Characterization of Patients with Embolic Strokes of Undetermined Source in the NAVIGATE ESUS Randomized Trial
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu klinické zkoušky, fáze III, srovnávací studie, časopisecké články, multicentrická studie, randomizované kontrolované studie
Grantová podpora
K23 HL127227
NHLBI NIH HHS - United States
PubMed
29525076
PubMed Central
PMC6701183
DOI
10.1016/j.jstrokecerebrovasdis.2018.01.027
PII: S1052-3057(18)30043-0
Knihovny.cz E-zdroje
- Klíčová slova
- Embolic Stroke of Undetermined Source (ESUS), Stroke, aspirin, cerebral embolism, cryptogenic stroke, randomized trial, rivaroxaban, stroke prevention,
- MeSH
- Aspirin terapeutické užití MeSH
- cévní mozková příhoda diagnóza farmakoterapie epidemiologie MeSH
- dvojitá slepá metoda MeSH
- fibrinolytika terapeutické užití MeSH
- inhibitory agregace trombocytů terapeutické užití MeSH
- inhibitory faktoru Xa terapeutické užití MeSH
- intrakraniální embolie diagnóza farmakoterapie epidemiologie MeSH
- komorbidita MeSH
- lidé středního věku MeSH
- lidé MeSH
- rasové skupiny MeSH
- rivaroxaban terapeutické užití MeSH
- rizikové faktory MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- sexuální faktory MeSH
- tranzitorní ischemická ataka diagnóza farmakoterapie epidemiologie MeSH
- věkové faktory MeSH
- výsledek terapie MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- multicentrická studie MeSH
- randomizované kontrolované studie MeSH
- srovnávací studie MeSH
- Názvy látek
- Aspirin MeSH
- fibrinolytika MeSH
- inhibitory agregace trombocytů MeSH
- inhibitory faktoru Xa MeSH
- rivaroxaban MeSH
BACKGROUND: The New Approach Rivaroxaban Inhibition of Factor Xa in a Global Trial vs. ASA to Prevent Embolism in Embolic Stroke of Undetermined Source (NAVIGATE-ESUS) trial is a randomized phase-III trial comparing rivaroxaban versus aspirin in patients with recent ESUS. AIMS: We aimed to describe the baseline characteristics of this large ESUS cohort to explore relationships among key subgroups. METHODS: We enrolled 7213 patients at 459 sites in 31 countries. Prespecified subgroups for primary safety and efficacy analyses included age, sex, race, global region, stroke or transient ischemic attack prior to qualifying event, time to randomization, hypertension, and diabetes mellitus. RESULTS: Mean age was 66.9 ± 9.8 years; 24% were under 60 years. Older patients had more hypertension, coronary disease, and cancer. Strokes in older subjects were more frequently cortical and accompanied by radiographic evidence of prior infarction. Women comprised 38% of participants and were older than men. Patients from East Asia were oldest whereas those from Latin America were youngest. Patients in the Americas more frequently were on aspirin prior to the qualifying stroke. Acute cortical infarction was more common in the United States, Canada, and Western Europe, whereas prior radiographic infarctions were most common in East Asia. Approximately forty-five percent of subjects were enrolled within 30 days of the qualifying stroke, with earliest enrollments in Asia and Eastern Europe. CONCLUSIONS: NAVIGATE-ESUS is the largest randomized trial comparing antithrombotic strategies for secondary stroke prevention in patients with ESUS. The study population encompasses a broad array of patients across multiple continents and these subgroups provide ample opportunities for future research.
Bayer Healthcare Pharmaceuticals Parsipanny New Jersey USA
Bayer Pharma AG Berlin Germany
Bayer Pharma AG Wuppertal Germany
Bayer Vital Leverkusen Germany
Baylor College of Medicine Houston USA
Centro Hospitalar e Universitário de Coimbra Coimbra Portugal
Clinica Alemana de Santiago Universidad del Desarrollo Universidad de Chile Santiago Chile
Departament of Neuroscencies Hospital Universitari Germans Trias i Pujol Barcelona Spain
Department of Innere Medizin Universitätsspital Basel Basel Switzerland
Department of Medicine University of Thessaly Larissa Greece
Department of Neurology and Psychiatry Sapienza University of Rome Rome Italy
Department of Neurology Beijing Tiantan Hospital Capital Medical University Beijing China
Department of Neurology Bichat Hospital Paris France
Department of Neurology Helsinki University Central Hospital Helsinki Finland
Department of Neurology Selcuk University Konya Turkey
Department of Neurology Semmelweis University Budapest Hungary
Department of Neurology Seoul National University Hospital Seoul Korea
Department of Neurology University of Pennsylvania Philadelphia United States
Hospital St John of God Medical Faculty Sigmund Freud University Vienna Austria
Imperial College London London United Kingdom
Instituto Nacional de Neurologia y Neurocirugia Mexico D F Mexico
Irmandade da Santa Casa de Misericórdia de São Paulo Sao Paulo Brazil
Janssen Research and Development LLC Spring House United States
National University of Ireland Galway Ireland
Pirogov Russian National Research Medical University Moscow Russia
Population Health Research Institute Hamilton Canada
Population Health Research Institute McMaster University Hamilton Health Sciences Hamilton Canada
Sanno Hospital and Sanno Medical Center Tokyo Japan
Shaare Zedek Medical Center Jerusalem Israel
Thrombosis and Atherosclerosis Research Institute McMaster University Hamilton Canada
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