Population pharmacokinetics of unfractionated heparin and multivariable analysis of activated clotting time in patients undergoing radiofrequency ablation of atrial fibrillation
Research article published in Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie (2024)
Abstract
INTRODUCTION: Atrial fibrillation (AF) increases cardiovascular morbidity and mortality. To reduce thrombosis and bleeding risks, and due to high variability of unfractionated heparin (UFH) effect, activated clotting time (ACT) is used during radiofrequency catheter ablation (RFCA) of AF to guide UFH dose. This study aimed to develop a population PK-PD model and perform multivariable analysis in order to identify the most significant covariates associated with interindividual variability of UFH. METHODS: Electronic medical records from 668 patients undergoing RFCA were analyzed, including relevant covariates. The relationship between UFH dose and ACT and the impact of the main covariates were characterized using a mixed-effect PK-PD model. Multivariable analysis was then used to identify predictors of ACT 15 minutes after UFH administration (ACT15). RESULTS: A two-compartment PK model with linear elimination and a direct Emax PD model with a baseline and sigmoidicity best described the observed ACT values. Pretreatment with dabigatran, warfarin, or fluindione significantly influenced baseline ACT. Pretreatment with vitamin K antagonists or low molecular weight heparin explained Emax variability. The multivariable model identified baseline ACT, initial UFH dose, and previous anticoagulant as the main predictors of ACT15. Model evaluation through resampling and external validation showed accurate ACT15 predictions. CONCLUSION: This study presents the first population PK-PD model characterizing the relationship between UFH doses and ACT during RFCA, along with multivariable analysis. Additionally, predictive calculators for ACT15 and UFH dose based on patient and procedural characteristics were developed, enhancing personalized anticoagulation management during RFCA.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Peer-reviewed pharmacology and drug-development research relevant to anticoagulants and leech-derived compounds. Indexed in PubMed and verified against the NCBI record.
Por qué esto importa para la hirudoterapia
Este estudio desarrolló el primer modelo farmacocinético-farmacodinámico poblacional que vincula la dosis de heparina no fraccionada con el tiempo de coagulación activado (ACT) durante la ablación por radiofrecuencia de la fibrilación auricular en 668 pacientes, identificando el ACT basal, la dosis inicial de heparina y el uso previo de anticoagulantes como los principales predictores del ACT a los 15 minutos y produciendo calculadoras de dosificación validadas para la anticoagulación personalizada. En cuanto a la hirudoterapia, es contextual: muestra la variabilidad y los desafíos de monitoreo de la anticoagulación basada en heparina, las mismas limitaciones que motivaron el interés en inhibidores directos de trombina derivados de sanguijuelas como la hirudina como alternativas. El trabajo modela un agente sintético (heparina) y no hace referencia a la terapia con sanguijuelas ni a los anticoagulantes derivados de sanguijuelas; como un solo cohorte de modelado con validación externa, informa sobre la dosificación de heparina en lugar de cualquier pregunta específica de sanguijuelas.
Citación
Population pharmacokinetics of unfractionated heparin and multivariable analysis of activated clotting time in patients undergoing radiofrequency ablation of atrial fibrillation.
Konecki et al. · Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 2024
Contexto clínico relacionado
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Añadido a la biblioteca ASH: May 29, 2026 · Última actualización del sitio: June 18, 2026