Validation of Risk-Adapted Venous Thromboembolism Prediction in Multiple Myeloma Patients.

direct oral anticoagulants multiple myeloma thromboprophylaxis venous thromboembolism

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
12 Aug 2021
Historique:
received: 20 05 2021
revised: 04 08 2021
accepted: 09 08 2021
entrez: 27 8 2021
pubmed: 28 8 2021
medline: 28 8 2021
Statut: epublish

Résumé

Multiple myeloma (MM) is associated with an increased risk of venous thrombosis (VTE). In the United Kingdom Medical Research Council (MRC) XI study of patients treated with immunomodulatory therapy, the VTE rate was 11.8% despite 87.7% of the patients being on thromboprophylaxis at the time of thrombosis. In order to effectively prevent VTE events in MM patients, a better understanding of patient and disease risk factors that might predict thrombosis is required. We performed a retrospective cohort analysis of over 300 newly diagnosed MM patients at a tertiary referral centre to determine the VTE rate, predictive factors for VTE, value of the Khorana score for MM VTE events and long-term mortality outcomes. Fifty-four percent of the patients were receiving thromboprophylaxis at the time of the VTE event. The mortality odds ratio was 3.3 (95% CI, 2.4-4.5) in patients who developed VTE in comparison to age-matched controls with MM. A younger age at diagnosis and higher white cell count (WCC) were found to be predictive of VTE events. Our data suggest that standard thromboprophylaxis may not be effective in preventing VTE events in myeloma patients, and alternative strategies, which could include higher-intensity thromboprophylaxis in young patients with a high WCC, are necessary.

Identifiants

pubmed: 34441832
pii: jcm10163536
doi: 10.3390/jcm10163536
pmc: PMC8396929
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Aisling Barrett (A)

Department of Haematology, Beaumont Hospital, D09 V2N0 Dublin, Ireland.

John Quinn (J)

Department of Haematology, Beaumont Hospital, D09 V2N0 Dublin, Ireland.

Michelle Lavin (M)

Irish Centre for Vascular Biology, Royal College of Surgeons in Ireland, D02 VN51 Dublin, Ireland.

Patrick Thornton (P)

Department of Haematology, Beaumont Hospital, D09 V2N0 Dublin, Ireland.

James O'Donnell (J)

Irish Centre for Vascular Biology, Royal College of Surgeons in Ireland, D02 VN51 Dublin, Ireland.

Philip Murphy (P)

Department of Haematology, Beaumont Hospital, D09 V2N0 Dublin, Ireland.

Siobhán Glavey (S)

Department of Haematology, Beaumont Hospital, D09 V2N0 Dublin, Ireland.
Departments of Pathology and Haematology, Royal College of Surgeons in Ireland, D02 VN51 Dublin, Ireland.

Classifications MeSH