Anticoagulant Reversal, Blood Pressure Levels, and Anticoagulant Resumption in Patients With Anticoagulation-Related Intracerebral Hemorrhage

Joji B. Kuramatsu(Friedrich-Alexander-Universität Erlangen-Nürnberg), Stefan T. Gerner(Friedrich-Alexander-Universität Erlangen-Nürnberg), Peter D. Schellinger(Johannes Wesling Klinikum Minden), Jörg Glahn(Johannes Wesling Klinikum Minden), Matthias Endres(German Centre for Cardiovascular Research), Jan Sobesky(Charité - Universitätsmedizin Berlin), Julia Flechsenhar(Charité - Universitätsmedizin Berlin), Hermann Neugebauer(Charité - Universitätsmedizin Berlin), Eric Jüttler(Charité - Universitätsmedizin Berlin), Armin Grau(Klinikum Ludwigshafen), Frederick Palm(Klinikum Ludwigshafen), Joachim Röther(Asklepios Klinik Altona), Peter Michels(Asklepios Klinik Altona), Gerhard F. Hamann(Helios Dr. Horst Schmidt Kliniken Wiesbaden), J. Hüwel(Helios Dr. Horst Schmidt Kliniken Wiesbaden), Georg Hagemann(Helios Hospital Berlin-Buch), Beatrice Barber(Helios Hospital Berlin-Buch), Christoph Terborg(Asklepios Klinik St. Georg), Frank Trostdorf(Asklepios Klinik St. Georg), Hansjörg Bäzner(Klinikum Stuttgart), Aletta Roth(Klinikum Stuttgart), Johannes C. Wöhrle(Katholisches Klinikum Koblenz), Moritz Keller(Katholisches Klinikum Koblenz), Michael Schwarz(Klinikum Dortmund), Gernot Reimann(Klinikum Dortmund), Jens Volkmann(University of Würzburg), Wolfgang Müllges(University of Würzburg), Peter Kraft(University of Würzburg), Joseph Claßen(Leipzig University), Carsten Hobohm(Leipzig University), Markus Horn, Angelika Milewski, Heinz Reichmann(Technische Universität Dresden), Hauke Schneider(Technische Universität Dresden), Eik Schimmel(Technische Universität Dresden), Gereon R. Fink(University of Cologne), Christian Dohmen(University of Cologne), Henning Stetefeld(University of Cologne), Otto W. Witte(Friedrich Schiller University Jena), Albrecht Günther(Friedrich Schiller University Jena), Tobias Neumann‐Haefelin, Andras E. Racs, Martin Nueckel(Nuremberg Hospital), Frank Erbguth(Nuremberg Hospital), Stephan Kloska(Friedrich-Alexander-Universität Erlangen-Nürnberg), Arnd Dörfler(Friedrich-Alexander-Universität Erlangen-Nürnberg), Martin Köhrmann(Friedrich-Alexander-Universität Erlangen-Nürnberg), Stefan Schwab(Friedrich-Alexander-Universität Erlangen-Nürnberg), Hagen B. Huttner(Friedrich-Alexander-Universität Erlangen-Nürnberg)
JAMA
February 24, 2015
Cited by 558

Abstract

IMPORTANCE: Although use of oral anticoagulants (OACs) is increasing, there is a substantial lack of data on how to treat OAC-associated intracerebral hemorrhage (ICH). OBJECTIVE: To assess the association of anticoagulation reversal and blood pressure (BP) with hematoma enlargement and the effects of OAC resumption. DESIGN, SETTING, AND PARTICIPANTS: Retrospective cohort study at 19 German tertiary care centers (2006-2012) including 1176 individuals for analysis of long-term functional outcome, 853 for analysis of hematoma enlargement, and 719 for analysis of OAC resumption. EXPOSURES: Reversal of anticoagulation during acute phase, systolic BP at 4 hours, and reinitiation of OAC for long-term treatment. MAIN OUTCOMES AND MEASURES: Frequency of hematoma enlargement in relation to international normalized ratio (INR) and BP. Incidence analysis of ischemic and hemorrhagic events with or without OAC resumption. Factors associated with favorable (modified Rankin Scale score, 0-3) vs unfavorable functional outcome. RESULTS: Hemorrhage enlargement occurred in 307 of 853 patients (36.0%). Reduced rates of hematoma enlargement were associated with reversal of INR levels <1.3 within 4 hours after admission (43/217 [19.8%]) vs INR of ≥1.3 (264/636 [41.5%]; P < .001) and systolic BP <160 mm Hg at 4 hours (167/504 [33.1%]) vs ≥160 mm Hg (98/187 [52.4%]; P < .001). The combination of INR reversal <1.3 within 4 hours and systolic BP of <160 mm Hg at 4 hours was associated with lower rates of hematoma enlargement (35/193 [18.1%] vs 220/498 [44.2%] not achieving these values; OR, 0.28; 95% CI, 0.19-0.42; P < .001) and lower rates of in-hospital mortality (26/193 [13.5%] vs 103/498 [20.7%]; OR, 0.60; 95% CI, 0.37-0.95; P = .03). OAC was resumed in 172 of 719 survivors (23.9%). OAC resumption showed fewer ischemic complications (OAC: 9/172 [5.2%] vs no OAC: 82/547 [15.0%]; P < .001) and not significantly different hemorrhagic complications (OAC: 14/172 [8.1%] vs no OAC: 36/547 [6.6%]; P = .48). Propensity-matched survival analysis in patients with atrial fibrillation who restarted OAC showed a decreased HR of 0.258 (95% CI, 0.125-0.534; P < .001) for long-term mortality. Functional long-term outcome was unfavorable in 786 of 1083 patients (72.6%). CONCLUSIONS AND RELEVANCE: Among patients with OAC-associated ICH, reversal of INR <1.3 within 4 hours and systolic BP <160 mm Hg at 4 hours were associated with lower rates of hematoma enlargement, and resumption of OAC therapy was associated with lower risk of ischemic events. These findings require replication and assessment in prospective studies. TRIAL REGISTRATION: clinicaltrials.gov Identifier: NCT01829581.


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