Impact of extracorporeal membrane oxygenation (ECMO) support on piperacillin exposure in septic patients: a case-control study.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
13 04 2021
Historique:
received: 07 08 2020
accepted: 14 01 2021
pubmed: 12 2 2021
medline: 9 7 2021
entrez: 11 2 2021
Statut: ppublish

Résumé

To describe the impact of extracorporeal membrane oxygenation (ECMO) devices on piperacillin exposure in ICU patients. This observational, prospective, multicentre, case-control study was performed in the ICUs of two tertiary care hospitals in France. ECMO patients with sepsis treated with piperacillin/tazobactam were enrolled. Control patients were matched according to SOFA score and creatinine clearance. The pharmacokinetics of piperacillin were described based on a population pharmacokinetic model, calculating the proportion of time the piperacillin plasma concentration was above 64 mg/L (i.e. 4× MIC breakpoint for Pseudomonas aeruginosa). Forty-two patients were included. Median (IQR) age was 60 years (49-66), SOFA score was 11 (9-14) and creatinine clearance was 47 mL/min (5-95). There was no significant difference in the proportion of time piperacillin concentrations were ≥64 mg/L in patients treated with ECMO and controls during the first administration (P = 0.184) or at steady state (P = 0.309). Following the first administration, 36/42 (86%) patients had trough piperacillin concentrations <64 mg/L. Trough concentrations at steady state were similar in patients with ECMO and controls (P = 0.535). Creatinine clearance ≥40 mL/min was independently associated with piperacillin trough concentration <64 mg/L at steady state [OR = 4.3 (95% CI 1.1-17.7), P = 0.043], while ECMO support was not [OR = 0.5 (95% CI 0.1-2.1), P = 0.378]. ECMO support has no impact on piperacillin exposure. ICU patients with sepsis are frequently underexposed to piperacillin, which suggests that therapeutic drug monitoring should be strongly recommended for severe infections.

Identifiants

pubmed: 33569597
pii: 6132745
doi: 10.1093/jac/dkab031
doi:

Substances chimiques

Anti-Bacterial Agents 0
Piperacillin X00B0D5O0E

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1242-1249

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

P Fillâtre (P)

St Brieuc Hospital, Réanimation Polyvalente, F-22000 St Brieuc, France.

F Lemaitre (F)

Univ Rennes, Rennes University Hospital, Inserm, EHESP, Irset (Institut de Recherche en santé, Environnement et Travail) - UMR_S 1085, F-35000 Rennes, France.

N Nesseler (N)

Rennes University Hospital, Service de Réanimation de Chirurgie Cardiothoracique et de Chirurgie Vasculaire, F-35000 Rennes, France.
Univ Rennes, Inra, Inserm, Institut NUMECAN - UMR_A 1341, UMR_S 1241, CIC 1414, F35000 Rennes, France.

M Schmidt (M)

Sorbonne Université, Institute of Cardiometabolism and Nutrition, APHP, Pitié-Salpêtrière Hospital, Medical Intensive Care Unit, Paris, France.

S Besset (S)

Louis Mourier Hospital, Médecine Intensive-Réanimation, AP-HP, F92700 Colombes, France.

Y Launey (Y)

Univ Rennes, Inra, Inserm, Institut NUMECAN - UMR_A 1341, UMR_S 1241, CIC 1414, F35000 Rennes, France.
Rennes University Hospital, Surgical Critical Care Unit, Department of Anaesthesia, Critical Care and Perioperative Medicine, F-35033 Rennes, France.

A Maamar (A)

Rennes University Hospital, Infectious Diseases and Intensive Care Unit, F-35033 Rennes, France.
Univ Rennes, Faculté de Médecine, Biosit, F-35043 Rennes, France.
Univ Rennes, Inserm-CIC-1414, IFR 140, F-35033 Rennes, France.

P Daufresne (P)

Rennes University Hospital, Haematology Unit, F-35033 Rennes, France.

E Flecher (E)

Rennes University Hospital, Department of Thoracic and Cardiovascular Surgery, F-35033 Rennes, France.
Univ Rennes, Inserm U1099, Signal and Image Treatment Laboratory (LTSI), F-35033 Rennes, France.

Y Le Tulzo (Y)

Rennes University Hospital, Infectious Diseases and Intensive Care Unit, F-35033 Rennes, France.
Univ Rennes, Faculté de Médecine, Biosit, F-35043 Rennes, France.
Univ Rennes, Inserm-CIC-1414, IFR 140, F-35033 Rennes, France.

J M Tadie (JM)

Rennes University Hospital, Infectious Diseases and Intensive Care Unit, F-35033 Rennes, France.
Univ Rennes, Faculté de Médecine, Biosit, F-35043 Rennes, France.
Univ Rennes, Inserm-CIC-1414, IFR 140, F-35033 Rennes, France.

P Tattevin (P)

Rennes University Hospital, Infectious Diseases and Intensive Care Unit, F-35033 Rennes, France.
Univ Rennes, Faculté de Médecine, Biosit, F-35043 Rennes, France.
Univ Rennes, Inserm-CIC-1414, IFR 140, F-35033 Rennes, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH