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Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage.

Publication ,  Journal Article
Kidwell, CS; Rosand, J; Norato, G; Dixon, S; Worrall, BB; James, ML; Elkind, MSV; Flaherty, ML; Osborne, J; Vashkevich, A; Langefeld, CD ...
Published in: Neurology
February 21, 2017

OBJECTIVE: To evaluate the associations among diffusion-weighted imaging (DWI) lesions, blood pressure (BP) dysregulation, MRI markers of small vessel disease, and poor outcome in a large, prospective study of primary intracerebral hemorrhage (ICH). METHODS: The Ethnic/Racial Variations of Intracerebral Hemorrhage (ERICH) study is a multicenter, observational study of ICH among white, black, and Hispanic patients. RESULTS: Of 600 patients, mean (±SD) age was 60.8 ± 13.6 years, median (interquartile range) ICH volume was 9.1 mL (3.5-20.8), and 79.6% had hypertension. Overall, 26.5% of cases had DWI lesions, and this frequency differed by race/ethnicity (black 33.8%, Hispanic 24.9%, white 20.2%, overall p = 0.006). A logistic regression model of variables associated with DWI lesions included lower age (odds ratio [OR] 0.721, p = 0.002), higher first recorded systolic BP (10-unit OR 1.12, p = 0.002), greater change in mean arterial pressure (MAP) prior to the MRI (10-unit OR 1.10, p = 0.037), microbleeds (OR 1.99, p = 0.008), and higher white matter hyperintensity (WMH) score (1-unit OR 1.16, p = 0.002) after controlling for race/ethnicity, leukocyte count, and acute in-hospital antihypertensive treatment. A second model of variables associated with poor 90-day functional outcome (modified Rankin Scale scores 4-6) included DWI lesion count (OR 1.085, p = 0.034) as well as age, ICH volume, intraventricular hemorrhage, Glasgow Coma Scale score, WMH score, race/ethnicity, acute in-hospital antihypertensive treatment, and ICH location. CONCLUSIONS: These results support the hypotheses that acute BP dysregulation is associated with the development of DWI lesions in primary ICH and that DWI lesions are, in turn, associated with poor outcomes.

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Published In

Neurology

DOI

EISSN

1526-632X

Publication Date

February 21, 2017

Volume

88

Issue

8

Start / End Page

782 / 788

Location

United States

Related Subject Headings

  • United States
  • Treatment Outcome
  • Prospective Studies
  • Neurology & Neurosurgery
  • Multivariate Analysis
  • Middle Aged
  • Male
  • Logistic Models
  • Humans
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
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Kidwell, C. S., Rosand, J., Norato, G., Dixon, S., Worrall, B. B., James, M. L., … Woo, D. (2017). Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage. Neurology, 88(8), 782–788. https://doi.org/10.1212/WNL.0000000000003630
Kidwell, Chelsea S., Jonathan Rosand, Gina Norato, Simone Dixon, Bradford B. Worrall, Michael L. James, Mitchell S. V. Elkind, et al. “Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage.Neurology 88, no. 8 (February 21, 2017): 782–88. https://doi.org/10.1212/WNL.0000000000003630.
Kidwell CS, Rosand J, Norato G, Dixon S, Worrall BB, James ML, et al. Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage. Neurology. 2017 Feb 21;88(8):782–8.
Kidwell, Chelsea S., et al. “Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage.Neurology, vol. 88, no. 8, Feb. 2017, pp. 782–88. Pubmed, doi:10.1212/WNL.0000000000003630.
Kidwell CS, Rosand J, Norato G, Dixon S, Worrall BB, James ML, Elkind MSV, Flaherty ML, Osborne J, Vashkevich A, Langefeld CD, Moomaw CJ, Woo D. Ischemic lesions, blood pressure dysregulation, and poor outcomes in intracerebral hemorrhage. Neurology. 2017 Feb 21;88(8):782–788.

Published In

Neurology

DOI

EISSN

1526-632X

Publication Date

February 21, 2017

Volume

88

Issue

8

Start / End Page

782 / 788

Location

United States

Related Subject Headings

  • United States
  • Treatment Outcome
  • Prospective Studies
  • Neurology & Neurosurgery
  • Multivariate Analysis
  • Middle Aged
  • Male
  • Logistic Models
  • Humans
  • Female