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Optimal medical therapy at discharge in patients with acute coronary syndromes: Temporal changes, characteristics, and 1-year outcome - 16/08/11

Doi : 10.1016/j.ahj.2007.07.040 
Andrew T. Yan, MD a, , Raymond T. Yan, MD a, Mary Tan, BSc a, Thao Huynh, MD b, Kamyar Soghrati, MD a, Lawrence J. Brunner, PhD c, Paul DeYoung, MD d, David H. Fitchett, MD a, Anatoly Langer, MD, MSc a, Shaun G. Goodman, MD, MSc a,

for the Canadian ACS Registries Investigatorse

a Division of Cardiology, Canadian Heart Research Centre and Terrence Donnelly Heart Centre, St. Michael's Hospital, University of Toronto, Toronto, Ontario, Canada 
b Montréal General Hospital, Montréal, Québec, Canada 
c Department of Statistics, University of Toronto, Toronto, Ontario, Canada 
d Hotel Dieu Hospital, Cornwall, Ontario, Canada 
e A list of participating Canadian ACS Registry Investigators and Coordinators may be found in Arch Intern Med 2007;167:1009-1016 

Reprint requests: Andrew T. Yan is to be contacted at Division of Cardiology, St. Michael’s Hospital, 30 Bond Street, Room 6_030 Queen, Toronto, Ontario, Canada M5B 1W8. Shaun G. Goodman, Division of Cardiology, St. Michael’s Hospital, 30 Bond Street, Room 6-030 Queen, Toronto, Ontario, Canada M5B 1W8.

Résumé

Background

There are limited data on the recent trend in the use of optimal evidence-based medical therapies after acute coronary syndromes (ACSs). We sought to evaluate (1) the temporal changes in medical management of patients discharged after an ACS; (2) patient and practice characteristics associated with optimal medical therapy at discharge; and (3) the association between discharge medication use and 1-year outcome.

Methods

The Canadian ACS I (September 1999-June 2001) and ACS II (October 2002-December 2003) Registries were prospective, multicenter, observational studies of 6853 patients admitted for ACS. We examined the discharge use of medications among 5833 hospital survivors who did not have any contraindications to antiplatelet/anticoagulant, β-blocker, angiotensin-converting enzyme inhibitor, or lipid-modifying therapies. Optimal medical therapy was defined as the use of all indicated medications. Follow-up data at 1 year were collected by telephone interview. We performed hierarchical logistic regression to identify patient characteristics and care patterns associated with optimal medical treatment and to examine its relationship with 1-year mortality.

Results

There were significant increases in the discharge use of all 4 classes of medications over time; 28.9% and 51.8% of patients in ACS I and ACS II Registries, respectively, were prescribed optimal medical therapy (P < .001). Advanced age, female sex, prior heart failure, renal dysfunction, and coronary bypass surgery during hospitalization were negative independent predictors of optimal medical therapy. Conversely, enrollment in ACS II Registry, history of dyslipidemia, presence of ST elevation and abnormal cardiac biomarker, previous myocardial infarction, and previous coronary revascularization were independently associated with the use of combination therapy. After adjusting for other validated prognosticators, patients receiving optimal medical therapy had significantly lower 1-year mortality (adjusted odds ratio 0.54, 95% confidence interval 0.36-0.81, P = .003) compared with those given 0 or 1 drug at discharge. Over the 1-year follow-up period, substantial numbers of patients discontinued therapies, whereas others were initiated on treatment.

Conclusions

Despite the temporal increases in the combined use of evidence-based pharmacologic therapies, which is associated with improved outcome, medical management of ACS remains suboptimal. Quality improvement strategies are needed to enhance the appropriate use of effective therapies, targeting specifically the high-risk but undertreated patients who may derive the greatest therapeutic benefit.

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Plan


 The Canadian ACS Registries were sponsored by the Canadian Heart Research Centre (a federally incorporated not-for-profit academic research organization) and Key Pharmaceuticals, Division of Schering Canada Inc (ACS I), Pfizer Canada Inc (ACS II), Sanofi Aventis Canada Inc (ACS II), and Bristol-Myers Squibb Canada Inc (ACS II). The industrial sponsors had no involvement in the study conception or design; in the collection, analysis, and interpretation of data; in the writing, review, or approval of the manuscript; and in the decision to submit the manuscript for publication.


© 2007  Mosby, Inc. Tous droits réservés.
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Vol 154 - N° 6

P. null - décembre 2007 Retour au numéro
Article précédent Article précédent
  • Clinical presentation and investigation findings in cardiac myxomas: new insights from the developing world
  • Suneil Kumar Aggarwal, Ramachandra Barik, T.C.S.R. Sarma, V. Ramnath Iyer, Vijay Sai, Jitendra Mishra, Choudary D. Voleti
| Article suivant Article suivant
  • Coronary dominance and prognosis of patients with acute coronary syndrome
  • Alexander Goldberg, Danielle A. Southern, P. Diane Galbraith, Mouhieddin Traboulsi, Merril L. Knudtson, William A. Ghali, for the Alberta Provincial Project for Outcome Assessment in Coronary Heart Disease (APPROACH) Investigators

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