Pharmacokinetics of intravenous immunoglobulin in very low birth weight neonates
- 1 November 1989
- journal article
- research article
- Published by Wolters Kluwer Health in The Pediatric Infectious Disease Journal
- Vol. 8 (11) , 759-762
- https://doi.org/10.1097/00006454-198911000-00006
Abstract
We studied the pharmacokinetics of single doses of intravenous immunoglobulin (IVIG) of 1000, 750 and 500 mg/kg administered to 21 neonates with birth weights from 750 to 1500 g. No adverse effects were detected. Mean pharmacokinetic values for the large, intermediate and small dose groups, respectively, were: elimination half-life, 19.6, 28.7 and 22.1 days; clearance, 5.2, 5.6 and 3.7 ml/kg/day; volume of distribution, 151, 255 and 130 ml/kg. Mean peak IgG concentrations in serum were 1826, 1476 and 1257 mg/dl for the large, intermediate and small dose groups, respectively. Mean IgG on post-infusion Days 1 to 28 were similar for the intermediate and small dose groups but were higher in the larger dose group. Both large and intermediate doses achieved larger increases in IgG over preinfusion values (ΔIgG) than the small dose. The differences in ΔIgG between the large and intermediate doses were less notable. The wide variability observed indicates that individualization of intravenous immunoglobulin dosage will be required in these patients.This publication has 5 references indexed in Scilit:
- Analysis of Lymphocyte Proliferative Response Subpopulations in Very Low Birth Weight Infants and during the First 8 Weeks of LifePediatric Research, 1988
- Intravenous immunoglobulin for prophylaxis of neonatal sepsis in premature infants.Archives of Disease in Childhood, 1988
- Disposition of an immunoglobulin intravenous preparation in very low birth weight neonatesThe Journal of Pediatrics, 1988
- Intravenous gammaglobulin therapy for prophylaxis of infection in high-risk neonatesThe Journal of Pediatrics, 1987
- Alterations in the half-life and clearance of IgG during therapy with intravenous ?-globulin in 16 patients with severe primary humoral immunodeficiencyJournal of Clinical Immunology, 1986