Antecedent hypertension and the effect of captopril on the risk of adverse cardiovascular outcomes after acute myocardial infarction with left ventricular systolic dysfunction: Insights from the survival and ventricular enlargement trial

被引:31
作者
Kenchaiah, S
Davis, BR
Braunwald, E
Rouleau, JL
Dagenais, GR
Sussex, B
Steingart, RM
Brown, EJ
Lamas, GA
Gordon, D
Bernstein, V
Pfeffer, MA
机构
[1] Harvard Univ, Div Cardiovasc, Sch Med, Brigham & Womens Hosp, Boston, MA 02115 USA
[2] Boston Univ, Sch Med, Boston, MA 02118 USA
[3] Univ Texas, Hlth Sci Ctr, Houston, TX USA
[4] Partners Healthcare Syst, Boston, MA USA
[5] Toronto Gen Hosp, Toronto, ON, Canada
[6] Univ Laval, Heart & Lung Inst, St Foy, PQ G1K 7P4, Canada
[7] Mem Univ Newfoundland, St Johns, NF, Canada
[8] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[9] Bronx Lebanon Hosp Ctr, Bronx, NY 10456 USA
[10] Mt Sinai Med Ctr, Miami Beach, FL USA
[11] Iowa Heart Ctr, Des Moines, IA USA
[12] Vancouver Hosp & Hlth Sci Ctr, Vancouver, BC V5Z 1M9, Canada
关键词
D O I
10.1016/j.ahj.2004.02.011
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background Hypertension is a well-established risk factor for myocardial infarction (MI), but its prognostic importance in survivors of an acute MI is less clear. Methods We used Cox proportional hazards models to examine the risk of any major cardiovascular event (cardiovascular death, heart failure, recurrent MI, or stroke) -combined or individual components-and all-cause death and evaluate the efficacy of captopril in 906 patients with hypertension and 1325 patients without hypertension in the Survival and Ventricular Enlargement (SAVE) clinical trial. All patients had survived an acute MI with resultant left ventricular (LV) systolic dysfunction, but without overt heart failure, and were randomized within 3 to 16 days after the index MI to receive either captopril or placebo. The mean (+/- SD) follow-up period was 42 10 months. Results After adjustment for known risk factors, medication use at enrollment, and baseline systolic blood pressure, patients with hypertension had a significant increase in the risk of experiencing a combined cardiovascular event (47.7% vs 31.3%; hazard ratio [HR], 1.49; 95% CI, 1.28-1.74), cardiovascular death (23.4% vs 15.9%; HR, 1.40; 95% CI, 1.12-1.74), heart failure (27.7% vs 15.5%; HR, 1.64; 95% CI, 1.34-2.02), and all-cause death (27.4 vs 19.3%; HR, 1.25; 95% CI, 1.02-1.53), and a similar but statistically non-significant increase in the risk of non-fatal or fatal recurrent MI (17.4% vs 10.9%; HR, 1.27; 95% CI, 0.98-1.65), and non-fatal or fatal stroke (5.0% vs 3.6%; HR, 1.31; 95% CI, 0.81-2.09). Captopril resulted in similar benefits for both patients with and patients without hypertension. The number of combined cardiovascular events prevented for every 100 patients treated with captopril was 7.0 (95% CI, 0.5-13.5) in patients with hypertension and 7.5 (95% CI, 2.6-12.5) in patients without hypertension. Conclusions In survivors of an acute MI with LV systolic dysfunction, antecedent hypertension was associated with a greater risk of subsequent adverse cardiovascular events, not directly explained by elevated blood pressure levels. Captopril use was beneficial in both patients with and patients without hypertenson.
引用
收藏
页码:356 / 364
页数:9
相关论文
共 51 条
[1]
Hypertension control at hospital discharge after acute coronary event:: influence on cardiovascular prognosis -: the PREVENIR study [J].
Amar, J ;
Chamontin, B ;
Ferrières, J ;
Danchin, N ;
Grenier, O ;
Cantet, C ;
Cambou, JP .
HEART, 2002, 88 (06) :587-591
[2]
THE EFFECT OF THE ANGIOTENSIN-CONVERTING ENZYME-INHIBITOR ZOFENOPRIL ON MORTALITY AND MORBIDITY AFTER ANTERIOR MYOCARDIAL-INFARCTION [J].
AMBROSIONI, E ;
BORGHI, C ;
MAGNANI, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (02) :80-85
[3]
ASTRUP J, 1976, LANCET, V6, P903
[4]
Relation of increased arterial blood pressure to mortality and stroke in the context of contemporary thrombolytic therapy for acute myocardial infarction - A randomized trial [J].
Aylward, PE ;
Wilcox, RG ;
Horgan, JH ;
White, HD ;
Granger, CB ;
Califf, RM ;
Topol, EJ .
ANNALS OF INTERNAL MEDICINE, 1996, 125 (11) :891-+
[5]
BALL SG, 1993, LANCET, V342, P821
[6]
RELATION OF LOW DIASTOLIC BLOOD-PRESSURE TO CORONARY HEART-DISEASE DEATH IN PRESENCE OF MYOCARDIAL-INFARCTION - THE FRAMINGHAM-STUDY [J].
DAGOSTINO, RB ;
BELANGER, AJ ;
KANNEL, WB ;
CRUICKSHANK, JM .
BRITISH MEDICAL JOURNAL, 1991, 303 (6799) :385-389
[7]
Coronary disease - The pathophysiology of acute coronary syndromes [J].
Davies, MJ .
HEART, 2000, 83 (03) :361-366
[8]
DZAU VJ, 1990, J CARDIOVASC PHARM, V15, pS59, DOI 10.1097/00005344-199000155-00009
[9]
CORONARY PLAQUE DISRUPTION [J].
FALK, E ;
SHAH, PK ;
FUSTER, V .
CIRCULATION, 1995, 92 (03) :657-671
[10]
BLOOD-PRESSURE AND MORTALITY AMONG MEN WITH PRIOR MYOCARDIAL-INFARCTION [J].
FLACK, JM ;
NEATON, J ;
GRIMM, R ;
SHIH, J ;
CUTLER, J ;
ENSRUD, K ;
MACMAHON, S .
CIRCULATION, 1995, 92 (09) :2437-2445