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Abstract Details

Analysis of Ischemic Stroke Cases Eligible for Novel Treatment of Hypertriglyceridemia
Cerebrovascular Disease and Interventional Neurology
P16 - Poster Session 16 (8:00 AM-9:00 AM)
13-005

We proposed to evaluate the eligibility of patients presenting with Acute Ischemic Strokes (AIS) for Icosapent Ethyl (IPE) with regards to risk factors, demographics, and stroke subtype.

Hypertriglyceridemia (HTG) is known to be associated with metabolic syndrome and type 2 DM. It can result in accelerated atherosclerosis, a major stroke risk factor. IPE has been recently approved as a novel treatment for HTG in patients older than 45.

A total of 743 patients older than 45 admitted with AIS between Jan 2018 – Dec 2020 were identified.  Those on a statin at admission were categorized into eligible for IPE (LDL 41-100 and Triglyceride 150-499) vs. not eligible. Chi squared tests of proportion were performed to evaluate differences in demographics, risk factors, and stroke subtype between those eligible vs non eligible.

We identified 365 patients taking a statin on admission and 378 not on a statin. Of those that were on a statin at admission, 39 (5%) were eligible for IPE by LDL and TG criteria. Mean age of eligible patients was 68.5 and 51% were women. Patients eligible for IPE were more likely to be white (67% vs. 44%, p=0.006), have a history of DM (67% vs. 47%, p=0.018), and HTN (97% vs. 86%, p=0.042), as well as a trend for prior MI or CAD (46% vs. 33%, p=0.09). The most common stroke subtype in those eligible was cardioembolic (CE) (0.33%, p=.015).  

A substantial proportion of our population was not on a statin on admission underscoring the need for better primary prevention in these cases. About 5% of patients on a statin qualified for IPE. This population was more likely to have DM, HTN and CAD.  Stroke patients newly initiated on a statin should have follow-up TG measurement to assess eligibility for HTG treatment.

Authors/Disclosures
Adam P. Klein, DO
PRESENTER
Dr. Klein has nothing to disclose.
Karen Yarbrough (University of Maryland Medical Center) No disclosure on file
Prachi Mehndiratta, MD Dr. Mehndiratta has nothing to disclose.
Carolyn Cronin, MD, PhD, FAAN (Vanderbilt University Medical Center) Dr. Cronin has nothing to disclose.
John Cole, MD (UMD SOM) Dr. Cole has nothing to disclose.
Marcella A. Wozniak, MD, PhD (U of MD Department of Neurology) Dr. Wozniak has nothing to disclose.
Steven J. Kittner, MD, MPH (Dept of Neurology) The institution of Dr. Kittner has received research support from NINDS.
Seemant Chaturvedi, MD, FAHA, FAAN (University of Maryland) Dr. Chaturvedi has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Bayer. Dr. Chaturvedi has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Novartis. Dr. Chaturvedi has received personal compensation in the range of $10,000-$49,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for American Heart Association. The institution of Dr. Chaturvedi has received research support from NINDS.