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Abstract Details

Frequency of Guideline-Ineligible Large Vessel Occlusion Strokes
Cerebrovascular Disease and Interventional Neurology
P1 - Poster Session 1 (5:30 PM-6:30 PM)
3-053
To explore the frequency and reasons for EVT ineligiblity of acute ischemic strokes per AHA guidelines

The natural history of large vessel occlusion (LVO) strokes is poor. Currently AHA guidelines recommend endovascular thrombectomy (EVT) upto 24 hours since time last seen well in highly selected patient populations. We aim to understand the frequency of guideline ineligible patients, reasons for ineligibility and the required sample size for a trial exploring the effect of EVT in ineligible subgroups.

Retrospective chart review of consecutive acute ischemic stroke discharges was performed at a single comprehensive stroke center between November 2014 and February 2017. Demographic, clinical (stroke severity, time from stroke onset and mode of presentation) and radiological imaging data (occlusion location, stroke burden- ischemic core volume and ASPECTS score) were collected and analyzed for eligibility for EVT per AHA 2018 guidelines.

17.5% of acute ischemic strokes in the 0-6-hour and 9.2% in the 6-24-hour time window were EVT candidates per AHA guidelines. Of the patients harboring an intracranial vessel occlusion (639 of total 2667), the most common reasons for ineligibility were a large stroke burden (17%, ASPECTS ≤5), non-proximal occlusions (MCA-M2- 17%, MCA-M3/ ACA/ PCA-4%), vertebra-basilar occlusions (17%) and mild stroke symptoms (9%, NIHSS score ≤5). Assuming a 10% treatment effect of EVT concerning relevant endpoints, a sample size of 712, 774 and 602 would be required to study the effect of EVT in LVO strokes with ASPECTS ≤5, NIHSS score ≤5 and MCA-M2 occlusions, respectively. 

The frequency of acute ischemic strokes due to LVO eligible for EVT per AHA guidelines is low with only one in eight patients meeting AHA eligibility.  Common reasons for non-guideline eligibility are distal location, posterior circulation location, large core and low NIHSS.  These data outline opportunities for indication expansion.

Authors/Disclosures
Shashvat Desai, MD (University of Pittsburgh Medical Center)
PRESENTER
Dr. Desai has nothing to disclose.
Bradley Molyneaux, MD, PhD (Brigham and Women's Hospital) Dr. Molyneaux has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Biogen. Dr. Molyneaux has received personal compensation in the range of $500-$4,999 for serving as an Expert Witness for Billing, Cochran, Lyles, Mauro and Ramsey. The institution of Dr. Molyneaux has received research support from NIH. Dr. Molyneaux has received publishing royalties from a publication relating to health care.
Marcelo Rocha, MD, PhD (UPMC) The institution of Dr. Rocha has received research support from NIH.
Matthew T. Starr, MD (University of Pittsburgh Medical Center) Dr. Starr has nothing to disclose.
Tudor G. Jovin, MD (Cooper University Healthcare) Dr. Jovin has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Cerenovus. Dr. Jovin has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Contego Medical. Dr. Jovin has received personal compensation in the range of $5,000-$9,999 for serving as an Expert Witness for Several law firms. Dr. Jovin has stock in Corindus. Dr. Jovin has stock in Methinks. Dr. Jovin has stock in Viz.ai. Dr. Jovin has stock in Route92. Dr. Jovin has stock in FreeOx Biotech. Dr. Jovin has stock in Galaxy. Dr. Jovin has stock in Kandu. The institution of Dr. Jovin has received research support from Stryker. The institution of Dr. Jovin has received research support from Medtronic.
Ashutosh P. Jadhav, MD, FAAN (Barrow Neurological Institute) Dr. Jadhav has nothing to disclose.