Disposition of Chloramphenicol in Low Birth Weight Infants
- 1 October 1980
- journal article
- research article
- Published by American Academy of Pediatrics (AAP) in Pediatrics
- Vol. 66 (4), 573-578
- https://doi.org/10.1542/peds.66.4.573
Abstract
Although infrequently an antibiotic of first choice for neonates, chloramphenicol (CL) may be indicated in selected instances of infection caused by aminoglycoside-resistant Enterobacteriaciae, anaerobes and ampicillin-resistant Haemophilus influenzae. Use of CL in neonates is limited since the recognition that vascular collapse may occur as a consequence of dosage regimens tolerated by adults. With an assay that detects only active CL, drug disposition was studied in 13 low birth weight infants, 8 between 1-8 days of age (group I) and 5 between 11 days and 8 wk of age (group II). Peak serum CL concentrations ranged from 11.2-36.2 .mu.g/ml in group I and from 10.0-36.2 .mu.g/ml in group II, at doses ranging from 15-50 mg/kg per day and 25-50 mg/kg per day, in groups I and II, respectively. Serum CL half-lives (t1/2) ranged from 10-36 h in 4 of the 8 group I patients; 3 of the remaining patients had t1/2 greater than 48 h and the 4th patient accumulated CL in the interval between doses. The t1/2 in group II ranged from 5.5-15.7 h. Observed differences in t1/2 between groups I and II were statistically significant (P = .05) and could not be accounted for by factors other than postnatal age. These preliminary data suggest that although there appears to be an inverse relationship between CL t1/2 and postnatal age, there is sufficient variability in serum levels that monitoring must be performed in low birth weight infants treated with this drug.This publication has 3 references indexed in Scilit:
- Central nervous system chloramphenicol concentration in premature infantsAntimicrobial Agents and Chemotherapy, 1978
- Quantitative gas-chromatographic flame-ionization method for chloramphenicol in human serum.Clinical Chemistry, 1977
- An Enzymatic Assay for Chloramphenicol with Partially Purified Chloramphenicol AcetyltransferaseThe Journal of Infectious Diseases, 1976