Untreated brain arteriovenous malformation: Patient-level meta-analysis of hemorrhage predictors

OBJECTIVE:To identify risk factors for intracranial hemorrhage in the natural history course of brain arteriovenous malformations (AVMs) using individual patient data meta-analysis of 4 existing cohorts. METHODS:We harmonized data from Kaiser Permanente of Northern California (n = 856), University o...

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Veröffentlicht in:Neurology 2014-08, Vol.83 (7), p.590-597
Hauptverfasser: Kim, Helen, Al-Shahi Salman, Rustam, McCulloch, Charles E, Stapf, Christian, Young, William L
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container_end_page 597
container_issue 7
container_start_page 590
container_title Neurology
container_volume 83
creator Kim, Helen
Al-Shahi Salman, Rustam
McCulloch, Charles E
Stapf, Christian
Young, William L
description OBJECTIVE:To identify risk factors for intracranial hemorrhage in the natural history course of brain arteriovenous malformations (AVMs) using individual patient data meta-analysis of 4 existing cohorts. METHODS:We harmonized data from Kaiser Permanente of Northern California (n = 856), University of California San Francisco (n = 787), Columbia University (n = 672), and the Scottish Intracranial Vascular Malformation Study (n = 210). We censored patients at first treatment, death, last visit, or 10-year follow-up, and performed stratified Cox regression analysis of time-to-hemorrhage after evaluating hemorrhagic presentation, sex, age at diagnosis, deep venous drainage, and AVM size as predictors. Multiple imputation was performed to assess impact of missing data. RESULTS:A total of 141 hemorrhage events occurred during 6,074 patient-years of follow-up (annual rate of 2.3%, 95% confidence interval [CI] 2.0%–2.7%), higher for ruptured (4.8%, 3.9%–5.9%) than unruptured (1.3%, 1.0%–1.7%) AVMs at presentation. Hemorrhagic presentation (hazard ratio 3.86, 95% CI 2.42–6.14) and increasing age (1.34 per decade, 1.17–1.53) independently predicted hemorrhage and remained significant predictors in the imputed dataset. Female sex (1.49, 95% CI 0.96–2.30) and exclusively deep venous drainage (1.60, 0.95–2.68, p = 0.02 in imputed dataset) may be additional predictors. AVM size was not associated with intracerebral hemorrhage in multivariable models (p > 0.5). CONCLUSION:This large, individual patient data meta-analysis identified hemorrhagic presentation and increasing age as independent predictors of hemorrhage during follow-up. Additional AVM cohort data may further improve precision of estimates, identify new risk factors, and allow validation of prediction models.
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METHODS:We harmonized data from Kaiser Permanente of Northern California (n = 856), University of California San Francisco (n = 787), Columbia University (n = 672), and the Scottish Intracranial Vascular Malformation Study (n = 210). We censored patients at first treatment, death, last visit, or 10-year follow-up, and performed stratified Cox regression analysis of time-to-hemorrhage after evaluating hemorrhagic presentation, sex, age at diagnosis, deep venous drainage, and AVM size as predictors. Multiple imputation was performed to assess impact of missing data. RESULTS:A total of 141 hemorrhage events occurred during 6,074 patient-years of follow-up (annual rate of 2.3%, 95% confidence interval [CI] 2.0%–2.7%), higher for ruptured (4.8%, 3.9%–5.9%) than unruptured (1.3%, 1.0%–1.7%) AVMs at presentation. Hemorrhagic presentation (hazard ratio 3.86, 95% CI 2.42–6.14) and increasing age (1.34 per decade, 1.17–1.53) independently predicted hemorrhage and remained significant predictors in the imputed dataset. Female sex (1.49, 95% CI 0.96–2.30) and exclusively deep venous drainage (1.60, 0.95–2.68, p = 0.02 in imputed dataset) may be additional predictors. AVM size was not associated with intracerebral hemorrhage in multivariable models (p &gt; 0.5). CONCLUSION:This large, individual patient data meta-analysis identified hemorrhagic presentation and increasing age as independent predictors of hemorrhage during follow-up. Additional AVM cohort data may further improve precision of estimates, identify new risk factors, and allow validation of prediction models.</description><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/WNL.0000000000000688</identifier><identifier>PMID: 25015366</identifier><identifier>CODEN: NEURAI</identifier><language>eng</language><publisher>Hagerstown, MD: American Academy of Neurology</publisher><subject>Adult ; Age Factors ; Biological and medical sciences ; Cerebral Hemorrhage - diagnosis ; Cerebral Hemorrhage - epidemiology ; Cerebral Hemorrhage - etiology ; Cerebrovascular Circulation ; Female ; Follow-Up Studies ; Humans ; Intracranial Arteriovenous Malformations - complications ; Intracranial Arteriovenous Malformations - epidemiology ; Intracranial Arteriovenous Malformations - pathology ; Intracranial Arteriovenous Malformations - physiopathology ; Male ; Medical sciences ; Middle Aged ; Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis ; Multivariate Analysis ; Neurology ; Prognosis ; Regression Analysis ; Risk Factors ; Sex Factors ; Survival Analysis ; Time Factors ; Vascular diseases and vascular malformations of the nervous system</subject><ispartof>Neurology, 2014-08, Vol.83 (7), p.590-597</ispartof><rights>2014 American Academy of Neurology</rights><rights>2015 INIST-CNRS</rights><rights>2014 American Academy of Neurology.</rights><rights>2014 American Academy of Neurology 2014 American Academy of Neurology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3898-e04ecf9a244afdbf2762b8fc3439274890b56e9bee4fab21433c035295eb48833</citedby><cites>FETCH-LOGICAL-c3898-e04ecf9a244afdbf2762b8fc3439274890b56e9bee4fab21433c035295eb48833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28739974$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25015366$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Helen</creatorcontrib><creatorcontrib>Al-Shahi Salman, Rustam</creatorcontrib><creatorcontrib>McCulloch, Charles E</creatorcontrib><creatorcontrib>Stapf, Christian</creatorcontrib><creatorcontrib>Young, William L</creatorcontrib><creatorcontrib>MARS Coinvestigators</creatorcontrib><creatorcontrib>For the MARS Coinvestigators</creatorcontrib><title>Untreated brain arteriovenous malformation: Patient-level meta-analysis of hemorrhage predictors</title><title>Neurology</title><addtitle>Neurology</addtitle><description>OBJECTIVE:To identify risk factors for intracranial hemorrhage in the natural history course of brain arteriovenous malformations (AVMs) using individual patient data meta-analysis of 4 existing cohorts. METHODS:We harmonized data from Kaiser Permanente of Northern California (n = 856), University of California San Francisco (n = 787), Columbia University (n = 672), and the Scottish Intracranial Vascular Malformation Study (n = 210). We censored patients at first treatment, death, last visit, or 10-year follow-up, and performed stratified Cox regression analysis of time-to-hemorrhage after evaluating hemorrhagic presentation, sex, age at diagnosis, deep venous drainage, and AVM size as predictors. Multiple imputation was performed to assess impact of missing data. RESULTS:A total of 141 hemorrhage events occurred during 6,074 patient-years of follow-up (annual rate of 2.3%, 95% confidence interval [CI] 2.0%–2.7%), higher for ruptured (4.8%, 3.9%–5.9%) than unruptured (1.3%, 1.0%–1.7%) AVMs at presentation. Hemorrhagic presentation (hazard ratio 3.86, 95% CI 2.42–6.14) and increasing age (1.34 per decade, 1.17–1.53) independently predicted hemorrhage and remained significant predictors in the imputed dataset. Female sex (1.49, 95% CI 0.96–2.30) and exclusively deep venous drainage (1.60, 0.95–2.68, p = 0.02 in imputed dataset) may be additional predictors. AVM size was not associated with intracerebral hemorrhage in multivariable models (p &gt; 0.5). CONCLUSION:This large, individual patient data meta-analysis identified hemorrhagic presentation and increasing age as independent predictors of hemorrhage during follow-up. 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Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</subject><subject>Multivariate Analysis</subject><subject>Neurology</subject><subject>Prognosis</subject><subject>Regression Analysis</subject><subject>Risk Factors</subject><subject>Sex Factors</subject><subject>Survival Analysis</subject><subject>Time Factors</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><issn>0028-3878</issn><issn>1526-632X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EokvhHyCUC1IvKf5KYnNAQlUpSKvCgQpuZuIdNwYnXuzsVv33uNqllB7Al7E0z4xe-yHkOaPHjDP-6sv58pjePa1SD8iCNbytW8G_PiQLSrmqherUAXmS83dKS7PTj8kBb8pVtO2CfLuY5oQw46rqE_ipgjRj8nGLU9zkaoTgYhph9nF6XX0qFae5DrjFUI04Qw0ThOvscxVdNeAYUxrgEqt1wpW3c0z5KXnkIGR8tq-H5OLd6eeT9_Xy49mHk7fL2gqlVY1UonUauJTgVr3jXct75ayQQvNOKk37pkXdI0oHPWdSCEtFw3WDvVRKiEPyZrd3velHXNmSM0Ew6-RHSNcmgjd_dyY_mMu4NZJJpnVbFhztF6T4c4N5NqPPFkOACctXGNbKjvKG0e7_aNMIRmXX6ILKHWpTzDmhu03EqLnxaIpHc99jGXtx9zW3Q7_FFeDlHoBsi6QEk_X5D6c6oXUnC6d23FUMRWz-ETZXmMyAEObh3xl-AfIfuTA</recordid><startdate>20140812</startdate><enddate>20140812</enddate><creator>Kim, Helen</creator><creator>Al-Shahi Salman, Rustam</creator><creator>McCulloch, Charles E</creator><creator>Stapf, Christian</creator><creator>Young, William L</creator><general>American Academy of Neurology</general><general>Lippincott Williams &amp; Wilkins</general><scope>IQODW</scope><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><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20140812</creationdate><title>Untreated brain arteriovenous malformation: Patient-level meta-analysis of hemorrhage predictors</title><author>Kim, Helen ; Al-Shahi Salman, Rustam ; McCulloch, Charles E ; Stapf, Christian ; Young, William L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3898-e04ecf9a244afdbf2762b8fc3439274890b56e9bee4fab21433c035295eb48833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Age Factors</topic><topic>Biological and medical sciences</topic><topic>Cerebral Hemorrhage - diagnosis</topic><topic>Cerebral Hemorrhage - epidemiology</topic><topic>Cerebral Hemorrhage - etiology</topic><topic>Cerebrovascular Circulation</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Intracranial Arteriovenous Malformations - complications</topic><topic>Intracranial Arteriovenous Malformations - epidemiology</topic><topic>Intracranial Arteriovenous Malformations - pathology</topic><topic>Intracranial Arteriovenous Malformations - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis</topic><topic>Multivariate Analysis</topic><topic>Neurology</topic><topic>Prognosis</topic><topic>Regression Analysis</topic><topic>Risk Factors</topic><topic>Sex Factors</topic><topic>Survival Analysis</topic><topic>Time Factors</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Helen</creatorcontrib><creatorcontrib>Al-Shahi Salman, Rustam</creatorcontrib><creatorcontrib>McCulloch, Charles E</creatorcontrib><creatorcontrib>Stapf, Christian</creatorcontrib><creatorcontrib>Young, William L</creatorcontrib><creatorcontrib>MARS Coinvestigators</creatorcontrib><creatorcontrib>For the MARS Coinvestigators</creatorcontrib><collection>Pascal-Francis</collection><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><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Helen</au><au>Al-Shahi Salman, Rustam</au><au>McCulloch, Charles E</au><au>Stapf, Christian</au><au>Young, William L</au><aucorp>MARS Coinvestigators</aucorp><aucorp>For the MARS Coinvestigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Untreated brain arteriovenous malformation: Patient-level meta-analysis of hemorrhage predictors</atitle><jtitle>Neurology</jtitle><addtitle>Neurology</addtitle><date>2014-08-12</date><risdate>2014</risdate><volume>83</volume><issue>7</issue><spage>590</spage><epage>597</epage><pages>590-597</pages><issn>0028-3878</issn><eissn>1526-632X</eissn><coden>NEURAI</coden><abstract>OBJECTIVE:To identify risk factors for intracranial hemorrhage in the natural history course of brain arteriovenous malformations (AVMs) using individual patient data meta-analysis of 4 existing cohorts. METHODS:We harmonized data from Kaiser Permanente of Northern California (n = 856), University of California San Francisco (n = 787), Columbia University (n = 672), and the Scottish Intracranial Vascular Malformation Study (n = 210). We censored patients at first treatment, death, last visit, or 10-year follow-up, and performed stratified Cox regression analysis of time-to-hemorrhage after evaluating hemorrhagic presentation, sex, age at diagnosis, deep venous drainage, and AVM size as predictors. Multiple imputation was performed to assess impact of missing data. RESULTS:A total of 141 hemorrhage events occurred during 6,074 patient-years of follow-up (annual rate of 2.3%, 95% confidence interval [CI] 2.0%–2.7%), higher for ruptured (4.8%, 3.9%–5.9%) than unruptured (1.3%, 1.0%–1.7%) AVMs at presentation. Hemorrhagic presentation (hazard ratio 3.86, 95% CI 2.42–6.14) and increasing age (1.34 per decade, 1.17–1.53) independently predicted hemorrhage and remained significant predictors in the imputed dataset. Female sex (1.49, 95% CI 0.96–2.30) and exclusively deep venous drainage (1.60, 0.95–2.68, p = 0.02 in imputed dataset) may be additional predictors. AVM size was not associated with intracerebral hemorrhage in multivariable models (p &gt; 0.5). CONCLUSION:This large, individual patient data meta-analysis identified hemorrhagic presentation and increasing age as independent predictors of hemorrhage during follow-up. Additional AVM cohort data may further improve precision of estimates, identify new risk factors, and allow validation of prediction models.</abstract><cop>Hagerstown, MD</cop><pub>American Academy of Neurology</pub><pmid>25015366</pmid><doi>10.1212/WNL.0000000000000688</doi><tpages>8</tpages></addata></record>
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source MEDLINE; Alma/SFX Local Collection; Journals@Ovid Complete
subjects Adult
Age Factors
Biological and medical sciences
Cerebral Hemorrhage - diagnosis
Cerebral Hemorrhage - epidemiology
Cerebral Hemorrhage - etiology
Cerebrovascular Circulation
Female
Follow-Up Studies
Humans
Intracranial Arteriovenous Malformations - complications
Intracranial Arteriovenous Malformations - epidemiology
Intracranial Arteriovenous Malformations - pathology
Intracranial Arteriovenous Malformations - physiopathology
Male
Medical sciences
Middle Aged
Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis
Multivariate Analysis
Neurology
Prognosis
Regression Analysis
Risk Factors
Sex Factors
Survival Analysis
Time Factors
Vascular diseases and vascular malformations of the nervous system
title Untreated brain arteriovenous malformation: Patient-level meta-analysis of hemorrhage predictors
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