CT Perfusion Does Not Modify the Effect of Reperfusion in Patients with Acute Ischemic Stroke Undergoing Endovascular Treatment in the ESCAPE-NA1 Trial.


Journal

AJNR. American journal of neuroradiology
ISSN: 1936-959X
Titre abrégé: AJNR Am J Neuroradiol
Pays: United States
ID NLM: 8003708

Informations de publication

Date de publication:
09 2023
Historique:
received: 28 03 2023
accepted: 27 06 2023
pmc-release: 01 09 2024
medline: 13 9 2023
pubmed: 25 8 2023
entrez: 24 8 2023
Statut: ppublish

Résumé

Although reperfusion is associated with improved outcomes in patients with acute ischemic stroke undergoing endovascular treatment, many patients still do poorly. We investigated whether CTP modifies the effect of near-complete reperfusion on clinical outcomes, ie, whether poor clinical outcomes despite near-complete reperfusion can be partly or fully explained by CTP findings. Data are from the Safety and Efficacy of Nerinetide in Subjects Undergoing Endovascular Thrombectomy for Stroke (ESCAPE-NA1) trial. Admission CTP was processed using RAPID software, generating relative CBF and CBV volume maps at standard thresholds. CTP lesion volumes were compared in patients with-versus-without near-complete reperfusion. Associations between each CTP metric and clinical outcome (90-day mRS) were tested using multivariable logistic regression, adjusted for baseline imaging and clinical variables. Treatment-effect modification was assessed by introducing CTP lesion volume × reperfusion interaction terms in the models. CTP lesion volumes and reperfusion status were available in 410/1105 patients. CTP lesion volumes were overall larger in patients without near-complete reperfusion, albeit not always statistically significant. Increased CBF <34%, CBV <34%, CBV <38%, and CBV <42% lesion volumes were associated with worse clinical outcome (ordinal mRS) at 90 days. CTP core lesion volumes did not modify the treatment effect of near-complete recanalization on clinical outcome. CTP did not modify the effect of near-complete reperfusion on clinical outcomes. Thus, CTP cannot explain why some patients with near-complete reperfusion have poor clinical outcomes.

Sections du résumé

BACKGROUND AND PURPOSE
Although reperfusion is associated with improved outcomes in patients with acute ischemic stroke undergoing endovascular treatment, many patients still do poorly. We investigated whether CTP modifies the effect of near-complete reperfusion on clinical outcomes, ie, whether poor clinical outcomes despite near-complete reperfusion can be partly or fully explained by CTP findings.
MATERIALS AND METHODS
Data are from the Safety and Efficacy of Nerinetide in Subjects Undergoing Endovascular Thrombectomy for Stroke (ESCAPE-NA1) trial. Admission CTP was processed using RAPID software, generating relative CBF and CBV volume maps at standard thresholds. CTP lesion volumes were compared in patients with-versus-without near-complete reperfusion. Associations between each CTP metric and clinical outcome (90-day mRS) were tested using multivariable logistic regression, adjusted for baseline imaging and clinical variables. Treatment-effect modification was assessed by introducing CTP lesion volume × reperfusion interaction terms in the models.
RESULTS
CTP lesion volumes and reperfusion status were available in 410/1105 patients. CTP lesion volumes were overall larger in patients without near-complete reperfusion, albeit not always statistically significant. Increased CBF <34%, CBV <34%, CBV <38%, and CBV <42% lesion volumes were associated with worse clinical outcome (ordinal mRS) at 90 days. CTP core lesion volumes did not modify the treatment effect of near-complete recanalization on clinical outcome.
CONCLUSIONS
CTP did not modify the effect of near-complete reperfusion on clinical outcomes. Thus, CTP cannot explain why some patients with near-complete reperfusion have poor clinical outcomes.

Identifiants

pubmed: 37620153
pii: ajnr.A7954
doi: 10.3174/ajnr.A7954
pmc: PMC10494951
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1045-1049

Informations de copyright

© 2023 by American Journal of Neuroradiology.

Références

Lancet. 2020 Mar 14;395(10227):878-887
pubmed: 32087818
Interv Neurol. 2018 Oct;7(6):513-521
pubmed: 30410531
N Engl J Med. 2018 Feb 22;378(8):708-718
pubmed: 29364767
Stroke. 2017 Apr;48(4):932-938
pubmed: 28283606
Emerg Radiol. 2019 Aug;26(4):401-408
pubmed: 30929145
Neurology. 2021 Nov 16;97(20 Suppl 2):S60-S67
pubmed: 34785605
N Engl J Med. 2018 Jan 4;378(1):11-21
pubmed: 29129157
Stroke. 2020 Oct;51(10):3147-3155
pubmed: 32933417
Neurology. 2021 Sep 14;97(11):e1075-e1084
pubmed: 34261783
Stroke. 2015 Nov;46(11):3241-8
pubmed: 26443832
Neurotherapeutics. 2023 Apr;20(3):679-692
pubmed: 37014594
Stroke. 2015 Jun;46(6):1582-9
pubmed: 25908463
Eur Stroke J. 2022 Mar;7(1):I-XXVI
pubmed: 35300256
Stroke. 2019 Dec;50(12):e344-e418
pubmed: 31662037

Auteurs

N B Rex (NB)

From the Department of Diagnostic Imaging (N.B.R., R.A.M.), Brown University, Providence, Rhode Island.
Department of Diagnostic Imaging (N.B.R., R.V.M., J.M.O., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.

R V McDonough (RV)

Department of Diagnostic Imaging (N.B.R., R.V.M., J.M.O., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.

J M Ospel (JM)

Department of Diagnostic Imaging (N.B.R., R.V.M., J.M.O., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences (J.M.O., A.S., J.C.F., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.

N Kashani (N)

Department of Neurosurgery (N.K.), University of Saskatchewan, Saskatoon, Saskatchewan, Canada.

A Sehgal (A)

Department of Clinical Neurosciences (J.M.O., A.S., J.C.F., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.

J C Fladt (JC)

Department of Clinical Neurosciences (J.M.O., A.S., J.C.F., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.
Department of Neurology and Stroke Center (J.C.F.), University Hospital Basel, Basel, Switzerland.

R A McTaggart (RA)

From the Department of Diagnostic Imaging (N.B.R., R.A.M.), Brown University, Providence, Rhode Island.

R Nogueira (R)

Department of Neurology and Neurosurgery (R.N.), University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.

B Menon (B)

Department of Diagnostic Imaging (N.B.R., R.V.M., J.M.O., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences (J.M.O., A.S., J.C.F., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.

A M Demchuk (AM)

Department of Diagnostic Imaging (N.B.R., R.V.M., J.M.O., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences (J.M.O., A.S., J.C.F., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.

M Tymianski (M)

NoNO Inc (M.T.), Toronto, Ontario, Canada.

M D Hill (MD)

Department of Diagnostic Imaging (N.B.R., R.V.M., J.M.O., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.
Department of Clinical Neurosciences (J.M.O., A.S., J.C.F., B.M., A.M.D., M.D.H., M.G.), University of Calgary, Calgary, Alberta, Canada.

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