Collateral Circulation in Thrombectomy for Stroke After 6 to 24 Hours in the DAWN Trial.


Journal

Stroke
ISSN: 1524-4628
Titre abrégé: Stroke
Pays: United States
ID NLM: 0235266

Informations de publication

Date de publication:
03 2022
Historique:
pubmed: 4 11 2021
medline: 11 3 2022
entrez: 3 11 2021
Statut: ppublish

Résumé

Collaterals govern the pace and severity of cerebral ischemia, distinguishing fast or slow progressors and corresponding therapeutic opportunities. The fate of sustained collateral perfusion or collateral failure is poorly characterized. We evaluated the nature and impact of collaterals on outcomes in the late time window DAWN trial (Diffusion-Weighted Imaging or Computed Tomography Perfusion Assessment With Clinical Mismatch in the Triage of Wake-Up and Late Presenting Strokes Undergoing Neurointervention With Trevo). The DAWN Imaging Core Lab prospectively scored collateral grade on baseline computed tomography angiography (CTA; endovascular and control arms) and digital subtraction angiography (DSA; endovascular arm only), blinded to all other data. CTA collaterals were graded with the Tan scale and DSA collaterals were scored by ASITN grade (American Society of Interventional and Therapeutic Neuroradiology collateral score). Descriptive statistics characterized CTA collateral grade in all DAWN subjects and DSA collaterals in the endovascular arm. The relationship between collateral grade and day 90 outcomes were separately analyzed for each treatment arm. Collateral circulation to the ischemic territory was evaluated on CTA (n=144; median 2, 0-3) and DSA (n=57; median 2, 1-4) before thrombectomy in 161 DAWN subjects (mean age 69.8±13.6 years; 55.3% women; 91 endovascular therapy, 70 control). CTA revealed a broad range of collaterals (Tan grade 3, n=64 [44%]; 2, n=45 [31%]; 1, n=31 [22%]; 0, n=4 [3%]). DSA also showed a diverse range of collateral grades (ASITN grade 4, n=4; 3, n=22; 2, n=27; 1, n=4). Across treatment arms, baseline demographics, clinical variables except atrial fibrillation (41.6% endovascular versus 25.0% controls, DAWN subjects enrolled at 6 to 24 hours after onset with limited infarct cores had a wide range of collateral grades on both CTA and DSA. Even in this late time window, better collaterals lead to slower stroke progression and better functional outcomes. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02142283.

Sections du résumé

BACKGROUND AND PURPOSE
Collaterals govern the pace and severity of cerebral ischemia, distinguishing fast or slow progressors and corresponding therapeutic opportunities. The fate of sustained collateral perfusion or collateral failure is poorly characterized. We evaluated the nature and impact of collaterals on outcomes in the late time window DAWN trial (Diffusion-Weighted Imaging or Computed Tomography Perfusion Assessment With Clinical Mismatch in the Triage of Wake-Up and Late Presenting Strokes Undergoing Neurointervention With Trevo).
METHODS
The DAWN Imaging Core Lab prospectively scored collateral grade on baseline computed tomography angiography (CTA; endovascular and control arms) and digital subtraction angiography (DSA; endovascular arm only), blinded to all other data. CTA collaterals were graded with the Tan scale and DSA collaterals were scored by ASITN grade (American Society of Interventional and Therapeutic Neuroradiology collateral score). Descriptive statistics characterized CTA collateral grade in all DAWN subjects and DSA collaterals in the endovascular arm. The relationship between collateral grade and day 90 outcomes were separately analyzed for each treatment arm.
RESULTS
Collateral circulation to the ischemic territory was evaluated on CTA (n=144; median 2, 0-3) and DSA (n=57; median 2, 1-4) before thrombectomy in 161 DAWN subjects (mean age 69.8±13.6 years; 55.3% women; 91 endovascular therapy, 70 control). CTA revealed a broad range of collaterals (Tan grade 3, n=64 [44%]; 2, n=45 [31%]; 1, n=31 [22%]; 0, n=4 [3%]). DSA also showed a diverse range of collateral grades (ASITN grade 4, n=4; 3, n=22; 2, n=27; 1, n=4). Across treatment arms, baseline demographics, clinical variables except atrial fibrillation (41.6% endovascular versus 25.0% controls,
CONCLUSIONS
DAWN subjects enrolled at 6 to 24 hours after onset with limited infarct cores had a wide range of collateral grades on both CTA and DSA. Even in this late time window, better collaterals lead to slower stroke progression and better functional outcomes. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT02142283.

Identifiants

pubmed: 34727737
doi: 10.1161/STROKEAHA.121.034471
doi:

Banques de données

ClinicalTrials.gov
['NCT02142283']

Types de publication

Clinical Trial Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

742-748

Auteurs

David S Liebeskind (DS)

Neurovascular Imaging Research Core, UCLA (D.S.L., H.S.).

Hamidreza Saber (H)

Neurovascular Imaging Research Core, UCLA (D.S.L., H.S.).

Bin Xiang (B)

Prospect Analytical, Inc, San Jose, CA (B.X.).

Ashutosh P Jadhav (AP)

Barrow Neurological Institute, Phoenix, AZ (A.P.J., T.G.J.).

Tudor G Jovin (TG)

Barrow Neurological Institute, Phoenix, AZ (A.P.J., T.G.J.).

Diogo C Haussen (DC)

Emory University School of Medicine/Grady Memorial Hospital, Atlanta, GA (D.C.H., R.G.N.).

Ronald F Budzik (RF)

OhioHealth Riverside Methodist Hospital, Columbus, OH (R.F.B.).

Alain Bonafe (A)

Hôpital Gui-de-Chauliac, Montpellier, France (A.B.).

Parita Bhuva (P)

Texas Stroke Institute, Dallas-Fort Worth (P.B.).

Dileep R Yavagal (DR)

University of Miami Miller School of Medicine-Jackson Memorial Hospital, Miami, FL (D.R.Y.).

Ricardo A Hanel (RA)

Baptist Jacksonville, Jacksonville, FL (R.A.H.).

Marc Ribo (M)

Hospital Vall d'Hebrón, Barcelona, Spain (M.R.).

Christophe Cognard (C)

University Hospital of Toulouse, France (C.C.).

Cathy Sila (C)

University Hospital of Cleveland, OH (C.S.).

Ameer E Hassan (AE)

University of Texas Rio Grande Valley-Valley Baptist Medical Center, Harlingen (A.E.H.).

Wade S Smith (WS)

University of California, San Francisco, San Francisco (W.S.S.).

Jeffrey L Saver (JL)

UCLA, Los Angeles, CA (J.L.S.).

Raul G Nogueira (RG)

Emory University School of Medicine/Grady Memorial Hospital, Atlanta, GA (D.C.H., R.G.N.).

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Classifications MeSH