Branch atheromatous disease diagnosed as embolic stroke of undetermined source: A sub-analysis of NAVIGATE ESUS.


Journal

International journal of stroke : official journal of the International Stroke Society
ISSN: 1747-4949
Titre abrégé: Int J Stroke
Pays: United States
ID NLM: 101274068

Informations de publication

Date de publication:
12 2019
Historique:
pubmed: 28 5 2019
medline: 2 6 2020
entrez: 29 5 2019
Statut: ppublish

Résumé

Branch atheromatous disease (BAD) is distinctive from large and small arterial diseases, which is single subcortical infarction larger than lacunar stroke in the territories of deep perforators without relevant arterial stenosis. BAD meets the current criteria of embolic stroke of undetermined source. We performed an exploratory analysis of BAD in patients recruited to NAVIGATE embolic stroke of undetermined source, a randomized controlled trial to compare rivaroxaban and aspirin in embolic stroke of undetermined source patients. Among 3972 stroke patients in cerebral hemispheres with intracranial arterial imaging, 502 (12.6%) patients met the criteria for BAD. BAD was associated with younger age (years; OR: 0.97, 95% CI: 0.96-0.98), race (Asian; OR: 1.78, 95% CI: 1.44-2.21), region (Eastern Europe; OR: 2.49, 95% CI: 1.87-3.32), and higher National Institute of Health Stroke Scale (OR: 1.17, 95% CI: 1.12-1.22) at randomization. During follow-up, stroke or systemic embolism (2.5%/year vs. 6.2%/year, BAD was relatively common, especially in Asian and from Eastern Europe among embolic stroke of undetermined source patients. Stroke severity was higher at randomization but recurrence of stroke was fewer in BAD than non-BAD patients. The efficacy and safety of rivaroxaban and aspirin did not differ among BAD patients.

Sections du résumé

BACKGROUND
Branch atheromatous disease (BAD) is distinctive from large and small arterial diseases, which is single subcortical infarction larger than lacunar stroke in the territories of deep perforators without relevant arterial stenosis. BAD meets the current criteria of embolic stroke of undetermined source. We performed an exploratory analysis of BAD in patients recruited to NAVIGATE embolic stroke of undetermined source, a randomized controlled trial to compare rivaroxaban and aspirin in embolic stroke of undetermined source patients.
METHODS AND RESULTS
Among 3972 stroke patients in cerebral hemispheres with intracranial arterial imaging, 502 (12.6%) patients met the criteria for BAD. BAD was associated with younger age (years; OR: 0.97, 95% CI: 0.96-0.98), race (Asian; OR: 1.78, 95% CI: 1.44-2.21), region (Eastern Europe; OR: 2.49, 95% CI: 1.87-3.32), and higher National Institute of Health Stroke Scale (OR: 1.17, 95% CI: 1.12-1.22) at randomization. During follow-up, stroke or systemic embolism (2.5%/year vs. 6.2%/year,
CONCLUSIONS
BAD was relatively common, especially in Asian and from Eastern Europe among embolic stroke of undetermined source patients. Stroke severity was higher at randomization but recurrence of stroke was fewer in BAD than non-BAD patients. The efficacy and safety of rivaroxaban and aspirin did not differ among BAD patients.

Identifiants

pubmed: 31132967
doi: 10.1177/1747493019852177
doi:

Substances chimiques

Factor Xa Inhibitors 0
Platelet Aggregation Inhibitors 0
Rivaroxaban 9NDF7JZ4M3
Aspirin R16CO5Y76E

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

915-922

Auteurs

Shinichiro Uchiyama (S)

Clinical Research Center for Medicine, International University of Health and Welfare, Center for Brain and Cerebral Vessels, Sanno Hospital and Sanno Medical Center, Tokyo, Japan.

Kazunori Toyoda (K)

National Cerebral and Cardiovascular Center, Osaka, Japan.

Kazuo Kitagawa (K)

Department of Neurology, Tokyo Women's Medical University, Tokyo, Japan.

Yasushi Okada (Y)

National Hospital Organization Kyushu Medical Center, Fukuoka, Japan.

Sebastian Ameriso (S)

Institute for Neurological Research-FLENI, Buenos Aires, Argentina.

Hardi Mundl (H)

Bayer AG, Wuppertal, Germany.

Scott Berkowitz (S)

Bayer U.S. LLC, Pharmaceuticals Clinical Development Thrombosis, Whippany, NJ, USA.

Takashi Yamada (T)

Bayer Yakuhin, Ltd., Osaka, Japan.

Yan Yun Liu (YY)

Population Health Research Institute, Hamilton, Canada.

Robert G Hart (RG)

Population Health Research Institute, Hamilton, Canada.

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Classifications MeSH