Can the Charlson Comorbidity Index help to guide DOAC dosing in patients with atrial fibrillation and improve the efficacy and safety of treatment? A subanalysis of the MAS study: Charlson index and DOAC dosing in AF patients.

Charlson comorbidity index DOAC atrial fibrillation dosing

Journal

Current problems in cardiology
ISSN: 1535-6280
Titre abrégé: Curr Probl Cardiol
Pays: Netherlands
ID NLM: 7701802

Informations de publication

Date de publication:
29 Oct 2024
Historique:
received: 22 10 2024
accepted: 27 10 2024
medline: 1 11 2024
pubmed: 1 11 2024
entrez: 31 10 2024
Statut: aheadofprint

Résumé

Frailty influences the effectiveness and safety of anticoagulant therapy in patients with atrial fibrillation (AF). The age-weighted Charlson Comorbidity Index may offer a valuable tool to assess the risk of adverse events in AF patients treated with direct oral anticoagulants (DOACs). This sub-analysis of MAS trial data aimed to assess whether using the Charlson index, instead of the standard criteria, would have led to different dosing and improved adverse event occurrence during treatment. The MAS study looked for a relationship between DOAC levels assessed at baseline and adverse events during follow-up. The study is described in detail elsewhere. Among the 1,657 patients studied, 832 (50.2%) had a relatively low Charlson index (up to 6, general median class), of whom 132 (15.9%) were treated with reduced doses. Conversely, among the 825 patients with a high Charlson index (≥7), 257 (31.1%) received standard doses. A weak but statistically significant positive correlation (r = 0.1413, p = 0.0001 by ANOVA) was observed between increasing Charlson classes and DOAC levels standardized to allow comparability among drug results. However, no significant differences were found in the incidence or number of adverse events during follow-up, or in other parameters, between patients with low and high Charlson scores. Utilizing the Charlson index would have led to notable differences in DOAC dosing compared to standard criteria. However, we found no evidence that its use would have improved the prediction of adverse events in AF patients enrolled in the MAS study.

Sections du résumé

BACKGROUND BACKGROUND
Frailty influences the effectiveness and safety of anticoagulant therapy in patients with atrial fibrillation (AF). The age-weighted Charlson Comorbidity Index may offer a valuable tool to assess the risk of adverse events in AF patients treated with direct oral anticoagulants (DOACs). This sub-analysis of MAS trial data aimed to assess whether using the Charlson index, instead of the standard criteria, would have led to different dosing and improved adverse event occurrence during treatment.
METHODS METHODS
The MAS study looked for a relationship between DOAC levels assessed at baseline and adverse events during follow-up. The study is described in detail elsewhere.
RESULTS RESULTS
Among the 1,657 patients studied, 832 (50.2%) had a relatively low Charlson index (up to 6, general median class), of whom 132 (15.9%) were treated with reduced doses. Conversely, among the 825 patients with a high Charlson index (≥7), 257 (31.1%) received standard doses. A weak but statistically significant positive correlation (r = 0.1413, p = 0.0001 by ANOVA) was observed between increasing Charlson classes and DOAC levels standardized to allow comparability among drug results. However, no significant differences were found in the incidence or number of adverse events during follow-up, or in other parameters, between patients with low and high Charlson scores.
CONCLUSIONS CONCLUSIONS
Utilizing the Charlson index would have led to notable differences in DOAC dosing compared to standard criteria. However, we found no evidence that its use would have improved the prediction of adverse events in AF patients enrolled in the MAS study.

Identifiants

pubmed: 39481583
pii: S0146-2806(24)00548-6
doi: 10.1016/j.cpcardiol.2024.102913
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

102913

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: PALARETI GUALTIERO reports financial support was provided by Fondazione Cassa di Risparmio di Bologna. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Gualtiero Palareti (G)

Fondazione Arianna Anticoagulazione, Bologna, Italy. Electronic address: gualtiero.palareti@unibo.it.

Cristina Legnani (C)

Fondazione Arianna Anticoagulazione, Bologna, Italy.

Sophie Testa (S)

Centro Emostasi e Trombosi, Laboratorio Analisi Chimico-Cliniche e Microbiologiche, ASST Cremona, Cremona, Italy.

Oriana Paoletti (O)

Centro Emostasi e Trombosi, Laboratorio Analisi Chimico-Cliniche e Microbiologiche, ASST Cremona, Cremona, Italy.

Michela Cini (M)

Fondazione Arianna Anticoagulazione, Bologna, Italy.

Emilia Antonucci (E)

Fondazione Arianna Anticoagulazione, Bologna, Italy.

Vittorio Pengo (V)

Clinica Cardiologica, Centro Trombosi, Dipartimento di Scienze Cardio-Toraco-Vascolare, Università di Padova, Italy.

Daniela Poli (D)

Malattie Aterotrombotiche, AOU Careggi, Firenze, Italy.

Walter Ageno (W)

Ospedale Regionale di Bellinzona e Valli, Ente Ospedaliero Cantonale, Bellinzona, Switzerland.

Paolo Prandoni (P)

Fondazione Arianna Anticoagulazione, Bologna, Italy.

Domenico Prisco (D)

Dipartimento di Medicina Sperimentale e Clinica, Università di Firenze.

Alberto Tosetto (A)

UOC Ematologia, Centro Malattie Emorragiche e Trombotiche (CMET), AULSS 8 Berica Ospedale S. Bortolo, Vicenza, Italy.

Classifications MeSH