Serum concentrations and safety of single daily dosing of amikacin in children undergoing bone marrow transplantation
- PMID: 1856140
- DOI: 10.1093/jac/27.suppl_c.113
Serum concentrations and safety of single daily dosing of amikacin in children undergoing bone marrow transplantation
Abstract
The serum concentrations and safety of single daily dosing of amikacin were studied in 16 episodes of fever and granulocytopenia in children undergoing bone marrow transplantation. Amikacin (20 mg/kg) was administered as a 20 min iv infusion once daily for 7 to 19 days; all patients received concomitant therapy with ceftazidime. Peak amikacin concentrations measured immediately after infusion on day 1 and 4 of therapy averaged 72.29 +/- 11.6 mg/l and 74.02 +/- 19.29 mg/l respectively. A slight but statistically significant increase 30 minute post-infusion concentrations was observed in most patients during therapy. Serum amikacin were less than 3 mg/l in all trough samples and within 6 h post-infusion in most patients. A significant increase in serum creatinine was observed in one patient, who was also receiving cyclosporin A. Auditory function was evaluated in 10 patients and showed no changes. Although other drugs were added to cover Gram-positive or fungal pathogens, all patients survived. These data combined with the recent experience of single daily dose amikacin in adults supports further evaluation of novel dosage regimens of aminoglycosides in children.
Similar articles
-
Efficacy and toxicity of single daily doses of amikacin and ceftriaxone versus multiple daily doses of amikacin and ceftazidime for infection in patients with cancer and granulocytopenia. The International Antimicrobial Therapy Cooperative Group of the European Organization for Research and Treatment of Cancer.Ann Intern Med. 1993 Oct 1;119(7 Pt 1):584-93. doi: 10.7326/0003-4819-119-7_Part_1-199310010-00006. Ann Intern Med. 1993. PMID: 8363169 Clinical Trial.
-
The pharmacokinetic of amikacin in critically ill adult and paediatric patients: comparison of once- versus twice-daily dosing regimens.J Antimicrob Chemother. 1991 May;27 Suppl C:81-9. doi: 10.1093/jac/27.suppl_c.81. J Antimicrob Chemother. 1991. PMID: 1856148 Clinical Trial.
-
Single daily dose amikacin in paediatric patients with severe gram-negative infections.J Antimicrob Chemother. 1991 May;27 Suppl C:141-7. doi: 10.1093/jac/27.suppl_c.141. J Antimicrob Chemother. 1991. PMID: 1856143
-
Clinical and pharmacokinetic study of a single daily dose of amikacin in paediatric patients with severe gram-negative infections.J Antimicrob Chemother. 1991 May;27 Suppl C:105-12. doi: 10.1093/jac/27.suppl_c.105. J Antimicrob Chemother. 1991. PMID: 1906861 Clinical Trial.
-
Pharmacokinetic evaluation of single daily dose amikacin.J Antimicrob Chemother. 1991 May;27 Suppl C:63-71. doi: 10.1093/jac/27.suppl_c.63. J Antimicrob Chemother. 1991. PMID: 1856147 Review.
Cited by
-
Efficacy and tolerability of extended-interval aminoglycoside administration in pediatric patients.Paediatr Drugs. 2002;4(7):469-84. doi: 10.2165/00128072-200204070-00005. Paediatr Drugs. 2002. PMID: 12083974
-
Once daily antibiotic regimen in paediatric oncology.Arch Dis Child. 1994 Jun;70(6):484-7. doi: 10.1136/adc.70.6.484. Arch Dis Child. 1994. PMID: 8048816 Free PMC article. Clinical Trial.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical