Risk of symptomatic intracerebral hemorrhage after intravenous thrombolysis in patients with acute ischemic stroke and high cerebral microbleed burden ameta-analysis

Journal article


Tsivgoulis, Georgios, Zand, Ramin, Katsanos, Aristeidis H., Turc, Guillaume, Nolte, Christian H., Jung, Simon, Cordonnier, Charlotte, Fiebach, Jochen B., Scheitz, Jan F., Klinger-Gratz, Pascal P., Oppenheim, Catherine, Goyal, Nitin, Safouris, Apostolos, Mattle, Heinrich P., Alexandrov, Anne W., Schellinger, Peter D. and Alexandrov, Andrei V.. (2016). Risk of symptomatic intracerebral hemorrhage after intravenous thrombolysis in patients with acute ischemic stroke and high cerebral microbleed burden ameta-analysis. JAMA Neurology. 73(6), pp. 675 - 683. https://doi.org/10.1001/jamaneurol.2016.0292
AuthorsTsivgoulis, Georgios, Zand, Ramin, Katsanos, Aristeidis H., Turc, Guillaume, Nolte, Christian H., Jung, Simon, Cordonnier, Charlotte, Fiebach, Jochen B., Scheitz, Jan F., Klinger-Gratz, Pascal P., Oppenheim, Catherine, Goyal, Nitin, Safouris, Apostolos, Mattle, Heinrich P., Alexandrov, Anne W., Schellinger, Peter D. and Alexandrov, Andrei V.
Abstract

Importance Cerebral microbleeds (CMBs) have been established as an independent predictor of cerebral bleeding. There are contradictory data regarding the potential association of CMB burden with the risk of symptomatic intracerebral hemorrhage (sICH) in patients with acute ischemic stroke (AIS) treated with intravenous thrombolysis (IVT). Objective To investigate the association of high CMB burden (>10 CMBs on a pre-IVT magnetic image resonance [MRI] scan) with the risk of sICH following IVT for AIS. Data Sources: Eligible studies were identified by searching Medline and Scopus databases. No language or other restrictions were imposed. The literature search was conducted on October 7, 2015. This meta-analysis has adopted the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and was written according to the Meta-analysis of Observational Studies in Epidemiology (MOOSE) proposal. Study Selection: Eligible prospective study protocols that reported sICH rates in patients with AIS who underwent MRI for CMB screening prior to IVT. Data Extraction and Synthesis: The reported rates of sICH complicating IVT in patients with AIS with pretreatment MRI were extracted independently for groups of patients with 0 CMBs (CMB absence), 1 or more CMBs (CMB presence), 1 to 10 CMBs (low to moderate CMB burden), and more than 10 CMBs (high CMB burden). An individual-patient data meta-analysis was also performed in the included studies that provided complete patient data sets. Main Outcomes and Measures: Symptomatic intracerebral hemorrhage based on the European Cooperative Acute Stroke Study–II definition (any intracranial bleed with ≥4 points worsening on the National Institutes of Health Stroke Scale score). Results: We included 9 studies comprising 2479 patients with AIS. The risk of sICH after IVT was found to be higher in patients with evidence of CMB presence, compared with patients without CMBs (risk ratio [RR], 2.36; 95% CI, 1.21-4.61; P = .01). A higher risk for sICH after IVT was detected in patients with high CMB burden (>10 CMBs) when compared with patients with 0 to 10 CMBs (RR, 12.10; 95% CI, 4.36-33.57; P < .001) or 1 to 10 CMBs (RR, 7.01; 95% CI, 3.20-15.38; P < .001) on pretreatment MRI. In the individual-patient data meta-analysis, high CMB burden was associated with increased likelihood of sICH before (unadjusted odds ratio, 31.06; 95% CI, 7.12-135.44; P < .001) and after (adjusted odds ratio, 18.17; 95% CI, 2.39-138.22; P = .005) adjusting for potential confounders. Conclusions and Relevance: Presence of CMB and high CMB burdens on pretreatment MRI were independently associated with sICH in patients with AIS treated with IVT. High CMB burden may be included in individual risk stratification scores predicting sICH risk following IVT for AIS.

Year2016
JournalJAMA Neurology
Journal citation73 (6), pp. 675 - 683
PublisherAmerican Medical Association
ISSN2168-6149
Digital Object Identifier (DOI)https://doi.org/10.1001/jamaneurol.2016.0292
Scopus EID2-s2.0-84974625093
Page range675 - 683
Publisher's version
File Access Level
Controlled
Place of publicationUnited States of America
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