARCTION [J].
FORRESTER, AW ;
LIPSEY, JR ;
TEITELBAUM, ML ;
DEPAULO, JR ;
ANDRZEJEWSKI, PL ;
ROBINSON, RG .
INTERNATIONAL JOURNAL OF PSYCHIATRY IN MEDICINE, 1992, 22 (01) :33-46
[14]   DEPRESSION FOLLOWING MYOCARDIAL-INFARCTION - IMPACT ON 6-MONTH SURVIVAL [J].
FRASURESMITH, N ;
LESPERANCE, F ;
TALAJIC, M .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 270 (15) :1819-1825
[15]   The Depression Interview and Structured Hamilton (DISH): Rationale, development, characteristics, and clinical validity [J].
Freedland, KE ;
Skala, JA ;
Carney, RM ;
Raczynski, JM ;
Taylor, CB ;
de Leon, CFM ;
Ironson, G ;
Youngblood, ME ;
Krishnan, KRR ;
Veith, RC .
PSYCHOSOMATIC MEDICINE, 2002, 64 (06) :897-905
[16]   THE SAFETY OF TRICYCLIC ANTIDEPRESSANTS IN CARDIAC PATIENTS - RISK-BENEFIT RECONSIDERED [J].
GLASSMAN, AH ;
ROOSE, SP ;
BIGGER, JT .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 269 (20) :2673-2675
[17]   Sertraline treatment of major depression in patients with acute MI or unstable angina [J].
Glassman, AH ;
O'Connor, CM ;
Califf, RM ;
Swedberg, K ;
Schwartz, P ;
Bigger, JT ;
Krishnan, KRR ;
van Zyl, LT ;
Swenson, JR ;
Finkel, MS ;
Landau, C ;
Shapiro, PA ;
Pepine, CJ ;
Mardekian, J ;
Harrison, WM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 288 (06) :701-709
[18]   Depression in patients with coronary heart disease - A 12-month follow-up [J].
Hance, M ;
Carney, RM ;
Freedland, KE ;
Skala, J .
GENERAL HOSPITAL PSYCHIATRY, 1996, 18 (01) :61-65
[19]   DECREASED HEART-RATE-VARIABILITY AND ITS ASSOCIATION WITH INCREASED MORTALITY AFTER ACUTE MYOCARDIAL-INFARCTION [J].
KLEIGER, RE ;
MILLER, JP ;
BIGGER, JT ;
MOSS, AJ .
AMERICAN JOURNAL OF CARDIOLOGY, 1987, 59 (04) :256-262
[20]   Elevated platelet factor 4 and beta-thromboglobulin plasma levels in depressed patients with ischemic heart disease [J].
LaghrissiThode, F ;
Wagner, WR ;
Pollock, BG ;
Johnson, PC ;
Finkel, MS .
BIOLOGICAL PSYCHIATRY, 1997, 42 (04) :290-295