Meropenem pharmacokinetics during extracorporeal membrane oxygenation and continuous haemodialysis: a case report.


Journal

Journal of global antimicrobial resistance
ISSN: 2213-7173
Titre abrégé: J Glob Antimicrob Resist
Pays: Netherlands
ID NLM: 101622459

Informations de publication

Date de publication:
09 2020
Historique:
received: 04 03 2020
revised: 09 04 2020
accepted: 21 04 2020
pubmed: 18 5 2020
medline: 1 6 2021
entrez: 18 5 2020
Statut: ppublish

Résumé

Pharmacokinetic (PK) parameters can change significantly during extracorporeal membrane oxygenation (ECMO) and continuous haemodialysis. This case report describes the pharmacokinetics of a 3-h meropenem infusion in an infantile anuric patient on ECMO with continuous haemodialysis. A 19-month-old female patient with asplenia syndrome was admitted to the paediatric intensive care unit for postoperative management of an extracardiac total cavopulmonary connection procedure. Veno-arterial ECMO and continuous haemodialysis were initiated on postoperative Day 2 for circulatory insufficiency due to septic shock and thrombosis of the inferior vena cava extending to the pulmonary artery. Blood and ascites cultures were positive for extended-spectrum β-lactamase-producing Escherichia coli, and 3-h meropenem infusions [120-300 mg/kg/day divided every 8 h (q8h)] were commenced. Following dose escalation to 300 mg/kg/day q8h, sustained negative blood cultures were confirmed. The estimated meropenem clearance and volume of distribution (V To optimise meropenem dosing in paediatric patients on ECMO and continuous haemodialysis, further study and PK monitoring are warranted.

Identifiants

pubmed: 32417590
pii: S2213-7165(20)30120-X
doi: 10.1016/j.jgar.2020.04.029
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Meropenem FV9J3JU8B1

Types de publication

Case Reports Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

651-655

Informations de copyright

Copyright © 2020 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Auteurs

Jumpei Saito (J)

Department of Pharmacy, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-0074, Japan. Electronic address: saito-jn@ncchd.go.jp.

Kensuke Shoji (K)

Division of Infectious Diseases, Department of Medical Subspecialties, National Center for Child Health and Development, Tokyo, Japan.

Yusuke Oho (Y)

Department of Pharmacy, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-0074, Japan.

Satoshi Aoki (S)

Critical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.

Shotaro Matsumoto (S)

Critical Care Medicine, National Center for Child Health and Development, Tokyo, Japan.

Michiko Yoshida (M)

Office for Infection Control, National Center for Child Health and Development, Tokyo, Japan.

Hidefumi Nakamura (H)

Clinical Research Center, National Center for Child Health and Development, Tokyo, Japan.

Yukihiro Kaneko (Y)

Department of Cardiovascular Surgery, National Center for Child Health and Development, Tokyo, Japan.

Taiyu Hayashi (T)

Department of Cardiology, National Center for Child Health and Development, Tokyo, Japan.

Akimasa Yamatani (A)

Department of Pharmacy, National Center for Child Health and Development, 2-10-1 Okura, Setagaya-ku, Tokyo 157-0074, Japan.

Edmund Capparelli (E)

University of California at San Diego, Division of Host-Microbe Systems and Therapeutics, University of California at San Diego, La Jolla, CA, USA.

Isao Miyairi (I)

Division of Infectious Diseases, Department of Medical Subspecialties, National Center for Child Health and Development, Tokyo, Japan; Department of Microbiology, Immunology and Biochemistry, University of Tennessee Health Science Center, Memphis, TN, USA.

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Classifications MeSH