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 |
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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. |
doi_str_mv | 10.1212/WNL.0000000000000688 |
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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 > 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&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 > 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><subject>Adult</subject><subject>Age Factors</subject><subject>Biological and medical sciences</subject><subject>Cerebral Hemorrhage - diagnosis</subject><subject>Cerebral Hemorrhage - epidemiology</subject><subject>Cerebral Hemorrhage - etiology</subject><subject>Cerebrovascular Circulation</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Intracranial Arteriovenous Malformations - complications</subject><subject>Intracranial Arteriovenous Malformations - epidemiology</subject><subject>Intracranial Arteriovenous Malformations - pathology</subject><subject>Intracranial Arteriovenous Malformations - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multiple sclerosis and variants. 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 & 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 > 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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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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