Reconsidering low-dose aspirin therapy for cardiovascular disease: a study protocol for physician and patient behavioral change
Open accessAbstract
Background: There are often disparities between current evidence and current practice. Decreasing the gap between desired practice outcomes and observed practice outcomes in the healthcare system is not always easy. Stopping previously recommended or variably recommended interventions may be even harder to achieve than increasing the use of a desired but under-performed activity. For over a decade, aspirin has been prescribed for primary prevention of cardiovascular disease and for patients with the coronary artery disease risk equivalents; yet, there is no substantial evidence of an appropriate risk-benefit ratio to support this practice. This paper describes the protocol of a randomized trial being conducted in six primary care practices in the Denver metropolitan area to examine the effectiveness of three interventional strategies to change physician behavior regarding prescription of low-dose aspirin. Methods: All practices received academic detailing, one arm received clinician reminders to reconsider aspirin, a second arm received both clinician and patient messages to reconsider aspirin. The intervention will run for 15 to 18 months. Data collected at baseline and for outcomes from an electronic health record will be used to assess pre- and post-interventional prescribing, as well as to explore any inappropriate decrease in aspirin use by patients with known cardiovascular disease. Discussion: This study was designed to investigate effective methods of changing physician behavior to decrease the use of aspirin for primary cardiovascular disease prevention. The results of this study will contribute to the small pool of knowledge currently available on the topic of ceasing previously supported practices. Trial Registration: ClinicalTrials.gov: NCT01247454
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Across diverse fields, reasonable consensus has developed about when particular designs should be used and what sample size and design protocols are needed to maximize internal validity.
“Within this growing family of randomized, nonrandomized, and mixed method designs, reasonable consensus has grown across diverse fields about when certain designs should be used and what sample size requirements and design protocols are necessary to maximize internal validity (42, 87).”
From An Overview of Research and Evaluation Designs for Dissemination and Implementation (2017) · cites this paper as [42]
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- Authors
- Folks, B., LeBlanc, W. G., Staton, E. W., & Pace, W. D.
- Affiliations
- University of Colorado Denver (US)
- Corresponding author
- Staton, Elizabeth W
- Venue
- Implementation Science
- Published
- 2011-06-26
- Volume
- 6
- Issue
- 1
- Pages
- 65-65
- ISSN
- 1748-5908 (ISSN-L)
- PMC
- PMC3141566
- OpenAlex
- W2163363279
- Cited by
- 5
- References
- 42
- Citations by year
- 2026: 1 · 2022: 1 · 2017: 1 · 2014: 2
- FWCI
- 0.63
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Implementation Science (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Clinical practice guidelines implementation
- Health Sciences › Health Professions › General Health Professions › Health Policy Implementation Science
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Antiplatelet Therapy and Cardiovascular Diseases
- Keywords
- low-dose aspirin, aspirin prescribing, primary prevention of cardiovascular disease, physician behavior change, academic detailing, knowledge-practice gap, primary care, electronic health records
- MeSH terms
- Aspirin, Cardiovascular Diseases, Clinical Protocols, Colorado, Coronary Artery Disease, Decision Support Techniques, Education, Medical, Continuing, Humans, Practice Patterns, Physicians'
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