Benefits of aspirin and beta-blockade after myocardial infarction in patients with chronic kidney disease

被引:171
作者
McCullough, PA
Sandberg, KR
Borzak, S
Hudson, MP
Garg, M
Manley, HJ
机构
[1] Univ Missouri, Truman Med Ctr, Sch Med, Dept Internal Med,Cardiol Sect, Kansas City, MO 64108 USA
[2] Univ Missouri, Truman Med Ctr, Sch Med, Dept Basic Sci,Cardiol Sect, Kansas City, MO 64108 USA
[3] Univ Missouri, Truman Med Ctr, Sch Pharm, Dept Basic Sci,Cardiol Sect, Kansas City, MO 64108 USA
[4] Univ Missouri, Truman Med Ctr, Sch Pharm, Dept Internal Med,Cardiol Sect, Kansas City, MO 64108 USA
[5] Henry Ford Heart & Vasc Inst, Detroit, MI USA
关键词
D O I
10.1067/mhj.2002.125513
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background There have been no randomized trials of cardioprotective therapy after acute myocardial infarction in patients with chronic kidney disease who should be largely eligible for aspirin (acetylsalicylic acid; ASA) and beta-blockers (BB) as a base of therapy. Methods We analyzed a prospective coronary care unit registry of 1724 patients with ST-segment elevation myocardial infarction. Results Usage rates were 52.3%, 19.0%, 15.2%, and 13.5% for ASA and BB (ASA+BB), BB alone, ASA alone, and no ASA or BB therapy. Patients who received ASA+BB were more likely to be male, free of earlier cardiac disease, and recipients of thrombolysis. Conversely, the absence of ASA+BB was observed in patients with heart failure on admission, left bundle branch block, atrial and ventricular arrhythmias, and shock. The combination of ASA+BB was used in 63.9%, 55.8%, 48.2%, and 35.5% of patients with corrected creatinine clearance values of >81.5, 81.5 to 63.1, 63.1 to 46.2, and <46.2 mL/min/72 kg (P <.0001). ASA+BB was used in 40.4% of patients undergoing dialysis. The age-adjusted relative risk reduction for the inhospital mortality rate was similar among all renal groups and ranged from 64.3% to 80.0% (all P <.0001). Conclusion ASA+BB is an underused therapy in patients with acute myocardial infarction who have underlying kidney disease.
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页码:226 / 232
页数:7
相关论文
共 25 条
[1]   CARDIOVASCULAR-DISEASE RISK PROFILES [J].
ANDERSON, KM ;
ODELL, PM ;
WILSON, PWF ;
KANNEL, WB .
AMERICAN HEART JOURNAL, 1991, 121 (01) :293-298
[2]  
Baracskay D, 1997, CLIN NEPHROL, V47, P222
[3]   Determinants of mortality after myocardial infarction in patients with advanced renal dysfunction [J].
Beattie, JN ;
Soman, SS ;
Sandberg, KR ;
Yee, J ;
Borzak, S ;
Garg, M ;
McCullough, PA .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 37 (06) :1191-1200
[4]   Survival after acute myocardial infarction in patients with end-stage renal disease: Results from the Cooperative Cardiovascular Project [J].
Chertow, GM ;
Normand, SLT ;
Silva, LR ;
McNeil, BJ .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 35 (06) :1044-1051
[5]  
Chertow GM, 1997, CIRCULATION, V95, P878
[6]   PREDICTION OF CREATININE CLEARANCE FROM SERUM CREATININE [J].
COCKCROFT, DW ;
GAULT, MH .
NEPHRON, 1976, 16 (01) :31-41
[7]   Effect of carvedilol on outcome after myocardial infarction in patients with left-ventricular dysfunction: the CAPRICORN randomised trial [J].
Dargie, HJ ;
Colucci, Y ;
Ford, I ;
Sendon, JLL ;
Remme, W ;
Sharpe, N ;
Blank, A ;
Holcslaw, TL .
LANCET, 2001, 357 (9266) :1385-1390
[8]  
Demers RY, 1998, CANCER, V82, P2043, DOI 10.1002/(SICI)1097-0142(19980515)82:10+<2043::AID-CNCR12>3.0.CO
[9]  
2-B
[10]   ASPIRIN PROLONGS BLEEDING-TIME IN UREMIA BY A MECHANISM DISTINCT FROM PLATELET CYCLOOXYGENASE INHIBITION [J].
GASPARI, F ;
VIGANO, G ;
ORISIO, S ;
BONATI, M ;
LIVIO, M ;
REMUZZI, G .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (06) :1788-1797