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Icosapent Ethyl for Primary Versus Secondary Prevention of Major Adverse Cardiovascular Events in Hypertriglyceridemia: Value for Money Analysis - 25/06/21

Doi : 10.1016/j.amjmed.2020.12.023 
Ronen Arbel, PhD a, , Enis Aboalhasan, BA a, Ariel Hammerman, PhD b, Joseph Azuri, MD, MHA c, d
a Maximizing Health Outcomes Research Lab, Sapir College, Sderot, Israel 
b Department of Pharmaceutical Technology Assessment, Clalit Health Services Headquarters, Tel-Aviv, Israel 
c Diabetes Clinic, Central District, Maccabi Healthcare Services, Tel Aviv, Israel 
d Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel 

Requests for reprints should be addressed to Ronen Arbel, PhD, Director, Maximizing Health Outcomes Research Lab, Department of Technology Marketing, Sapir College, Sderot, Israel.Maximizing Health Outcomes Research Lab, Department of Technology MarketingSapir CollegeSderotIsrael

Abstract

Background

Icosapent ethyl (IPE) is approved for the prevention of major adverse cardiovascular events (MACE) in patients with hypertriglyceridemia. However, due to budget constraints, access to IPE will inevitably be limited to a fraction of eligible patients. To help maximize value for money spent, we estimated the number of preventable MACE when providing IPE for primary versus secondary prevention.

Methods

The number of preventable MACE was estimated by dividing the available budget by the cost needed to treat (CNT) to prevent one MACE. CNT was calculated as the product of the number needed to treat (NNT) to prevent 1 MACE by therapy cost. NNT values were determined according to the Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (REDUCE-IT) results. The budget limit was set as the United States’ threshold suggested by the Institute for Clinical and Economic Review. Sensitivity analysis was performed regarding the cost of IPE in the United States.

Results

The NNT to prevent 1 MACE over 4.9 years in the Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial primary prevention cohort was 59 (95% confidence interval [CI]: 24-∞) versus 14 (11-21) for secondary prevention. At an annual IPE cost of $2915, the CNT to prevent 1 MACE was $842,726 (95% CI: $342,804-∞) and $199,969 ($157,118-$299,953) accordingly. A total of $819 million worth of IPE can avoid 4762 MACE (95% CI: 0-11,707) versus 20,069 (13,379-25,541), when provided as primary versus secondary prevention therapy; P < .001. The number of avoided MACE is sensitive to IPE price.

Conclusions

Prioritizing IPE therapy for patients with an established cardiovascular disease may provide significantly more value for money than primary prevention.

El texto completo de este artículo está disponible en PDF.

Keywords : Hypertriglyceridemia, Icosapent ethyl, Major adverse cardiovascular events, Outcomes research


Esquema


 Funding: None.
 Conflicts of Interest: JA has received nonfinancial support from Janssen Pharmaceuticals and speaker and consulting honorarium from Pfizer and NovoNordisk. RA, EA, AH report none.
 Authorship: All authors had access to the data and a role in writing this manuscript.


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Vol 134 - N° 7

P. e415-e419 - juillet 2021 Regresar al número
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