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Abstract Details

Comparison of NIHSS Within 7-day and 90-day mRS Outcomes in Randomized-controlled Trials of Acute Ischemic Stroke: A Systematic Review and Meta-analysis
Cerebrovascular Disease and Interventional Neurology
P1 - Poster Session 1 (8:00 AM-9:00 AM)
5-024

To evaluate agreement between National Institutes of Health Stroke Scale (NIHSS) assessed within 7-days follow-up and 90-day modified Rankin Scale (mRS) outcomes in randomized-controlled trials (RCTs).

Since factors independent of acute ischemic stroke (AIS) can confound 90-day outcomes in RCTs of acute treatments, early NIHSS may be a suitable alternative.

We conducted a meta-analysis including RCTs of acute therapies for AIS published until 01-April-2023, with available data for both 90-day mRS and NIHSS within 7-days. Primary outcome was agreement between trial results (classified as positive versus negative/neutral) based on 24-hour NIHSS and 90-day mRS. We additionally assessed agreement for 2-hours, 48-hours, 72-hours, 4-days, 5-days, 6-days and 7-days NIHSS. We aimed to validate our study-level findings using individual patient data from the ESCAPE and ESCAPE-NA1 RCTs, comparing NIHSS at 2-hours, 24-hours, 48-hours, and 5-7 days with 90-day mRS (both dichotomized at 0-2).

We included 116 trials (44,387 patients, median age 68 [IQR 66-72] years, 25,218 [56.8%] men), contributing 170 NIHSS assessments performed across the 8 timepoints. For 24-hour NIHSS, there was agreement with 90-day mRS assessments in 63/74 (85%) trials. Agreement varied numerically by timing of NIHSS assessments, ranging from 80%–100%, but differences were not statistically significant (p=0.76). Whereas ESCAPE and ESCAPE-NA1 data showed agreement in overall trial results for all timepoints except 2-hour NIHSS, agreement with 90-day mRS for individual patient outcomes was lower (3523/5195, 67.8%) but improved with later assessments (2-hours: 56.6%; 24-hours: 66.6%; 48-hours: 72.7%; 5-7 days: 76.5%,p<0.01).

NIHSS assessed between 24-hours and 7-days follow-up results in similar overall conclusions as 90-day mRS in identifying positive versus neutral/negative RCTs, indicating its value as an alternative primary outcome measure for AIS treatments. However, individual patient level data showed that NIHSS within 7-days risks misclassifying 1 in 3 patients with respect to 90-day mRS, although agreement improves with later assessments.

Authors/Disclosures
Aravind Ganesh
PRESENTER
No disclosure on file
Leon Rinkel Mr. Rinkel has received research support from the Niels Stensen Foundation. Mr. Rinkel has received research support from Hartstichting.
Johanna Ospel No disclosure on file
Manon Kappelhof No disclosure on file
Arshia Sehgal No disclosure on file
Rosalie McDonough No disclosure on file
Michael Tymianski, MD, PhD, FRCSC Michael Tymianski, MD, PHD, FRCSC has received personal compensation for serving as an employee of NoNO Inc.. Michael Tymianski, MD, PHD, FRCSC has stock in NoNO Inc.
Michael D. Hill, MD (University of Calgary) Dr. Hill has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Boehringer Ingelheim. Dr. Hill has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Sun Pharma. Dr. Hill has received stock or an ownership interest from Circle Neurovascular.
Mayank Goyal, MD, PhD No disclosure on file