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  3. Intracerebral haemorrhage in patients taking different types of oral anticoagulants: a pooled individual patient data analysis from two national stroke registries.
 

Intracerebral haemorrhage in patients taking different types of oral anticoagulants: a pooled individual patient data analysis from two national stroke registries.

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BORIS DOI
10.48350/192780
Publisher DOI
10.1136/svn-2023-002813
PubMed ID
38336370
Description
BACKGROUND

We investigated outcomes in patients with intracerebral haemorrhage (ICH) according to prior anticoagulation treatment with Vitamin K antagonists (VKAs), direct oral anticoagulants (DOACs) or no anticoagulation.

METHODS

This is an individual patient data study combining two prospective national stroke registries from Switzerland and Norway (2013-2019). We included all consecutive patients with ICH from both registries. The main outcomes were favourable functional outcome (modified Rankin Scale 0-2) and mortality at 3 months.

RESULTS

Among 11 349 patients with ICH (mean age 73.6 years; 47.6% women), 1491 (13.1%) were taking VKAs and 1205 (10.6%) DOACs (95.2% factor Xa inhibitors). The median percentage of patients on prior anticoagulation was 23.7 (IQR 22.6-25.1) with VKAs decreasing (from 18.3% to 7.6%) and DOACs increasing (from 3.0% to 18.0%) over time. Prior VKA therapy (n=209 (22.3%); adjusted ORs (aOR), 0.64; 95% CI, 0.49 to 0.84) and prior DOAC therapy (n=184 (25.7%); aOR, 0.64; 95% CI, 0.47 to 0.87) were independently associated with lower odds of favourable outcome compared with patients without anticoagulation (n=2037 (38.8%)). Prior VKA therapy (n=720 (49.4%); aOR, 1.71; 95% CI, 1.41 to 2.08) and prior DOAC therapy (n=460 (39.7%); aOR, 1.28; 95% CI, 1.02 to 1.60) were independently associated with higher odds of mortality compared with patients without anticoagulation (n=2512 (30.2%)).

CONCLUSIONS

The spectrum of anticoagulation-associated ICH changed over time. Compared with patients without prior anticoagulation, prior VKA treatment and prior DOAC treatment were independently associated with lower odds of favourable outcome and higher odds of mortality at 3 months. Specific reversal agents unavailable during the study period might improve outcomes of DOAC-associated ICH in the future.
Date of Publication
2024-12-30
Publication Type
Article
Subject(s)
600 - Technology::610 - Medicine & health
Keyword(s)
Anticoagulants Hemorrhage Stroke
Language(s)
en
Contributor(s)
Siepen, Bernhard Matthias
Universitätsklinik für Neurologie
Forfang, Elisabeth
Branca, Mattia
Clinical Trials Unit Bern (CTU) - Statistics & Methodology (Bütikofer)
Department of Clinical Research (DCR)
Drop, Boudewijn Roderick Hinne
Universitätsklinik für Neurologie
Müller, Madlaine
Universitätsklinik für Neurologie
Göldlin, Martina Béatriceorcid-logo
Universitätsklinik für Neurologie
Katan, Mira
Michel, Patrik
Cereda, Carlo
Medlin, Friedrich
Peters, Nils
Renaud, Susanne
Niederhauser, Julien
Carrera, Emmanuel
Kahles, Timo
Kägi, Georg Heinrich
Universitätsklinik für Neurologie
Bolognese, Manuel
Salmen, Stephan
Mono, Marie-Luise
Polymeris, Alexandros A
Wegener, Susanne
Z'Graggen, Werner Josef
Universitätsklinik für Neurochirurgie
Universitätsklinik für Neurologie
Kaesmacher, Johannes
Universitätsinstitut für Diagnostische und Interventionelle Neuroradiologie (DIN)
Schaerer, Michael
Rodic, Biljana
Kristoffersen, Espen Saxhaug
Larsen, Kristin T
Wyller, Torgeir Bruun
Volbers, Bastian
Universitätsklinik für Neurologie
Meinel, Thomas Raphaelorcid-logo
Universitätsklinik für Neurologie
Arnold, Marcel
Universitätsklinik für Neurologie
Engelter, Stefan T
Bonati, Leo H
Fischer, Urs Martin
Universitätsklinik für Neurologie
Rønning, Ole Morten
Seiffge, David Julian
Universitätsklinik für Neurologie
Additional Credits
Universitätsklinik für Neurochirurgie
Universitätsinstitut für Diagnostische und Interventionelle Neuroradiologie (DIN)
Universitätsklinik für Neurologie
Clinical Trials Unit Bern (CTU) - Statistics & Methodology (Bütikofer)
Series
Stroke and vascular neurology
Publisher
BMJ
ISSN
2059-8696
Access(Rights)
open.access
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