Increased Arbekacin Clearance in Patients With Febrile Neutropenia.


Journal

Therapeutic drug monitoring
ISSN: 1536-3694
Titre abrégé: Ther Drug Monit
Pays: United States
ID NLM: 7909660

Informations de publication

Date de publication:
02 2020
Historique:
pubmed: 20 7 2019
medline: 29 4 2021
entrez: 20 7 2019
Statut: ppublish

Résumé

Arbekacin (ABK) is used to treat infections caused by methicillin-resistant Staphylococcus aureus and is used widely for the treatment of febrile neutropenia (FN). As ABK has a narrow therapeutic concentration window, the dosage must be adjusted via therapeutic drug monitoring. However, the influence of the physiology of patients with FN on the pharmacokinetic (PK) parameters of ABK remains unclear. Therefore, we examined this influence on ABK PK parameters. We performed a retrospective cohort study using data from patients with a hematologic malignancy who were ≥18 years and had been administered ABK. We excluded patients who did not receive therapeutic drug monitoring and had an estimated glomerular filtration rate (eGFR) of <30 mL/min, because clinically sufficient data would not be available. Of the 99 enrolled patients, 25 did not have FN and 74 had FN. Arbekacin clearance (CLabk) was shown to correlate with eGFR in patients with FN (r = 0.32, P = 0.0062) and without FN (r = 0.50, P = 0.01). CLabk was higher in patients with FN than in those without FN. In addition, in the eGFR of <100 mL/min group (normal renal function), CLabk and CLabk/eGFR were also higher in patients with FN than in those without FN. CLabk was increased in patients with FN and normal renal function; therefore, we propose an increased ABK dose for patients with FN and normal renal function.

Sections du résumé

BACKGROUND
Arbekacin (ABK) is used to treat infections caused by methicillin-resistant Staphylococcus aureus and is used widely for the treatment of febrile neutropenia (FN). As ABK has a narrow therapeutic concentration window, the dosage must be adjusted via therapeutic drug monitoring. However, the influence of the physiology of patients with FN on the pharmacokinetic (PK) parameters of ABK remains unclear. Therefore, we examined this influence on ABK PK parameters.
METHOD
We performed a retrospective cohort study using data from patients with a hematologic malignancy who were ≥18 years and had been administered ABK. We excluded patients who did not receive therapeutic drug monitoring and had an estimated glomerular filtration rate (eGFR) of <30 mL/min, because clinically sufficient data would not be available.
RESULT
Of the 99 enrolled patients, 25 did not have FN and 74 had FN. Arbekacin clearance (CLabk) was shown to correlate with eGFR in patients with FN (r = 0.32, P = 0.0062) and without FN (r = 0.50, P = 0.01). CLabk was higher in patients with FN than in those without FN. In addition, in the eGFR of <100 mL/min group (normal renal function), CLabk and CLabk/eGFR were also higher in patients with FN than in those without FN.
CONCLUSIONS
CLabk was increased in patients with FN and normal renal function; therefore, we propose an increased ABK dose for patients with FN and normal renal function.

Identifiants

pubmed: 31323015
doi: 10.1097/FTD.0000000000000678
pii: 00007691-202002000-00016
doi:

Substances chimiques

Anti-Infective Agents 0
Dibekacin 45ZFO9E525
arbekacin G7V6SLI20L

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

133-138

Références

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Auteurs

Takahiro Nakayama (T)

Department of Pharmacy, Nihon University Itabashi Hospital, Tokyo, Japan. Dr. Chuma is now Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan; and.

Masayuki Chuma (M)

Department of Pharmacy, Nihon University Itabashi Hospital, Tokyo, Japan. Dr. Chuma is now Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan; and.

Naohiro Tochikura (N)

Department of Pharmacy, Nihon University Itabashi Hospital, Tokyo, Japan. Dr. Chuma is now Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan; and.

So Iwabuchi (S)

Department of Pharmacy, Nihon University Itabashi Hospital, Tokyo, Japan. Dr. Chuma is now Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan; and.

Shinichiro Suzuki (S)

Department of Pharmacy, Nihon University Itabashi Hospital, Tokyo, Japan. Dr. Chuma is now Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan; and.

Chiaki Matsumoto (C)

Department of Pharmacy, Nihon University Itabashi Hospital, Tokyo, Japan. Dr. Chuma is now Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan; and.

Toru Imai (T)

Department of Pharmacy, Nihon University Itabashi Hospital, Tokyo, Japan. Dr. Chuma is now Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan; and.

Takashi Hamada (T)

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Masaru Nakagawa (M)

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Hiromichi Takahashi (H)

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Yoshihito Uchino (Y)

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Katsuhiro Miura (K)

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Noriyoshi Iriyama (N)

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Yoshihiro Hatta (Y)

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Masami Takei (M)

Division of Hematology and Rheumatology, Department of Medicine, Nihon University School of Medicine, Tokyo, Japan.

Takahisa Kimura (T)

Department of Pharmacy, Nihon University Itabashi Hospital, Tokyo, Japan. Dr. Chuma is now Clinical Trial Center for Developmental Therapeutics, Tokushima University Hospital, Tokushima, Japan; and.

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