Oral Anticoagulation and Functional Outcome after Intracerebral Hemorrhage

Alessandro Biffi(Massachusetts General Hospital), Joji B. Kuramatsu(Friedrich-Alexander-Universität Erlangen-Nürnberg), Audrey C. Leasure(Yale University), Hooman Kamel(Cornell University), Christina Kourkoulis(Massachusetts General Hospital), Kristin Schwab(Massachusetts General Hospital), Alison Ayres(Massachusetts General Hospital), Jordan Elm(Medical University of South Carolina), M. Edip Gurol(Massachusetts General Hospital), Steven M. Greenberg(Massachusetts General Hospital), Anand Viswanathan(Massachusetts General Hospital), Christopher D. Anderson(Massachusetts General Hospital), Stefan Schwab(Friedrich-Alexander-Universität Erlangen-Nürnberg), Jonathan Rosand(Massachusetts General Hospital), Fernando D. Testai(Illinois College), Daniel Woo(University of Cincinnati), Hagen B. Huttner(Friedrich-Alexander-Universität Erlangen-Nürnberg), Kevin N. Sheth(Yale University)
Annals of Neurology
October 13, 2017
Cited by 151Open Access
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Abstract

OBJECTIVE: Oral anticoagulation treatment (OAT) resumption is a therapeutic dilemma in intracerebral hemorrhage (ICH) care, particularly for lobar hemorrhages related to amyloid angiopathy. We sought to determine whether OAT resumption after ICH is associated with long-term outcome, accounting for ICH location (ie, lobar vs nonlobar). METHODS: We meta-analyzed individual patient data from: (1) the multicenter RETRACE study (n = 542), (2) a U.S.-based single-center ICH study (n = 261), and (3) the Ethnic/Racial Variations of Intracerebral Hemorrhage study (n = 209). We determined whether, within 1 year from ICH, OAT resumption was associated with: (1) mortality, (2) favorable functional outcome (modified Rankin Scale = 0-3), and (3) stroke incidence. We separately analyzed nonlobar and lobar ICH cases using propensity score matching and Cox regression models. RESULTS: We included 1,012 OAT-related ICH survivors (633 nonlobar and 379 lobar). Among nonlobar ICH survivors, 178/633 (28%) resumed OAT, whereas 86/379 (23%) lobar ICH survivors did. In multivariate analyses, OAT resumption after nonlobar ICH was associated with decreased mortality (hazard ratio [HR] = 0.25, 95% confidence interval [CI] = 0.14-0.44, p < 0.0001) and improved functional outcome (HR = 4.22, 95% CI = 2.57-6.94, p < 0.0001). OAT resumption after lobar ICH was also associated with decreased mortality (HR = 0.29, 95% CI = 0.17-0.45, p < 0.0001) and favorable functional outcome (HR = 4.08, 95% CI = 2.48-6.72, p < 0.0001). Furthermore, OAT resumption was associated with decreased all-cause stroke incidence in both lobar and nonlobar ICH (both p < 0.01). INTERPRETATION: These results suggest novel evidence of an association between OAT resumption and outcome following ICH, regardless of hematoma location. These findings support conducting randomized trials to explore risks and benefits of OAT resumption after ICH. Ann Neurol 2017;82:755-765.


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