Characteristics of Ischemic Versus Hemorrhagic Stroke in Patients Receiving Oral Anticoagulants: Results of the PASTA Study.

atrial fibrillation intracerebral hemorrhage ischemic stroke non-vitamin K antagonist oral anticoagulant vitamin K antagonist

Journal

Internal medicine (Tokyo, Japan)
ISSN: 1349-7235
Titre abrégé: Intern Med
Pays: Japan
ID NLM: 9204241

Informations de publication

Date de publication:
15 Mar 2022
Historique:
pubmed: 7 9 2021
medline: 19 3 2022
entrez: 6 9 2021
Statut: ppublish

Résumé

Objective Limited data exist regarding the comparative detailed clinical characteristics of patients with ischemic stroke (IS)/transient ischemic attack (TIA) and intracerebral hemorrhage (ICH) receiving oral anticoagulants (OACs). Methods The prospective analysis of stroke patients taking oral anticoagulants (PASTA) registry, a multicenter registry of 1,043 stroke patients receiving OACs [vitamin K antagonists (VKAs) or non-vitamin K antagonist oral anticoagulant (NOACs)] across 25 medical institutions throughout Japan, was used. Univariate and multivariable analyses were used to analyze differences in clinical characteristics between IS/TIA and ICH patients with atrial fibrillation (AF) who were registered in the PASTA registry. Results There was no significant differences in cardiovascular risk factors, such as hypertension, diabetes mellitus, dyslipidemia, smoking, or alcohol consumption (all p>0.05), between IS/TIA and ICH among both NOAC and VKA users. Cerebral microbleeds (CMBs) [odds ratio (OR), 4.77; p<0.0001] were independently associated with ICH, and high brain natriuretic peptide/N-terminal pro B-type natriuretic peptide levels (OR, 1.89; p=0.0390) were independently associated with IS/TIA among NOAC users. A history of ICH (OR, 13.59; p=0.0279) and the high prothrombin time-international normalized ratio (PT-INR) (OR, 1.17; p<0.0001) were independently associated with ICH, and a history of IS/TIA (OR, 3.37; 95% CI, 1.34-8.49; p=0.0101) and high D-dimer levels (OR, 2.47; 95% CI, 1.05-5.82; p=0.0377) were independently associated with IS/TIA among VKA users. Conclusion The presence of CMBs, a history of stroke, natriuretic peptide and D-dimer levels, and PT-INR may be useful for risk stratification of either IS/TIA or ICH development in patients with AF receiving OACs.

Identifiants

pubmed: 34483213
doi: 10.2169/internalmedicine.8113-21
pmc: PMC8987259
doi:

Substances chimiques

Anticoagulants 0
Vitamin K 12001-79-5

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

801-810

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Auteurs

Satoshi Suda (S)

Department of Neurology, Nippon Medical School, Japan.

Arata Abe (A)

Department of Neurology and Stroke Medicine, Tokyo Metropolitan Tama Medical Center, Japan.

Yasuyuki Iguchi (Y)

Department of Neurology, The Jikei University School of Medicine, Japan.

Yoshiki Yagita (Y)

Department of Stroke Medicine, Kawasaki Medical School, Japan.

Takao Kanzawa (T)

Department of Stroke Medicine, Institute of Brain and Blood Vessels, Mihara Memorial Hospital, Japan.

Seiji Okubo (S)

Department of Cerebrovascular Medicine, NTT Medical Center Tokyo, Japan.

Nobuyuki Ohara (N)

Department of Neurology, Kobe City Medical Center General Hospital, Japan.

Takayuki Mizunari (T)

Department of Neurosurgery, Nippon Medical School Chiba Hokusoh Hospital, Japan.

Mineo Yamazaki (M)

Department of Neurology, Nippon Medical School Chiba Hokusoh Hospital, Japan.

Nobuhito Nakajima (N)

Department of Neurology, Kitamurayama Hospital, Japan.

Kimito Kondo (K)

Department of Neurology, Hokuto Hospital, Japan.

Shigeru Fujimoto (S)

Division of Neurology, Department of Medicine, Jichi Medical University Hospital, Japan.

Takeshi Inoue (T)

Department of Stroke Medicine, Kawasaki Medical School General Medical Center, Japan.

Takeshi Iwanaga (T)

Department of Stroke Medicine, Japanese Red Cross Okayama Hospital, Japan.

Yuka Terasawa (Y)

Department of Neurology, Brain Attack Center Ota Memorial Hospital, Japan.

Kensaku Shibazaki (K)

Department of Stroke Medicine, Kurashiki Heisei Hospital, Japan.

Yu Kono (Y)

Department of Neurology, Fuji City General Hospital, Japan.

Makoto Nakajima (M)

Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Japan.

Masataka Nakajima (M)

Department of Neurology, Heisei-Tateishi Hospital, Japan.

Masahiro Mishina (M)

Department of Neuro-pathophysiological Imaging, Graduate School of Medicine, Nippon Medical School, Japan.

Koji Adachi (K)

Department of Neurological Surgery, Nippon Medical School Musashi-Kosugi Hospital, Japan.

Ichiro Imafuku (I)

Department of Neurology, Yokohama Rosai Hospital, Japan.

Koichi Nomura (K)

Department of Neurology, Shioda Hospital, Japan.

Takehiko Nagao (T)

Department of Neurology, Nippon Medical School Tama Nagayama Hospital, Japan.

Hiroshi Yaguchi (H)

Department of Neurology, The Jikei University Kashiwa Hospital, Japan.

Sadahisa Okamoto (S)

Department of Neurology, Omuta Tenryo Hospital, Japan.

Masato Osaki (M)

Department of Cerebrovascular Medicine, Steel Memorial Yawata Hospital, Japan.

Kazumi Kimura (K)

Department of Neurology, Nippon Medical School, Japan.

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