Microbleeds, Cerebral Hemorrhage, and Functional Outcome After Stroke Thrombolysis

Andreas Charidimou(Université Paris Cité), Guillaume Turc(Université Paris Cité), Catherine Oppenheim(Université Paris Cité), Shenqiang Yan(Université Paris Cité), Jan F. Scheitz(Université Paris Cité), Hebun Erdur(Université Paris Cité), Pascal P. Klinger-Gratz(Université Paris Cité), Marwan El‐Koussy(Université Paris Cité), Wakoh Takahashi(Université Paris Cité), Yusuke Moriya(Université Paris Cité), Duncan Wilson(Université Paris Cité), Chelsea S. Kidwell(Université Paris Cité), Jeffrey L. Saver(Université Paris Cité), Asma Sallem(Université Paris Cité), Solène Moulin(Université Paris Cité), Myriam Edjlali(Université Paris Cité), Vincent Thijs(Université Paris Cité), Zoë Fox(Université Paris Cité), Ashkan Shoamanesh(Université Paris Cité), Gregory W. Albers(Université Paris Cité), Heinrich P. Mattle(Université Paris Cité), Oscar Benavente(Université Paris Cité), Hans Rolf Jäger(Université Paris Cité), Gareth Ambler(Université Paris Cité), Junya Aoki(Université Paris Cité), Jean‐Claude Baron(Université Paris Cité), Kazumi Kimura(Université Paris Cité), Wataru Kakuda(Université Paris Cité), Shunya Takizawa(Université Paris Cité), Simon Jung(Université Paris Cité), Christian H. Nolte(Université Paris Cité), Min Lou(Université Paris Cité), Charlotte Cordonnier(Université Paris Cité), David J. Werring(Université Paris Cité)
Stroke
July 19, 2017
Cited by 138Open Access
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Abstract

Background and Purpose- We assessed whether the presence, number, and distribution of cerebral microbleeds (CMBs) on pre-intravenous thrombolysis MRI scans of acute ischemic stroke patients are associated with an increased risk of intracerebral hemorrhage (ICH) or poor functional outcome. Methods- We performed an individual patient data meta-analysis, including prospective and retrospective studies of acute ischemic stroke treated with intravenous tissue-type plasminogen activator. Using multilevel mixed-effects logistic regression, we investigated associations of pre-treatment CMB presence, burden (1, 2-4, ≥5, and >10), and presumed pathogenesis (cerebral amyloid angiopathy defined as strictly lobar CMBs and noncerebral amyloid angiopathy) with symptomatic ICH, parenchymal hematoma (within [parenchymal hemorrhage, PH] and remote from the ischemic area [remote parenchymal hemorrhage, PHr]), and poor 3- to 6-month functional outcome (modified Rankin score >2). Results- In 1973 patients from 8 centers, the crude prevalence of CMBs was 526 of 1973 (26.7%). A total of 77 of 1973 (3.9%) patients experienced symptomatic ICH, 210 of 1806 (11.6%) experienced PH, and 56 of 1720 (3.3%) experienced PHr. In adjusted analyses, patients with CMBs (compared with those without CMBs) had increased risk of PH (odds ratio: 1.50; 95% confidence interval: 1.09-2.07; P=0.013) and PHr (odds ratio: 3.04; 95% confidence interval: 1.73-5.35; P<0.001) but not symptomatic ICH. Both cerebral amyloid angiopathy and noncerebral amyloid angiopathy patterns of CMBs were associated with PH and PHr. Increasing CMB burden category was associated with the risk of symptomatic ICH ( P=0.014), PH ( P=0.013), and PHr ( P<0.00001). Five or more and >10 CMBs independently predicted poor 3- to 6-month outcome (odds ratio: 1.85; 95% confidence interval: 1.10-3.12; P=0.020; and odds ratio: 3.99; 95% confidence interval: 1.55-10.22; P=0.004, respectively). Conclusions- Increasing CMB burden is associated with increased risk of ICH (including PHr) and poor 3- to 6-month functional outcome after intravenous thrombolysis for acute ischemic stroke.


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