Amikacin pharmacokinetic/pharmacodynamic in intensive care unit: a prospective database.

Amikacin Intensive care unit Pharmacodynamic Pharmacokinetic

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
08 Jun 2020
Historique:
received: 10 03 2020
accepted: 20 05 2020
entrez: 10 6 2020
pubmed: 10 6 2020
medline: 10 6 2020
Statut: epublish

Résumé

Aminoglycosides have a concentration-dependent therapeutic effect when peak serum concentration (C Retrospective analysis from February 2016 to December 2017 of a prospective database conducted in 2 intensive care units (ICU). All patients with documented severe GNB infections treated with amikacin (single daily dose of 25 mg/kg of total body weight (TBW)) with both MIC and C 93 patients with 98 GNB-documented infections were included. The median C According to PK/PD parameters observed in our study, single daily dose of amikacin 25 mg/kg of TBW appears to be sufficient in most critically ill patients treated for severe GNB infections.

Sections du résumé

BACKGROUND BACKGROUND
Aminoglycosides have a concentration-dependent therapeutic effect when peak serum concentration (C
METHODS METHODS
Retrospective analysis from February 2016 to December 2017 of a prospective database conducted in 2 intensive care units (ICU). All patients with documented severe GNB infections treated with amikacin (single daily dose of 25 mg/kg of total body weight (TBW)) with both MIC and C
RESULTS RESULTS
93 patients with 98 GNB-documented infections were included. The median C
CONCLUSION CONCLUSIONS
According to PK/PD parameters observed in our study, single daily dose of amikacin 25 mg/kg of TBW appears to be sufficient in most critically ill patients treated for severe GNB infections.

Identifiants

pubmed: 32514769
doi: 10.1186/s13613-020-00685-5
pii: 10.1186/s13613-020-00685-5
pmc: PMC7276966
doi:

Types de publication

Journal Article

Langues

eng

Pagination

75

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Auteurs

Elsa Logre (E)

CH Argenteuil, réanimation polyvalente, 69 rue du Lieutenant-Colonel Prudhon, Argenteuil, France. elsa.logre@gmail.com.

Maya Enser (M)

CH Argenteuil, réanimation polyvalente, 69 rue du Lieutenant-Colonel Prudhon, Argenteuil, France.

Sébastien Tanaka (S)

CHU Bichat, réanimation chirurgicale, Paris, France.
INSERM UMR1188 Diabète - Athérothrombose - Thérapies Réunion Océan Indien (DéTROI), Saint-Denis de la Réunion, Université de la Réunion, Réunion, France.

Marie Dubert (M)

CHU Bichat, maladies infectieuses et tropicales, Paris, France.

Aurore Claudinon (A)

CH Argenteuil, microbiologie, Argenteuil, France.

Nathalie Grall (N)

CHU Bichat, microbiologie, Paris, France.

Hervé Mentec (H)

CH Argenteuil, réanimation polyvalente, 69 rue du Lieutenant-Colonel Prudhon, Argenteuil, France.

Philippe Montravers (P)

CHU Bichat, réanimation chirurgicale, Paris, France.

Olivier Pajot (O)

CH Argenteuil, réanimation polyvalente, 69 rue du Lieutenant-Colonel Prudhon, Argenteuil, France.

Classifications MeSH