Simple, personalized alerts embedded in a patients’ electronic health record (EHR) led to a wider use of guideline recommended lipid-lowering therapies at 90-days, according to a study by Yale School of Medicine researchers.
The PROMPT-Lipid Intervention
For patients with cardiovascular disease, lowering LDL-cholesterol has been shown to reduce the risk of future adverse events, including heart attack and stroke. Despite this evidence and guidelines recommending their use, lipid-lowering therapies are underused in clinical practice. Funded by Amgen, PROMPT-LIPID (Pragmatic Trial of Messaging to Providers about Treatment of Hyperlipidemia) is a pragmatic, randomized trial focused on improving the management of a common condition — hyperlipidemia or high cholesterol — using real-time, individualized, informational, automated electronic alerts. The results could help improve clinical decision-making and optimize use of evidence-based lipid-lowering therapies.
The results were presented Nov. 7 at the American Heart Association’s Scientific Sessions.
Led by Nihar Desai, MD, MPH, associate professor and the principal investigator of this study, F. Perry Wilson, MD, associate professor and director of Yale’s Clinical and Translational Research Accelerator (CTRA), and Tariq Ahmad, MD, MPH, associate professor and chief of the Heart Failure Program, PROMPT-LIPID, enrolled 2,500 patients from 100 outpatient providers within the Yale New Haven Health System. Providers were divided into two groups where one cohort received real-time, targeted, and tailored alerts about the opportunity to intensify lipid-lowering therapy to reduce the risk of cardiovascular disease.
Overall, there were important increases in the use of evidence-based lipid-lowering therapies, numerically higher among providers receiving alerts. Importantly, among the subset of providers who positively interacted with the decision alert, there was a significant, two-fold, increase in the intensification of treatment.