Literature DB >> 15260513

Strategies to increase HMG-CoA reductase inhibitor use after acute myocardial infarction.

Joseph B Muhlestein1.   

Abstract

Coronary artery disease with its accompanying complication of acute myocardial infarction (MI) is one of the major causes of death in the modern world. A variety of both primary and secondary prevention strategies have been developed for the treatment of acute MI. One of the more important of these strategies is the prescription of HMG-CoA reductase inhibitors. HMG-CoA reductase inhibitors have the potential to positively affect the outcome of acute MI in a variety of ways including the reduction of low-density lipoprotein-cholesterol levels and stabilisation of the atherosclerotic plaque. Multiple large randomised clinical trials have documented the potential of HMG-CoA reductase inhibitors to reduce both short- and long-term mortality after acute MI. This benefit exists regardless of age, gender, clinical presentation, or even baseline lipid levels. However, despite this overwhelming amount of evidence supporting the use of HMG-CoA reductase inhibitors in the post-MI setting, multiple studies have documented the presence of a significant 'treatment gap'. Indeed, often, less than half of acute MI patients who would benefit from HMG-CoA reductase inhibitor therapy actually receive it. The reasons for the low utilisation of HMG-CoA reductase inhibitors in the acute MI patient are many, but may include poor communication, the high cost of treatment, the lack of associated symptoms and confusion regarding appropriate lipid levels to target. One approach that has been tried to address these issues is the development of institutional programmes specifically targeted to increase the use of HMG-CoA reductase inhibitors in acute MI patients. These programmes, often managed by nurses or pharmacists, have been piloted in several institutions. They have been effectively implemented in both inpatient and outpatient settings. In most cases they have been implemented without a great increase in expense. They have often increased the use of HMG-CoA reductase inhibitors to >90%. Most importantly, they have documented a significant improvement in the long-term survival of acute MI patients. Based on these preliminary studies, it is recommended that the implementation of these strategies be considered by most healthcare institutions.

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Year:  2004        PMID: 15260513     DOI: 10.2165/00002512-200421090-00003

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   3.923


  43 in total

1.  In-hospital initiation of lipid-lowering therapy for patients with coronary heart disease: the time is now.

Authors:  G C Fonarow; C M Ballantyne
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2.  Statin therapy, lipid levels, C-reactive protein and the survival of patients with angiographically severe coronary artery disease.

Authors:  B D Horne; J B Muhlestein; J F Carlquist; T L Bair; T E Madsen; N I Hart; J L Anderson
Journal:  J Am Coll Cardiol       Date:  2000-11-15       Impact factor: 24.094

3.  Effect of statin therapy on C-reactive protein levels: the pravastatin inflammation/CRP evaluation (PRINCE): a randomized trial and cohort study.

Authors:  M A Albert; E Danielson; N Rifai; P M Ridker
Journal:  JAMA       Date:  2001-07-04       Impact factor: 56.272

Review 4.  Cholesterol in the prediction of atherosclerotic disease. New perspectives based on the Framingham study.

Authors:  W B Kannel; W P Castelli; T Gordon
Journal:  Ann Intern Med       Date:  1979-01       Impact factor: 25.391

5.  Summary of the second report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel II)

Authors: 
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6.  Physician noncompliance with the 1993 National Cholesterol Education Program (NCEP-ATPII) guidelines.

Authors:  J P Frolkis; S J Zyzanski; J M Schwartz; P S Suhan
Journal:  Circulation       Date:  1998-09-01       Impact factor: 29.690

7.  Multicentric inflammation in epicardial coronary arteries of patients dying of acute myocardial infarction.

Authors:  Luigi Giusto Spagnoli; Elena Bonanno; Alessandro Mauriello; Giampiero Palmieri; Antonietta Partenzi; Giuseppe Sangiorgi; Filippo Crea
Journal:  J Am Coll Cardiol       Date:  2002-11-06       Impact factor: 24.094

8.  Sex bias and underutilization of lipid-lowering therapy in patients with coronary artery disease at academic medical centers in the United States and Canada. Prospective Randomized Evaluation of the Vascular Effects of Norvasc Trial (PREVENT) Investigators.

Authors:  M Miller; R Byington; D Hunninghake; B Pitt; C D Furberg
Journal:  Arch Intern Med       Date:  2000-02-14

9.  The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. Cholesterol and Recurrent Events Trial investigators.

Authors:  F M Sacks; M A Pfeffer; L A Moye; J L Rouleau; J D Rutherford; T G Cole; L Brown; J W Warnica; J M Arnold; C C Wun; B R Davis; E Braunwald
Journal:  N Engl J Med       Date:  1996-10-03       Impact factor: 91.245

10.  Primary prevention of acute coronary events with lovastatin in men and women with average cholesterol levels: results of AFCAPS/TexCAPS. Air Force/Texas Coronary Atherosclerosis Prevention Study.

Authors:  J R Downs; M Clearfield; S Weis; E Whitney; D R Shapiro; P A Beere; A Langendorfer; E A Stein; W Kruyer; A M Gotto
Journal:  JAMA       Date:  1998-05-27       Impact factor: 56.272

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