Optimal medical therapy with or without PCI for stable coronary disease

被引:3404
作者
Boden, William E.
O'Rourke, Robert A.
Teo, Koon K.
Hartigan, Pamela M.
Maron, David J.
Kostuk, William J.
Knudtson, Merril
Dada, Marcin
Casperson, Paul
Harris, Crystal L.
Chaitman, Bernard R.
Shaw, Leslee
Gosselin, Gilbert
Nawaz, Shah
Title, Lawrence M.
Gau, Gerald
Blaustein, Alvin S.
Booth, David C.
Bates, Eric R.
Spertus, John A.
Berman, Daniel S.
Mancini, G. B. John
Weintraub, William S.
Boden, W.
O'Rourke, R.
Teo, K.
Hartigan, P.
Weintraub, W.
Maron, D.
Mancini, J.
Weintraub, W.
Boden, W.
O'Rourke, R.
Teo, K.
Hartigan, P.
Knudtson, M.
Maron, D.
Bates, E.
Blaustein, A.
Booth, D.
Carere, R.
Ellis, S.
Gosselin, G.
Gau, G.
Jacobs, A.
King, S., III
Kostuk, W.
Harris, C.
Spertus, J.
Peduzzi, P.
机构
[1] SUNY Buffalo, Buffalo Gen Hosp, Div Cardiol, Buffalo, NY 14203 USA
[2] Western New York Vet Affairs VA Healthcare Networ, Buffalo, NY USA
[3] S Texas Vet Hlth Care Syst, San Antonio, TX USA
[4] McMaster Univ, Med Ctr, Hamilton, ON, Canada
[5] VA Connecticut Healthcare Syst, Cooperat Studies Program Coordinating Ctr, West Haven, CT USA
[6] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[7] London Hlth Sci Ctr, London, ON, Canada
[8] Foothills Prov Gen Hosp, Calgary, AB T2N 2T9, Canada
[9] Hartford Hosp, Hartford, CT 06115 USA
[10] VA Cooperat Studies Program Clin Res Pharm Coordi, Albuquerque, NM USA
[11] St Louis Univ, St Louis, MO 63103 USA
[12] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[13] Montreal Heart Inst, Montreal, PQ H1T 1C8, Canada
[14] Sudbury Reg Hosp, Sudbury, ON, Canada
[15] Queen Elizabeth 2 Hlth Sci Ctr, Halifax, NS, Canada
[16] Mayo Clin, Rochester, MN USA
[17] Houston VA Med Ctr, Houston, TX USA
[18] Lexington VA Med Ctr, Lexington, KY USA
[19] Univ Michigan, Med Ctr, Ann Arbor, MI USA
[20] St Lukes Hosp, Mid Amer Heart Inst, Kansas City, MO 64111 USA
[21] Vancouver Hosp & Hlth Sci Ctr, Vancouver, BC V5Z 1M9, Canada
[22] Christiana Care Hlth Syst, Newark, DE USA
关键词
D O I
10.1056/NEJMoa070829
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In patients with stable coronary artery disease, it remains unclear whether an initial management strategy of percutaneous coronary intervention (PCI) with intensive pharmacologic therapy and lifestyle intervention (optimal medical therapy) is superior to optimal medical therapy alone in reducing the risk of cardiovascular events. Methods: We conducted a randomized trial involving 2287 patients who had objective evidence of myocardial ischemia and significant coronary artery disease at 50 U.S. and Canadian centers. Between 1999 and 2004, we assigned 1149 patients to undergo PCI with optimal medical therapy (PCI group) and 1138 to receive optimal medical therapy alone (medical-therapy group). The primary outcome was death from any cause and nonfatal myocardial infarction during a follow-up period of 2.5 to 7.0 years (median, 4.6). Results: There were 211 primary events in the PCI group and 202 events in the medical-therapy group. The 4.6-year cumulative primary-event rates were 19.0% in the PCI group and 18.5% in the medical-therapy group (hazard ratio for the PCI group, 1.05; 95% confidence interval [CI], 0.87 to 1.27; P=0.62). There were no significant differences between the PCI group and the medical-therapy group in the composite of death, myocardial infarction, and stroke (20.0% vs. 19.5%; hazard ratio, 1.05; 95% CI, 0.87 to 1.27; P=0.62); hospitalization for acute coronary syndrome (12.4% vs. 11.8%; hazard ratio, 1.07; 95% CI, 0.84 to 1.37; P=0.56); or myocardial infarction (13.2% vs. 12.3%; hazard ratio, 1.13; 95% CI, 0.89 to 1.43; P=0.33). Conclusions: As an initial management strategy in patients with stable coronary artery disease, PCI did not reduce the risk of death, myocardial infarction, or other major cardiovascular events when added to optimal medical therapy.
引用
收藏
页码:1503 / 1516
页数:14
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