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...
Gespeichert in:
Veröffentlicht in: | Lancet neurology 2016-02, Vol.15 (2), p.166-173 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4710581</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S1474442215003038</els_id><sourcerecordid>1826641223</sourcerecordid><originalsourceid>FETCH-LOGICAL-c719t-a0f1d7b5e0ec14b0d63fb03aa5268da0dd7ff92ddee5f8193b70b3ef85f488583</originalsourceid><addsrcrecordid>eNqFUk1v1DAUtBCIlsJPAEXiUg6h_owdDkVoBbRSJQ7A2XLsZ3BJ4sVOVtp_j7O7LKWXnmz5zcx7b8YIvST4LcGkufhKuOQ155SeE_EGY4ZZrR6h08NzIx4f75SeoGc532JMCVfkKTqhTSM4VfIUhVUfxmBNX9k4pwxV9NU8TgnMBK6ykKBLS9FsII1xztVgeh_TYKYQx_yuMtUAk6nNaPptDnmhh9GFTXBzoa0LDMapcmYyz9ETb_oMLw7nGfr-6eO31VV98-Xz9erDTW0laafaYE-c7ARgsIR32DXMd5gZI2ijnMHOSe9b6hyA8Iq0rJO4Y-CV8FwpodgZutzrruduAGdL_7KBXqcwmLTV0QT9f2UMP_WPuNFcEiwUKQLnB4EUf8-QJz2EbKHvzQjFAU1UsY8TStnDUNlQJiWWbYG-vge9LYYX2xaUaDFt6W54sUfZFHNO4I9zE6yX3PUud72EqonQu9z1wnt1d-kj62_QBfB-D4Bi_SZA0tmWaCy4kMBO2sXwYIvLewr28HV-wRbyv210phrvRRYNInYKiv0B5WLT8A</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1759029258</pqid></control><display><type>article</type><title>Clinical course of untreated cerebral cavernous malformations: a meta-analysis of individual patient data</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><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</creator><creatorcontrib>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 ; Cerebral Cavernous Malformations Individual Patient Data Meta-analysis Collaborators</creatorcontrib><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.</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. Funding UK Medical Research Council, Chief Scientist Office of the Scottish Government, and UK Stroke Association.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Brain Neoplasms - complications</subject><subject>Brain research</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Hemangioma, Cavernous, Central Nervous System - complications</subject><subject>Humans</subject><subject>Intracranial Hemorrhages - etiology</subject><subject>Male</subject><subject>Meta-analysis</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Statistical analysis</subject><subject>Studies</subject><subject>Systematic review</subject><subject>Young Adult</subject><issn>1474-4422</issn><issn>1474-4465</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFUk1v1DAUtBCIlsJPAEXiUg6h_owdDkVoBbRSJQ7A2XLsZ3BJ4sVOVtp_j7O7LKWXnmz5zcx7b8YIvST4LcGkufhKuOQ155SeE_EGY4ZZrR6h08NzIx4f75SeoGc532JMCVfkKTqhTSM4VfIUhVUfxmBNX9k4pwxV9NU8TgnMBK6ykKBLS9FsII1xztVgeh_TYKYQx_yuMtUAk6nNaPptDnmhh9GFTXBzoa0LDMapcmYyz9ETb_oMLw7nGfr-6eO31VV98-Xz9erDTW0laafaYE-c7ARgsIR32DXMd5gZI2ijnMHOSe9b6hyA8Iq0rJO4Y-CV8FwpodgZutzrruduAGdL_7KBXqcwmLTV0QT9f2UMP_WPuNFcEiwUKQLnB4EUf8-QJz2EbKHvzQjFAU1UsY8TStnDUNlQJiWWbYG-vge9LYYX2xaUaDFt6W54sUfZFHNO4I9zE6yX3PUud72EqonQu9z1wnt1d-kj62_QBfB-D4Bi_SZA0tmWaCy4kMBO2sXwYIvLewr28HV-wRbyv210phrvRRYNInYKiv0B5WLT8A</recordid><startdate>20160201</startdate><enddate>20160201</enddate><creator>Horne, Margaret A, PhD</creator><creator>Flemming, Kelly D, MD</creator><creator>Su, I-Chang, MD</creator><creator>Stapf, Christian, Prof</creator><creator>Jeon, Jin Pyeong, MD</creator><creator>Li, Da, MD</creator><creator>Maxwell, Susanne S, MBChB</creator><creator>White, Philip, Prof</creator><creator>Christianson, Teresa J, BSc</creator><creator>Agid, Ronit, MD</creator><creator>Cho, Won-Sang, MD</creator><creator>Oh, Chang Wan, Prof</creator><creator>Wu, Zhen, Prof</creator><creator>Zhang, Jun-Ting, Prof</creator><creator>Kim, Jeong Eun, PhD</creator><creator>ter Brugge, Karel, Prof</creator><creator>Willinsky, Robert, FRCPC</creator><creator>Brown, Robert D, Prof</creator><creator>Murray, Gordon D, Prof</creator><creator>Salman, Rustam Al-Shahi, Prof</creator><general>Elsevier Ltd</general><general>Elsevier Limited</general><general>Lancet Pub. Group</general><scope>6I.</scope><scope>AAFTH</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>0TZ</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8C2</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160201</creationdate><title>Clinical course of untreated cerebral cavernous malformations: a meta-analysis of individual patient data</title><author>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</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 & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Lancet Titles</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Lancet neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horne, Margaret A, PhD</au><au>Flemming, Kelly D, MD</au><au>Su, I-Chang, MD</au><au>Stapf, Christian, Prof</au><au>Jeon, Jin Pyeong, MD</au><au>Li, Da, MD</au><au>Maxwell, Susanne S, MBChB</au><au>White, Philip, Prof</au><au>Christianson, Teresa J, BSc</au><au>Agid, Ronit, MD</au><au>Cho, Won-Sang, MD</au><au>Oh, Chang Wan, Prof</au><au>Wu, Zhen, Prof</au><au>Zhang, Jun-Ting, Prof</au><au>Kim, Jeong Eun, PhD</au><au>ter Brugge, Karel, Prof</au><au>Willinsky, Robert, FRCPC</au><au>Brown, Robert D, Prof</au><au>Murray, Gordon D, Prof</au><au>Salman, Rustam Al-Shahi, Prof</au><aucorp>Cerebral Cavernous Malformations Individual Patient Data Meta-analysis Collaborators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical course of untreated cerebral cavernous malformations: a meta-analysis of individual patient data</atitle><jtitle>Lancet neurology</jtitle><addtitle>Lancet Neurol</addtitle><date>2016-02-01</date><risdate>2016</risdate><volume>15</volume><issue>2</issue><spage>166</spage><epage>173</epage><pages>166-173</pages><issn>1474-4422</issn><eissn>1474-4465</eissn><coden>LANCAO</coden><abstract>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.</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> |
fulltext | fulltext |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T10%3A12%3A44IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Clinical%20course%20of%20untreated%20cerebral%20cavernous%20malformations:%20a%20meta-analysis%20of%20individual%20patient%20data&rft.jtitle=Lancet%20neurology&rft.au=Horne,%20Margaret%20A,%20PhD&rft.aucorp=Cerebral%20Cavernous%20Malformations%20Individual%20Patient%20Data%20Meta-analysis%20Collaborators&rft.date=2016-02-01&rft.volume=15&rft.issue=2&rft.spage=166&rft.epage=173&rft.pages=166-173&rft.issn=1474-4422&rft.eissn=1474-4465&rft.coden=LANCAO&rft_id=info:doi/10.1016/S1474-4422(15)00303-8&rft_dat=%3Cproquest_pubme%3E1826641223%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1759029258&rft_id=info:pmid/26654287&rft_els_id=1_s2_0_S1474442215003038&rfr_iscdi=true |