American Society of Hirudotherapy

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)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportDrug DevelopmentKonecki et al. · 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.

Publication typeJournal Article
Indexed MeSH termsHumansAtrial FibrillationMaleHeparinFemaleMiddle AgedAgedAnticoagulantsMultivariate AnalysisWhole Blood Coagulation TimeCatheter AblationBlood Coagulation

Summary

Peer-reviewed pharmacology and drug-development research relevant to anticoagulants and leech-derived compounds. Indexed in PubMed and verified against the NCBI record.

Why This Matters for Hirudotherapy

This study built the first population pharmacokinetic-pharmacodynamic model linking unfractionated heparin dose to activated clotting time (ACT) during radiofrequency ablation of atrial fibrillation in 668 patients, identifying baseline ACT, initial heparin dose, and prior anticoagulant use as the main predictors of ACT at 15 minutes and producing validated dosing calculators for personalized anticoagulation. For hirudotherapy it is contextual: it shows the variability and monitoring challenges of heparin-based anticoagulation, the very limitations that motivated interest in leech-derived direct thrombin inhibitors like hirudin as alternatives. The work models a synthetic agent (heparin) and makes no reference to leech therapy or leech-derived anticoagulants; as a single modeling cohort with external validation it informs heparin dosing rather than any leech-specific question.

Citation

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

Added to ASH library: May 29, 2026 · Site last updated: June 18, 2026

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