Association Between Adoption of Evidence-Based Treatment and Survival for Patients With ST-Elevation Myocardial Infarction

被引:312
作者
Jernberg, Tomas [1 ,2 ]
Johanson, Per [3 ]
Held, Claes [4 ]
Svennblad, Bodil [4 ]
Lindback, Johan [4 ]
Wallentin, Lars [4 ]
机构
[1] Dept Med, Cardiol Sect, Huddinge, Sweden
[2] Karolinska Inst, Karolinska Univ Hosp, S-14186 Huddinge, Sweden
[3] Sahlgrens Univ Hosp, Dept Cardiol, Gothenburg, Sweden
[4] Uppsala Univ, Uppsala Clin Res Ctr, Uppsala, Sweden
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2011年 / 305卷 / 16期
关键词
THERAPY; METAANALYSIS; REPERFUSION; OUTCOMES; DISEASE; TRENDS; STATIN;
D O I
10.1001/jama.2011.522
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Only limited information is available on the speed of implementation of new evidence-based and guideline-recommended treatments and its association with survival in real life health care of patients with ST-elevation myocardial infarction (STEMI). Objective To describe the adoption of new treatments and the related chances of short-and long-term survival in consecutive patients with STEMI in a single country over a 12-year period. Design, Setting, and Participants The Register of Information and Knowledge about Swedish Heart Intensive Care Admission (RIKS-HIA) records baseline characteristics, treatments, and outcome of consecutive patients with acute coronary syndrome admitted to almost all hospitals in Sweden. This study includes 61 238 patients with a first-time diagnosis of STEMI between 1996 and 2007. Main Outcome Measures Estimated and crude proportions of patients treated with different medications and invasive procedures and mortality over time. Results Of evidence based-treatments, reperfusion increased from 66% (95%, confidence interval [CI], 52%-79%) to 79% (95% CI, 69%-89%; P<.001), primary percutaneous coronary intervention from 12% (95% CI, 11%-14%) to 61% (95% CI, 45%-77%; P<.001), and revascularization from 10% (96% CI, 6%-14%) to 84% (95% CI, 73%-95%; P<.001). The use of aspirin, clopidogrel, beta-blockers, statins, and angiotensin-converting enzyme (ACE) inhibitors all increased: clopidogrel from 0% to 82% (95% CI, 69%-95%; P<.001), statins from 23% (95% CI, 12%-33%) to 83% (95% CI, 75%-91%; P<.001), and ACE inhibitor or angiotensin II receptor blockers from 39% (95% CI, 26%-52%) to 69% (95% CI, 58%-70%; P<.001). The estimated in-hospital, 30-day and 1-year mortality decreased from 12.5% (95% CI, 4.3%-20.6%) to 7.2% (95% CI, 1.7%-12.6%; P<.001); from 15.0% (95% CI, 6.2%-23.7%) to 8.6% (95% CI, 2.7%-14.5%; P<.001); and from 21.0% (95% CI, 11.0%-30.9%) to 13.3% (95% CI, 6.0%-20.4%; P<.001), respectively. After adjustment, there was still a consistent trend with lower standardized mortality over the years. The 12-year survival analyses showed that the decrease of mortality was sustained over time. Conclusion In a Swedish registry of patients with STEMI, between 1996 and 2007, there was an increase in the prevalence of evidence-based treatments. During this same time, there was a decrease in 30-day and 1-year mortality that was sustained during long-term follow-up. JAMA. 2011;305(16):1677-1684 www.jama.com
引用
收藏
页码:1677 / 1684
页数:8
相关论文
共 30 条
  • [1] [Anonymous], [No title captured], DOI 10.1053/eurj.2000.2305
  • [2] [Anonymous], 2006, Generalized additive models: an introduction with R. Chapman and Hall/CRC
  • [3] Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins
    Baigent, C
    Keech, A
    Kearney, PM
    Blackwell, L
    Buck, G
    Pollicino, C
    Kirby, A
    Sourjina, T
    Peto, R
    Collins, R
    Simes, J
    [J]. LANCET, 2005, 366 (9493) : 1267 - 1278
  • [4] Angiotensin-converting-enzyme inhibitors in stable vascular disease without left ventricular systolic dysfunction or heart failure: a combined analysis of three trials
    Dagenais, Gilles R.
    Pogue, Janice
    Fox, Kim
    Simoons, Marteen L.
    Yusuf, Salim
    [J]. LANCET, 2006, 368 (9535) : 581 - 588
  • [5] Abciximab as adjunctive therapy to reperfusion in acute ST-segment elevation myocardial infarction - A meta-analysis of randomized trials
    De Luca, G
    Suryapranata, H
    Stone, GW
    Antoniucci, D
    Tcheng, JE
    Neumann, FJ
    Van de Werf, F
    Antman, EM
    Topol, EJ
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 293 (14): : 1759 - 1765
  • [6] Acute Myocardial Infarction Hospitalization in the United States, 1979 to 2005
    Fang, Jing
    Alderman, Michael H.
    Keenan, Nora L.
    Ayala, Carma
    [J]. AMERICAN JOURNAL OF MEDICINE, 2010, 123 (03) : 259 - 266
  • [7] A 30-Year Perspective (1975-2005) Into the Changing Landscape of Patients Hospitalized With Initial Acute Myocardial Infarction Worcester Heart Attack Study
    Floyd, Kevin C.
    Yarzebski, Jorge
    Spencer, Frederick A.
    Lessard, Darleen
    Dalen, James E.
    Alpert, Joseph S.
    Gore, Joel M.
    Goldberg, Robert J.
    [J]. CIRCULATION-CARDIOVASCULAR QUALITY AND OUTCOMES, 2009, 2 (02): : 88 - 95
  • [8] The Cardiology Audit and Registration Data Standards (CARDS), European data standards for clinical cardiology practice
    Flynn, MR
    Barrett, C
    Cosío, FG
    Gitt, AK
    Wallentin, L
    Kearney, P
    Lonergan, M
    Shelley, E
    Simoons, ML
    [J]. EUROPEAN HEART JOURNAL, 2005, 26 (03) : 308 - 313
  • [9] Indications for ACE inhibitors in the early treatment of acute myocardial infarction -: Systematic overview of individual data from 100,000 patients in randomized trials
    Franzosi, MG
    Santoro, E
    Zuanetti, G
    Baigent, C
    Collins, R
    Flather, M
    Kjekshus, J
    Latini, R
    Liu, LS
    Maggioni, AP
    Sleight, P
    Swedberg, K
    Tognoni, G
    Yusuf, S
    Tavazzi, L
    Ball, S
    Kober, L
    Torp-Pedersen, C
    Braunwald, E
    Moyé, L
    Pfeffer, M
    Santoro, L
    Pogue, J
    Wang, Y
    [J]. CIRCULATION, 1998, 97 (22) : 2202 - 2212
  • [10] 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