Blood pressure reduction and noncontrast CT markers of intracerebral hemorrhage expansion

To validate various noncontrast CT (NCCT) predictors of hematoma expansion in a large international cohort of ICH patients and investigate whether intensive blood pressure (BP) treatment reduces ICH growth and improves outcome in patients with these markers. We analyzed patients enrolled in the Anti...

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Veröffentlicht in:Neurology 2017-08, Vol.89 (6), p.548-554
Hauptverfasser: Morotti, Andrea, Boulouis, Gregoire, Romero, Javier M, Brouwers, H Bart, Jessel, Michael J, Vashkevich, Anastasia, Schwab, Kristin, Afzal, Mohammad Rauf, Cassarly, Christy, Greenberg, Steven M, Martin, Reneé Hebert, Qureshi, Adnan I, Rosand, Jonathan, Goldstein, Joshua N
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Sprache:eng
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Zusammenfassung:To validate various noncontrast CT (NCCT) predictors of hematoma expansion in a large international cohort of ICH patients and investigate whether intensive blood pressure (BP) treatment reduces ICH growth and improves outcome in patients with these markers. We analyzed patients enrolled in the Antihypertensive Treatment of Acute Cerebral Hemorrhage II (ATACH-II) randomized controlled trial. Participants were assigned to intensive (systolic BP 3 at 90 days. Logistic regression was used to identify predictors of ICH expansion and explore the association between NCCT signs and clinical benefit from intensive BP treatment. A total of 989 patients were included (mean age 62 years, 61.9% male), of whom 186/869 experienced hematoma expansion (21.4%) and 361/952 (37.9%) had unfavorable outcome. NCCT markers independently predicted ICH expansion (all < 0.01) with overall accuracy ranging from 61% to 78% and good interrater reliability ( > 0.6 for all markers). There was no evidence of an interaction between NCCT markers and benefit from intensive BP reduction (all for interaction >0.10). NCCT signs reliably identify ICH patients at high risk of hematoma growth. However, we found no evidence that patients with these markers specifically benefit from intensive BP reduction. NCT01176565.
ISSN:0028-3878
1526-632X
DOI:10.1212/WNL.0000000000004210