Cerebrospinal Pharmacokinetic Analysis and Pharmacodynamic Evaluation of Ceftriaxone in Pediatric Patients with Bacterial Meningitis
What Is Known? and Objective. Ceftriaxone has been widely used to treat bacterial meningitis in pediatric patients. Ceftriaxone dosing regimens of 80–120 mg/kg/day have been recommended for bacterial meningitis in pediatric patients, and the usual duration of therapy is 7–14 days. Although the targe...
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Published in | Journal of clinical pharmacy and therapeutics Vol. 2024; no. 1 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Hindawi
2024
John Wiley & Sons, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0269-4727 1365-2710 |
DOI | 10.1155/2024/4684986 |
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Abstract | What Is Known? and Objective. Ceftriaxone has been widely used to treat bacterial meningitis in pediatric patients. Ceftriaxone dosing regimens of 80–120 mg/kg/day have been recommended for bacterial meningitis in pediatric patients, and the usual duration of therapy is 7–14 days. Although the target site for meningitis is cerebrospinal fluid (CSF), a CSF pharmacokinetic (PK) model in pediatric patients has not been reported. We aimed to develop a CSF PK model of ceftriaxone, using not only serum but also CSF concentration data, and to evaluate the appropriateness of dosing regimens for pediatric patients with bacterial meningitis. Methods. The population PK model was developed by simultaneously fitting serum and CSF data from pediatric patients described in nine published articles. Probabilities of attaining a pharmacodynamic target (100% T > MIC, 100% of time that drug concentrations above the minimum inhibitory concentration) in CSF were estimated for some dosing regimens. Results and Discussion. Twenty-four pediatric patients with meningitis were the subjects for PK modeling (0.52–13 years old, and 3.5–50 kg of body weight). Sixty-eight serum concentrations and 98 CSF samples were used to develop the CSF PK model. The CSF/serum concentration ratio at the same sampling time was 0.0628 ± 0.0689. Age was not a statistically significant covariate in the PK parameter. In the CSF PK model, 40–60 mg/kg q12 h achieved a target attainment probability >90% against causative bacteria for bacterial meningitis. However, 4-h infusion (rather than 0.5-h infusion) dosing regimens were required for efficacy against antimicrobial-resistant bacteria with high MICs. What Is New? and Conclusion. Ceftriaxone-dosing regimens with prolonged infusion times might be reasonably effective for treating antimicrobial-resistant pathogens in empiric therapy. |
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AbstractList | What Is Known? and Objective. Ceftriaxone has been widely used to treat bacterial meningitis in pediatric patients. Ceftriaxone dosing regimens of 80–120 mg/kg/day have been recommended for bacterial meningitis in pediatric patients, and the usual duration of therapy is 7–14 days. Although the target site for meningitis is cerebrospinal fluid (CSF), a CSF pharmacokinetic (PK) model in pediatric patients has not been reported. We aimed to develop a CSF PK model of ceftriaxone, using not only serum but also CSF concentration data, and to evaluate the appropriateness of dosing regimens for pediatric patients with bacterial meningitis. Methods. The population PK model was developed by simultaneously fitting serum and CSF data from pediatric patients described in nine published articles. Probabilities of attaining a pharmacodynamic target (100% T > MIC, 100% of time that drug concentrations above the minimum inhibitory concentration) in CSF were estimated for some dosing regimens. Results and Discussion. Twenty-four pediatric patients with meningitis were the subjects for PK modeling (0.52–13 years old, and 3.5–50 kg of body weight). Sixty-eight serum concentrations and 98 CSF samples were used to develop the CSF PK model. The CSF/serum concentration ratio at the same sampling time was 0.0628 ± 0.0689. Age was not a statistically significant covariate in the PK parameter. In the CSF PK model, 40–60 mg/kg q12 h achieved a target attainment probability >90% against causative bacteria for bacterial meningitis. However, 4-h infusion (rather than 0.5-h infusion) dosing regimens were required for efficacy against antimicrobial-resistant bacteria with high MICs. What Is New? and Conclusion. Ceftriaxone-dosing regimens with prolonged infusion times might be reasonably effective for treating antimicrobial-resistant pathogens in empiric therapy. What Is Known? and Objective . Ceftriaxone has been widely used to treat bacterial meningitis in pediatric patients. Ceftriaxone dosing regimens of 80–120 mg/kg/day have been recommended for bacterial meningitis in pediatric patients, and the usual duration of therapy is 7–14 days. Although the target site for meningitis is cerebrospinal fluid (CSF), a CSF pharmacokinetic (PK) model in pediatric patients has not been reported. We aimed to develop a CSF PK model of ceftriaxone, using not only serum but also CSF concentration data, and to evaluate the appropriateness of dosing regimens for pediatric patients with bacterial meningitis. Methods . The population PK model was developed by simultaneously fitting serum and CSF data from pediatric patients described in nine published articles. Probabilities of attaining a pharmacodynamic target (100% T > MIC, 100% of time that drug concentrations above the minimum inhibitory concentration) in CSF were estimated for some dosing regimens. Results and Discussion . Twenty‐four pediatric patients with meningitis were the subjects for PK modeling (0.52–13 years old, and 3.5–50 kg of body weight). Sixty‐eight serum concentrations and 98 CSF samples were used to develop the CSF PK model. The CSF/serum concentration ratio at the same sampling time was 0.0628 ± 0.0689. Age was not a statistically significant covariate in the PK parameter. In the CSF PK model, 40–60 mg/kg q12 h achieved a target attainment probability >90% against causative bacteria for bacterial meningitis. However, 4‐h infusion (rather than 0.5‐h infusion) dosing regimens were required for efficacy against antimicrobial‐resistant bacteria with high MICs. What Is New? and Conclusion . Ceftriaxone‐dosing regimens with prolonged infusion times might be reasonably effective for treating antimicrobial‐resistant pathogens in empiric therapy. |
Author | Tamaki, Hiroki Ikawa, Kazuro Yano, Takahisa Ishihara, Noriyuki Naora, Kohji Morikawa, Norifumi Onita, Tetsushu |
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Cites_doi | 10.1086/321854 10.1007/s40262-021-01035-9 10.1128/aac.23.2.341 10.1007/s00228-020-02939-4 10.1097/00006454-199807000-00022 10.1016/s1473-3099(09)70306-8 10.1111/j.2042-7158.2010.01179.x 10.1007/s10156-012-0448-x 10.1086/516284 10.1016/j.cmpb.2003.11.003 10.1016/s0022-3476(84)80032-3 10.1128/aac.01412-20 10.1542/peds.2013-0621 10.2165/00003495-200565080-00005 10.1097/00006454-198611000-00026 10.1128/aac.21.2.248 10.1128/aac.01427-21 10.1097/00006454-198806000-00018 10.1016/s0140-6736(88)90596-x 10.1128/aac.22.4.622 10.1542/peds.98.1.133 10.1186/s12866-020-01808-5 10.1128/aac.23.2.191 10.1097/inf.0b013e31829b5880 10.1038/s41598-022-06950-w 10.1097/inf.0000000000003496 10.1128/aac.23.1.46 10.1542/peds.2011-3453 10.1016/j.ijid.2018.06.023 10.1016/s0891-5520(20)30369-x 10.7326/0003-4819-115-9-712 |
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Copyright | Copyright © 2024 Tetsushu Onita et al. Copyright © 2024 Tetsushu Onita et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0 |
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Snippet | What Is Known? and Objective. Ceftriaxone has been widely used to treat bacterial meningitis in pediatric patients. Ceftriaxone dosing regimens of 80–120... What Is Known? and Objective . Ceftriaxone has been widely used to treat bacterial meningitis in pediatric patients. Ceftriaxone dosing regimens of 80–120... |
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SubjectTerms | Antibiotics Antimicrobial agents Bacteria Body weight Ceftriaxone Cerebrospinal fluid Data integrity Dosage Drug dosages Estimates Meningitis Minimum inhibitory concentration Mortality Pathogens Patients Pediatrics Pharmacodynamics Pharmacokinetics Population Random variables Statistical analysis Streptococcus infections |
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Title | Cerebrospinal Pharmacokinetic Analysis and Pharmacodynamic Evaluation of Ceftriaxone in Pediatric Patients with Bacterial Meningitis |
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