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Cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome

Restoring blood flow to brain tissue at risk of infarction is essential for tissue survival and clinical outcome. We used cerebral blood flow (CBF) quantified with multiple post-labeling delay (PLD) pseudocontinuous arterial spin labeling (ASL) MRI after ischemic stroke and assessed the association...

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Autores principales: Luijten, Sven P.R., Bos, Daniel, van Doormaal, Pieter-Jan, Goyal, Mayank, Dijkhuizen, Rick M., Dippel, Diederik W.J., Roozenbeek, Bob, van der Lugt, Aad, Warnert, Esther A.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9932490/
https://www.ncbi.nlm.nih.gov/pubmed/36739791
http://dx.doi.org/10.1016/j.nicl.2023.103340
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author Luijten, Sven P.R.
Bos, Daniel
van Doormaal, Pieter-Jan
Goyal, Mayank
Dijkhuizen, Rick M.
Dippel, Diederik W.J.
Roozenbeek, Bob
van der Lugt, Aad
Warnert, Esther A.H.
author_facet Luijten, Sven P.R.
Bos, Daniel
van Doormaal, Pieter-Jan
Goyal, Mayank
Dijkhuizen, Rick M.
Dippel, Diederik W.J.
Roozenbeek, Bob
van der Lugt, Aad
Warnert, Esther A.H.
author_sort Luijten, Sven P.R.
collection PubMed
description Restoring blood flow to brain tissue at risk of infarction is essential for tissue survival and clinical outcome. We used cerebral blood flow (CBF) quantified with multiple post-labeling delay (PLD) pseudocontinuous arterial spin labeling (ASL) MRI after ischemic stroke and assessed the association between CBF and early neurological outcome. We acquired ASL with 7 PLDs at 3.0 T in large vessel occlusion stroke patients at 24 h. We quantified CBF relative to the contralateral hemisphere (rCBF) and defined hyperperfusion as a ≥30% increase and hypoperfusion as a ≥40% decrease in rCBF. We included 44 patients (median age: 70 years, median NIHSS: 13, 40 treated with endovascular thrombectomy) of whom 37 were recanalized. Hyperperfusion in ischemic core occurred in recanalized but not in non-recanalized patients (65.8% vs 0%, p = 0.006). Hypoperfusion occurred only in the latter group (0% vs 85.7%, p < 0.001). In recanalized patients, hyperperfusion was also seen in salvaged penumbra (38.9%). Higher rCBF in ischemic core (aβ, −2.75 [95% CI: −4.11 to −1.40]) and salvaged penumbra (aβ, −5.62 [95% CI: −9.57 to −1.68]) was associated with lower NIHSS scores at 24 h. In conclusion, hyperperfusion frequently occurs in infarcted and salvaged brain tissue following successful recanalization and early neurological outcome is positively associated with the level of reperfusion.
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spelling pubmed-99324902023-02-17 Cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome Luijten, Sven P.R. Bos, Daniel van Doormaal, Pieter-Jan Goyal, Mayank Dijkhuizen, Rick M. Dippel, Diederik W.J. Roozenbeek, Bob van der Lugt, Aad Warnert, Esther A.H. Neuroimage Clin Regular Article Restoring blood flow to brain tissue at risk of infarction is essential for tissue survival and clinical outcome. We used cerebral blood flow (CBF) quantified with multiple post-labeling delay (PLD) pseudocontinuous arterial spin labeling (ASL) MRI after ischemic stroke and assessed the association between CBF and early neurological outcome. We acquired ASL with 7 PLDs at 3.0 T in large vessel occlusion stroke patients at 24 h. We quantified CBF relative to the contralateral hemisphere (rCBF) and defined hyperperfusion as a ≥30% increase and hypoperfusion as a ≥40% decrease in rCBF. We included 44 patients (median age: 70 years, median NIHSS: 13, 40 treated with endovascular thrombectomy) of whom 37 were recanalized. Hyperperfusion in ischemic core occurred in recanalized but not in non-recanalized patients (65.8% vs 0%, p = 0.006). Hypoperfusion occurred only in the latter group (0% vs 85.7%, p < 0.001). In recanalized patients, hyperperfusion was also seen in salvaged penumbra (38.9%). Higher rCBF in ischemic core (aβ, −2.75 [95% CI: −4.11 to −1.40]) and salvaged penumbra (aβ, −5.62 [95% CI: −9.57 to −1.68]) was associated with lower NIHSS scores at 24 h. In conclusion, hyperperfusion frequently occurs in infarcted and salvaged brain tissue following successful recanalization and early neurological outcome is positively associated with the level of reperfusion. Elsevier 2023-01-31 /pmc/articles/PMC9932490/ /pubmed/36739791 http://dx.doi.org/10.1016/j.nicl.2023.103340 Text en © 2023 Erasmus MC University Medical Center https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Luijten, Sven P.R.
Bos, Daniel
van Doormaal, Pieter-Jan
Goyal, Mayank
Dijkhuizen, Rick M.
Dippel, Diederik W.J.
Roozenbeek, Bob
van der Lugt, Aad
Warnert, Esther A.H.
Cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome
title Cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome
title_full Cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome
title_fullStr Cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome
title_full_unstemmed Cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome
title_short Cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome
title_sort cerebral blood flow quantification with multi-delay arterial spin labeling in ischemic stroke and the association with early neurological outcome
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9932490/
https://www.ncbi.nlm.nih.gov/pubmed/36739791
http://dx.doi.org/10.1016/j.nicl.2023.103340
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