Characteristics in Non–Vitamin K Antagonist Oral Anticoagulant–Related Intracerebral Hemorrhage

BACKGROUND AND PURPOSE—Given inconclusive studies, it is debated whether clinical and imaging characteristics, as well as functional outcome, differ among patients with intracerebral hemorrhage (ICH) related to vitamin K antagonists (VKA) versus non–vitamin K antagonist (NOAC)-related ICH. Notably,...

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Veröffentlicht in:Stroke (1970) 2019-06, Vol.50 (6), p.1392-1402
Hauptverfasser: Gerner, Stefan T, Kuramatsu, Joji B, Sembill, Jochen A, Sprügel, Maximilian I, Hagen, Manuel, Knappe, Ruben U, Endres, Matthias, Haeusler, Karl Georg, Sobesky, Jan, Schurig, Johannes, Zweynert, Sarah, Bauer, Miriam, Vajkoczy, Peter, Ringleb, Peter A, Purrucker, Jan C, Rizos, Timolaos, Volkmann, Jens, Müllges, Wolfgang, Kraft, Peter, Schubert, Anna-Lena, Erbguth, Frank, Nueckel, Martin, Schellinger, Peter D, Glahn, Jörg, Knappe, Ulrich J, Fink, Gereon R, Dohmen, Christian, Stetefeld, Henning, Fisse, Anna Lena, Minnerup, Jens, Hagemann, Georg, Rakers, Florian, Reichmann, Heinz, Schneider, Hauke, Rahmig, Jan, Ludolph, Albert Christian, Stösser, Sebastian, Neugebauer, Hermann, Röther, Joachim, Michels, Peter, Schwarz, Michael, Reimann, Gernot, Bäzner, Hansjörg, Schwert, Henning, Claßen, Joseph, Michalski, Dominik, Grau, Armin, Palm, Frederick, Urbanek, Christian, Wöhrle, Johannes C, Alshammari, Fahid, Horn, Markus, Bahner, Dirk, Witte, Otto W, Günther, Albrecht, Hamann, Gerhard F, Engelhorn, Tobias, Lücking, Hannes, Dörfler, Arnd, Schwab, Stefan, Huttner, Hagen B
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container_end_page 1402
container_issue 6
container_start_page 1392
container_title Stroke (1970)
container_volume 50
creator Gerner, Stefan T
Kuramatsu, Joji B
Sembill, Jochen A
Sprügel, Maximilian I
Hagen, Manuel
Knappe, Ruben U
Endres, Matthias
Haeusler, Karl Georg
Sobesky, Jan
Schurig, Johannes
Zweynert, Sarah
Bauer, Miriam
Vajkoczy, Peter
Ringleb, Peter A
Purrucker, Jan C
Rizos, Timolaos
Volkmann, Jens
Müllges, Wolfgang
Kraft, Peter
Schubert, Anna-Lena
Erbguth, Frank
Nueckel, Martin
Schellinger, Peter D
Glahn, Jörg
Knappe, Ulrich J
Fink, Gereon R
Dohmen, Christian
Stetefeld, Henning
Fisse, Anna Lena
Minnerup, Jens
Hagemann, Georg
Rakers, Florian
Reichmann, Heinz
Schneider, Hauke
Rahmig, Jan
Ludolph, Albert Christian
Stösser, Sebastian
Neugebauer, Hermann
Röther, Joachim
Michels, Peter
Schwarz, Michael
Reimann, Gernot
Bäzner, Hansjörg
Schwert, Henning
Claßen, Joseph
Michalski, Dominik
Grau, Armin
Palm, Frederick
Urbanek, Christian
Wöhrle, Johannes C
Alshammari, Fahid
Horn, Markus
Bahner, Dirk
Witte, Otto W
Günther, Albrecht
Hamann, Gerhard F
Engelhorn, Tobias
Lücking, Hannes
Dörfler, Arnd
Schwab, Stefan
Huttner, Hagen B
description BACKGROUND AND PURPOSE—Given inconclusive studies, it is debated whether clinical and imaging characteristics, as well as functional outcome, differ among patients with intracerebral hemorrhage (ICH) related to vitamin K antagonists (VKA) versus non–vitamin K antagonist (NOAC)-related ICH. Notably, clinical characteristics according to different NOAC agents and dosages are not established. METHODS—Multicenter observational cohort study integrating individual patient data of 1328 patients with oral anticoagulation–associated ICH, including 190 NOAC-related ICH patients, recruited from 2011 to 2015 at 19 tertiary centers across Germany. Imaging, clinical characteristics, and 3-months modified Rankin Scale (mRS) outcomes were compared in NOAC- versus VKA-related ICH patients. Propensity score matching was conducted to adjust for clinically relevant differences in baseline parameters. Subgroup analyses were performed regarding NOAC agent, dosing and present clinically relevant anticoagulatory activity (last intake 30 ng/mL). RESULTS—Despite older age in NOAC patients, there were no relevant differences in clinical and hematoma characteristics between NOAC- and VKA-related ICH regarding baseline hematoma volume (median [interquartile range]NOAC, 14.7 [5.1–42.3] mL versus VKA, 16.4 [5.8–40.6] mL; P=0.33), rate of hematoma expansion (NOAC, 49/146 [33.6%] versus VKA, 235/688 [34.2%]; P=0.89), and the proportion of patients with unfavorable outcome at 3 months (mRS, 4–6NOAC 126/179 [70.4%] versus VKA 473/682 [69.4%]; P=0.79). Subgroup analyses revealed that NOAC patients with clinically relevant anticoagulatory effect had higher rates of intraventricular hemorrhage (n/N [%]present 52/109 [47.7%] versus absent 9/35 [25.7%]; P=0.022) and hematoma expansion (present 35/90 [38.9%] versus absent 5/30 [16.7%]; P=0.040), whereas type of NOAC agent or different NOAC-dosing regimens did not result in relevant differences in imaging characteristics or outcome. CONCLUSIONS—If effectively anticoagulated, there are no differences in hematoma characteristics and functional outcome among patients with NOAC- or VKA-related ICH. CLINICAL TRIAL REGISTRATION—URLhttps://www.clinicaltrials.gov. Unique identifierNCT03093233.
doi_str_mv 10.1161/STROKEAHA.118.023492
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Notably, clinical characteristics according to different NOAC agents and dosages are not established. METHODS—Multicenter observational cohort study integrating individual patient data of 1328 patients with oral anticoagulation–associated ICH, including 190 NOAC-related ICH patients, recruited from 2011 to 2015 at 19 tertiary centers across Germany. Imaging, clinical characteristics, and 3-months modified Rankin Scale (mRS) outcomes were compared in NOAC- versus VKA-related ICH patients. Propensity score matching was conducted to adjust for clinically relevant differences in baseline parameters. Subgroup analyses were performed regarding NOAC agent, dosing and present clinically relevant anticoagulatory activity (last intake &lt;12h/24h or NOAC level &gt;30 ng/mL). RESULTS—Despite older age in NOAC patients, there were no relevant differences in clinical and hematoma characteristics between NOAC- and VKA-related ICH regarding baseline hematoma volume (median [interquartile range]NOAC, 14.7 [5.1–42.3] mL versus VKA, 16.4 [5.8–40.6] mL; P=0.33), rate of hematoma expansion (NOAC, 49/146 [33.6%] versus VKA, 235/688 [34.2%]; P=0.89), and the proportion of patients with unfavorable outcome at 3 months (mRS, 4–6NOAC 126/179 [70.4%] versus VKA 473/682 [69.4%]; P=0.79). Subgroup analyses revealed that NOAC patients with clinically relevant anticoagulatory effect had higher rates of intraventricular hemorrhage (n/N [%]present 52/109 [47.7%] versus absent 9/35 [25.7%]; P=0.022) and hematoma expansion (present 35/90 [38.9%] versus absent 5/30 [16.7%]; P=0.040), whereas type of NOAC agent or different NOAC-dosing regimens did not result in relevant differences in imaging characteristics or outcome. CONCLUSIONS—If effectively anticoagulated, there are no differences in hematoma characteristics and functional outcome among patients with NOAC- or VKA-related ICH. CLINICAL TRIAL REGISTRATION—URLhttps://www.clinicaltrials.gov. 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Notably, clinical characteristics according to different NOAC agents and dosages are not established. METHODS—Multicenter observational cohort study integrating individual patient data of 1328 patients with oral anticoagulation–associated ICH, including 190 NOAC-related ICH patients, recruited from 2011 to 2015 at 19 tertiary centers across Germany. Imaging, clinical characteristics, and 3-months modified Rankin Scale (mRS) outcomes were compared in NOAC- versus VKA-related ICH patients. Propensity score matching was conducted to adjust for clinically relevant differences in baseline parameters. Subgroup analyses were performed regarding NOAC agent, dosing and present clinically relevant anticoagulatory activity (last intake &lt;12h/24h or NOAC level &gt;30 ng/mL). RESULTS—Despite older age in NOAC patients, there were no relevant differences in clinical and hematoma characteristics between NOAC- and VKA-related ICH regarding baseline hematoma volume (median [interquartile range]NOAC, 14.7 [5.1–42.3] mL versus VKA, 16.4 [5.8–40.6] mL; P=0.33), rate of hematoma expansion (NOAC, 49/146 [33.6%] versus VKA, 235/688 [34.2%]; P=0.89), and the proportion of patients with unfavorable outcome at 3 months (mRS, 4–6NOAC 126/179 [70.4%] versus VKA 473/682 [69.4%]; P=0.79). Subgroup analyses revealed that NOAC patients with clinically relevant anticoagulatory effect had higher rates of intraventricular hemorrhage (n/N [%]present 52/109 [47.7%] versus absent 9/35 [25.7%]; P=0.022) and hematoma expansion (present 35/90 [38.9%] versus absent 5/30 [16.7%]; P=0.040), whereas type of NOAC agent or different NOAC-dosing regimens did not result in relevant differences in imaging characteristics or outcome. CONCLUSIONS—If effectively anticoagulated, there are no differences in hematoma characteristics and functional outcome among patients with NOAC- or VKA-related ICH. CLINICAL TRIAL REGISTRATION—URLhttps://www.clinicaltrials.gov. Unique identifierNCT03093233.</description><subject>Administration, Oral</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anticoagulants - administration &amp; dosage</subject><subject>Cerebral Hemorrhage - diagnostic imaging</subject><subject>Cerebral Hemorrhage - drug therapy</subject><subject>Cerebral Hemorrhage - epidemiology</subject><subject>Female</subject><subject>Fibrinolytic Agents - administration &amp; dosage</subject><subject>Germany - epidemiology</subject><subject>Humans</subject><subject>Male</subject><subject>Retrospective Studies</subject><subject>Vitamin K - antagonists &amp; 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Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201906</creationdate><title>Characteristics in Non–Vitamin K Antagonist Oral Anticoagulant–Related Intracerebral Hemorrhage</title><author>Gerner, Stefan T ; Kuramatsu, Joji B ; Sembill, Jochen A ; Sprügel, Maximilian I ; Hagen, Manuel ; Knappe, Ruben U ; Endres, Matthias ; Haeusler, Karl Georg ; Sobesky, Jan ; Schurig, Johannes ; Zweynert, Sarah ; Bauer, Miriam ; Vajkoczy, Peter ; Ringleb, Peter A ; Purrucker, Jan C ; Rizos, Timolaos ; Volkmann, Jens ; Müllges, Wolfgang ; Kraft, Peter ; Schubert, Anna-Lena ; Erbguth, Frank ; Nueckel, Martin ; Schellinger, Peter D ; Glahn, Jörg ; Knappe, Ulrich J ; Fink, Gereon R ; Dohmen, Christian ; Stetefeld, Henning ; Fisse, Anna Lena ; Minnerup, Jens ; Hagemann, Georg ; Rakers, Florian ; Reichmann, Heinz ; Schneider, Hauke ; Rahmig, Jan ; Ludolph, Albert Christian ; Stösser, Sebastian ; Neugebauer, Hermann ; Röther, Joachim ; Michels, Peter ; Schwarz, Michael ; Reimann, Gernot ; Bäzner, Hansjörg ; Schwert, Henning ; Claßen, Joseph ; Michalski, Dominik ; Grau, Armin ; Palm, Frederick ; Urbanek, Christian ; Wöhrle, Johannes C ; Alshammari, Fahid ; Horn, Markus ; Bahner, Dirk ; Witte, Otto W ; Günther, Albrecht ; Hamann, Gerhard F ; Engelhorn, Tobias ; Lücking, Hannes ; Dörfler, Arnd ; Schwab, Stefan ; Huttner, Hagen B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4532-541fbf04b933342218de33f641cd2add15b99b6c02a7c6b6c04477a762a7c6033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Administration, Oral</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anticoagulants - administration &amp; dosage</topic><topic>Cerebral Hemorrhage - diagnostic imaging</topic><topic>Cerebral Hemorrhage - drug therapy</topic><topic>Cerebral Hemorrhage - epidemiology</topic><topic>Female</topic><topic>Fibrinolytic Agents - administration &amp; dosage</topic><topic>Germany - epidemiology</topic><topic>Humans</topic><topic>Male</topic><topic>Retrospective Studies</topic><topic>Vitamin K - antagonists &amp; inhibitors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gerner, Stefan T</creatorcontrib><creatorcontrib>Kuramatsu, Joji B</creatorcontrib><creatorcontrib>Sembill, Jochen A</creatorcontrib><creatorcontrib>Sprügel, Maximilian I</creatorcontrib><creatorcontrib>Hagen, Manuel</creatorcontrib><creatorcontrib>Knappe, Ruben U</creatorcontrib><creatorcontrib>Endres, Matthias</creatorcontrib><creatorcontrib>Haeusler, Karl Georg</creatorcontrib><creatorcontrib>Sobesky, Jan</creatorcontrib><creatorcontrib>Schurig, Johannes</creatorcontrib><creatorcontrib>Zweynert, Sarah</creatorcontrib><creatorcontrib>Bauer, Miriam</creatorcontrib><creatorcontrib>Vajkoczy, Peter</creatorcontrib><creatorcontrib>Ringleb, Peter A</creatorcontrib><creatorcontrib>Purrucker, Jan C</creatorcontrib><creatorcontrib>Rizos, Timolaos</creatorcontrib><creatorcontrib>Volkmann, Jens</creatorcontrib><creatorcontrib>Müllges, Wolfgang</creatorcontrib><creatorcontrib>Kraft, Peter</creatorcontrib><creatorcontrib>Schubert, Anna-Lena</creatorcontrib><creatorcontrib>Erbguth, Frank</creatorcontrib><creatorcontrib>Nueckel, Martin</creatorcontrib><creatorcontrib>Schellinger, Peter D</creatorcontrib><creatorcontrib>Glahn, Jörg</creatorcontrib><creatorcontrib>Knappe, Ulrich J</creatorcontrib><creatorcontrib>Fink, Gereon R</creatorcontrib><creatorcontrib>Dohmen, Christian</creatorcontrib><creatorcontrib>Stetefeld, Henning</creatorcontrib><creatorcontrib>Fisse, Anna Lena</creatorcontrib><creatorcontrib>Minnerup, Jens</creatorcontrib><creatorcontrib>Hagemann, Georg</creatorcontrib><creatorcontrib>Rakers, Florian</creatorcontrib><creatorcontrib>Reichmann, Heinz</creatorcontrib><creatorcontrib>Schneider, Hauke</creatorcontrib><creatorcontrib>Rahmig, Jan</creatorcontrib><creatorcontrib>Ludolph, Albert Christian</creatorcontrib><creatorcontrib>Stösser, Sebastian</creatorcontrib><creatorcontrib>Neugebauer, Hermann</creatorcontrib><creatorcontrib>Röther, Joachim</creatorcontrib><creatorcontrib>Michels, Peter</creatorcontrib><creatorcontrib>Schwarz, Michael</creatorcontrib><creatorcontrib>Reimann, Gernot</creatorcontrib><creatorcontrib>Bäzner, Hansjörg</creatorcontrib><creatorcontrib>Schwert, Henning</creatorcontrib><creatorcontrib>Claßen, Joseph</creatorcontrib><creatorcontrib>Michalski, Dominik</creatorcontrib><creatorcontrib>Grau, Armin</creatorcontrib><creatorcontrib>Palm, Frederick</creatorcontrib><creatorcontrib>Urbanek, Christian</creatorcontrib><creatorcontrib>Wöhrle, Johannes C</creatorcontrib><creatorcontrib>Alshammari, Fahid</creatorcontrib><creatorcontrib>Horn, Markus</creatorcontrib><creatorcontrib>Bahner, Dirk</creatorcontrib><creatorcontrib>Witte, Otto W</creatorcontrib><creatorcontrib>Günther, Albrecht</creatorcontrib><creatorcontrib>Hamann, Gerhard F</creatorcontrib><creatorcontrib>Engelhorn, Tobias</creatorcontrib><creatorcontrib>Lücking, Hannes</creatorcontrib><creatorcontrib>Dörfler, Arnd</creatorcontrib><creatorcontrib>Schwab, Stefan</creatorcontrib><creatorcontrib>Huttner, Hagen B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Stroke (1970)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gerner, Stefan T</au><au>Kuramatsu, Joji B</au><au>Sembill, Jochen A</au><au>Sprügel, Maximilian I</au><au>Hagen, Manuel</au><au>Knappe, Ruben U</au><au>Endres, Matthias</au><au>Haeusler, Karl Georg</au><au>Sobesky, Jan</au><au>Schurig, Johannes</au><au>Zweynert, Sarah</au><au>Bauer, Miriam</au><au>Vajkoczy, Peter</au><au>Ringleb, Peter A</au><au>Purrucker, Jan C</au><au>Rizos, Timolaos</au><au>Volkmann, Jens</au><au>Müllges, Wolfgang</au><au>Kraft, Peter</au><au>Schubert, Anna-Lena</au><au>Erbguth, Frank</au><au>Nueckel, Martin</au><au>Schellinger, Peter D</au><au>Glahn, Jörg</au><au>Knappe, Ulrich J</au><au>Fink, Gereon R</au><au>Dohmen, Christian</au><au>Stetefeld, Henning</au><au>Fisse, Anna Lena</au><au>Minnerup, Jens</au><au>Hagemann, Georg</au><au>Rakers, Florian</au><au>Reichmann, Heinz</au><au>Schneider, Hauke</au><au>Rahmig, Jan</au><au>Ludolph, Albert Christian</au><au>Stösser, Sebastian</au><au>Neugebauer, Hermann</au><au>Röther, Joachim</au><au>Michels, Peter</au><au>Schwarz, Michael</au><au>Reimann, Gernot</au><au>Bäzner, Hansjörg</au><au>Schwert, Henning</au><au>Claßen, Joseph</au><au>Michalski, Dominik</au><au>Grau, Armin</au><au>Palm, Frederick</au><au>Urbanek, Christian</au><au>Wöhrle, Johannes C</au><au>Alshammari, Fahid</au><au>Horn, Markus</au><au>Bahner, Dirk</au><au>Witte, Otto W</au><au>Günther, Albrecht</au><au>Hamann, Gerhard F</au><au>Engelhorn, Tobias</au><au>Lücking, Hannes</au><au>Dörfler, Arnd</au><au>Schwab, Stefan</au><au>Huttner, Hagen B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characteristics in Non–Vitamin K Antagonist Oral Anticoagulant–Related Intracerebral Hemorrhage</atitle><jtitle>Stroke (1970)</jtitle><addtitle>Stroke</addtitle><date>2019-06</date><risdate>2019</risdate><volume>50</volume><issue>6</issue><spage>1392</spage><epage>1402</epage><pages>1392-1402</pages><issn>0039-2499</issn><eissn>1524-4628</eissn><abstract>BACKGROUND AND PURPOSE—Given inconclusive studies, it is debated whether clinical and imaging characteristics, as well as functional outcome, differ among patients with intracerebral hemorrhage (ICH) related to vitamin K antagonists (VKA) versus non–vitamin K antagonist (NOAC)-related ICH. Notably, clinical characteristics according to different NOAC agents and dosages are not established. METHODS—Multicenter observational cohort study integrating individual patient data of 1328 patients with oral anticoagulation–associated ICH, including 190 NOAC-related ICH patients, recruited from 2011 to 2015 at 19 tertiary centers across Germany. Imaging, clinical characteristics, and 3-months modified Rankin Scale (mRS) outcomes were compared in NOAC- versus VKA-related ICH patients. Propensity score matching was conducted to adjust for clinically relevant differences in baseline parameters. Subgroup analyses were performed regarding NOAC agent, dosing and present clinically relevant anticoagulatory activity (last intake &lt;12h/24h or NOAC level &gt;30 ng/mL). RESULTS—Despite older age in NOAC patients, there were no relevant differences in clinical and hematoma characteristics between NOAC- and VKA-related ICH regarding baseline hematoma volume (median [interquartile range]NOAC, 14.7 [5.1–42.3] mL versus VKA, 16.4 [5.8–40.6] mL; P=0.33), rate of hematoma expansion (NOAC, 49/146 [33.6%] versus VKA, 235/688 [34.2%]; P=0.89), and the proportion of patients with unfavorable outcome at 3 months (mRS, 4–6NOAC 126/179 [70.4%] versus VKA 473/682 [69.4%]; P=0.79). Subgroup analyses revealed that NOAC patients with clinically relevant anticoagulatory effect had higher rates of intraventricular hemorrhage (n/N [%]present 52/109 [47.7%] versus absent 9/35 [25.7%]; P=0.022) and hematoma expansion (present 35/90 [38.9%] versus absent 5/30 [16.7%]; P=0.040), whereas type of NOAC agent or different NOAC-dosing regimens did not result in relevant differences in imaging characteristics or outcome. CONCLUSIONS—If effectively anticoagulated, there are no differences in hematoma characteristics and functional outcome among patients with NOAC- or VKA-related ICH. CLINICAL TRIAL REGISTRATION—URLhttps://www.clinicaltrials.gov. Unique identifierNCT03093233.</abstract><cop>United States</cop><pub>American Heart Association, Inc</pub><pmid>31092170</pmid><doi>10.1161/STROKEAHA.118.023492</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; American Heart Association Journals; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Administration, Oral
Aged
Aged, 80 and over
Anticoagulants - administration & dosage
Cerebral Hemorrhage - diagnostic imaging
Cerebral Hemorrhage - drug therapy
Cerebral Hemorrhage - epidemiology
Female
Fibrinolytic Agents - administration & dosage
Germany - epidemiology
Humans
Male
Retrospective Studies
Vitamin K - antagonists & inhibitors
title Characteristics in Non–Vitamin K Antagonist Oral Anticoagulant–Related Intracerebral Hemorrhage
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