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2002, The American Journal of Medicine
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3 pages
1 file
AI-generated Abstract
This article examines the challenges in translating clinical research evidence into practice within the medical field, grounding the discussion in findings from the GUSTO-1 and SAVE trials. It highlights the slow adoption of evidence-based practices despite the depth of research available, referencing historical reviews that emphasize the ineffectiveness of simple educational strategies for behavior change. The article also discusses the need for multifaceted, context-sensitive approaches to effect change in clinical decision-making, while suggesting areas for future research to enhance the integration of evidence into routine medical practice.
The American Journal of Cardiology, 1999
This study was undertaken to examine recent trends in the use of angiotensin-converting enzyme (ACE) inhibitors within 24 hours of admission in patients hospitalized for acute myocardial infarction (AMI) and to identify clinical factors associated with ACE inhibitor-prescribing patterns. Demographic, procedural, and acute medication use from 202,438 patients with AMI were collected at 1,470 US hospitals participating in the National Registry of Myocardial Infarction 2 from June 1994 through June 1996. Acute ACE inhibitor use increased from 14.0% in 1994 to 17.3% in 1996. After controlling for all important clinical variables, we found that there was a significant increase in the odds of acute ACE inhibitor treatment over time (odds ratio [OR]1.07 for each 180day period; 95% confidence intervals [CI] 1.06 to 1.08; p <0.0001). Univariate data suggested that patients treated acutely with ACE inhibitors tended to be older (70.9 vs 67.2 years) and had lower rates of in-hospital mortality (8.8% vs 11.0%). Independent predictors of receiving an ACE inhibitor acutely included anterior wall infarction (OR 1.36; 95% CI 1.32 to 1.40), Killip class 2 or 3 (OR 1.77; 95% CI 1.72 to 1.83), prior myocardial infarction (OR 1.33; 95% CI 1.30 to 1.37), prior history of congestive heart failure (OR 1.88; 95% CI 1.82 to 1.95), and diabetes mellitus (OR 1.34; 95% CI 1.30 to 1.38). Physicians are prescribing ACE inhibitors acutely in patients with AMI with increasing frequency. Patients with evidence of congestive heart failure and those with anterior myocardial infarction have the greatest expected benefit from such therapy, and these persons receive such treatment most often. However, most patients hospitalized with AMI do not receive this potentially life-saving therapy. ᮊ1999 by Excerpta Medica, Inc.
The American Journal of Cardiology, 1997
We sought to determine how often angiotensin-converting enzyme (ACE) inhibitors are prescribed as a discharge medication among eligible patients ¢65 years old with an acute myocardial infarction; to identify patient characteristics associated with the decision to prescribe ACE inhibitors; and to determine the factors associated with the decision to obtain an evaluation of left ventricular function among patients who have no contraindications to ACE inhibitors. We addressed these aims with an observational study of consecutive elderly Medicare beneficiary survivors of an acute myocardial infarction hospitalized in Alabama, Connecticut, Iowa, and Wisconsin between June 1992 and February 1993. Among the 5,453 patients without a contraindication to ACE inhibitors at discharge, 3,528 (65%) had an evaluation of left ventricular function. Of the 1,228 patients without a contraindication to ACE inhibitors who had a left ventric-ular ejection fraction°40%, 548 (45%) were prescribed the medication at discharge. In a multivariable analysis, an increased prescribed use of ACE inhibitors at discharge was correlated with several factors, including diabetes mellitus, congestive heart failure, ventricular tachycardia, and loop diuretics as a discharge medication. Patients admitted after the publication of the Survival and Ventricular Enlargement (SAVE) trial were significantly more likely to receive ACE inhibitors, although the absolute improvement in utilization was small in the 6 months after the trial results were published. In conclusion, improving the identification of appropriate patients for ACE inhibitors and increasing the prescription of ACE inhibitors for ideal patients may provide an excellent opportunity to improve care.
Medical Journal of …, 2007
European Heart Journal, 2009
Aims Angiotensin-converting enzyme (ACE) inhibitors have been shown to reduce cardiovascular risk in different groups of patients. Whether these effects can be generalized to the broad group of patients with vascular disease is unknown. Therefore, we undertook a combined analysis using individual data from ADVANCE, EUROPA, and PROGRESS to determine the consistency of the treatment effect of perindopril-based regimen in patients with vascular disease or at high risk of vascular disease. Methods and results We studied all-cause mortality and major cardiovascular outcomes during a follow-up of about 4 years in the 29 463 patients randomly assigned a perindopril-based treatment regimen or placebo. The perindopril-based regimens were associated with a significant reduction in all-cause mortality [hazard ratio (HR) 0.89; 95% confidence interval (CI) 0.82-0.96; P ¼ 0.006], cardiovascular mortality (HR 0.85; 95% CI 0.76-0.95; P ¼ 0.004), non-fatal myocardial infarction (HR 0.80; 95% CI 0.71-0.90; P , 0.001), stroke (HR 0.82; 95% CI 0.74-0.92; P ¼ 0.002), and heart failure (HR 0.84; 95% CI 0.72-0.96; P ¼ 0.015). Results were consistent in subgroups with different clinical characteristics, concomitant medication use, and across all strata of baseline blood pressure. Conclusion This study provides strong evidence for a consistent cardiovascular protection with an ACE-inhibitor treatment regimen (perindopril-indapamide) by improving survival and reducing the risk of major cardiovascular events across a broad spectrum of patients with vascular disease.
European Journal of Clinical Pharmacology, 2004
Objective: The use of angiotensin-converting enzyme (ACE) inhibitors has increased markedly during the last decade. It has been claimed that doses of ACE inhibitors prescribed in clinical practice are considerably lower than the target doses used in randomized clinical trials. The aim of the study was to investigate dosing of ACE inhibitors in patients discharged from the hospital after an acute myocardial infarction (AMI) and, furthermore, to compare these doses with the doses actually reached in clinical trials. Methods: From 16 hospitals, we drew a sample of patients who were discharged alive with the diagnosis of AMI during a 3-month period in 1999/2000. From medical records, physicians in each hospital obtained the observed rate of cardiovascular drugs at discharge, including type and doses of ACE inhibitors. The clinicians' main indication for ACE inhibitor use was also reported. Outcome variables, including deaths and drug utilization with dosing after 6 months, were collected. Results: Of a total of 767 patients discharged alive, 274 patients received an ACE inhibitor. The daily mean doses of the four ACE inhibitors used in the study were as follows: captopril 69.8±36.9 mg (n=44), enalapril 13.6±8.1 mg (n=75), lisinopril 11.0±7.2 mg (n=114), and ramipril 8.4±4.5 mg (n=38). The doses were unchanged after 6 months except for captopril, which showed a rise in mean daily dose to 84.4±36.7 mg. Ramipril compared most favorably with clinical trial medications, while captopril deviated most. The indication of hypertension was associated with slightly higher doses than the indication of secondary prevention. Conclusion: AMI patients were discharged from the hospital with ACE inhibitor doses fairly close to the ones achieved in clinical trials showing survival benefits for ACE inhibitors. A distinction should be made between target doses and doses actually obtained in clinical trials.
European Journal of Preventive Cardiology, 2018
The American Journal of Medicine, 2010
Background-Guidelines for the management of patients with acute myocardial infarction recommend the routine use of 4 effective cardiac medications: angiotensin converting enzyme (ACE) inhibitors, aspirin, β-blockers, and lipid lowering agents. Limited data are available, however, about the contemporary, and changing, use of these therapies, particularly from a population-based perspective. The study describes differences in the use of these medications during hospitalization for acute myocardial infarction according to age, sex, and period of hospitalization. The study population consisted of 6,334 women and men treated at 11 hospitals in the Worcester (MA) metropolitan area for acute myocardial infarction in 6 annual periods between 1995 and 2005. Results-Increases in the use of all 4 cardiac medications during hospitalization for acute myocardial infarction were noted between 1995 and 2005 for all men as well as in those of different age strata (<65 years: 4% to 47%); 65-74 years (4% to 46%); 75-84 years (2% to 48%); and ≥85 years (0% to 23%). Increases in the use of all 4 cardiac medications were also observed in all women as well as in those of all ages over time (2% to 42%); 65-74 years (8% to 47%); 75-84 years (1% to 44%); and ≥85 years (1% to 44%). Conclusions-The present results suggest marked increases over time in the use of evidence-based therapies in patients hospitalized with acute myocardial infarction. Educational efforts to augment the utilization of these effective cardiac therapies, as well as attempts to identify sub-optimally treated groups, remain warranted.
Journal of Internal Medicine, 1999
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