Literature DB >> 30255970

Neuroimaging and clinical outcomes of oral anticoagulant-associated intracerebral hemorrhage.

Georgios Tsivgoulis1,2, Duncan Wilson3, Aristeidis H Katsanos1,4, João Sargento-Freitas5,6, Cláudia Marques-Matos7,8, Elsa Azevedo7,8, Tomohide Adachi9, Christian von der Brelie10, Yoshifusa Aizawa11, Hiroshi Abe11, Hirofumi Tomita12, Ken Okumura13, Joji Hagii14, David J Seiffge15, Vasileios-Arsenios Lioutas16, Christopher Traenka15, Panayiotis Varelas17, Ghazala Basir18, Christos Krogias19, Jan C Purrucker20, Vijay K Sharma21, Timolaos Rizos20, Robert Mikulik22, Oluwaseun A Sobowale23, Kristian Barlinn24, Hanne Sallinen25, Nitin Goyal2, Shin-Joe Yeh26, Theodore Karapanayiotides27, Teddy Y Wu28, Konstantinos Vadikolias29, Marc Ferrigno30, Georgios Hadjigeorgiou31, Rik Houben32, Sotirios Giannopoulos4, Floris H B M Schreuder32,33, Jason J Chang2, Luke A Perry34, Maximilian Mehdorn10, João-Pedro Marto35,36, João Pinho37, Jun Tanaka38, Marion Boulanger39, Rustam Al-Shahi Salman39, Hans R Jäger40, Clare Shakeshaft3, Yusuke Yakushiji38, Philip M C Choi34, Julie Staals32, Charlotte Cordonnier30, Jiann-Shing Jeng26, Roland Veltkamp41, Dar Dowlatshahi18, Stefan T Engelter15,42, Adrian R Parry-Jones23, Atte Meretoja25,43, Panayiotis D Mitsias17,44, Andrei V Alexandrov2, Gareth Ambler45, David J Werring3.   

Abstract

OBJECTIVE: Whether intracerebral hemorrhage (ICH) associated with non-vitamin K antagonist oral anticoagulants (NOAC-ICH) has a better outcome compared to ICH associated with vitamin K antagonists (VKA-ICH) is uncertain.
METHODS: We performed a systematic review and individual patient data meta-analysis of cohort studies comparing clinical and radiological outcomes between NOAC-ICH and VKA-ICH patients. The primary outcome measure was 30-day all-cause mortality. All outcomes were assessed in multivariate regression analyses adjusted for age, sex, ICH location, and intraventricular hemorrhage extension.
RESULTS: We included 7 eligible studies comprising 219 NOAC-ICH and 831 VKA-ICH patients (mean age = 77 years, 52.5% females). The 30-day mortality was similar between NOAC-ICH and VKA-ICH (24.3% vs 26.5%; hazard ratio = 0.94, 95% confidence interval [CI] = 0.67-1.31). However, in multivariate analyses adjusting for potential confounders, NOAC-ICH was associated with lower admission National Institutes of Health Stroke Scale (NIHSS) score (linear regression coefficient = -2.83, 95% CI = -5.28 to -0.38), lower likelihood of severe stroke (NIHSS > 10 points) on admission (odds ratio [OR] = 0.50, 95% CI = 0.30-0.84), and smaller baseline hematoma volume (linear regression coefficient = -0.24, 95% CI = -0.47 to -0.16). The two groups did not differ in the likelihood of baseline hematoma volume < 30cm3 (OR = 1.14, 95% CI = 0.81-1.62), hematoma expansion (OR = 0.97, 95% CI = 0.63-1.48), in-hospital mortality (OR = 0.73, 95% CI = 0.49-1.11), functional status at discharge (common OR = 0.78, 95% CI = 0.57-1.07), or functional status at 3 months (common OR = 1.03, 95% CI = 0.75-1.43).
INTERPRETATION: Although functional outcome at discharge, 1 month, or 3 months was comparable after NOAC-ICH and VKA-ICH, patients with NOAC-ICH had smaller baseline hematoma volumes and less severe acute stroke syndromes. Ann Neurol 2018;84:702-712.
© 2018 American Neurological Association.

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Year:  2018        PMID: 30255970     DOI: 10.1002/ana.25342

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


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