Dosing optimisation of intravenous lidocaine in patients with class 1-3 obesity by population pharmacokinetic analysis.

Autor: Tognolini AR; Department of Anaesthesia and Perioperative Medicine, The Royal Brisbane and Women's Hospital, Brisbane, Australia.; Faculty of Medicine, The University of Queensland, Brisbane, Australia., Liu X; The University of Queensland Centre for Clinical Research, The University of Queensland, Brisbane, Australia., Pandey S; The University of Queensland Centre for Clinical Research, The University of Queensland, Brisbane, Australia., Roberts JA; The University of Queensland Centre for Clinical Research, The University of Queensland, Brisbane, Australia.; Herston Infectious Diseases Institute (HeIDI), Metro North Health, Brisbane, Australia., Wallis SC; The University of Queensland Centre for Clinical Research, The University of Queensland, Brisbane, Australia., Jackson D; Department of Anaesthesia and Perioperative Medicine, The Royal Brisbane and Women's Hospital, Brisbane, Australia.; Faculty of Medicine, The University of Queensland, Brisbane, Australia., Eley VA; Department of Anaesthesia and Perioperative Medicine, The Royal Brisbane and Women's Hospital, Brisbane, Australia.; Faculty of Medicine, The University of Queensland, Brisbane, Australia.
Jazyk: angličtina
Zdroj: Anaesthesia [Anaesthesia] 2025 Jan 02. Date of Electronic Publication: 2025 Jan 02.
DOI: 10.1111/anae.16531
Abstrakt: Introduction: Evidence to support intra-operative lidocaine infusion regimens in patients with obesity is lacking, risking underdosing or toxicity. We aimed to measure the plasma concentrations of lidocaine and its active metabolites to develop a pharmacokinetic model and optimised dosing regimen in patients with obesity.
Methods: A standardised weight-based intravenous lidocaine regimen was administered to patients with a BMI ≥ 30 kg.m -2 undergoing elective laparoscopic abdominal surgery. Using lean body weight, a 1.5 mg.kg -1 loading dose over 10 min and infusion of 1.5 mg.kg -1 .h -1 was administered intra-operatively. Arterial blood was sampled during and after the infusion. The total and unbound plasma concentrations of lidocaine, monoethylglycinexylidide and glycinexylidide were measured using liquid chromatography-mass spectrometry. Monolix was used for population pharmacokinetic analysis. Dosing simulations were performed using Simulx to develop a regimen that best targeted a therapeutic plasma concentration between 2.5 and 5 μg.ml -1 .
Results: Thirty patients provided 221 plasma samples (median (IQR [range]) age 51 (44-61 [32-76]) y and 21 female). Median (IQR [range]) total body weight was 107.0 (91.8-132.5 [80.0-189.0]) kg and BMI was 37.7 (33.6-46.5 [30.2-58.4]) kg.m -2 . Using total and unbound plasma concentrations of lidocaine, monoethylglycinexylidide and glycinexylidide, a four-compartment model was developed. Unbound lidocaine volume of distribution was 2.1 l.kg -1 and clearance 1.7 l.kg -1 .h -1 . Simulations showed that doses used currently had a low probability of target attainment of 0%. A loading dose of 2 mg.kg -1 over 20 min followed by an infusion of 3 mg.kg -1 .h -1 based on lean body weight improved probability of target attainment to 18.6%. The infusion should be reduced to 2 mg.kg -1 .h -1 after 80 min.
Discussion: Our simulated dosing regimen achieved therapeutic concentrations more successfully in patients with obesity. Further studies should evaluate the clinical safety and efficacy of this dosing regimen.
(© 2025 Association of Anaesthetists.)
Databáze: MEDLINE
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