Key result
An educational presentation and strategy package had varied clinician uptake, and icosapent ethyl use remained minimal at 1.1% among eligible post-ACS patients with hypertriglyceridemia.
Why the study?
Does a co-designed implementation strategy package improve the standardized management of hypertriglyceridemia and increase guideline-directed therapy use in post-ACS patients?
Does a co-designed implementation strategy package improve the standardized management of hypertriglyceridemia and increase guideline-directed therapy use in post-ACS patients?
An educational and resource-based implementation strategy package had low clinician uptake and did not significantly increase the minimal baseline use of icosapent ethyl for hypertriglyceridemia in post-ACS patients, highlighting the need for more robust standardized clinical pathways.
Answers are grounded in this paper and cite their sources.
Implementation barriers persist for icosapent ethyl post-ACS despite co-designed strategies; leaves open more effective approaches to boost uptake.
Objectives Patients on statin therapy with persistent hypertriglyceridemia (HTG) (TG > 150 mg/dL) post-acute coronary syndrome (ACS) are at increased risk of residual cardiovascular disease (CVD). Despite recommendations to incorporate icosapent ethyl (IPE) to reduce recurrent CV events, HTG care is not standardized. We aimed to 1) co-design a strategy package to improve CV risk management in post-ACS patients with HTG, and 2) assess TG care changes following the pilot. Methods A pre-implementation survey assessed clinician perspectives of standardizing HTG management. Contextual inquiries informed a deliberative engagement session to co-design implementation strategies. One cardiology clinic piloted the final package. Resource use and electronic health record data were assessed for outcomes and care patterns. Results Survey responses (N = 16) indicated that a standardized TG management approach is acceptable, appropriate, and feasible. Clinician interviews (N = 7) highlighted lack of priority in HTG care. IPE is favored for CV benefit, but coverage concerns persisted despite established institutional routinization. A strategy package to overcome identified barriers was finalized following deliberative engagement. 50% (20/40) of invited clinicians attended the pilot presentation, and 7.5% used additional resources and workflow strategies. Medication use was consistent among eligible patients, but 1.1% received IPE, limited to severe HTG (>500 mg/dL). Conclusion Operationalized clinician strategies had varied uptake, and IPE use remained minimal. An educational presentation from experts demonstrated importance of intervention but did not translate to clinician motivation. Findings highlight areas for improvement and inform early development of a standardized clinical pathway to reduce CVD risk in post-ACS patients with HTG.
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Salvati et al. (2026) studied Post-acute coronary syndrome with hypertriglyceridemia (n=176). Co-designed implementation strategy package (clinician education and resources) was evaluated on Icosapent ethyl (IPE) prescription rate. An educational presentation and strategy package had varied clinician uptake, and icosapent ethyl use remained minimal at 1.1% among eligible post-ACS patients with hypertriglyceridemia.
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