Late Neurological Deterioration after Acute Intracerebral Hemorrhage: A post hoc Analysis of the ATACH-2 Trial.


Journal

Cerebrovascular diseases (Basel, Switzerland)
ISSN: 1421-9786
Titre abrégé: Cerebrovasc Dis
Pays: Switzerland
ID NLM: 9100851

Informations de publication

Date de publication:
2020
Historique:
received: 21 09 2019
accepted: 24 01 2020
pubmed: 12 2 2020
medline: 24 9 2020
entrez: 12 2 2020
Statut: ppublish

Résumé

Neurological deterioration (ND) has a major influence on the prognosis of intracerebral hemorrhage (ICH); however, factors associated with ND occurring after 24 h of ICH onset are unknown. We performed exploratory analyses of data from the Antihypertensive Treatment of Acute Cerebral Hemorrhage 2 trial, which compared intensive and standard blood pressure lowering treatment in ICH. NDs were captured on the adverse event case report form. Logistic regression analysis was performed to examine the independent predictors of late ND. Among 1,000 participants with acute ICH, 82 patients (8.2%) developed early ND (≤24 h), and 64 (6.4%) had late ND. Baseline hematoma volume (adjusted OR [aOR] per 1-cm3 increase 1.04, 95% CI 1.02-1.06, p < 0.0001), hematoma volume increase in 24 h (aOR 2.24, 95% CI 1.23-4.07, p = 0.008), and the presence of intraventricular hemorrhage (IVH; aOR 2.38, 95% CI 1.32-4.29, p = 0.004) were independent predictors of late ND (vs. no late ND). Late ND was a significant risk factor for poor 90-day outcome (OR 3.46, 95% CI 1.82-6.56). No statistically significant difference in the incidence of late ND was noted between the 2 treatment groups. Initial hematoma volume, early hematoma volume expansion, and IVH are independent predictors of late ND after ICH. Intensive reduction in the systolic blood pressure level does not prevent the development of late ND.

Sections du résumé

BACKGROUND
Neurological deterioration (ND) has a major influence on the prognosis of intracerebral hemorrhage (ICH); however, factors associated with ND occurring after 24 h of ICH onset are unknown.
METHODS
We performed exploratory analyses of data from the Antihypertensive Treatment of Acute Cerebral Hemorrhage 2 trial, which compared intensive and standard blood pressure lowering treatment in ICH. NDs were captured on the adverse event case report form. Logistic regression analysis was performed to examine the independent predictors of late ND.
RESULTS
Among 1,000 participants with acute ICH, 82 patients (8.2%) developed early ND (≤24 h), and 64 (6.4%) had late ND. Baseline hematoma volume (adjusted OR [aOR] per 1-cm3 increase 1.04, 95% CI 1.02-1.06, p < 0.0001), hematoma volume increase in 24 h (aOR 2.24, 95% CI 1.23-4.07, p = 0.008), and the presence of intraventricular hemorrhage (IVH; aOR 2.38, 95% CI 1.32-4.29, p = 0.004) were independent predictors of late ND (vs. no late ND). Late ND was a significant risk factor for poor 90-day outcome (OR 3.46, 95% CI 1.82-6.56). No statistically significant difference in the incidence of late ND was noted between the 2 treatment groups.
CONCLUSIONS
Initial hematoma volume, early hematoma volume expansion, and IVH are independent predictors of late ND after ICH. Intensive reduction in the systolic blood pressure level does not prevent the development of late ND.

Identifiants

pubmed: 32045911
pii: 000506117
doi: 10.1159/000506117
doi:

Substances chimiques

Antihypertensive Agents 0

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

26-31

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Shuhei Okazaki (S)

Department of Data Science, National Cerebral and Cardiovascular Center, Osaka, Japan, s-okazaki@umin.ac.jp.
Department of Neurology, National Cerebral and Cardiovascular Center, Osaka, Japan, s-okazaki@umin.ac.jp.
Department of Neurology, Osaka University Graduate School of Medicine, Osaka, Japan, s-okazaki@umin.ac.jp.

Haruko Yamamoto (H)

Department of Data Science, National Cerebral and Cardiovascular Center, Osaka, Japan.

Lydia D Foster (LD)

Department of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.

Mayumi Fukuda-Doi (M)

Department of Data Science, National Cerebral and Cardiovascular Center, Osaka, Japan.
Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.

Masatoshi Koga (M)

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.

Masafumi Ihara (M)

Department of Neurology, National Cerebral and Cardiovascular Center, Osaka, Japan.

Kazunori Toyoda (K)

Department of Cerebrovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.

Yuko Y Palesch (YY)

Department of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.

Adnan I Qureshi (AI)

Department of Neurology, University of Missouri, Columbia, Missouri, USA.

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