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Trends in teicoplanin loading dose implementation from 2010 to 2019 and evaluation of safety and efficacy factors: a retrospective cohort study based on a Japanese administrative claims database.
Goto, Ryota; Muraki, Yuichi; Inose, Ryo; Ichii, Moeno; Sawada, Keisuke; Mizuno, Kanako; Koizumi, Ryuji; Tsuzuki, Shinya; Ishikane, Masahiro; Ohmagari, Norio.
Afiliación
  • Goto R; Department of Clinical Pharmacoepidemiology, Kyoto Pharmaceutical University, 5 Misasagi Nakauchi-Cho, Yamashina-Ku, Kyoto, 607-8414, Japan.
  • Muraki Y; Department of Clinical Pharmacoepidemiology, Kyoto Pharmaceutical University, 5 Misasagi Nakauchi-Cho, Yamashina-Ku, Kyoto, 607-8414, Japan. y-muraki@mb.kyoto-phu.ac.jp.
  • Inose R; Department of Clinical Pharmacoepidemiology, Kyoto Pharmaceutical University, 5 Misasagi Nakauchi-Cho, Yamashina-Ku, Kyoto, 607-8414, Japan.
  • Ichii M; Department of Clinical Pharmacoepidemiology, Kyoto Pharmaceutical University, 5 Misasagi Nakauchi-Cho, Yamashina-Ku, Kyoto, 607-8414, Japan.
  • Sawada K; Department of Clinical Pharmacoepidemiology, Kyoto Pharmaceutical University, 5 Misasagi Nakauchi-Cho, Yamashina-Ku, Kyoto, 607-8414, Japan.
  • Mizuno K; Department of Pharmacy, Federation of National Public Service Personnel Mutual Aid Associations, Hirakata Kohsai Hospital, 1-2-1 Fujisaka Higashimachi, Osaka, 573-0153, Japan.
  • Koizumi R; Department of Clinical Pharmacoepidemiology, Kyoto Pharmaceutical University, 5 Misasagi Nakauchi-Cho, Yamashina-Ku, Kyoto, 607-8414, Japan.
  • Tsuzuki S; AMR Clinical Reference Center, Disease Control and Prevention Center, National Center for Global Health and Medicine, 1-21-1 Toyama Shinjuku-Ku, Tokyo, 162-8655, Japan.
  • Ishikane M; AMR Clinical Reference Center, Disease Control and Prevention Center, National Center for Global Health and Medicine, 1-21-1 Toyama Shinjuku-Ku, Tokyo, 162-8655, Japan.
  • Ohmagari N; AMR Clinical Reference Center, Disease Control and Prevention Center, National Center for Global Health and Medicine, 1-21-1 Toyama Shinjuku-Ku, Tokyo, 162-8655, Japan.
J Pharm Health Care Sci ; 9(1): 35, 2023 Nov 01.
Article en En | MEDLINE | ID: mdl-37908001
ABSTRACT

BACKGROUND:

The loading dose of teicoplanin (TEIC) is recommended for implementation. However, there is significant discrepancy between the dose settings in the package insert and, in the guidelines, and the actual status of loading doses in Japan is unclear. Furthermore, TEIC causes liver injury as side effect. Although the risk of developing liver injury has not been reported to be increased following a loading dose based on the guidelines, there is a lack of reports in large populations. Therefore, we evaluated the trend in the loading dose and factors affecting the efficacy and safety of TEIC administration.

METHODS:

A Japanese administrative claims database was used in this study. Trends in loading doses were evaluated in target populations administered TEIC between 2010 and 2019. Patient characteristics were adjusted by propensity score matching based on the guideline group (total dose of 3 days > 1,600 mg) and non-guideline group (≤ 1,600 mg) of the loading dose. Finally, univariable and multivariable conditional logistic regression analysis was performed to evaluate factors affecting 30-day mortality and liver injury.

RESULTS:

A total of 10,030 patients were selected based on these criteria. The proportion of loading doses based on the recommended guidelines showed an increase over time, regardless of the implementation of therapeutic drug monitoring (TDM), but especially so in cases where TDM was implemented, the loading doses were administered in accordance with the recommendations of the guidelines. Conditional logistic regression analysis showed a relationship between drug management and guidance fees (odds ratio [OR] 0.45, 95% confidence interval [CI] 0.36‒0.55), a reimbursement indicating pharmacist intervention, and a reduction in 30-day mortality. In addition, loading doses based on the recommended guidelines had no influence on liver injury, and other factors were not significantly associated with increased incidence of liver injury.

CONCLUSION:

Thus, this study implies the benefits of pharmacological management as indicated by drug management and guidance fee and supports the implementation of loading doses based on the guideline on TEIC administration.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Pharm Health Care Sci Año: 2023 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Pharm Health Care Sci Año: 2023 Tipo del documento: Article País de afiliación: Japón