» Articles » PMID: 1759825

Pharmacokinetics of Cefuroxime Axetil Suspension in Infants and Children

Overview
Specialty Pharmacology
Date 1991 Oct 1
PMID 1759825
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

The pharmacokinetics of cefuroxime axetil suspension in 28 infants and children, ranging in age from 3 months to 12 years (mean, 23 months), were studied. Mean maximum serum cefuroxime concentrations of 3.3, 5.1, and 7.0 micrograms/ml were achieved 3.6, 2.7, and 3.1 h after the administration of doses of 10, 15, and 20 mg, respectively, of cefuroxime axetil suspension per kg of body weight together with milk or milk formula. These concentrations exceed the MICs for common respiratory tract pathogens, including beta-lactamase-producing strains of Haemophilus influenzae and Moraxella (Branhamella) catarrhalis. Following a 10- or 15-mg/kg dose, serum cefuroxime concentrations are similar to those achieved in adults following the administration of a 250-mg cefuroxime axetil tablet. There were linear relationships between dose and both maximum serum cefuroxime concentration and area under the serum drug concentration-verus-time curve. The mean half-life of cefuroxime in serum was independent of dose and ranged from 1.4 to 1.9 h. No cefuroxime axetil (intact ester) was detected in the blood. The intact ester in the urine of four children was measured; however, the amount recovered represented less than 0.1% of the administered dose.

Citing Articles

Developmental Pharmacokinetics of Antibiotics Used in Neonatal ICU: Focus on Preterm Infants.

Butranova O, Ushkalova E, Zyryanov S, Chenkurov M Biomedicines. 2023; 11(3).

PMID: 36979919 PMC: 10046592. DOI: 10.3390/biomedicines11030940.


Are children undergoing cardiac surgery receiving antibiotics at subtherapeutic levels?.

Huang J, Sunstrom R, Munar M, Cherala G, Legg A, Olyeai A J Thorac Cardiovasc Surg. 2014; 148(4):1591-6.

PMID: 24521951 PMC: 4099311. DOI: 10.1016/j.jtcvs.2013.12.043.


Commonly used antibacterial and antifungal agents for hospitalised paediatric patients: implications for therapy with an emphasis on clinical pharmacokinetics.

Singh J, Burr B, Stringham D, Arrieta A Paediatr Drugs. 2001; 3(10):733-61.

PMID: 11706924 DOI: 10.2165/00128072-200103100-00003.


Clinical use of cefuroxime in paediatric community-acquired pneumonia.

Olivier C Paediatr Drugs. 2000; 2(5):331-43.

PMID: 11022795 DOI: 10.2165/00128072-200002050-00001.


Stereoselective absorption and hydrolysis of cefuroxime axetil diastereomers using the Caco-2 cell monolayer model.

Barrett M, Lawrence M, Hutt A, Lansley A Eur J Drug Metab Pharmacokinet. 1998; 22(4):409-13.

PMID: 9512942 DOI: 10.1007/BF03190978.


References
1.
Harding S, Williams P, Ayrton J . Pharmacology of Cefuroxime as the 1-acetoxyethyl ester in volunteers. Antimicrob Agents Chemother. 1984; 25(1):78-82. PMC: 185439. DOI: 10.1128/AAC.25.1.78. View

2.
Sommers D, van Wyk M, Williams P, Harding S . Pharmacokinetics and tolerance of cefuroxime axetil in volunteers during repeated dosing. Antimicrob Agents Chemother. 1984; 25(3):344-7. PMC: 185514. DOI: 10.1128/AAC.25.3.344. View

3.
Neu H, Fu K . Cefuroxime, a beta-lactamase-resistant cephalosporin with a broad spectrum of gram-positive and -negative activity. Antimicrob Agents Chemother. 1978; 13(4):657-64. PMC: 352306. DOI: 10.1128/AAC.13.4.657. View

4.
McCracken Jr G, Ginsburg C, Clahsen J, Thomas M . Pharmacologic evaluation of orally administered antibiotics in infants and children: effect of feeding on bioavailability. Pediatrics. 1978; 62(5):738-43. View

5.
Ginsburg C, McCracken Jr G . Pharmacokinetics of cephradine suspension infants and children. Antimicrob Agents Chemother. 1979; 16(1):74-6. PMC: 352791. DOI: 10.1128/AAC.16.1.74. View