The impact of extracorporeal membrane oxygenation on antifungal pharmacokinetics: A systematic review

被引:8
作者
Jendoubi, Ali [1 ,2 ]
Pressiat, Claire [1 ,3 ,4 ]
De Roux, Quentin [1 ,2 ]
Hulin, Anne [1 ,3 ,4 ]
Ghaleh, Bijan [1 ,3 ,4 ]
Tissier, Renaud [1 ]
Kohlhauer, Matthias [1 ]
Mongardon, Nicolas [1 ,2 ,3 ,5 ]
机构
[1] Univ Paris Est Creteil UPEC, Ecole Natl Veterinaire Alfort EnVA, Equipe Pharmacol & Technol Malad Cardiovasc PROTEC, Inserm U955 IMRB, Maisons Alfort, France
[2] Hop Univ Henri Mondor, Assistance Publ Hop Paris AP HP, Serv Anesthesie Reanimat Chirurgicale, DMU CARE, Creteil, France
[3] Univ Paris Est Creteil, Fac Sante, Creteil, France
[4] Hop Univ Henri Mondor, Assistance Publ Hop Paris APHP, Lab Pharmacol, DMU Biol Pathol, Creteil, France
[5] Univ Paris Est Creteil UPEC, Assistance Publ Hop Paris APHP,Inserm,IMRB U955, Dept Anesthesiol & Crit Care Med,Equipe Pharmacolo, Ecole Natl Veterinaire Alfort EnVA,Henri Mondor Un, F-94700 Maisons Alfort, France
关键词
Antifungals; Pharmacokinetics; Extracorporeal membrane oxygenation; Critically ill patients; CRITICALLY-ILL PATIENTS; POPULATION PHARMACOKINETICS; VORICONAZOLE; CASPOFUNGIN; SEQUESTRATION; FLUCONAZOLE; PATIENT; SAFETY;
D O I
10.1016/j.ijantimicag.2023.107078
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background and Objective: The use of extracorporeal membrane oxygenation (ECMO) as a cardiocirculatory or respiratory support has tremendously increased in critically ill patients. In the setting of ECMO support, invasive fungal infections are a severe cause of morbidity and mortality. This vulnerable population is at risk of suboptimal antifungal exposure due to an increased volume of distribution (Vd), drug sequestration and decreased clearance. Here, we aimed to summarize ex -vivo and clinical studies on the potential impact of ECMO on the pharmacokinetics (PK) of antifungal agents and dosing requirements. Methods: A systematic search of the literature within electronic databases PubMed and EMBASE was conducted from database inception to 30 April 2023. Inclusion criteria were as follows: critically ill patients receiving ECMO regardless of age and reporting at least one PK parameter. Results: Thirty-six studies met inclusion criteria, including seven ex -vivo experiments and 29 clinical studies evaluating three classes of antifungals: polyenes, triazoles and echinocandins. Based on the available ex -vivo PK data, we found a significant sequestration of highly lipophilic and protein -bound antifungals within the ECMO circuit such as voriconazole, posaconazole and micafungin but the PK of several antifungals remains to be addressed such as amphotericin B, isavuconazole and anidulafungin. Most clinical studies have shown increased Vd of some antifungals like fluconazole and micafungin, particularly in the pediatric population. Conflicting data exist about caspofungin exposure. Conclusions: The available literature on the antifungal PK changes in ECMO setting is scarce. Whenever possible, therapeutic drug monitoring is highly advised to personalize antifungal therapy. (c) 2023 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved.
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页数:19
相关论文
共 80 条
[1]   ECLS-associated infections in adults: what we know and what we don't yet know [J].
Abrams, Darryl ;
Grasselli, Giacomo ;
Schmidt, Matthieu ;
Mueller, Thomas ;
Brodie, Daniel .
INTENSIVE CARE MEDICINE, 2020, 46 (02) :182-191
[2]   Pharmacokinetics of anidulafungin during venovenous extracorporeal membrane oxygenation [J].
Aguilar, Gerardo ;
Ferriols, Rafael ;
Carbonell, Jose A. ;
Ezquer, Carlos ;
Miguel Alonso, Jose ;
Villena, Abigail ;
Puig, Jaume ;
Navarro, David ;
Alos, Manuel ;
Javier Belda, F. .
CRITICAL CARE, 2016, 20
[3]   High Incidence of Candidemia in Critically Ill COVID-19 Patients Supported by Veno-Venous Extracorporeal Membrane Oxygenation: A Retrospective Study [J].
Alessandri, Francesco ;
Ceccarelli, Giancarlo ;
Migliara, Giuseppe ;
Baccolini, Valentina ;
Russo, Alessandro ;
Marzuillo, Carolina ;
Ceparano, Mariateresa ;
Giordano, Giovanni ;
Tozzi, Pierfrancesco ;
Galardo, Gioacchini ;
Raponi, Giammarco ;
Mastroianni, Claudio ;
Venditti, Mario ;
Pugliese, Francesco ;
d'Ettorre, Gabriella .
JOURNAL OF FUNGI, 2023, 9 (01)
[4]   Pharmacokinetics and pharmacodynamics of antifungals [J].
Andes, David .
INFECTIOUS DISEASE CLINICS OF NORTH AMERICA, 2006, 20 (03) :679-+
[5]  
[Anonymous], 1996, Guide to Clinical Preventive Services, V2nd, P209
[6]   Therapeutic drug monitoring (TDM) of antifungal agents: guidelines from the British Society for Medical Mycology [J].
Ashbee, H. Ruth ;
Barnes, Rosemary A. ;
Johnson, Elizabeth M. ;
Richardson, Malcolm D. ;
Gorton, Rebecca ;
Hope, William W. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2014, 69 (05) :1162-1176
[7]   Pharmacokinetics and Safety of Micafungin in Infants Supported With Extracorporeal Membrane Oxygenation [J].
Autmizguine, Julie ;
Hornik, Christoph P. ;
Benjamin, Daniel K., Jr. ;
Brouwer, Kim L. R. ;
Hupp, Susan R. ;
Cohen-Wolkowiez, Michael ;
Watt, Kevin M. .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2016, 35 (11) :1204-1210
[8]   Pharmacokinetics, excretion, and mass balance of liposomal amphotericin B (AmBisome) and amphotericin B deoxycholate in humans [J].
Bekersky, I ;
Fielding, RM ;
Dressler, DE ;
Lee, JW ;
Buell, DN ;
Walsh, TJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (03) :828-833
[9]   Clinical Pharmacokinetics of Systemically Administered Antimycotics [J].
Bellmann, Romuald .
CURRENT CLINICAL PHARMACOLOGY, 2007, 2 (01) :37-58
[10]   Pharmacokinetics of antifungal drugs: practical implications for optimized treatment of patients [J].
Bellmann, Romuald ;
Smuszkiewicz, Piotr .
INFECTION, 2017, 45 (06) :737-779