Primary intraventricular hemorrhage outcomes in the CLEAR III trial.


Journal

International journal of stroke : official journal of the International Stroke Society
ISSN: 1747-4949
Titre abrégé: Int J Stroke
Pays: United States
ID NLM: 101274068

Informations de publication

Date de publication:
10 2020
Historique:
pubmed: 23 2 2020
medline: 26 10 2021
entrez: 21 2 2020
Statut: ppublish

Résumé

Intraventricular hemorrhage occurs due to intracerebral hemorrhage with intraventricular extension or without apparent parenchymal involvement, known as primary intraventricular hemorrhage. We evaluated the prognosis of primary intraventricular hemorrhage patients in the CLEAR III trial (Clot Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage). In patients with primary intraventricular hemorrhage versus those with secondary intraventricular hemorrhage, we compared intraventricular alteplase response and outcomes including modified Rankin Scale, Barthel Index, National Institutes of Health Stroke Scale (NIHSS), and extended Glasgow Outcome Scale (eGOS) at 30, 180, and 365 days. Outcomes were also compared in primary intraventricular hemorrhage patients who received intraventricular alteplase versus placebo (normal saline) and in matched primary and secondary intraventricular hemorrhage patients using inverse-probability-weighted regression adjustment. Of 500 patients enrolled in CLEAR III, 46 (9.2%) had primary intraventricular hemorrhage. Combining both treatment groups, primary intraventricular hemorrhage patients had larger intraventricular hemorrhage volumes (median: 34.2 mL vs. 20.8 mL, In CLEAR III, primary intraventricular hemorrhage patients who survived achieved better long-term outcomes than surviving secondary intraventricular hemorrhage patients with similar mortality. Outcomes and safety were similar between primary intraventricular hemorrhage patients receiving alteplase and those receiving saline.

Sections du résumé

BACKGROUND
Intraventricular hemorrhage occurs due to intracerebral hemorrhage with intraventricular extension or without apparent parenchymal involvement, known as primary intraventricular hemorrhage.
AIMS
We evaluated the prognosis of primary intraventricular hemorrhage patients in the CLEAR III trial (Clot Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage).
METHODS
In patients with primary intraventricular hemorrhage versus those with secondary intraventricular hemorrhage, we compared intraventricular alteplase response and outcomes including modified Rankin Scale, Barthel Index, National Institutes of Health Stroke Scale (NIHSS), and extended Glasgow Outcome Scale (eGOS) at 30, 180, and 365 days. Outcomes were also compared in primary intraventricular hemorrhage patients who received intraventricular alteplase versus placebo (normal saline) and in matched primary and secondary intraventricular hemorrhage patients using inverse-probability-weighted regression adjustment.
RESULTS
Of 500 patients enrolled in CLEAR III, 46 (9.2%) had primary intraventricular hemorrhage. Combining both treatment groups, primary intraventricular hemorrhage patients had larger intraventricular hemorrhage volumes (median: 34.2 mL vs. 20.8 mL,
CONCLUSIONS
In CLEAR III, primary intraventricular hemorrhage patients who survived achieved better long-term outcomes than surviving secondary intraventricular hemorrhage patients with similar mortality. Outcomes and safety were similar between primary intraventricular hemorrhage patients receiving alteplase and those receiving saline.

Identifiants

pubmed: 32075571
doi: 10.1177/1747493020908146
pmc: PMC7837409
mid: NIHMS1660387
doi:

Substances chimiques

Fibrinolytic Agents 0
Tissue Plasminogen Activator EC 3.4.21.68

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

872-880

Subventions

Organisme : NINDS NIH HHS
ID : U01 NS062851
Pays : United States

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Auteurs

Sarah E Nelson (SE)

Departments of Neurology and Anesthesiology/Critical Care Medicine, 1466Johns Hopkins University, Baltimore, MD, USA.

W Andrew Mould (WA)

Division of Brain Injury Outcomes, 1466Johns Hopkins University, Baltimore, MD, USA.

Dheeraj Gandhi (D)

Department of Diagnostic Radiology and Nuclear Medicine, University of Maryland, Baltimore, MD, USA.

Richard E Thompson (RE)

Department of Biostatistics, 1466Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.

Sarah Salter (S)

Department of Biostatistics, 1466Johns Hopkins University Bloomberg School of Public Health, Baltimore, MD, USA.

Rachel Dlugash (R)

Division of Brain Injury Outcomes, 1466Johns Hopkins University, Baltimore, MD, USA.

Issam A Awad (IA)

Section of Neurosurgery, University of Chicago, Chicago, IL, USA.

Daniel F Hanley (DF)

Departments of Neurology and Anesthesiology/Critical Care Medicine, 1466Johns Hopkins University, Baltimore, MD, USA.
Division of Brain Injury Outcomes, 1466Johns Hopkins University, Baltimore, MD, USA.

Wendy Ziai (W)

Departments of Neurology and Anesthesiology/Critical Care Medicine, 1466Johns Hopkins University, Baltimore, MD, USA.

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