Population pharmacokinetic–pharmacodynamic modeling and dosing simulation of propofol maintenance anesthesia in severely obese adolescents. Issue 9 (13th May 2015)

• Record Type: Journal Article
• Authors: Chidambaran, Vidya; Venkatasubramanian, Raja; Sadhasivam, Senthilkumar; Esslinger, Hope; Cox, Shareen; Diepstraten, Jeroen; Fukuda, Tsuyoshi; Inge, Thomas; Knibbe, Catherijne A.J.; Vinks, Alexander A.; Anderson, Brian
• Is Part Of: Paediatric anaesthesia. Volume 25:Issue 9(2015)
• Page Start: 911
• Page End: 923
• Publication Date: 2015-05-13
• Subjects: Pediatric anesthesia -- Periodicals; 617.96798
• DOI: 10.1111/pan.12684
• Languages: English
• ISSNs: 1155-5645

Abstract

<abstract abstract-type="main" id="pan12684-abs-0001"> <title>Summary</title> <sec id="pan12684-sec-0001" sec-type="section"> <title>Background</title> <p>Optimal dosing of propofol to maintain appropriate anesthetic depth is challenging in severely obese (SO) adolescents. We previously reported that total body weight (TBW) is predictive of propofol clearance. This study was aimed at characterizing pharmacokinetics (PK) and pharmacodynamics (PD) of propofol in SO adolescents, using bispectral index (BIS), and toward developing PK/PD model‐based dosing guidelines.</p> </sec> <sec id="pan12684-sec-0002" sec-type="section"> <title>Methods</title> <p>A prospective PK/PD study was conducted in 26 SO children and adolescents aged 9–18 years (body mass index 31–69 kg·m<sup>−2</sup>), undergoing surgery with intravenous propofol anesthesia clinically titrated by providers blinded to BIS. BIS data and propofol infusion schemes were recorded. Venous blood samples collected during and after propofol infusion were assayed for propofol concentrations. A propofol PK/PD model was developed using NONMEM and model‐based simulations were performed to determine propofol dosing regimens targeting BIS of 50 ± 10.</p> </sec> <sec id="pan12684-sec-0003" sec-type="section"> <title>Results</title> <p>A three‐compartment PK model linked to a sigmoidal inhibitory <italic>E</italic><sub>max</sub> PD model by a first‐order rate constant, adequately described the propofol concentration (<italic>n</italic> = 375) and BIS (<italic>n</italic> = 3334) data. TBW was the most predictive covariate for propofol clearance [CL (l·min<sup>−1</sup>) = 1.65 × (TBW/70)<sup>0.75</sup>]. An effect‐site propofol concentration of 3.19 μg·ml<sup>−1</sup> was estimated for half‐maximal effect, with no identifiable predictive covariates. The proposed maintenance dosing regimen targeted to a BIS of 50 ± 10, based on our PK/PD model, was able to predict desired propofol concentrations and BIS in a representative obese teen when used in conjunction with accepted PK/PD models for children/obese adults (PK:Eleveld/PD: Cortinez), further supporting evidence for the dosing based on TBW.</p> </sec> <sec id="pan12684-sec-0004" sec-type="section"> <title>Conclusion</title> <p>This is the first study to describe the PK/PD of propofol in SO adolescents. The proposed maintenance dosing regimen for propofol uses TBW in an allometric function as a dosing scalar, with an exponent of 0.75. Our results suggest no relevant effect of obesity on the propofol concentration–BIS relationship.</p> </sec> </abstract>