Academic Journal
973. Pharmacokinetic/Pharmacodynamic Evaluation and Dose Optimization of Daptomycin in Pediatric Patients with Staphylococcus aureus Bacteremia
| العنوان: | 973. Pharmacokinetic/Pharmacodynamic Evaluation and Dose Optimization of Daptomycin in Pediatric Patients with Staphylococcus aureus Bacteremia |
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| المؤلفون: | Olney, Katie B, Howard, Joel I, Burgess, David |
| المصدر: | Open Forum Infectious Diseases ; volume 10, issue Supplement_2 ; ISSN 2328-8957 |
| بيانات النشر: | Oxford University Press (OUP) |
| سنة النشر: | 2023 |
| مصطلحات موضوعية: | Infectious Diseases, Oncology |
| الوصف: | Background Optimal dosing of daptomycin (DAP) in pediatric patients has not been elucidated in clinical practice. This study was conducted to examine DAP exposures achieved with package label dosing (PLD) and identify dosing regimens necessary to optimize efficacy and mitigate toxicity in pediatric patients being treated for Staphylococcus aureus bacteremia. Methods Pharmacokinetic/pharmacodynamic (PK/PD) models were constructed using age-specific pediatric PK parameters from previously published clinical trials in children to determine the probability of target attainment (PTA) for each of the following age cohorts: 3 to 6 months, 7 to 12 months, 13 to 24 months, 2 to 6 years, 7 to 11 years, and 12 to 17 years. Achievement of area under the curve over 24 hours (AUC0-24) ≥ 666 mg*hr/L was used as the PD target to determine the PTA for efficacy (PTAE). The probability for which the trough concentration (Cmin) exceeded 24.3 mg/L was the PD target used to determine the PTA for toxicity (PTAT). These PD targets were selected based on prior adult data correlating DAP exposure with efficacy and safety outcomes. Optimal dosing regimens were considered to be those which achieved the combined target of PTAE ≥ 90% and PTAT ≤ 5%. Results If targeting previously validated efficacy (AUC0-24 ≥ 666 mg*hr/L) and safety (Cmin < 24.3 mg*hr/L) endpoints, current pediatric dosing regimens do not achieve adequate DAP exposure for treatment of Staphylococcus aureus bacteremia. PLD failed to achieve adequate PTAE in all age groups with only 26.3% PTAE in children 13 to 24 months, 39.5% PTAE in children 2 to 6 years, 30.1% PTAE in children 7 to 11 years, and 50.1% PTAE in children 12 to 17 years of age. Optimal dosing regimens, defined as achieving at least 90% PTAE with PTAT ≤ 5%, are displayed in Table 1. Conclusion Current PLD of DAP resulted in inadequate exposure for all pediatric patients evaluated. If using validated PD targets for efficacy and safety, adequate PTAE and minimal PTAT were achieved with DAP at ... |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| DOI: | 10.1093/ofid/ofad500.028 |
| الاتاحة: | http://dx.doi.org/10.1093/ofid/ofad500.028 https://academic.oup.com/ofid/article-pdf/10/Supplement_2/ofad500.028/53764018/ofad500.028.pdf |
| Rights: | https://creativecommons.org/licenses/by/4.0/ |
| رقم الانضمام: | edsbas.86B10A71 |
| قاعدة البيانات: | BASE |
| DOI: | 10.1093/ofid/ofad500.028 |
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