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Effects of dalteparin on anti‐Xa activities cannot be predicted in critically ill COVID‐19 patients
Author(s) -
Heijden Charlotte D. C. C.,
Heine Rob,
Kooistra Emma J.,
Brüggemann Roger J.,
Walburgh Schmidt Jesper W. J.,
Grouw Elke P. L. M.,
Frenzel Tim,
Pickkers Peter,
Leentjens Jenneke
Publication year - 2022
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/bcp.15208
Subject(s) - medicine , critically ill , covid-19 , pharmacokinetics , pharmacodynamics , heparin , low molecular weight heparin , intensity (physics) , covariate , intensive care medicine , statistics , physics , mathematics , disease , quantum mechanics , infectious disease (medical specialty)
Critically ill COVID‐19 patients are at high risk of thromboembolic events despite routine‐dosed low‐molecular‐weight heparin thromboprophylaxis. However, in recent randomized trials increased‐intensity thromboprophylaxis seemed futile and possibly even harmful. In this explorative pharmacokinetic (PK) study we measured anti‐Xa activities on frequent timepoints in 15 critically ill COVID‐19 patients receiving dalteparin and performed PK analysis by nonlinear mixed‐effect modelling. A linear one‐compartment model with first‐order kinetics provided a good fit. However, wide interindividual variation in dalteparin absorption (variance 78%) and clearance (variance 34%) was observed, unexplained by routine clinical covariates. Using the final PK model for Monte Carlo simulations, we predicted increased‐intensity dalteparin to result in anti‐Xa activities well over prophylactic targets (0.2‐0.4 IU/mL) in the majority of patients. Therapeutic‐intensity dalteparin results in supratherapeutic anti‐Xa levels (target 0.6‐1.0 IU/mL) in 19% of patients and subtherapeutic levels in 22%. Therefore, anti‐Xa measurements should guide high‐intensity dalteparin in critically ill COVID‐19 patients.