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Essential medicines containing ethanol elevate blood acetaldehyde concentrations in neonates
H C Pandya1, H Mulla2, M Hubbard3
1Department of Infection, Immunity and Inflammation, University of Leicester, University Road, Leicester, LE1 9HN, UK. hp28@le.ac.uk.
Insights
Ethanol-containing medicines given to neonates resulted in low blood ethanol levels but elevated acetaldehyde concentrations, a potentially toxic metabolite. This suggests acetaldehyde
Area of Science:
- Neonatal pharmacology
- Toxicology
- Drug metabolism
Background:
- Neonates often receive medications containing ethanol, like iron and furosemide.
- There is limited data on the impact of these medications on blood ethanol and acetaldehyde levels in neonates.
Purpose of the Study:
- To determine blood ethanol and acetaldehyde concentrations in preterm infants receiving ethanol-containing medications.
- To assess the potential risks associated with ethanol and acetaldehyde exposure in neonates.
Main Methods:
- Measured blood ethanol and acetaldehyde concentrations in 49 preterm infants dosed with iron or furosemide.
- Included 11 control infants not receiving medications.
- Analyzed concentrations in relation to medication type and time.
Main Results:
- Infants receiving iron or furosemide had low median blood ethanol concentrations (0.33-0.39 mg/L).
- Median blood acetaldehyde concentrations were elevated in infants receiving these medications (0.16-0.21 mg/L), indicating moderate alcohol exposure.
- No clear correlation was found between concentrations and time post-dose.
Conclusions:
- Ethanol-containing medicines in neonates lead to low blood ethanol but potentially concerning acetaldehyde levels.
- The toxic effects of acetaldehyde should be considered in the risk-benefit analysis of these medications for neonates.
Unlabelled:
Neonates administered ethanol-containing medicines are potentially at risk of dose-dependent injury through exposure to ethanol and its metabolite, acetaldehyde. Here, we determine blood ethanol and acetaldehyde concentrations in 49 preterm infants (median birth weight = 1190 g) dosed with iron or furosemide, medicines that contain different amounts of ethanol, and in 11 control group infants (median birth weight = 1920 g) who were not on any medications. Median ethanol concentrations in neonates administered iron or furosemide were 0.33 (range = 0-4.92) mg/L, 0.39 (range = 0-72.77) mg/L and in control group infants were 0.15 (range = 0.03-5.4) mg/L. Median acetaldehyde concentrations in neonates administered iron or furosemide were 0.16 (range = 0-8.89) mg/L, 0.21 (range = 0-2.43) mg/L and in control group infants were 0.01 (range = 0-0.14) mg/L. There was no discernible relationship between blood ethanol or acetaldehyde concentrations and time after medication dose.
Conclusion:
Although infants dosed with iron or furosemide had low blood ethanol concentrations, blood acetaldehyde concentrations were consistent with moderate alcohol exposure. The data suggest the need to account for the effects of acetaldehyde in the benefit-risk analysis of administering ethanol-containing medicines to neonates.
What Is Known:
• Neonates are commonly treated with ethanol-containing medicines, such as iron and furosemide. • However, there is no data on whether this leads to appreciable increases in blood concentrations of ethanol or its metabolite, acetaldehyde. What is New: • In this study, we find low blood ethanol concentrations in neonates administered iron and/or furosemide but markedly elevated blood acetaldehyde concentrations in some infants receiving these medicines. • Our data suggest that ethanol in drugs may cause elevation of blood acetaldehyde, a potentially toxic metabolite.
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