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Bridging Therapy With Heparin Before Starting Rivaroxaban in Ischemic Stroke or Transient Ischemic Attack With Non-Valvular Atrial Fibrillation.
Tokunaga, Keisuke; Yasaka, Masahiro; Toyoda, Kazunori; Mori, Etsuro; Hirano, Teruyuki; Hamasaki, Toshimitsu; Yamagami, Hiroshi; Nagao, Takehiko; Yoshimura, Shinichi; Uchiyama, Shinichiro; Minematsu, Kazuo.
Afiliação
  • Tokunaga K; Department of Cerebrovascular Medicine and Neurology, Clinical Research Institute, National Hospital Organization Kyushu Medical Center.
  • Yasaka M; Department of Cerebrovascular Medicine and Neurology, Clinical Research Institute, National Hospital Organization Kyushu Medical Center.
  • Toyoda K; Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center.
  • Mori E; Department of Behavioral Neurology and Neuropsychiatry, United Graduate School of Child Development, Osaka University.
  • Hirano T; Department of Stroke and Cerebrovascular Medicine, Kyorin University.
  • Hamasaki T; The George Washington University Biostatistics Center.
  • Yamagami H; Department of Stroke Neurology, National Hospital Organization Osaka National Hospital.
  • Nagao T; Department of Neurology, Nippon Medical School, Tama-Nagayama Hospital.
  • Yoshimura S; Department of Neurosurgery, Hyogo College of Medicine.
  • Uchiyama S; International University of Health and Welfare Director, Center for Brain and Cerebral Vessels, Sanno Medical Center.
  • Minematsu K; Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center.
Circ J ; 86(6): 958-963, 2022 05 25.
Article em En | MEDLINE | ID: mdl-34789635
BACKGROUND: The present observational study aimed to clarify the association between bridging therapy with heparin before starting rivaroxaban and clinical outcomes after ischemic stroke or transient ischemic attack (TIA) in patients with non-valvular atrial fibrillation (NVAF).Methods and Results: Patients with NVAF who experienced acute ischemic stroke or TIA of the middle cerebral artery territory and started rivaroxaban within 30 days after onset were enrolled and were followed up for 90 days. Outcome measures were ischemic events, major bleeding, their composite, and death or disability 90 days after onset. Ischemic events were defined as ischemic stroke, TIA, and systemic embolism. Of 1,308 analyzed patients, 638 received bridging therapy with unfractionated or low-molecular-weight heparin with a median of 10,000 IU/day. Associations between bridging therapy and ischemic events or major bleeding were not statistically significant individually, but the association between bridging therapy and their composite was statistically significant (multivariable-adjusted hazard ratio, 1.80; 95% confidence interval, 1.01-3.29). The association between bridging therapy and death or disability 90 days after onset was not statistically significant. CONCLUSIONS: The composite of ischemic events and major bleeding was more frequent in patients with NVAF who received bridging therapy with low-dose heparin than in those who started treatment directly with rivaroxaban after ischemic stroke or TIA.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Ataque Isquêmico Transitório / Acidente Vascular Cerebral / AVC Isquêmico Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Ataque Isquêmico Transitório / Acidente Vascular Cerebral / AVC Isquêmico Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article