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Sökning: WFRF:(Tanne David) > Andexanet for Facto...

Andexanet for Factor Xa Inhibitor-Associated Acute Intracerebral Hemorrhage

Connolly, Stuart J. (författare)
Population Health Research Institute, Ontario
Sharma, Mukul (författare)
Population Health Research Institute, Ontario
Cohen, Alexander T. (författare)
Guy's and St Thomas' NHS Foundation Trust
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Demchuk, Andrew M. (författare)
Członkowska, Anna (författare)
Institute of Psychiatry and Neurology, Warszawa
Lindgren, Arne G. (författare)
Lund University,Lunds universitet,Neurologi, Lund,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Klinisk strokeforskning,Forskargrupper vid Lunds universitet,Neurology, Lund,Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine,Clinical Stroke Research Group,Lund University Research Groups,Skåne University Hospital
Molina, Carlos A. (författare)
Vall d'Hebron University Hospital
Bereczki, Daniel (författare)
Semmelweis University
Toni, Danilo (författare)
Sapienza University of Rome
Seiffge, David J. (författare)
Bern University Hospital
Tanne, David (författare)
Technion - Israel Institute of Technology
Sandset, Else Charlotte (författare)
Oslo university hospital
Tsivgoulis, Georgios (författare)
National and Kapodistrian University of Athens
Christensen, Hanne (författare)
Bispebjerg Hospital
Beyer-Westendorf, Jan (författare)
University Hospitals Leuven
Coutinho, Jonathan M. (författare)
Academic Medical Center of University of Amsterdam (AMC)
Crowther, Mark (författare)
University Hospitals Leuven
Verhamme, Peter (författare)
University Hospitals Leuven
Amarenco, Pierre (författare)
Hopital Bichat-Claude-Bernard AP-HP
Roine, Risto O. (författare)
Turku University Hospital
Mikulik, Robert (författare)
Lemmens, Robin (författare)
University Hospitals Leuven,Catholic University of Leuven
Veltkamp, Roland (författare)
Alfried Krupp Krankenhaus,Imperial College London
Middeldorp, Saskia (författare)
Radboud University Medical Center
Robinson, Thompson G. (författare)
University of Leicester
Milling, Truman John (författare)
University of Houston,Dell Medical School
Tedim-Cruz, Vitor (författare)
University of Porto
Lang, Wilfried (författare)
Sigmund Freud Private University
Himmelmann, Anders (författare)
University Clinic Carl Gustav Carus at the TU Dresden,AstraZeneca, UK
Ladenvall, Per (författare)
AstraZeneca, UK
Knutsson, Mikael (författare)
AstraZeneca, UK
Ekholm, Ella (författare)
AstraZeneca, UK
Law, Andrew (författare)
Semmelweis University
Taylor, Amanda (författare)
Bispebjerg Hospital
Karyakina, Tetyana (författare)
Alfried Krupp Krankenhaus
Xu, Lizhen (författare)
University of Tübingen
Tsiplova, Kate (författare)
Radboud University Medical Center
Poli, Sven (författare)
University of Tübingen
Kallmünzer, Bernd (författare)
University Hospital Erlangen
Gumbinger, Christoph (författare)
University Hospital Heidelberg
Shoamanesh, Ashkan (författare)
Academic Medical Center of University of Amsterdam (AMC)
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 (creator_code:org_t)
 
2024
2024
Engelska 11 s.
Ingår i: New England Journal of Medicine. - 0028-4793. ; 390:19, s. 1745-1755
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background Patients with acute intracerebral hemorrhage who are receiving factor Xa inhibitors have a risk of hematoma expansion. The effect of andexanet alfa, an agent that reverses the effects of factor Xa inhibitors, on hematoma volume expansion has not been well studied. Methods We randomly assigned, in a 1:1 ratio, patients who had taken factor Xa inhibitors within 15 hours before having an acute intracerebral hemorrhage to receive andexanet or usual care. The primary end point was hemostatic efficacy, defined by expansion of the hematoma volume by 35% or less at 12 hours after baseline, an increase in the score on the National Institutes of Health Stroke Scale of less than 7 points (scores range from 0 to 42, with higher scores indicating worse neurologic deficit) at 12 hours, and no receipt of rescue therapy between 3 hours and 12 hours. Safety end points were thrombotic events and death. Results A total of 263 patients were assigned to receive andexanet, and 267 to receive usual care. Efficacy was assessed in an interim analysis that included 452 patients, and safety was analyzed in all 530 enrolled patients. Atrial fibrillation was the most common indication for factor Xa inhibitors. Of the patients receiving usual care, 85.5% received prothrombin complex concentrate. Hemostatic efficacy was achieved in 150 of 224 patients (67.0%) receiving andexanet and in 121 of 228 (53.1%) receiving usual care (adjusted difference, 13.4 percentage points; 95% confidence interval [CI], 4.6 to 22.2; P=0.003). The median reduction from baseline to the 1-to-2-hour nadir in anti-factor Xa activity was 94.5% with andexanet and 26.9% with usual care (P<0.001). Thrombotic events occurred in 27 of 263 patients (10.3%) receiving andexanet and in 15 of 267 (5.6%) receiving usual care (difference, 4.6 percentage points; 95% CI, 0.1 to 9.2; P=0.048); ischemic stroke occurred in 17 patients (6.5%) and 4 patients (1.5%), respectively. There were no appreciable differences between the groups in the score on the modified Rankin scale or in death within 30 days. Conclusions Among patients with intracerebral hemorrhage who were receiving factor Xa inhibitors, andexanet resulted in better control of hematoma expansion than usual care but was associated with thrombotic events, including ischemic stroke. (Funded by Alexion AstraZeneca Rare Disease and others; ANNEXA-I ClinicalTrials.gov number, NCT03661528.).

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Nyckelord

Coagulation
Emergency Medicine
Emergency Medicine General
Hematology/Oncology
Neurology/Neurosurgery
Stroke

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