Antimicrobial Exposures in Critically Ill Patients Receiving Extracorporeal Membrane Oxygenation

Kiran Shekar(Bond University), Mohd H. Abdul‐Aziz(The University of Queensland), Vesa Cheng(The University of Queensland), Fay Burrows, Hergen Buscher(UNSW Sydney), Young‐Jae Cho(Seoul National University Bundang Hospital), Amanda Corley(Griffith University), Arne Diehl(The Alfred Hospital), Eileen Gilder(Monash University), Stephan M. Jakob(Auckland City Hospital), Hyung-Sook Kim(University of Bern), Bianca Levkovich(Seoul National University Bundang Hospital), Sung Yoon Lim(Seoul National University Bundang Hospital), Shay McGuinness(University of Auckland), Rachael Parke(Université de Montpellier), Vincent Pellegrino(The Alfred Hospital), Yok‐Ai Que(Auckland City Hospital), Claire Reynolds(St Vincent's Hospital Sydney), Sam Rudham(St Vincent's Hospital Sydney), Steven C. Wallis(The University of Queensland), Susan Welch, David G. Zacharias(Auckland City Hospital), John F. Fraser(Bond University), Jason A. Roberts(The University of Queensland)
American Journal of Respiratory and Critical Care Medicine
October 10, 2022
Cited by 57Open Access
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Abstract

Abstract Rationale Data suggest that altered antimicrobial concentrations are likely during extracorporeal membrane oxygenation (ECMO). Objectives The primary aim of this analysis was to describe the pharmacokinetics (PKs) of antimicrobials in critically ill adult patients receiving ECMO. Our secondary aim was to determine whether current antimicrobial dosing regimens achieve effective and safe exposure. Methods This study was a prospective, open-labeled, PK study in six ICUs in Australia, New Zealand, South Korea, and Switzerland. Serial blood samples were collected over a single dosing interval during ECMO for 11 antimicrobials. PK parameters were estimated using noncompartmental methods. Adequacy of antimicrobial dosing regimens were evaluated using predefined concentration exposures associated with maximal clinical outcomes and minimal toxicity risks. Measurements and Main Results We included 993 blood samples from 85 patients. The mean age was 44.7 ± 14.4 years, and 61.2% were male. Thirty-eight patients (44.7%) were receiving renal replacement therapy during the first PK sampling. Large variations (coefficient of variation of ≥30%) in antimicrobial concentrations were seen leading to more than fivefold variations in all PK parameters across all study antimicrobials. Overall, 70 (56.5%) concentration profiles achieved the predefined target concentration and exposure range. Target attainment rates were not significantly different between modes of ECMO and renal replacement therapy. Poor target attainment was observed across the most frequently used antimicrobials for ECMO recipients, including for oseltamivir (33.3%), piperacillin (44.4%), and vancomycin (27.3%). Conclusions Antimicrobial PKs were highly variable in critically ill patients receiving ECMO, leading to poor target attainment rates. Clinical trial registered with the Australian New Zealand Clinical Trials Registry (ACTRN12612000559819).


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