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Published on: August 25, 2014
Perinatal drug exposure and renal function in very preterm infants
R Vieux1, J Fresson, F Guillemin
1Maternité Régionale, Neonatal Department, Nancy, France. r.vieux@maternite.chu-nancy.fr
Insights
Ibuprofen was found to be nephrotoxic in very preterm infants, impacting glomerular filtration rate (GFR) for up to one month. Physicians should monitor GFR in infants treated with ibuprofen, as drug clearance may remain reduced.
Area of Science:
- Neonatal Medicine
- Pharmacology
- Nephrology
Background:
- Very preterm infants are vulnerable to kidney injury.
- Assessing the nephrotoxic potential of commonly prescribed drugs is crucial for this population.
Purpose of the Study:
- To evaluate the impact of first-week-of-life medications on glomerular filtration rate (GFR) and tubular function in very preterm infants.
Main Methods:
- Prospective multicentre cohort study involving infants born between 27-31 weeks gestation.
- GFR measured on day 2 and weekly for 1 month using a standardized kinetic Jaffe method.
- Infants categorized into 'Low GFR' and 'High GFR' groups based on day 7 GFR relative to gestational age median.
Main Results:
- 269 infants analyzed; 183 in 'Low GFR' and 86 in 'High GFR' group.
- Higher incidence of ibuprofen use in the 'Low GFR' group (30.0%) compared to the 'High GFR' group (17.4%).
- Aminoglycosides, glycopeptides, and other common drugs showed no significant nephrotoxic effect at therapeutic doses.
Conclusions:
- Ibuprofen was the only drug identified as nephrotoxic in very preterm infants during the 1-month follow-up.
- Reduced GFR post-ibuprofen treatment may persist for the first month, affecting drug clearance.
Objective:
To determine the impact on glomerular filtration rate (GFR) and tubular function of drugs prescribed to very preterm infants during the first week of life.
Design:
Prospective multicentre cohort study of infants aged 27-31 weeks gestation.
Methods:
GFR was measured on day 2, and then weekly for 1 month, with 12-h urine collection by a standardised kinetic Jaffe method. Infants were classified into two groups according to their GFR on day 7 ('Low GFR' and 'High GFR') with regard to the median reference GFR for their gestational age. Tubular function was also measured weekly for 1 month. Statistical analysis was performed using logistic regression and a repeated measure analysis.
Results:
Data from 269 infants were analysed, 183 in the 'Low GFR' group and 86 in the 'High GFR' group. Perinatal factors did not differ in both groups. Significantly more infants were treated with ibuprofen in the 'Low GFR' group than in the 'High GFR' group, respectively, n=55 (30.0%) versus n=15 (17.4%), whereas aminoglycosides, glycopeptides and all other drugs commonly prescribed during the first week of life did not show a nephrotoxic effect at usual therapeutic dosage.
Conclusions:
Among all drugs described as nephrotoxic in very preterm infants, ibuprofen alone proved to be nephrotoxic in this study for a 1-month span follow-up. If GFR is lower than the median reference value on day 7 after ibuprofen infusion, physicians should keep in mind that glomerular clearance of drugs may stay decreased for the first month of life.
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