Clinical course of untreated cerebral cavernous malformations: a meta-analysis of individual patient data

Summary Background Cerebral cavernous malformations (CCMs) can cause symptomatic intracranial haemorrhage (ICH), but the estimated risks are imprecise and predictors remain uncertain. We aimed to obtain precise estimates and predictors of the risk of ICH during untreated follow-up in an individual p...

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Veröffentlicht in:Lancet neurology 2016-02, Vol.15 (2), p.166-173
Hauptverfasser: Horne, Margaret A, PhD, Flemming, Kelly D, MD, Su, I-Chang, MD, Stapf, Christian, Prof, Jeon, Jin Pyeong, MD, Li, Da, MD, Maxwell, Susanne S, MBChB, White, Philip, Prof, Christianson, Teresa J, BSc, Agid, Ronit, MD, Cho, Won-Sang, MD, Oh, Chang Wan, Prof, Wu, Zhen, Prof, Zhang, Jun-Ting, Prof, Kim, Jeong Eun, PhD, ter Brugge, Karel, Prof, Willinsky, Robert, FRCPC, Brown, Robert D, Prof, Murray, Gordon D, Prof, Salman, Rustam Al-Shahi, Prof
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container_end_page 173
container_issue 2
container_start_page 166
container_title Lancet neurology
container_volume 15
creator Horne, Margaret A, PhD
Flemming, Kelly D, MD
Su, I-Chang, MD
Stapf, Christian, Prof
Jeon, Jin Pyeong, MD
Li, Da, MD
Maxwell, Susanne S, MBChB
White, Philip, Prof
Christianson, Teresa J, BSc
Agid, Ronit, MD
Cho, Won-Sang, MD
Oh, Chang Wan, Prof
Wu, Zhen, Prof
Zhang, Jun-Ting, Prof
Kim, Jeong Eun, PhD
ter Brugge, Karel, Prof
Willinsky, Robert, FRCPC
Brown, Robert D, Prof
Murray, Gordon D, Prof
Salman, Rustam Al-Shahi, Prof
description Summary Background Cerebral cavernous malformations (CCMs) can cause symptomatic intracranial haemorrhage (ICH), but the estimated risks are imprecise and predictors remain uncertain. We aimed to obtain precise estimates and predictors of the risk of ICH during untreated follow-up in an individual patient data meta-analysis. Methods We invited investigators of published cohorts of people aged at least 16 years, identified by a systematic review of Ovid MEDLINE and Embase from inception to April 30, 2015, to provide individual patient data on clinical course from CCM diagnosis until first CCM treatment or last available follow-up. We used survival analysis to estimate the 5-year risk of symptomatic ICH due to CCMs (primary outcome), multivariable Cox regression to identify baseline predictors of outcome, and random-effects models to pool estimates in a meta-analysis. Findings Among 1620 people in seven cohorts from six studies, 204 experienced ICH during 5197 person-years of follow-up (Kaplan-Meier estimated 5-year risk 15·8%, 95% CI 13·7–17·9). The primary outcome of ICH within 5 years of CCM diagnosis was associated with clinical presentation with ICH or new focal neurological deficit (FND) without brain imaging evidence of recent haemorrhage versus other modes of presentation (hazard ratio 5·6, 95% CI 3·2–9·7) and with brainstem CCM location versus other locations (4·4, 2·3–8·6), but age, sex, and CCM multiplicity did not add independent prognostic information. The 5-year estimated risk of ICH during untreated follow-up was 3·8% (95% CI 2·1–5·5) for 718 people with non-brainstem CCM presenting without ICH or FND, 8·0% (0·1–15·9) for 80 people with brainstem CCM presenting without ICH or FND, 18·4% (13·3–23·5) for 327 people with non-brainstem CCM presenting with ICH or FND, and 30·8% (26·3–35·2) for 495 people with brainstem CCM presenting with ICH or FND. Interpretation Mode of clinical presentation and CCM location are independently associated with ICH within 5 years of CCM diagnosis. These findings can inform decisions about CCM treatment. Funding UK Medical Research Council, Chief Scientist Office of the Scottish Government, and UK Stroke Association.
doi_str_mv 10.1016/S1474-4422(15)00303-8
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We aimed to obtain precise estimates and predictors of the risk of ICH during untreated follow-up in an individual patient data meta-analysis. Methods We invited investigators of published cohorts of people aged at least 16 years, identified by a systematic review of Ovid MEDLINE and Embase from inception to April 30, 2015, to provide individual patient data on clinical course from CCM diagnosis until first CCM treatment or last available follow-up. We used survival analysis to estimate the 5-year risk of symptomatic ICH due to CCMs (primary outcome), multivariable Cox regression to identify baseline predictors of outcome, and random-effects models to pool estimates in a meta-analysis. Findings Among 1620 people in seven cohorts from six studies, 204 experienced ICH during 5197 person-years of follow-up (Kaplan-Meier estimated 5-year risk 15·8%, 95% CI 13·7–17·9). The primary outcome of ICH within 5 years of CCM diagnosis was associated with clinical presentation with ICH or new focal neurological deficit (FND) without brain imaging evidence of recent haemorrhage versus other modes of presentation (hazard ratio 5·6, 95% CI 3·2–9·7) and with brainstem CCM location versus other locations (4·4, 2·3–8·6), but age, sex, and CCM multiplicity did not add independent prognostic information. The 5-year estimated risk of ICH during untreated follow-up was 3·8% (95% CI 2·1–5·5) for 718 people with non-brainstem CCM presenting without ICH or FND, 8·0% (0·1–15·9) for 80 people with brainstem CCM presenting without ICH or FND, 18·4% (13·3–23·5) for 327 people with non-brainstem CCM presenting with ICH or FND, and 30·8% (26·3–35·2) for 495 people with brainstem CCM presenting with ICH or FND. Interpretation Mode of clinical presentation and CCM location are independently associated with ICH within 5 years of CCM diagnosis. These findings can inform decisions about CCM treatment. Funding UK Medical Research Council, Chief Scientist Office of the Scottish Government, and UK Stroke Association.</description><identifier>ISSN: 1474-4422</identifier><identifier>EISSN: 1474-4465</identifier><identifier>DOI: 10.1016/S1474-4422(15)00303-8</identifier><identifier>PMID: 26654287</identifier><identifier>CODEN: LANCAO</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Brain Neoplasms - complications ; Brain research ; Disease Progression ; Female ; Hemangioma, Cavernous, Central Nervous System - complications ; Humans ; Intracranial Hemorrhages - etiology ; Male ; Meta-analysis ; Middle Aged ; Neurology ; Statistical analysis ; Studies ; Systematic review ; Young Adult</subject><ispartof>Lancet neurology, 2016-02, Vol.15 (2), p.166-173</ispartof><rights>Horne et al. Open Access article distributed under the terms of CC BY</rights><rights>2016 Horne et al. Open Access article distributed under the terms of CC BY</rights><rights>Copyright © 2016 Horne et al. Open Access article distributed under the terms of CC BY. Published by Elsevier Ltd.. All rights reserved.</rights><rights>Copyright Elsevier Limited Feb 2016</rights><rights>2016 Horne et al. Open Access article distributed under the terms of CC BY 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c719t-a0f1d7b5e0ec14b0d63fb03aa5268da0dd7ff92ddee5f8193b70b3ef85f488583</citedby><cites>FETCH-LOGICAL-c719t-a0f1d7b5e0ec14b0d63fb03aa5268da0dd7ff92ddee5f8193b70b3ef85f488583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1474442215003038$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26654287$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Horne, Margaret A, PhD</creatorcontrib><creatorcontrib>Flemming, Kelly D, MD</creatorcontrib><creatorcontrib>Su, I-Chang, MD</creatorcontrib><creatorcontrib>Stapf, Christian, Prof</creatorcontrib><creatorcontrib>Jeon, Jin Pyeong, MD</creatorcontrib><creatorcontrib>Li, Da, MD</creatorcontrib><creatorcontrib>Maxwell, Susanne S, MBChB</creatorcontrib><creatorcontrib>White, Philip, Prof</creatorcontrib><creatorcontrib>Christianson, Teresa J, BSc</creatorcontrib><creatorcontrib>Agid, Ronit, MD</creatorcontrib><creatorcontrib>Cho, Won-Sang, MD</creatorcontrib><creatorcontrib>Oh, Chang Wan, Prof</creatorcontrib><creatorcontrib>Wu, Zhen, Prof</creatorcontrib><creatorcontrib>Zhang, Jun-Ting, Prof</creatorcontrib><creatorcontrib>Kim, Jeong Eun, PhD</creatorcontrib><creatorcontrib>ter Brugge, Karel, Prof</creatorcontrib><creatorcontrib>Willinsky, Robert, FRCPC</creatorcontrib><creatorcontrib>Brown, Robert D, Prof</creatorcontrib><creatorcontrib>Murray, Gordon D, Prof</creatorcontrib><creatorcontrib>Salman, Rustam Al-Shahi, Prof</creatorcontrib><creatorcontrib>Cerebral Cavernous Malformations Individual Patient Data Meta-analysis Collaborators</creatorcontrib><title>Clinical course of untreated cerebral cavernous malformations: a meta-analysis of individual patient data</title><title>Lancet neurology</title><addtitle>Lancet Neurol</addtitle><description>Summary Background Cerebral cavernous malformations (CCMs) can cause symptomatic intracranial haemorrhage (ICH), but the estimated risks are imprecise and predictors remain uncertain. We aimed to obtain precise estimates and predictors of the risk of ICH during untreated follow-up in an individual patient data meta-analysis. Methods We invited investigators of published cohorts of people aged at least 16 years, identified by a systematic review of Ovid MEDLINE and Embase from inception to April 30, 2015, to provide individual patient data on clinical course from CCM diagnosis until first CCM treatment or last available follow-up. We used survival analysis to estimate the 5-year risk of symptomatic ICH due to CCMs (primary outcome), multivariable Cox regression to identify baseline predictors of outcome, and random-effects models to pool estimates in a meta-analysis. Findings Among 1620 people in seven cohorts from six studies, 204 experienced ICH during 5197 person-years of follow-up (Kaplan-Meier estimated 5-year risk 15·8%, 95% CI 13·7–17·9). The primary outcome of ICH within 5 years of CCM diagnosis was associated with clinical presentation with ICH or new focal neurological deficit (FND) without brain imaging evidence of recent haemorrhage versus other modes of presentation (hazard ratio 5·6, 95% CI 3·2–9·7) and with brainstem CCM location versus other locations (4·4, 2·3–8·6), but age, sex, and CCM multiplicity did not add independent prognostic information. The 5-year estimated risk of ICH during untreated follow-up was 3·8% (95% CI 2·1–5·5) for 718 people with non-brainstem CCM presenting without ICH or FND, 8·0% (0·1–15·9) for 80 people with brainstem CCM presenting without ICH or FND, 18·4% (13·3–23·5) for 327 people with non-brainstem CCM presenting with ICH or FND, and 30·8% (26·3–35·2) for 495 people with brainstem CCM presenting with ICH or FND. Interpretation Mode of clinical presentation and CCM location are independently associated with ICH within 5 years of CCM diagnosis. These findings can inform decisions about CCM treatment. 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Flemming, Kelly D, MD ; Su, I-Chang, MD ; Stapf, Christian, Prof ; Jeon, Jin Pyeong, MD ; Li, Da, MD ; Maxwell, Susanne S, MBChB ; White, Philip, Prof ; Christianson, Teresa J, BSc ; Agid, Ronit, MD ; Cho, Won-Sang, MD ; Oh, Chang Wan, Prof ; Wu, Zhen, Prof ; Zhang, Jun-Ting, Prof ; Kim, Jeong Eun, PhD ; ter Brugge, Karel, Prof ; Willinsky, Robert, FRCPC ; Brown, Robert D, Prof ; Murray, Gordon D, Prof ; Salman, Rustam Al-Shahi, Prof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c719t-a0f1d7b5e0ec14b0d63fb03aa5268da0dd7ff92ddee5f8193b70b3ef85f488583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Brain Neoplasms - complications</topic><topic>Brain research</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Hemangioma, Cavernous, Central Nervous System - complications</topic><topic>Humans</topic><topic>Intracranial Hemorrhages - etiology</topic><topic>Male</topic><topic>Meta-analysis</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Statistical analysis</topic><topic>Studies</topic><topic>Systematic review</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horne, Margaret A, PhD</creatorcontrib><creatorcontrib>Flemming, Kelly D, MD</creatorcontrib><creatorcontrib>Su, I-Chang, MD</creatorcontrib><creatorcontrib>Stapf, Christian, Prof</creatorcontrib><creatorcontrib>Jeon, Jin Pyeong, MD</creatorcontrib><creatorcontrib>Li, Da, MD</creatorcontrib><creatorcontrib>Maxwell, Susanne S, MBChB</creatorcontrib><creatorcontrib>White, Philip, Prof</creatorcontrib><creatorcontrib>Christianson, Teresa J, BSc</creatorcontrib><creatorcontrib>Agid, Ronit, MD</creatorcontrib><creatorcontrib>Cho, Won-Sang, MD</creatorcontrib><creatorcontrib>Oh, Chang Wan, Prof</creatorcontrib><creatorcontrib>Wu, Zhen, Prof</creatorcontrib><creatorcontrib>Zhang, Jun-Ting, Prof</creatorcontrib><creatorcontrib>Kim, Jeong Eun, PhD</creatorcontrib><creatorcontrib>ter Brugge, Karel, Prof</creatorcontrib><creatorcontrib>Willinsky, Robert, FRCPC</creatorcontrib><creatorcontrib>Brown, Robert D, Prof</creatorcontrib><creatorcontrib>Murray, Gordon D, Prof</creatorcontrib><creatorcontrib>Salman, Rustam Al-Shahi, Prof</creatorcontrib><creatorcontrib>Cerebral Cavernous Malformations Individual Patient Data Meta-analysis Collaborators</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Pharma and Biotech Premium PRO</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing &amp; 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We aimed to obtain precise estimates and predictors of the risk of ICH during untreated follow-up in an individual patient data meta-analysis. Methods We invited investigators of published cohorts of people aged at least 16 years, identified by a systematic review of Ovid MEDLINE and Embase from inception to April 30, 2015, to provide individual patient data on clinical course from CCM diagnosis until first CCM treatment or last available follow-up. We used survival analysis to estimate the 5-year risk of symptomatic ICH due to CCMs (primary outcome), multivariable Cox regression to identify baseline predictors of outcome, and random-effects models to pool estimates in a meta-analysis. Findings Among 1620 people in seven cohorts from six studies, 204 experienced ICH during 5197 person-years of follow-up (Kaplan-Meier estimated 5-year risk 15·8%, 95% CI 13·7–17·9). The primary outcome of ICH within 5 years of CCM diagnosis was associated with clinical presentation with ICH or new focal neurological deficit (FND) without brain imaging evidence of recent haemorrhage versus other modes of presentation (hazard ratio 5·6, 95% CI 3·2–9·7) and with brainstem CCM location versus other locations (4·4, 2·3–8·6), but age, sex, and CCM multiplicity did not add independent prognostic information. The 5-year estimated risk of ICH during untreated follow-up was 3·8% (95% CI 2·1–5·5) for 718 people with non-brainstem CCM presenting without ICH or FND, 8·0% (0·1–15·9) for 80 people with brainstem CCM presenting without ICH or FND, 18·4% (13·3–23·5) for 327 people with non-brainstem CCM presenting with ICH or FND, and 30·8% (26·3–35·2) for 495 people with brainstem CCM presenting with ICH or FND. Interpretation Mode of clinical presentation and CCM location are independently associated with ICH within 5 years of CCM diagnosis. These findings can inform decisions about CCM treatment. Funding UK Medical Research Council, Chief Scientist Office of the Scottish Government, and UK Stroke Association.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26654287</pmid><doi>10.1016/S1474-4422(15)00303-8</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 1474-4422
ispartof Lancet neurology, 2016-02, Vol.15 (2), p.166-173
issn 1474-4422
1474-4465
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4710581
source MEDLINE; Elsevier ScienceDirect Journals
subjects Adolescent
Adult
Aged
Aged, 80 and over
Brain Neoplasms - complications
Brain research
Disease Progression
Female
Hemangioma, Cavernous, Central Nervous System - complications
Humans
Intracranial Hemorrhages - etiology
Male
Meta-analysis
Middle Aged
Neurology
Statistical analysis
Studies
Systematic review
Young Adult
title Clinical course of untreated cerebral cavernous malformations: a meta-analysis of individual patient data
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