Intracerebral haemorrhage in patients with brain metastases receiving therapeutic anticoagulation.


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:
09 Mar 2021
Historique:
received: 04 07 2020
revised: 22 10 2020
accepted: 22 12 2020
entrez: 10 3 2021
pubmed: 11 3 2021
medline: 11 3 2021
Statut: aheadofprint

Résumé

Venous thromboembolism is common in patients with solid malignancies and brain metastases. Whether to anticoagulate such patients is controversial given the possibility of intracerebral haemorrhage (ICH). We evaluated the added risk of ICH in patients with brain metastases receiving therapeutic anticoagulation. We performed a matched, retrospective cohort study of 291 patients (100 receiving therapeutic anticoagulation vs 191 controls) with brain metastases managed at Brigham and Women's Hospital/Dana-Farber Cancer Institute between 1998 and 2015. For each patient, all MRI studies of the brain were reviewed to identify ICH. Propensity score matching and multivariable Cox regression were used to mitigate confounding. The risk of ICH was comparable in patients receiving anticoagulation versus controls preanticoagulation Anticoagulation is associated with clinically significant ICH in patients with brain metastases, especially those with melanoma or prior ICH. The indication for anticoagulation and risk of intracerebral bleeding should be considered on an individual basis among such patients.

Sections du résumé

BACKGROUND BACKGROUND
Venous thromboembolism is common in patients with solid malignancies and brain metastases. Whether to anticoagulate such patients is controversial given the possibility of intracerebral haemorrhage (ICH). We evaluated the added risk of ICH in patients with brain metastases receiving therapeutic anticoagulation.
METHODS METHODS
We performed a matched, retrospective cohort study of 291 patients (100 receiving therapeutic anticoagulation vs 191 controls) with brain metastases managed at Brigham and Women's Hospital/Dana-Farber Cancer Institute between 1998 and 2015. For each patient, all MRI studies of the brain were reviewed to identify ICH. Propensity score matching and multivariable Cox regression were used to mitigate confounding.
RESULTS RESULTS
The risk of ICH was comparable in patients receiving anticoagulation versus controls preanticoagulation
CONCLUSIONS CONCLUSIONS
Anticoagulation is associated with clinically significant ICH in patients with brain metastases, especially those with melanoma or prior ICH. The indication for anticoagulation and risk of intracerebral bleeding should be considered on an individual basis among such patients.

Identifiants

pubmed: 33687972
pii: jnnp-2020-324488
doi: 10.1136/jnnp-2020-324488
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: AA reports research funding from Varian Medical Systems.

Auteurs

Peter Wood (P)

Department of Radiology, Massachusetts General Hospital, Boston, MA, USA.

Giovanni Boyer (G)

Department of Radiation Oncology, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts, USA.

Elie Mehanna (E)

Harvard Radiation Oncology Program, Departments of Radiation Oncology, Brigham and Women's Hospital / Massachusetts General Hospital, Boston, MA, USA.

Daniel Cagney (D)

Department of Radiation Oncology, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts, USA.

Nayan Lamba (N)

Harvard Radiation Oncology Program, Departments of Radiation Oncology, Brigham and Women's Hospital / Massachusetts General Hospital, Boston, MA, USA.

Paul Catalano (P)

Department of Biostatistics, Harvard University T H Chan School of Public Health, Boston, Massachusetts, USA.
Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.

Jean M Connors (JM)

Division of Hematology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Liangge Hsu (L)

Department of Radiology, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Mallika Mendu (M)

Department of Quality and Safety, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Shyam Tanguturi (S)

Department of Radiation Oncology, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts, USA.

Brian Alexander (B)

Department of Radiation Oncology, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts, USA.

Daphne Haas-Kogan (D)

Department of Radiation Oncology, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts, USA.

Ayal Aizer (A)

Department of Radiation Oncology, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts, USA aaaizer@partners.org.

Classifications MeSH