Ceftriaxone Pharmacokinetics and Pharmacodynamic Target Attainment for Three Pediatric Patients Receiving Continuous Kidney Replacement Therapy

Author:

Hambrick H. Rhodes12,Cervantes Francisco3,Dong Min24,Tang Peter45,Arbough Trent6,Vinks Alexander A.24,Mizuno Tomoyuki24,Goldstein Stuart L.1247,Kaplan Jennifer48,Girdwood Sonya Tang49

Affiliation:

1. Division of Nephrology and Hypertension (HRH, SLG), Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;

2. Division of Clinical Pharmacology (HRH, MD, AAV, TM, STG), Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;

3. Department of Medical Education (FC), University of Cincinnati College of Medicine, Cincinnati, OH;

4. Department of Pediatrics (MD, PT, AAV, TM, SLG, JK, STG), University of Cincinnati College of Medicine, Cincinnati, OH;

5. Division of Pathology and Laboratory Medicine (PT), Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;

6. Department of Anesthesiology (TA), University of Kentucky College of Medicine, Lexington, KY;

7. Center for Acute Care Nephrology (SLG), Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;

8. Division of Critical Care Medicine (JK), Cincinnati Children’s Hospital Medical Center, Cincinnati, OH;

9. Division of Hospital Medicine (STG), Cincinnati Children’s Hospital Medical Center, Cincinnati, OH.

Abstract

Ceftriaxone is used commonly for sepsis, including in children requiring continuous kidney replacement therapy (CKRT). No reports exist of pharmacokinetic (PK) parameters for children receiving ceftriaxone on CKRT. We enrolled children admitted to our pediatric intensive care unit (PICU) who received CKRT for >24 hours and received >1 dose of ceftriaxone while on and off CKRT. We measured free ceftriaxone ­concentrations from residual blood samples then used Bayesian estimation with PK modeling software to generate concentration-time profiles and determine PK parameters and the percentage of time free ceftriaxone concentrations were above 1× or 4× MIC (% fT >MIC). Three patients aged 2 to 17 years were included; all were anuric at CKRT initiation and received 50 mg/kg (max 2000 mg) ceftriaxone every 12 to 24 hours. Total ceftriaxone clearance (CL) was 0.50 to 3.67 L/hr while receiving CKRT and 0.29 to 2.71 L/hr while off, indicating CKRT provided 25% to 42% of total ceftriaxone CL. All achieved 100% fT >1× and 4× MIC using an estimated MIC (1 mg/L) for patients 1 to 2 (no culture data) and a measured MIC (0.016 mg/L) for patient 3. Therefore, CKRT contributed significantly to total ceftriaxone clearance in 3 children though the dosing strategies used in each patient attained PD targets.

Publisher

Pediatric Pharmacy Advocacy Group

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