Use of MRI to predict symptomatic haemorrhagic transformation after thrombolysis for cerebral ischaemia.


Journal

Journal of neurology, neurosurgery, and psychiatry
ISSN: 1468-330X
Titre abrégé: J Neurol Neurosurg Psychiatry
Pays: England
ID NLM: 2985191R

Informations de publication

Date de publication:
04 2020
Historique:
received: 21 08 2019
revised: 14 01 2020
accepted: 16 01 2020
pubmed: 6 2 2020
medline: 18 8 2020
entrez: 5 2 2020
Statut: ppublish

Résumé

Predictors of symptomatic haemorrhagic transformation (s-HT) of cerebral ischaemia after intravenous recombinant tissue-plasminogen activator (rt-PA) were identified in studies using CT scans. We evaluated whether MRI can identify other predictors. We analysed predictors of s-HT in a cohort of consecutive patients who received intravenous rt-PA for cerebral ischaemia after MRI at baseline. We used receiver operating characteristic curves considering an area under the curve (AUC) of 0.70 or higher as indicating acceptable discrimination. Of 944 patients, 49 patients (5.2%) developed s-HT. Clinical factors independently associated with s-HT were age (adjusted OR (adjOR) 1.03 for 1 year increase; 95% CI 1.01 to 1.05), excessive alcohol consumption (adjOR 3.13; 95% CI 1.32 to 7.42), recent transient ischaemic attack (adjOR 2.88; 95% CI 1.04 to 7.95) and baseline national institutes of health stroke scale score (adjOR 1.06 for 1 point increase; 95% CI 1.02 to 1.10). MRI predictors were vascular hyperintensities (adjOR 3.89; 95% CI 1.50 to 10.08), old infarcts (adjOR 2.01; 95% CI 1.11 to 3.66) and volume of diffusion-weighted imaging (DWI) abnormality (adjOR 1.02 for 1 cm Although the volume of DWI abnormality predicts s-HT, other imaging characteristics that can only be assessed with MRI were not significantly associated with s-HT.

Sections du résumé

BACKGROUND AND OBJECTIVE
Predictors of symptomatic haemorrhagic transformation (s-HT) of cerebral ischaemia after intravenous recombinant tissue-plasminogen activator (rt-PA) were identified in studies using CT scans. We evaluated whether MRI can identify other predictors.
METHOD
We analysed predictors of s-HT in a cohort of consecutive patients who received intravenous rt-PA for cerebral ischaemia after MRI at baseline. We used receiver operating characteristic curves considering an area under the curve (AUC) of 0.70 or higher as indicating acceptable discrimination.
RESULTS
Of 944 patients, 49 patients (5.2%) developed s-HT. Clinical factors independently associated with s-HT were age (adjusted OR (adjOR) 1.03 for 1 year increase; 95% CI 1.01 to 1.05), excessive alcohol consumption (adjOR 3.13; 95% CI 1.32 to 7.42), recent transient ischaemic attack (adjOR 2.88; 95% CI 1.04 to 7.95) and baseline national institutes of health stroke scale score (adjOR 1.06 for 1 point increase; 95% CI 1.02 to 1.10). MRI predictors were vascular hyperintensities (adjOR 3.89; 95% CI 1.50 to 10.08), old infarcts (adjOR 2.01; 95% CI 1.11 to 3.66) and volume of diffusion-weighted imaging (DWI) abnormality (adjOR 1.02 for 1 cm
CONCLUSION
Although the volume of DWI abnormality predicts s-HT, other imaging characteristics that can only be assessed with MRI were not significantly associated with s-HT.

Identifiants

pubmed: 32015090
pii: jnnp-2019-321904
doi: 10.1136/jnnp-2019-321904
doi:

Substances chimiques

Fibrinolytic Agents 0
Tissue Plasminogen Activator EC 3.4.21.68

Banques de données

ClinicalTrials.gov
['NCT01614080']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

402-410

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: ND-P and HH reports participation in drug trials with Boehringer-Ingelheim (honoraria paid to the hospital). CC reports participation in symposia organised by Boehringer-Ingelheim and Pfizer, advisory board by BMS (honoraria paid to ADRINORD), drug trials with Boehringer-Ingelheim, Servier, Astra-Zeneca, Biogen (honoraria paid to the hospital), vice president of the European Stroke Organisation (unpaid), member of DSMBs for institutional trials (unpaid): ATTEST 2 (UK), FIV-HeMA (France). Research support from the French Ministry of Health (A3ICH). DL reports participation in symposia organised by Boehringer Ingelheim, Bayer, BMS and Pfizer (honoraria paid to Adrinord), drug trials with Boehringer-Ingelheim (honoraria paid to the hospital), vice editor of the European Stroke Journal (honoraria paid to Adrinord), vice president of the scientific committee of the Fondation de Recherche sur les AVC (unpaid) and member of the scientific committee of the Servier Institute (unpaid). Member of DSMBs for institutional trials (unpaid): INCH (Germany), TARDIS (UK), and TO-ACT (the Netherlands). Research support from a grant of the University of Heidelberg (Germany) for the ECASS4 trial.

Auteurs

François Caparros (F)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Gregory Kuchcinski (G)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Agathe Drelon (A)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Barbara Casolla (B)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Solene Moulin (S)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Nelly Dequatre-Ponchelle (N)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Hilde Henon (H)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Charlotte Cordonnier (C)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Jean-Pierre Pruvo (JP)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France.

Didier Leys (D)

Departments of Neurology and Neuroradiology, University of Lille, Inserm U1171-1, CHU Lille. Lille, France, Lille, France didier.leys@univ-lille.fr.

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Classifications MeSH