Volume and functional outcome of intracerebral hemorrhage according to oral anticoagulant type

Duncan Wilson(University College London Hospitals NHS Foundation Trust), Andreas Charidimou(University College London Hospitals NHS Foundation Trust), Clare Shakeshaft(University College London Hospitals NHS Foundation Trust), Gareth Ambler(University College London Hospitals NHS Foundation Trust), Mark White(University College London Hospitals NHS Foundation Trust), Hannah Cohen(University College London Hospitals NHS Foundation Trust), Tarek Yousry(University College London Hospitals NHS Foundation Trust), Rustam Al‐Shahi Salman(University College London Hospitals NHS Foundation Trust), Gregory Y.H. Lip(University College London Hospitals NHS Foundation Trust), Martin M. Brown(University College London Hospitals NHS Foundation Trust), Hans Rolf Jäger(University College London Hospitals NHS Foundation Trust), David J. Werring(University College London Hospitals NHS Foundation Trust), On behalf of the CROMIS-2 collaborators, Louise Shaw, Jane Sword, Azlisham Mohd, Pankaj Sharma, Deborah F. Kelly, Frances Harrington, Marc Randall, Matthew Smith, Karim Mahawish, Abduelbaset Elmarim, Bernard Esisi, Claire Cullen, Arumug Nallasivam, Christopher Price, Adrian Barry, Christine Roffe, John Coyle, Ahamad Hassan, Caroline Lovelock, Jonathan Birns(University College London Hospitals NHS Foundation Trust), David Cohen(University College London Hospitals NHS Foundation Trust), Lakshmanan Sekaran, Adrian Parry‐Jones, Anthea Parry(University College London Hospitals NHS Foundation Trust), David Hargroves, Harald Proschel, Prabel Datta, Khaled Darawil, Aravindakshan Manoj, Mathew Burn, C. C. Patterson, Elio Giallombardo, Nigel Smyth, Syed Mansoor, Ijaz Anwar, Rachel Marsh, Sissi Ispoglou, Dinesh Chadha, Mathuri Prabhakaran, Sanjeevikumar Meenakishundaram, Janice O’Connell, Jon Scott, Vinodh Krishnamurthy, Prasanna Aghoram, Michael McCormick, Paul O’Mahony(University College London Hospitals NHS Foundation Trust), Martin Cooper, Lillian Choy, Peter Wilkinson, Simon Leach, Sarah Caine, Ilse Burger, Gunaratam Gunathilagan, Paul Guyler, Hedley Emsley, Michelle Davis, Dulka Manawadu, Kath Pasco, Maam Mamun, Robert Luder, Mahmud Sajid, Ijaz Anwar, James Okwera, Julie Staals, Elizabeth A. Warburton, Kari Saastamoinen, Timothy J. England, Janet Putterill, Enrico Flossman, Mick Power, Krishna Dani(University College London Hospitals NHS Foundation Trust), David Mangion, Appu Suman, John Corrigan, Enas Lawrence, Djamil Vahidassr
Neurology
December 31, 2015
Cited by 115Open Access
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Abstract

OBJECTIVE: To compare intracerebral hemorrhage (ICH) volume and clinical outcome of non-vitamin K oral anticoagulants (NOAC)-associated ICH to warfarin-associated ICH. METHODS: In this multicenter cross-sectional observational study of patients with anticoagulant-associated ICH, consecutive patients with NOAC-ICH were compared to those with warfarin-ICH selected from a population of 344 patients with anticoagulant-associated ICH. ICH volume was measured by an observer blinded to clinical details. Outcome measures were ICH volume and clinical outcome adjusted for confounding factors. RESULTS: We compared 11 patients with NOAC-ICH to 52 patients with warfarin-ICH. The median ICH volume was 2.4 mL (interquartile range [IQR] 0.3-5.4 mL) for NOAC-ICH vs 8.9 mL (IQR 4.0-21.3 mL) for warfarin-ICH (p = 0.0028). In univariate linear regression, use of warfarin (difference in cube root volume 1.61; 95% confidence interval [CI] 0.69 to 2.53) and lobar ICH location (compared with nonlobar ICH; difference in cube root volume 1.52; 95% CI 2.20 to 0.85) were associated with larger ICH volumes. In multivariable linear regression adjusting for confounding factors (sex, hypertension, previous ischemic stroke, white matter disease burden, and premorbid modified Rankin Scale score [mRS]), warfarin use remained independently associated with larger ICH (cube root) volumes (coefficient 0.64; 95% CI 0.24 to 1.25; p = 0.042). Ordered logistic regression showed an increased odds of a worse clinical outcome (as measured by discharge mRS) in warfarin-ICH compared with NOAC-ICH: odds ratio 4.46 (95% CI 1.10 to 18.14; p = 0.037). CONCLUSIONS: In this small prospective observational study, patients with NOAC-associated ICH had smaller ICH volumes and better clinical outcomes compared with warfarin-associated ICH.


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