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Prognostic Significance of Perihematomal Edema in Acute Intracerebral Hemorrhage Pooled Analysis From the Intensive Blood Pressure Reduction in Acute Cerebral Hemorrhage Trial Studies

Authors
Yang, JieArima, HisatomiWu, GuojunHeeley, EmmaDelcourt, CandiceZhou, JunshanChen, GuofangWang, XiaZhang, ShihongYu, SungwookChalmers, JohnAnderson, Craig S.
Issue Date
4월-2015
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Keywords
cerebral hemorrhage; clinical trial; hypertension
Citation
STROKE, v.46, no.4, pp.1009 - +
Indexed
SCIE
SCOPUS
Journal Title
STROKE
Volume
46
Number
4
Start Page
1009
End Page
+
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/93985
DOI
10.1161/STROKEAHA.114.007154
ISSN
0039-2499
Abstract
Background and Purpose-Controversy exists over the prognostic significance of perihematomal edema (PHE) in intracerebral hemorrhage. We aimed to determine the association of early PHE and clinical outcome among participants of the Intensive Blood Pressure Reduction in Acute Cerebral Hemorrhage Trial (INTERACT) studies. Methods-Pooled analyses of computed tomographic substudies in the pilot phase (INTERACT1) and main phase (INTERACT2), both international, prospective, open, blinded end point, randomized controlled trials, of patients with spontaneous intracerebral hemorrhage (<6 hours) and elevated systolic blood pressure, randomly assigned to intensive (target systolic blood pressure, < 140 mm Hg) or guideline-based (systolic blood pressure, < 180 mm Hg) blood-pressure management. Substudy participants (n= 1310; 346 INTERACT1, 964 INTERACT2) had blinded central analyses of digital images from standardized baseline and 24-hour computed tomography. Predictors of death or dependency (modified >= Rankin scale scores, 3) at 90 days were assessed in logistic regression models and reported with odds ratios and 95% confidence intervals. INTERACT studies are registered at Clinical Trials. gov (NCT00226096 and NCT00716079). Results-Of 1138 (87%) patients with 2 CTs available for edema analysis and outcome information, time from intracerebral hemorrhage onset to baseline computed tomography, baseline hematoma volume, 24-hour hematoma growth, and intraventricular extension were independent predictors of 24-hour PHE growth. Absolute growth in PHE volume was significantly associated with death or dependency (adjusted odds ratio, 1.17; 95% confidence interval, 1.02-1.33 per 5 mL increase from baseline; P= 0.025) at 90 days after adjustment for demographic, clinical, and hematoma parameter prognostic factors. Associations were consistent across various sensitivity analyses. Conclusion-PHE growth is an independent prognostic factor in intracerebral hemorrhage.
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