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Factors Affecting the Initial Serum Concentration of Teicoplanin in Pediatric Patients: A Single-Center Retrospective
Tatsuo Kataoka1,2, Takanori Taogoshi1,2, Yoko Hiyama1,3
1Department of Pharmaceutical Services, Hiroshima University Hospital, Hiroshima, Japan.
Insights
Higher teicoplanin loading doses are safe for pediatric patients. Clinical factors like febrile neutropenia and bone marrow transplant influence teicoplanin levels, requiring personalized dosing strategies.
Area of Science:
- Pharmacology
- Pediatric Infectious Diseases
- Antibiotic Therapy
Background:
- Teicoplanin (TEIC) treats serious gram-positive bacterial infections, including MRSA.
- Current guidelines suggest higher TEIC trough concentrations, necessitating higher loading doses (LD).
- Factors influencing TEIC Ctrough and safety of high-LD regimens in pediatrics are not fully understood.
Purpose of the Study:
- Investigate factors influencing TEIC loading dose (LD) regimens in pediatric patients.
- Assess the safety and efficacy of higher TEIC LDs in this population.
Main Methods:
- Retrospective analysis of 108 pediatric patients (1-14 years) with TEIC concentrations.
- Examined factors affecting initial Ctrough and Ctrough/Dose ratio (C/D).
- Safety evaluated via serious adverse reactions at initial Ctrough measurement.
Main Results:
- 52% of patients receiving higher LD (avg. 54.2 mg/kg/3 days) did not reach target Ctrough (15 μg/mL).
- Initial Ctrough associated with age, eGFR, and serum albumin.
- C/D ratio linked to eGFR and febrile neutropenia (FN); BMT further impacted C/D in FN patients.
Conclusions:
- Clinical conditions like FN and BMT, affecting eGFR, influence pediatric TEIC Ctrough.
- Higher TEIC loading doses were well-tolerated in pediatric patients.
- Individualized LD determination considering clinical status is crucial for optimal TEIC therapy.
Background:
The glycopeptide antibiotic teicoplanin (TEIC) is used to treat infections caused by methicillin-resistant Staphylococcus aureus and other gram-positive bacteria. Because higher target trough concentrations are now recommended, higher loading dose (LD) regimens have been proposed. However, the factors affecting trough concentration (Ctrough) levels and the safety of high-dose regimens remain unclear. This study aimed to investigate the factors that should be considered in the LD regimen of TEIC in pediatric patients and assess the safety of a higher LD.
Methods:
We enrolled pediatric patients aged 1-14 years with available TEIC concentrations measured between August 2013 and December 2024. Factors affecting the initial Ctrough and the initial Ctrough divided by LD per kilogram of body weight (C/D ratio) were investigated. Safety assessment included serious adverse reactions at the time of initial Ctrough measurement.
Results:
In total, 108 patients were enrolled in this study. Of 108 enrolled patients, 64 patients were measured initial Ctrough on day 4. Fifty-four patients received higher LD (average 54.2 mg/kg/3 days) than the standard regimen, with 33 patients (52%) not achieving an initial Ctrough of 15 μg/mL. Linear regression analysis showed that the initial Ctrough was associated with age (P = .008), estimated glomerular filtration rate (eGFR; P < .001), and serum albumin level (P = .017). The C/D ratio on day 4 was associated with eGFR (P < .001) and the presence or absence of febrile neutropenia (FN) (P = .046). Further analysis restricted to patients with FN indicated that bone marrow transplantation (BMT) (P = .046) affected the C/D ratio. Serious adverse reactions occurred in 5 cases.
Conclusions:
Clinical conditions, such as FN and BMT, which cause an increase in eGFR, may affect the initial Ctrough in pediatric patients. Moreover, a higher LD was well-tolerated. When determining the LD, clinical conditions must be considered.
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