A comprehensive model for assessing and classifying patients with thrombotic microangiopathy: the TMA-INSIGHT score.

Atypical hemolytic uremic syndrome Complement mediated TMA Shiga toxin-mediated hemolytic uremic syndrome Thrombotic Thrombocytopenic Purpura Thrombotic microangiopathy

Journal

Thrombosis journal
ISSN: 1477-9560
Titre abrégé: Thromb J
Pays: England
ID NLM: 101170542

Informations de publication

Date de publication:
22 Nov 2023
Historique:
received: 15 08 2023
accepted: 13 11 2023
medline: 23 11 2023
pubmed: 23 11 2023
entrez: 23 11 2023
Statut: epublish

Résumé

Thrombotic Microangiopathy (TMA) is a syndrome characterized by the presence of anemia, thrombocytopenia and organ damage and has multiple etiologies. The primary aim is to develop an algorithm to classify TMA (TMA-INSIGHT score). This was a single-center retrospective cohort study including hospitalized patients with TMA at a single center. We included all consecutive patients diagnosed with TMA between 2012 and 2021. TMA was defined based on the presence of anemia (hemoglobin level < 10 g/dL) and thrombocytopenia (platelet count < 150,000/µL), signs of hemolysis, and organ damage. We classified patients in eight categories: infections; Malignant Hypertension; Transplant; Malignancy; Pregnancy; Thrombotic Thrombocytopenic Purpura (TTP); Shiga toxin-mediated hemolytic uremic syndrome (STEC-SHU) and Complement Mediated TMA (aHUS). We fitted a model to classify patients using clinical characteristics, biochemical exams, and mean arterial pressure at presentation. We retrospectively retrieved TMA phenotypes using automatic strategies in electronic health records in almost 10 years (n = 2407). Secondary TMA was found in 97.5% of the patients. Primary TMA was found in 2.47% of the patients (TTP and aHUS). The best model was LightGBM with accuracy of 0.979, and multiclass ROC-AUC of 0.966. The predictions had higher accuracy in most TMA classes, although the confidence was lower in aHUS and STEC-HUS cases. Secondary conditions were the most common etiologies of TMA. We retrieved comorbidities, associated conditions, and mean arterial pressure to fit a model to predict TMA and define TMA phenotypic characteristics. This is the first multiclass model to predict TMA including primary and secondary conditions.

Sections du résumé

BACKGROUND BACKGROUND
Thrombotic Microangiopathy (TMA) is a syndrome characterized by the presence of anemia, thrombocytopenia and organ damage and has multiple etiologies. The primary aim is to develop an algorithm to classify TMA (TMA-INSIGHT score).
METHODS METHODS
This was a single-center retrospective cohort study including hospitalized patients with TMA at a single center. We included all consecutive patients diagnosed with TMA between 2012 and 2021. TMA was defined based on the presence of anemia (hemoglobin level < 10 g/dL) and thrombocytopenia (platelet count < 150,000/µL), signs of hemolysis, and organ damage. We classified patients in eight categories: infections; Malignant Hypertension; Transplant; Malignancy; Pregnancy; Thrombotic Thrombocytopenic Purpura (TTP); Shiga toxin-mediated hemolytic uremic syndrome (STEC-SHU) and Complement Mediated TMA (aHUS). We fitted a model to classify patients using clinical characteristics, biochemical exams, and mean arterial pressure at presentation.
RESULTS RESULTS
We retrospectively retrieved TMA phenotypes using automatic strategies in electronic health records in almost 10 years (n = 2407). Secondary TMA was found in 97.5% of the patients. Primary TMA was found in 2.47% of the patients (TTP and aHUS). The best model was LightGBM with accuracy of 0.979, and multiclass ROC-AUC of 0.966. The predictions had higher accuracy in most TMA classes, although the confidence was lower in aHUS and STEC-HUS cases.
CONCLUSION CONCLUSIONS
Secondary conditions were the most common etiologies of TMA. We retrieved comorbidities, associated conditions, and mean arterial pressure to fit a model to predict TMA and define TMA phenotypic characteristics. This is the first multiclass model to predict TMA including primary and secondary conditions.

Identifiants

pubmed: 37993892
doi: 10.1186/s12959-023-00564-6
pii: 10.1186/s12959-023-00564-6
pmc: PMC10664252
doi:

Types de publication

Journal Article

Langues

eng

Pagination

119

Informations de copyright

© 2023. The Author(s).

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Auteurs

Vanessa Vilani Addad (VV)

Department of Internal Medicine - UNESP, Univ Estadual Paulista, Rubião Jr, s/n, Botucatu/SP, 18618-687, Brazil.

Lilian Monteiro Pereira Palma (LMP)

Department of Pediatrics, Universidade Estadual de Campinas, R. Tessália Vieira de Camargo, 126 - Cidade Universitária, Campinas/SP, 13083-887, Brazil.

Maria Helena Vaisbich (MH)

Pediatric Nephrology Service, Child Institute, University of São Paulo, Av. Dr. Enéas Carvalho de Aguiar, 647, São Paulo, SP, 05403-000, Brazil.

Abner Mácola Pacheco Barbosa (AM)

Department of Internal Medicine - UNESP, Univ Estadual Paulista, Rubião Jr, s/n, Botucatu/SP, 18618-687, Brazil.

Naila Camila da Rocha (NC)

Department of Internal Medicine - UNESP, Univ Estadual Paulista, Rubião Jr, s/n, Botucatu/SP, 18618-687, Brazil.

Marilia Mastrocolla de Almeida Cardoso (MM)

Health Technology Assessment Center of Hospital das Clínicas - HCFMB, Botucatu, SP, Brazil.

Juliana Tereza Coneglian de Almeida (JTC)

Health Technology Assessment Center of Hospital das Clínicas - HCFMB, Botucatu, SP, Brazil.

Monica Ap de Paula de Sordi (MA)

Health Technology Assessment Center of Hospital das Clínicas - HCFMB, Botucatu, SP, Brazil.

Juliana Machado-Rugolo (J)

Health Technology Assessment Center of Hospital das Clínicas - HCFMB, Botucatu, SP, Brazil.

Lucas Frederico Arantes (LF)

Health Technology Assessment Center of Hospital das Clínicas - HCFMB, Botucatu, SP, Brazil.

Luis Gustavo Modelli de Andrade (LGM)

Department of Internal Medicine - UNESP, Univ Estadual Paulista, Rubião Jr, s/n, Botucatu/SP, 18618-687, Brazil. Gustavo.modelli@unesp.br.

Classifications MeSH