3 results on '"Steve Kopecky"'
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2. Initiation of hormone replacement therapy after acute myocardial infarction is associated with more cardiac events during follow-up
- Author
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Robert Daly, Patrick T. O'Gara, Christopher M. O'Connor, Karen P. Alexander, Steven S. Khan, Anne S. Hellkamp, Steve Kopecky, Antoly Langer, Valentin Fuster, Robert M. Califf, Robert A. Harrington, Eric D. Peterson, and L. Kristin Newby
- Subjects
medicine.medical_specialty ,medicine.medical_treatment ,Myocardial Infarction ,Recurrence ,Internal medicine ,medicine ,Humans ,Myocardial infarction ,Angina, Unstable ,Aged ,Aspirin ,business.industry ,Unstable angina ,Incidence (epidemiology) ,Estrogen Replacement Therapy ,Absolute risk reduction ,Hormone replacement therapy (menopause) ,Middle Aged ,medicine.disease ,Surgery ,Relative risk ,Cohort ,Cardiology ,Female ,business ,Cardiology and Cardiovascular Medicine ,medicine.drug - Abstract
OBJECTIVES This study explored the association between the initiation of hormone replacement therapy (HRT) and early cardiac events ( BACKGROUND Observational studies have linked postmenopausal hormone use with a reduced risk of death from heart disease. However, a recent randomized trial of HRT found no long-term benefit, primarily due to an increase in cardiac events in the first year. METHODS The Coumadin Aspirin Reinfarction Study (CARS) database contains information on HRT use and menopausal status for women with a recent MI. We classified the 1,857 postmenopausal women in CARS as prior/current HRT users if they took HRT before enrollment, new users if they began HRT during the study period or never users. We assessed the incidence of cardiac events (death, MI, unstable angina [UA]) during follow-up. RESULTS In our cohort, 28% (n = 524) used HRT at some point. Of these, 21% (n = 111) began HRT after their MI. New users had a higher incidence of death/MI/UA (41% vs. 28%, p = 0.001) during follow-up than never users, largely due to a higher incidence of UA (39% vs. 20%, p = 0.001). After adjustment, new users still had a significantly higher risk of death/MI/UA than never users during follow-up (relative risk [RR] = 1.44 [1.05–1.99]). Prior/current users had no excess risk of the composite end point after adjustment. Users of estrogen/progestin had a lower incidence of death/MI/UA during follow-up than users of estrogen only (RR = 0.56 [0.37–0.85]). CONCLUSIONS Postmenopausal women who initiated HRT after a recent MI had an increased risk of cardiac events largely due to excess UA during follow-up.
- Published
- 2001
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3. Critical Pathways
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Judith S. Hochman, Richard C. Becker, Nathan R. Every, Steve Kopecky, and Christopher P. Cannon
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Protocol (science) ,medicine.medical_specialty ,Critical pathways ,business.industry ,Process (engineering) ,media_common.quotation_subject ,Guideline ,Surgery ,Identification (information) ,Risk analysis (engineering) ,Physiology (medical) ,Health care ,medicine ,Quality (business) ,Cardiology and Cardiovascular Medicine ,business ,media_common ,Coronary intensive care - Abstract
Critical pathways, also known as critical paths, clinical pathways, or care paths, are management plans that display goals for patients and provide the sequence and timing of actions necessary to achieve these goals with optimal efficiency.1 As competition in the healthcare industry has increased, managers have embraced critical pathways as a method to reduce variation in care, decrease resource utilization, and potentially improve healthcare quality. Cardiovascular medicine in particular is an area in which critical pathways have been embraced. This is due in part to the high volume and high cost associated with cardiovascular diseases and procedures. In addition, the relatively mature guideline process has also contributed to the growth in use of critical pathways in cardiology. Although anchored in clinical guidelines, the critical pathway is a distinct tool that details processes of care and highlights inefficiencies regardless of whether there is evidence to warrant changes in those processes. Clinical guidelines, on the other hand, are consensus statements that are systematically developed to assist practitioners in making patient management decisions related to specific clinical circumstances.2 Although clinical guidelines can and should be used in pathway development, the majority of processes included in a pathway have not been rigorously tested and are generally not addressed in guidelines. Another term that should also be distinguished from critical pathways is clinical protocols. Protocols are treatment recommendations that are often based on guidelines. Like the critical pathway, the goal of the clinical protocol may be to decrease treatment variation. However, protocols are most often focused on guideline compliance rather than the identification of rate-limiting steps in the patient care process. In further contrast to critical pathways, protocols may or may not include a continuous monitoring and data-evaluation component. Critical pathway techniques were first developed for use in industry as a tool to …
- Published
- 2000
- Full Text
- View/download PDF
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