Abstract DP136: Macrovascular angiographic and tissue-level perfusion collateral scoring to predict inter-hospital infarct growth rate

Introduction: In acute ischemic stroke patients, collateral circulation is an important target for neuroprotectant treatments as it influences tissue survival and clinical outcomes. Collateral status is determined with the expert-rated Tan score on CT Angiography (CTA) or tissue-level perfusion metrics on CT Perfusion (CTP). We developed a deep learning–based vessel segmentation method for CTA to quantify all vessels- and artery-only collateral scores (vesQCS, aQCS). We aim to (1) compare the performance of macrovascular and tissue-level collateral status for predicting inter-hospital infarct growth rate (IGR) and (2) evaluate if a mismatch in macrovascular and tissue-level collateral status influences IGR. Methods: We included patients recruited in a prospective, multicenter study who were transferred from a primary to a comprehensive stroke center for EVT (n=387). vesQCS and aQCS were defined as the ratio of deep learning–segmented vessel or artery volume in the infarcted versus contralateral hemisphere (Figure-1). Tan score was expert-rated, while tissue level collaterals such as the Hypoperfusion Intensity Ratio (HIR: Tmax>10s/Tmax>6s) and the mismatch volume (Tmax>6s-rCBF<30%) were derived from baseline CTP. Infarct growth was calculated using baseline rCBF<30% and DWI lesion segmentations obtained at primary and comprehensive stroke centers. Multivariable logistic regression was used to compare collateral scores with the adjusted odds ratio (aOR[95%CI]) and AUC for predicting IGR of >=5ml/hr. We used interaction analysis to evaluate if the association between HIR and fast IGR was affected by macrovascular collaterals. Results: Median inter-hospital growth rate was 3.9 (1.4-8.2) mL/hour and median transfer time was 3.6 (2.6-4.6) hours. All collateral scores, except mismatch volume, were significantly associated with fast IGR (Figure-2). AUC analysis shows similar performance between collateral scores for imputed and complete case sensitivity analyses (Figure-3). For lower Tan scores, the association of HIR with IGR was lower than for higher Tan scores (p for interaction = 0.03, Figure-3). Conclusion: Automated quantitative (vesQCS/aQCS), expert-rated Tan, and hypoperfusion intensity ratio perform similarly to predict inter-hospital infarct growth rate. Patients with poorer macrovascular collaterals are at higher risk of fast IGR despite favourable tissue-level collaterals.

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Journal
Stroke
Published
2026-01-29
DOI
https://doi.org/10.1161/str.57.suppl_1.dp136
Primary Topic
Acute Ischemic Stroke Management
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article
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article

Abstract DP136: Macrovascular angiographic and tissue-level perfusion collateral scoring to predict inter-hospital infarct growth rate

Stephanie Kemp, Anke Wouters, Henk van Voorst, Lieselotte Vandewalle et al.
Stroke
Acute Ischemic Stroke Management
article

Abstract DP136: Macrovascular angiographic and tissue-level perfusion collateral scoring to predict inter-hospital infarct growth rate

Stephanie Kemp, Anke Wouters, Henk van Voorst, Lieselotte Vandewalle, Pierre Seners, Michael Mlynash, Jeremy J. Heit, Adrien ter Schiphorst, Daniel de Wilde, Greg Zaharchuk, Maarten Lansberg, Gregory W. Albers, Soren Christensen
article en

Abstract

Introduction: In acute ischemic stroke patients, collateral circulation is an important target for neuroprotectant treatments as it influences tissue survival and clinical outcomes. Collateral status is determined with the expert-rated Tan score on CT Angiography (CTA) or tissue-level perfusion metrics on CT Perfusion (CTP). We developed a deep learning–based vessel segmentation method for CTA to quantify all vessels- and artery-only collateral scores (vesQCS, aQCS). We aim to (1) compare the performance of macrovascular and tissue-level collateral status for predicting inter-hospital infarct growth rate (IGR) and (2) evaluate if a mismatch in macrovascular and tissue-level collateral status influences IGR. Methods: We included patients recruited in a prospective, multicenter study who were transferred from a primary to a comprehensive stroke center for EVT (n=387). vesQCS and aQCS were defined as the ratio of deep learning–segmented vessel or artery volume in the infarcted versus contralateral hemisphere (Figure-1). Tan score was expert-rated, while tissue level collaterals such as the Hypoperfusion Intensity Ratio (HIR: Tmax>10s/Tmax>6s) and the mismatch volume (Tmax>6s-rCBF<30%) were derived from baseline CTP. Infarct growth was calculated using baseline rCBF<30% and DWI lesion segmentations obtained at primary and comprehensive stroke centers. Multivariable logistic regression was used to compare collateral scores with the adjusted odds ratio (aOR[95%CI]) and AUC for predicting IGR of >=5ml/hr. We used interaction analysis to evaluate if the association between HIR and fast IGR was affected by macrovascular collaterals. Results: Median inter-hospital growth rate was 3.9 (1.4-8.2) mL/hour and median transfer time was 3.6 (2.6-4.6) hours. All collateral scores, except mismatch volume, were significantly associated with fast IGR (Figure-2). AUC analysis shows similar performance between collateral scores for imputed and complete case sensitivity analyses (Figure-3). For lower Tan scores, the association of HIR with IGR was lower than for higher Tan scores (p for interaction = 0.03, Figure-3). Conclusion: Automated quantitative (vesQCS/aQCS), expert-rated Tan, and hypoperfusion intensity ratio perform similarly to predict inter-hospital infarct growth rate. Patients with poorer macrovascular collaterals are at higher risk of fast IGR despite favourable tissue-level collaterals.

StrokeVol. 57(Suppl_1)
Palo Alto University (US), Universitair Ziekenhuis Leuven (BE), Centre Hospitalier Universitaire de Montpellier (FR), Fondation de Rothschild (FR), Stanford Medicine (US), Stanford University (US), KU Leuven (BE)
Openalex Percentile: Top 74%
Acute Ischemic Stroke Management
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