Recent Vitamin K Antagonist Use and Intracranial Hemorrhage After Endovascular Thrombectomy for Acute Ischemic Stroke.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
20 06 2023
Historique:
pmc-release: 20 12 2023
medline: 22 6 2023
pubmed: 20 6 2023
entrez: 20 6 2023
Statut: ppublish

Résumé

Use of oral vitamin K antagonists (VKAs) may place patients undergoing endovascular thrombectomy (EVT) for acute ischemic stroke caused by large vessel occlusion at increased risk of complications. To determine the association between recent use of a VKA and outcomes among patients selected to undergo EVT in clinical practice. Retrospective, observational cohort study based on the American Heart Association's Get With the Guidelines-Stroke Program between October 2015 and March 2020. From 594 participating hospitals in the US, 32 715 patients with acute ischemic stroke selected to undergo EVT within 6 hours of time last known to be well were included. VKA use within the 7 days prior to hospital arrival. The primary end point was symptomatic intracranial hemorrhage (sICH). Secondary end points included life-threatening systemic hemorrhage, another serious complication, any complications of reperfusion therapy, in-hospital mortality, and in-hospital mortality or discharge to hospice. Of 32 715 patients (median age, 72 years; 50.7% female), 3087 (9.4%) had used a VKA (median international normalized ratio [INR], 1.5 [IQR, 1.2-1.9]) and 29 628 had not used a VKA prior to hospital presentation. Overall, prior VKA use was not significantly associated with an increased risk of sICH (211/3087 patients [6.8%] taking a VKA compared with 1904/29 628 patients [6.4%] not taking a VKA; adjusted odds ratio [OR], 1.12 [95% CI, 0.94-1.35]; adjusted risk difference, 0.69% [95% CI, -0.39% to 1.77%]). Among 830 patients taking a VKA with an INR greater than 1.7, sICH risk was significantly higher than in those not taking a VKA (8.3% vs 6.4%; adjusted OR, 1.88 [95% CI, 1.33-2.65]; adjusted risk difference, 4.03% [95% CI, 1.53%-6.53%]), while those with an INR of 1.7 or lower (n = 1585) had no significant difference in the risk of sICH (6.7% vs 6.4%; adjusted OR, 1.24 [95% CI, 0.87-1.76]; adjusted risk difference, 1.13% [95% CI, -0.79% to 3.04%]). Of 5 prespecified secondary end points, none showed a significant difference across VKA-exposed vs VKA-unexposed groups. Among patients with acute ischemic stroke selected to receive EVT, VKA use within the preceding 7 days was not associated with a significantly increased risk of sICH overall. However, recent VKA use with a presenting INR greater than 1.7 was associated with a significantly increased risk of sICH compared with no use of anticoagulants.

Identifiants

pubmed: 37338878
pii: 2806152
doi: 10.1001/jama.2023.8073
pmc: PMC10282891
doi:

Substances chimiques

Anticoagulants 0
Fibrinolytic Agents 0
Vitamin K 12001-79-5

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2038-2049

Commentaires et corrections

Type : CommentIn

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Auteurs

Brian Mac Grory (B)

Department of Neurology, Duke University School of Medicine, Durham, North Carolina.
Duke Clinical Research Institute, Durham, North Carolina.

DaJuanicia N Holmes (DN)

Duke Clinical Research Institute, Durham, North Carolina.

Roland A Matsouaka (RA)

Duke Clinical Research Institute, Durham, North Carolina.
Department of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina.

Shreyansh Shah (S)

Department of Neurology, Duke University School of Medicine, Durham, North Carolina.

Cherylee W J Chang (CWJ)

Department of Neurology, Duke University School of Medicine, Durham, North Carolina.

Richard Rison (R)

Department of Neurology, USC Keck School of Medicine, Los Angeles, California.

Jenelle Jindal (J)

Department of Neurology, Peter C. Fung, MD, Stroke Center, El Camino Hospital, Mountain View, California.

Christine Holmstedt (C)

Department of Neurology, Medical University of South Carolina, Charleston.

William R Logan (WR)

Department of Neurology, Mercy Hospital of St Louis, St Louis, Missouri.

Candy Corral (C)

Department of Neurology, Huntington Memorial Hospital, Pasadena, California.

Jason S Mackey (JS)

Department of Neurology, Indiana University School of Medicine, Indianapolis.

Joey R Gee (JR)

Department of Neurology, St Joseph's Heritage Medical Group, Irvine, California.

David Bonovich (D)

Department of Neurology, Sutter Health, Castro Valley, California.

James Walker (J)

Department of Anesthesiology, Critical Care, and Neurocritical Care, Ascension Via Christi Hospital and University of Kansas School of Medicine, Wichita.

Toby Gropen (T)

Department of Neurology, University of Alabama School of Medicine, Birmingham.

Curtis Benesch (C)

Department of Neurology, University of Rochester School of Medicine, Rochester, New York.

Jonathan Dissin (J)

Department of Neurology, Einstein Medical Center, Philadelphia, Pennsylvania.

Hemant Pandey (H)

Department of Neurology, Banner Baywood Medical Center, Chandler, Arizona.

David Wang (D)

Department of Neurology, OSF Healthcare, Peoria, Illinois.

Martin Unverdorben (M)

Global Specialty Medical Affairs, Daiichi Sankyo Inc, Basking Ridge, New Jersey.

Adrian F Hernandez (AF)

Duke Clinical Research Institute, Durham, North Carolina.
Department of Medicine, Duke University School of Medicine, Durham, North Carolina.

Mathew Reeves (M)

Department of Epidemiology and Biostatistics, Michigan State University, East Lansing.

Eric E Smith (EE)

Department of Clinical Neurosciences, University of Calgary, Calgary, Alberta, Canada.

Lee H Schwamm (LH)

Department of Neurology, Massachusetts General Hospital, Boston.
Yale School of Medicine, New Haven, Connecticut.

Deepak L Bhatt (DL)

Mount Sinai Heart, Icahn School of Medicine at Mount Sinai Health System, New Nork, New York.

Jeffrey L Saver (JL)

Department of Neurology, University of California, Los Angeles.

Gregg C Fonarow (GC)

Department of Medicine, University of California, Los Angeles.
Ahmanson-UCLA Cardiomyopathy Center, Los Angeles, California.

Eric D Peterson (ED)

Department of Medicine, UT Southwestern Medical Center, Dallas, Texas.

Ying Xian (Y)

Department of Neurology, UT Southwestern Medical Center, Dallas, Texas.
Department of Population and Data Science, UT Southwestern Medical Center, Dallas, Texas.

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