Impact of combined secondary prevention therapy after myocardial infarction:: Data from a nationwide French registry

被引:40
作者
Danchin, N
Cambou, JP
Hanania, G
Kadri, Z
Genès, N
Lablanche, JM
Blanchard, D
Vaur, L
Clerson, P
Guéret, P
机构
[1] Hop Europeen Georges Pompidou, Dept Cardiol, F-75015 Paris, France
[2] Fac Med Toulouse, INSERM, U558, F-31073 Toulouse, France
[3] Ctr Hosp Aulnay, Aulnay Sous Bois, France
[4] Lab Aventis, Paris, France
[5] CHU Lille, F-59037 Lille, France
[6] Clin St Gatien, Tours, France
[7] Orgametrie, Wasquehal, France
[8] CHU Henri Mondor, F-94010 Creteil, France
关键词
D O I
10.1016/j.ahj.2005.01.058
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Several classes of medications improve survival in patients with coronary artery disease. Whether these medications, as used in the real world, have additive efficacy remains speculative. Objectives To assess whether patients discharged on combined secondary prevention medications after acute myocardial infarction (AMI) have improved 1-year survival, compared with the action of any single class of medications. Design and setting Nationwide registry of consecutive patients admitted to intensive care units for AMI in November 2000 in France. Multivariate Cox regression analysis, including a propensity score for the prescription of combined therapy, was used. Results Of the 2119 patients discharged alive, 1095 (52%) were prescribed a combination of antiplatelet agents, beta-blockers, and statins (triple therapy), of whom 567 (27%) also received angiotensin-converting enzyme inhibitors (quadruple therapy) and 528 (25%) did not. One-year survival was 97% in patients receiving triple combination therapy versus 88% in those who received either none, 1, or 2 of these medications (P <.0001). After multivariate adjustment including the propensity score, the hazard ratio for 1-year mortality in patients with triple combination therapy was 0.52 (95% CI 0.33-0.81). In patients with ejection fraction <= 35%, beta-blockers and angiotensin-converting enzyme inhibitors were independent predictors of survival, and combination therapy had no additional prognostic value. Conclusions Compared with the prescription of any single class of secondary prevention medications, combination therapy offers additional protection in patients with AMI.
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页码:1147 / 1153
页数:7
相关论文
共 17 条
  • [1] Baigent C, 2002, BMJ-BRIT MED J, V324, P71, DOI 10.1136/bmj.324.7329.71
  • [2] Collins R, 2002, LANCET, V360, P7, DOI 10.1016/S0140-6736(02)09327-3
  • [3] Management of acute myocardial infarction in intensive care units in 1995: A nationwide French survey of practice and early hospital results
    Danchin, N
    Vaur, L
    Genes, N
    Renault, M
    Ferrieres, J
    Etienne, S
    Cambou, JP
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1997, 30 (07) : 1598 - 1605
  • [4] Danchin N., 2003, Annales de Cardiologie et d'Angeiologie, V52, P1, DOI 10.1016/S0003-3928(02)00181-6
  • [5] Use of secondary preventive drugs in patients with acute coronary syndromes treated medically or with coronary angioplasty:: results from the nationwide French PREVENIR survey
    Danchin, N
    Grenier, O
    Ferrières, J
    Cantet, C
    Cambou, JP
    [J]. HEART, 2002, 88 (02) : 159 - 162
  • [6] Fox KM, 2003, LANCET, V362, P782
  • [7] β Blockade after myocardial infarction:: systematic review and meta regression analysis
    Freemantle, N
    Cleland, J
    Young, P
    Mason, J
    Harrison, J
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 1999, 318 (7200): : 1730 - 1737
  • [8] Multifactorial intervention and cardiovascular disease in patients with type 2 diabetes
    Gaede, P
    Vedel, P
    Larsen, N
    Jensen, GVH
    Parving, H
    Pedersen, O
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (05) : 383 - 393
  • [9] Management and in-hospital outcome of patients with acute myocardial infarction admitted to intensive care units at the turn of the century:: results from the French nationwide USIC 2000 registry
    Hanania, G
    Cambou, JP
    Guéret, P
    Vaur, L
    Blanchard, D
    Lablanche, JM
    Boutalbi, Y
    Humbert, R
    Clerson, P
    Genès, N
    Danchin, N
    [J]. HEART, 2004, 90 (12) : 1404 - 1410
  • [10] Joffe MM, 1999, AM J EPIDEMIOL, V150, P327