The Prognostic Roles of Perihematomal Edema and Ventricular Size in Patients with Intracerebral Hemorrhage.


Journal

Neurocritical care
ISSN: 1556-0961
Titre abrégé: Neurocrit Care
Pays: United States
ID NLM: 101156086

Informations de publication

Date de publication:
10 2022
Historique:
received: 28 10 2021
accepted: 02 05 2022
pubmed: 9 6 2022
medline: 1 10 2022
entrez: 8 6 2022
Statut: ppublish

Résumé

Conflicting data exist regarding the association of perihematomal edema (PHE) with outcomes after intracerebral hemorrhage (ICH). We performed a post hoc analysis of the ICH Deferoxamine trial to examine whether an early change in ventricular size (VS), as a composite measure of PHE growth and mass effect, intraventricular hemorrhage, and hydrocephalus, is a more accurate predictor of outcome than PHE measures alone. Computerized tomography scans were performed at baseline and after 72-96 h. We evaluated measures of PHE and change in VS as predictors of outcome, assessed by a dichotomized modified Rankin Scale score (0-2 versus 3-6), primarily at 90 days and secondarily at 30 days. A multivariable logistic regression model was fitted for each predictor, with adjustment for the same confounders. A total of 248 participants were included after we excluded those requiring external ventricular drains. On univariate analyses, older age, female sex, lower Glasgow Coma Scale score and baseline temperature, greater ICH volume, absolute PHE volume, edema extension distance at presentation, lesser changes in relative PHE volume and edema extension distance, and an increase in VS were associated with poor outcome. In multivariable analyses, only the increase in VS was associated with lower odds of modified Rankin Scale scores 0-2 at 90 days (odds ratio 0.927, 95% confidence interval 0.866-0.970, p = 0.001) and 30 days (odds ratio 0.931, 95% confidence interval 0.888-0.975, p = 0.003). Within the context of a randomized controlled trial with standardized imaging and functional assessments, we did not find significant associations between measures of PHE and outcome but documented an independent association between early increase in VS and lower odds of good clinical outcome.

Sections du résumé

BACKGROUND
Conflicting data exist regarding the association of perihematomal edema (PHE) with outcomes after intracerebral hemorrhage (ICH). We performed a post hoc analysis of the ICH Deferoxamine trial to examine whether an early change in ventricular size (VS), as a composite measure of PHE growth and mass effect, intraventricular hemorrhage, and hydrocephalus, is a more accurate predictor of outcome than PHE measures alone.
METHODS
Computerized tomography scans were performed at baseline and after 72-96 h. We evaluated measures of PHE and change in VS as predictors of outcome, assessed by a dichotomized modified Rankin Scale score (0-2 versus 3-6), primarily at 90 days and secondarily at 30 days. A multivariable logistic regression model was fitted for each predictor, with adjustment for the same confounders.
RESULTS
A total of 248 participants were included after we excluded those requiring external ventricular drains. On univariate analyses, older age, female sex, lower Glasgow Coma Scale score and baseline temperature, greater ICH volume, absolute PHE volume, edema extension distance at presentation, lesser changes in relative PHE volume and edema extension distance, and an increase in VS were associated with poor outcome. In multivariable analyses, only the increase in VS was associated with lower odds of modified Rankin Scale scores 0-2 at 90 days (odds ratio 0.927, 95% confidence interval 0.866-0.970, p = 0.001) and 30 days (odds ratio 0.931, 95% confidence interval 0.888-0.975, p = 0.003).
CONCLUSIONS
Within the context of a randomized controlled trial with standardized imaging and functional assessments, we did not find significant associations between measures of PHE and outcome but documented an independent association between early increase in VS and lower odds of good clinical outcome.

Identifiants

pubmed: 35676589
doi: 10.1007/s12028-022-01532-0
pii: 10.1007/s12028-022-01532-0
doi:

Substances chimiques

Deferoxamine J06Y7MXW4D

Banques de données

ClinicalTrials.gov
['NCT02175225']

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

455-462

Subventions

Organisme : NINDS NIH HHS
ID : U01 NS074425
Pays : United States
Organisme : NINDS NIH HHS
ID : U01 NS102289
Pays : United States
Organisme : NINDS NIH HHS
ID : UF1 NS120871
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS017950
Pays : United States

Informations de copyright

© 2022. Springer Science+Business Media, LLC, part of Springer Nature and Neurocritical Care Society.

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Auteurs

Kun He Lee (KH)

Stroke Division, Department of Neurology, Beth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, MA, USA. khlee@bidmc.harvard.edu.

Vasileios-Arsenios Lioutas (VA)

Stroke Division, Department of Neurology, Beth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, MA, USA.

Sarah Marchina (S)

Stroke Division, Department of Neurology, Beth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, MA, USA.

Magdy Selim (M)

Stroke Division, Department of Neurology, Beth Israel Deaconess Medical Center, 330 Brookline Ave, Boston, MA, USA.

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