Intraperitoneally Administered Vancomycin in Patients with Peritoneal Dialysis-Associated Peritonitis: Population Pharmacokinetics and Dosing Implications

Author:

Hartinger Jan Miroslav1,Michaličková Danica1ORCID,Dvořáčková Eliška1,Hronová Karolína1,Krekels Elke H. J.2,Szonowská Barbora3,Bednářová Vladimíra4,Benáková Hana5,Kroneislová Gabriela5ORCID,Závora Jan5ORCID,Tesař Vladimír4ORCID,Slanař Ondřej1ORCID

Affiliation:

1. Department of Pharmacology, First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic

2. Division of Systems Pharmacology and Pharmacy, Leiden Academic Centre for Drug Research, Leiden University, 2311 EZ Leiden, The Netherlands

3. Internal Department of Strahov, General University Hospital in Prague, 128 00 Prague, Czech Republic

4. Department of Nephrology, First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic

5. Institute of Medical Biochemistry and Laboratory Diagnostics, First Faculty of Medicine, Charles University and General University Hospital in Prague, 128 00 Prague, Czech Republic

Abstract

Peritonitis is a limiting complication of peritoneal dialysis, which is treated by intraperitoneal administration of antibiotics. Various dosing strategies are recommended for intraperitoneally administered vancomycin, which leads to large differences in intraperitoneal vancomycin exposure. Based on data from therapeutic drug monitoring, we developed the first-ever population pharmacokinetic model for intraperitoneally administered vancomycin to evaluate intraperitoneal and plasma exposure after dosing schedules recommended by the International Society for Peritoneal Dialysis. According to our model, currently recommended dosing schedules lead to possible underdosing of a large proportion of patients. To prevent this, we suggest avoiding intermittent intraperitoneal vancomycin administration, and for the continuous dosing regimen, we suggest a loading dose of 20 mg/kg followed by maintenance doses of 50 mg/L in each dwell to improve the intraperitoneal exposure. Vancomycin plasma level measurement on the fifth day of treatment with subsequent dose adjustment would prevent it from reaching toxic levels in the few patients who are susceptible to overdose.

Funder

Open Access Fund of General University Hospital in Prague

research initiative of the Ministry of Health of Czech Republic

Publisher

MDPI AG

Subject

Pharmaceutical Science

Reference25 articles.

1. Peritoneal Dialysis;Teitelbaum;N. Engl. J. Med.,2021

2. Antimicrobial-resistant gram-positive bacteria in PD peritonitis and the newer antibiotics used to treat them;Salzer;Perit. Dial. Int.,2005

3. ISPD peritonitis guideline recommendations: 2022 update on prevention and treatment;Li;Perit. Dial. Int.,2022

4. Vancomycin absorption from the peritoneal cavity during dialysis-related peritonitis;Rubin;Perit. Dial. Int.,1990

5. Absorption of intraperitoneal antibiotics;Morse;Drug Intell. Clin. Pharm.,1988

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