Icosapent Ethyl (Vascepa) Cost-Effective in REDUCE-IT USA-Confirmed what we predicted and see in the trenches

Icosapent Ethyl (Vascepa) Cost-Effective in REDUCE-IT USA-Confirmed what we predicted and see in the trenches

Cost-Effectivess of Icosapent Ethyl in REDUCE-IT USA:Results From Patients Randomized in the United States"authored by William S. Weintraub MD et al,was just published in J.Am.Heart Assoc.2024;13:e032413.DOI:10.1161/JAHA.123.032413

There was incremental gain in quality-adjusted life-years with IPE compared with standard care using in-trial(3.28 versus 3.13) and lifetime (10.36 versus 9.83) horizons.

Using an IPE cost of $4.59 per day ,health care costs were lower with IPE compared with standard care for both in-trial ($29,420 versus $30,947) and lifetime ($216,243 versus $219,212) analysis.IPE versus standard care was a dominant strategy in trial and over the lifetime ,with 99.7% lifetime probability of an incremental cost-effectiveness ratio <$50,000 per quality-adjusted life-year gained

IPE is cost-effective at $11.48 per day for conventional willingness-to-pay thresholds.(The cost per quality-adjusted life-year gained was $36,208 in trial and $9,582 over the lifetime)

These results were not surprising to me as we published in the Journal of Medical Economics(Sephy Philip et al.2016.Vol19,No.10,1003-1010) over 7 1/2 years ago(7/14/2016),long before REDUCE-IT(1/3/2019) was published that prescription IPE would be cost-effective.

We published that EPA-plus-statin therapy compared with statin monotherapy resulted in cost savings(total 5-year costs $29,393 versus $30,587 per person,respectively) and improved utilities(average 3.627 versus 5.575,respectively).Furthermore,our model actually probably underestimated the cost-effectiveness as it allowed only a single event per patient.

One can appreciate this benefit in cost-effectiveness by just looking at the total CVD event rate reduction from IPE.The impact of total CVD event reduction in REDUCE-IT is substantial: for every 1,000 patients treated with IPE for 5 years,approximately 159 total primary endpoints could be prevented,including 12 CVD deaths,42 MI';s,14 strokes,76 coronary revascularizations and 16 episodes of hospitalization for unstable angina(Bhatt DL et al.JACC.2019;73(22):2791-2802)

Millions of Americans can benefit from IPE.Nathan D. Wong,PhD,MPH et al published in Am.J.Cardiol.2020;134:62-68 from NHANES data ,using FDA eligibility criteria,an estimated 4.6 million persons would be eligible for IPE,with 60,544 preventable primary CVD outcomes annually from REDUCE-IT USA event rates !!!


Beth Dunbar

--award winning executive sales representative in multi specialties. 8 time COE winner with Amarin Pharma. Dedicated, loyal and results driven.

10 个月

Thank you Dr Nelson

回复
David Revere, MD, FACC

Cardiologist at Austin Heart

10 个月

If only my patients could actually afford it.

回复
Om Ganda

Diabetes and Lipid Specialist, and Educator at Joslin Diabetes Center; Harvard Medical School, Boston

10 个月

Very informative analyses- thx for posting, John.

回复

要查看或添加评论,请登录

社区洞察

其他会员也浏览了