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Outcome of intracerebral hemorrhage associated with different oral anticoagulants

Identifieur interne : 000667 ( Main/Exploration ); précédent : 000666; suivant : 000668

Outcome of intracerebral hemorrhage associated with different oral anticoagulants

Auteurs : Duncan Wilson ; David J. Seiffge ; Christopher Traenka ; Ghazala Basir ; Jan C. Purrucker ; Timolaos Rizos ; Oluwaseun A. Sobowale ; Hanne Sallinen ; Shin-Joe Yeh ; Teddy Y. Wu ; Marc Ferrigno ; Rik Houben ; Floris H. B. M. Schreuder ; Luke A. Perry ; Jun Tanaka ; Marion Boulanger ; Rustam Al-Shahi Salman ; Hans R. J Ger ; Gareth Ambler ; Clare Shakeshaft ; Yusuke Yakushiji ; Philip M. C. Choi ; Julie Staals ; Charlotte Cordonnier ; Jiann-Shing Jeng ; Roland Veltkamp ; Dar Dowlatshahi ; Stefan T. Engelter ; Adrian R. Parry-Jones ; Atte Meretoja ; David J. Werring

Source :

RBID : PMC:5409844

Descripteurs français

English descriptors

Abstract

Objective:

In an international collaborative multicenter pooled analysis, we compared mortality, functional outcome, intracerebral hemorrhage (ICH) volume, and hematoma expansion (HE) between non–vitamin K antagonist oral anticoagulation–related ICH (NOAC-ICH) and vitamin K antagonist–associated ICH (VKA-ICH).

Methods:

We compared all-cause mortality within 90 days for NOAC-ICH and VKA-ICH using a Cox proportional hazards model adjusted for age; sex; baseline Glasgow Coma Scale score, ICH location, and log volume; intraventricular hemorrhage volume; and intracranial surgery. We addressed heterogeneity using a shared frailty term. Good functional outcome was defined as discharge modified Rankin Scale score ≤2 and investigated in multivariable logistic regression. ICH volume was measured by ABC/2 or a semiautomated planimetric method. HE was defined as an ICH volume increase >33% or >6 mL from baseline within 72 hours.

Results:

We included 500 patients (97 NOAC-ICH and 403 VKA-ICH). Median baseline ICH volume was 14.4 mL (interquartile range [IQR] 3.6–38.4) for NOAC-ICH vs 10.6 mL (IQR 4.0–27.9) for VKA-ICH (p = 0.78). We did not find any difference between NOAC-ICH and VKA-ICH for all-cause mortality within 90 days (33% for NOAC-ICH vs 31% for VKA-ICH [p = 0.64]; adjusted Cox hazard ratio (for NOAC-ICH vs VKA-ICH) 0.93 [95% confidence interval (CI) 0.52–1.64] [p = 0.79]), the rate of HE (NOAC-ICH n = 29/48 [40%] vs VKA-ICH n = 93/140 [34%] [p = 0.45]), or functional outcome at hospital discharge (NOAC-ICH vs VKA-ICH odds ratio 0.47; 95% CI 0.18–1.19 [p = 0.11]).

Conclusions:

In our international collaborative multicenter pooled analysis, baseline ICH volume, hematoma expansion, 90-day mortality, and functional outcome were similar following NOAC-ICH and VKA-ICH.


Url:
DOI: 10.1212/WNL.0000000000003886
PubMed: 28381513
PubMed Central: 5409844


Affiliations:


Links toward previous steps (curation, corpus...)


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<name sortKey="Sobowale, Oluwaseun A" sort="Sobowale, Oluwaseun A" uniqKey="Sobowale O" first="Oluwaseun A." last="Sobowale">Oluwaseun A. Sobowale</name>
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<name sortKey="Sallinen, Hanne" sort="Sallinen, Hanne" uniqKey="Sallinen H" first="Hanne" last="Sallinen">Hanne Sallinen</name>
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<name sortKey="Yeh, Shin Joe" sort="Yeh, Shin Joe" uniqKey="Yeh S" first="Shin-Joe" last="Yeh">Shin-Joe Yeh</name>
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<name sortKey="Wu, Teddy Y" sort="Wu, Teddy Y" uniqKey="Wu T" first="Teddy Y." last="Wu">Teddy Y. Wu</name>
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<name sortKey="Schreuder, Floris H B M" sort="Schreuder, Floris H B M" uniqKey="Schreuder F" first="Floris H. B. M." last="Schreuder">Floris H. B. M. Schreuder</name>
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<name sortKey="Perry, Luke A" sort="Perry, Luke A" uniqKey="Perry L" first="Luke A." last="Perry">Luke A. Perry</name>
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<name sortKey="Tanaka, Jun" sort="Tanaka, Jun" uniqKey="Tanaka J" first="Jun" last="Tanaka">Jun Tanaka</name>
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<name sortKey="Boulanger, Marion" sort="Boulanger, Marion" uniqKey="Boulanger M" first="Marion" last="Boulanger">Marion Boulanger</name>
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<name sortKey="Al Shahi Salman, Rustam" sort="Al Shahi Salman, Rustam" uniqKey="Al Shahi Salman R" first="Rustam" last="Al-Shahi Salman">Rustam Al-Shahi Salman</name>
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<name sortKey="J Ger, Hans R" sort="J Ger, Hans R" uniqKey="J Ger H" first="Hans R." last="J Ger">Hans R. J Ger</name>
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<name sortKey="Ambler, Gareth" sort="Ambler, Gareth" uniqKey="Ambler G" first="Gareth" last="Ambler">Gareth Ambler</name>
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<name sortKey="Shakeshaft, Clare" sort="Shakeshaft, Clare" uniqKey="Shakeshaft C" first="Clare" last="Shakeshaft">Clare Shakeshaft</name>
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<name sortKey="Yakushiji, Yusuke" sort="Yakushiji, Yusuke" uniqKey="Yakushiji Y" first="Yusuke" last="Yakushiji">Yusuke Yakushiji</name>
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<name sortKey="Choi, Philip M C" sort="Choi, Philip M C" uniqKey="Choi P" first="Philip M. C." last="Choi">Philip M. C. Choi</name>
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<name sortKey="Staals, Julie" sort="Staals, Julie" uniqKey="Staals J" first="Julie" last="Staals">Julie Staals</name>
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<name sortKey="Cordonnier, Charlotte" sort="Cordonnier, Charlotte" uniqKey="Cordonnier C" first="Charlotte" last="Cordonnier">Charlotte Cordonnier</name>
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<name sortKey="Jeng, Jiann Shing" sort="Jeng, Jiann Shing" uniqKey="Jeng J" first="Jiann-Shing" last="Jeng">Jiann-Shing Jeng</name>
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<name sortKey="Veltkamp, Roland" sort="Veltkamp, Roland" uniqKey="Veltkamp R" first="Roland" last="Veltkamp">Roland Veltkamp</name>
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<name sortKey="Dowlatshahi, Dar" sort="Dowlatshahi, Dar" uniqKey="Dowlatshahi D" first="Dar" last="Dowlatshahi">Dar Dowlatshahi</name>
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<name sortKey="Engelter, Stefan T" sort="Engelter, Stefan T" uniqKey="Engelter S" first="Stefan T." last="Engelter">Stefan T. Engelter</name>
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<name sortKey="Parry Jones, Adrian R" sort="Parry Jones, Adrian R" uniqKey="Parry Jones A" first="Adrian R." last="Parry-Jones">Adrian R. Parry-Jones</name>
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<name sortKey="Meretoja, Atte" sort="Meretoja, Atte" uniqKey="Meretoja A" first="Atte" last="Meretoja">Atte Meretoja</name>
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<name sortKey="Werring, David J" sort="Werring, David J" uniqKey="Werring D" first="David J." last="Werring">David J. Werring</name>
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<title level="j">Neurology</title>
<idno type="ISSN">0028-3878</idno>
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<date when="2017">2017</date>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Administration, Oral</term>
<term>Anticoagulants (administration & dosage)</term>
<term>Cerebral Hemorrhage (drug therapy)</term>
<term>Cerebral Hemorrhage (mortality)</term>
<term>Cerebral Hemorrhage (pathology)</term>
<term>Cerebral Hemorrhage (surgery)</term>
<term>Female</term>
<term>Glasgow Coma Scale</term>
<term>Humans</term>
<term>Logistic Models</term>
<term>Male</term>
<term>Multivariate Analysis</term>
<term>Proportional Hazards Models</term>
<term>Prospective Studies</term>
<term>Registries</term>
<term>Retrospective Studies</term>
<term>Survival Analysis</term>
<term>Treatment Outcome</term>
<term>Vitamin K (antagonists & inhibitors)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Administration par voie orale</term>
<term>Analyse de survie</term>
<term>Analyse multivariée</term>
<term>Anticoagulants (administration et posologie)</term>
<term>Enregistrements</term>
<term>Femelle</term>
<term>Humains</term>
<term>Hémorragie cérébrale ()</term>
<term>Hémorragie cérébrale (anatomopathologie)</term>
<term>Hémorragie cérébrale (mortalité)</term>
<term>Hémorragie cérébrale (traitement médicamenteux)</term>
<term>Modèles de hasards proportionnels</term>
<term>Modèles logistiques</term>
<term>Mâle</term>
<term>Résultat thérapeutique</term>
<term>Vitamine K (antagonistes et inhibiteurs)</term>
<term>Échelle de Glasgow</term>
<term>Études prospectives</term>
<term>Études rétrospectives</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en">
<term>Anticoagulants</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="antagonists & inhibitors" xml:lang="en">
<term>Vitamin K</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr">
<term>Anticoagulants</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr">
<term>Hémorragie cérébrale</term>
</keywords>
<keywords scheme="MESH" qualifier="antagonistes et inhibiteurs" xml:lang="fr">
<term>Vitamine K</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Cerebral Hemorrhage</term>
</keywords>
<keywords scheme="MESH" qualifier="mortality" xml:lang="en">
<term>Cerebral Hemorrhage</term>
</keywords>
<keywords scheme="MESH" qualifier="mortalité" xml:lang="fr">
<term>Hémorragie cérébrale</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Cerebral Hemorrhage</term>
</keywords>
<keywords scheme="MESH" qualifier="surgery" xml:lang="en">
<term>Cerebral Hemorrhage</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Hémorragie cérébrale</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Administration, Oral</term>
<term>Female</term>
<term>Glasgow Coma Scale</term>
<term>Humans</term>
<term>Logistic Models</term>
<term>Male</term>
<term>Multivariate Analysis</term>
<term>Proportional Hazards Models</term>
<term>Prospective Studies</term>
<term>Registries</term>
<term>Retrospective Studies</term>
<term>Survival Analysis</term>
<term>Treatment Outcome</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Administration par voie orale</term>
<term>Analyse de survie</term>
<term>Analyse multivariée</term>
<term>Enregistrements</term>
<term>Femelle</term>
<term>Humains</term>
<term>Hémorragie cérébrale</term>
<term>Modèles de hasards proportionnels</term>
<term>Modèles logistiques</term>
<term>Mâle</term>
<term>Résultat thérapeutique</term>
<term>Échelle de Glasgow</term>
<term>Études prospectives</term>
<term>Études rétrospectives</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">
<sec>
<title>Objective:</title>
<p>In an international collaborative multicenter pooled analysis, we compared mortality, functional outcome, intracerebral hemorrhage (ICH) volume, and hematoma expansion (HE) between non–vitamin K antagonist oral anticoagulation–related ICH (NOAC-ICH) and vitamin K antagonist–associated ICH (VKA-ICH).</p>
</sec>
<sec>
<title>Methods:</title>
<p>We compared all-cause mortality within 90 days for NOAC-ICH and VKA-ICH using a Cox proportional hazards model adjusted for age; sex; baseline Glasgow Coma Scale score, ICH location, and log volume; intraventricular hemorrhage volume; and intracranial surgery. We addressed heterogeneity using a shared frailty term. Good functional outcome was defined as discharge modified Rankin Scale score ≤2 and investigated in multivariable logistic regression. ICH volume was measured by ABC/2 or a semiautomated planimetric method. HE was defined as an ICH volume increase >33% or >6 mL from baseline within 72 hours.</p>
</sec>
<sec>
<title>Results:</title>
<p>We included 500 patients (97 NOAC-ICH and 403 VKA-ICH). Median baseline ICH volume was 14.4 mL (interquartile range [IQR] 3.6–38.4) for NOAC-ICH vs 10.6 mL (IQR 4.0–27.9) for VKA-ICH (
<italic>p</italic>
= 0.78). We did not find any difference between NOAC-ICH and VKA-ICH for all-cause mortality within 90 days (33% for NOAC-ICH vs 31% for VKA-ICH [
<italic>p</italic>
= 0.64]; adjusted Cox hazard ratio (for NOAC-ICH vs VKA-ICH) 0.93 [95% confidence interval (CI) 0.52–1.64] [
<italic>p</italic>
= 0.79]), the rate of HE (NOAC-ICH n = 29/48 [40%] vs VKA-ICH n = 93/140 [34%] [
<italic>p</italic>
= 0.45]), or functional outcome at hospital discharge (NOAC-ICH vs VKA-ICH odds ratio 0.47; 95% CI 0.18–1.19 [
<italic>p</italic>
= 0.11]).</p>
</sec>
<sec>
<title>Conclusions:</title>
<p>In our international collaborative multicenter pooled analysis, baseline ICH volume, hematoma expansion, 90-day mortality, and functional outcome were similar following NOAC-ICH and VKA-ICH.</p>
</sec>
</div>
</front>
<back>
<div1 type="bibliography">
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