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Abstract

Venous thromboembolism (VTE) is among the complications of Multiple Myeloma (MM) and may occur in up to 10% of this patient population. However, medications used in MM therapy such as immunomodulators (IMID) may raise these rates. Thus, risk prediction models have been developed to quantify the risk of VTE in MM patients. The aim of this study is to compare the performance of three risk assessment models for VTE in newly diagnosed MM (NDMM) patients using immunomodulatory agents. A historical cohort study during a 10-year period in a Brazilian metropolis with NDMM treated with IMID. Data were collected from patient’s medical charts for the period of one year to calculate the scores using IMPEDE VTE, SAVED, and International Myeloma Working Group (IMWG) guidelines. The area under the curve (AUC) of the Receiver Operating Characteristic curve analysis was calculated to assess the discriminative power of three risk assessment models. We included 131 patients (9 in the VTE group versus 122 in the non VTE group). According to IMPEDE, 19.1, 62.6, and 18.3% of patients were considered low, intermediate, and high risk, respectively. SAVED classified 32.1% as high risk and 64.9% had ≥2 risk factors based on IMWG guidelines. The AUC of the IMPEDE VTE score was 0.80 (95% CI 0.66–0.95, p = 0.002), of the SAVED score was 0.69 (95% CI 0.49–0.89, p = 0.057), and of the IMWG risk score was 0.68 (95% CI 0.48–0.88, p = 0.075). IMPEDE VTE was the most accurate in predicting the development of VTE in Brazilian patients on IMID therapy. The SAVED score and the IMWG guidelines did not show discriminative ability in predicting VTE based on the population involved in this study.

Details

Title
Comparison of three risk assessment models for thromboembolism in multiple myeloma patients receiving immunomodulators: a Brazilian historical cohort
Author
da Costa, Iwyson Henrique Fernandes 1   VIAFID ORCID Logo  ; de Pádua, Cristiane Aparecida Menezes 2 ; de Miranda Drummond, Paula Lana 3 ; Silveira, Lívia Pena 4 ; Malta, Jéssica Soares 5 ; dos Santos, Roberta Márcia Marques 6 ; Reis, Adriano Max Moreira 2 

 Universidade Federal de Minas Gerais, Programa de Pós-Graduação em Medicamentos e Assistência Farmacêutica, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888); Universidade Federal de Minas Gerais, Hospital das Clínicas, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888) 
 Universidade Federal de Minas Gerais, Programa de Pós-Graduação em Medicamentos e Assistência Farmacêutica, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888); Universidade Federal de Minas Gerais, Faculdade de Farmácia, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888) 
 Universidade Federal de Minas Gerais, Programa de Pós-Graduação em Medicamentos e Assistência Farmacêutica, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888); Fundação Ezequiel Dias, Belo Horizonte, Brazil (GRID:grid.472872.c) (ISNI:0000 0000 9688 4664) 
 Universidade Federal de Minas Gerais, Hospital das Clínicas, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888) 
 Universidade Federal de Minas Gerais, Faculdade de Farmácia, Belo Horizonte, Brazil (GRID:grid.8430.f) (ISNI:0000 0001 2181 4888) 
 Fundação Ezequiel Dias, Belo Horizonte, Brazil (GRID:grid.472872.c) (ISNI:0000 0000 9688 4664) 
Pages
147-155
Publication year
2023
Publication date
Jul 2023
Publisher
Springer Nature B.V.
ISSN
09295305
e-ISSN
1573742X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2828056707
Copyright
© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.