Increased Vancomycin Clearance in Patients with Solid Malignancies.


Journal

Biological & pharmaceutical bulletin
ISSN: 1347-5215
Titre abrégé: Biol Pharm Bull
Pays: Japan
ID NLM: 9311984

Informations de publication

Date de publication:
01 Jul 2020
Historique:
pubmed: 17 4 2020
medline: 1 4 2021
entrez: 17 4 2020
Statut: ppublish

Résumé

Vancomycin (VAN) is an anti-microbial agent used to treat a number of bacterial infections, which has a high incidence of nephrotoxicity. We examined the pharmacokinetics of VAN retrospectively based on trough concentrations at large scale and identified pharmacokinetic differences between Japanese patients having solid malignancy and non-malignancy patients. Data were analyzed from 162 solid malignancy patients and 261 non-malignancy patients, including the patient's background, VAN dose, and pharmacokinetics of VAN. We failed to detect differences in values for VAN clearance or shorter elimination half-lives between these two groups. In contrast, multiple regression analysis under adjusting for confounding factors by propensity score, showed that VAN clearance significantly increased in relation to solid malignancies in each stage. We conclude that VAN clearance in solid malignancy patients is increased and that the blood concentration of VAN becomes lower than expected. These results suggest that early monitoring of VAN levels in solid malignancy patients might be essential for maintaining desired effects without side-effects.

Identifiants

pubmed: 32295975
doi: 10.1248/bpb.b20-00083
doi:

Substances chimiques

Anti-Bacterial Agents 0
Vancomycin 6Q205EH1VU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1081-1087

Auteurs

Tomohiro Izumisawa (T)

Laboratory of Physiological Chemistry, Institute of Medicinal Chemistry, Hoshi University.
Department of Laboratory Medicine, The Jikei University Kashiwa Hospital.

Nobuyuki Wakui (N)

Division of Applied Pharmaceutical Education and Research, Hoshi University.

Tomoyoshi Kaneko (T)

Department of Laboratory Medicine, The Jikei University Kashiwa Hospital.

Masakazu Soma (M)

Department of Laboratory Medicine, The Jikei University Kashiwa Hospital.

Masahiko Imai (M)

Laboratory of Physiological Chemistry, Institute of Medicinal Chemistry, Hoshi University.

Daisuke Saito (D)

Laboratory of Physiological Chemistry, Institute of Medicinal Chemistry, Hoshi University.

Hideo Hasegawa (H)

Department of Laboratory Medicine, The Jikei University Kashiwa Hospital.

Tetsuya Horino (T)

Department of Infectious Diseases and Infection Control, Jikei University School of Medicine.

Noriko Takahashi (N)

Laboratory of Physiological Chemistry, Institute of Medicinal Chemistry, Hoshi University.

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Classifications MeSH