65 Is the developing lung susceptible to acetaminophen toxicity?

Abstract Acetaminophen exposures in the perinatal period are ubiquitous. In addition to being the most commonly used drug during pregnancy, clinicians have increasingly prescribed acetaminophen (APAP) for patients in the neonatal intensive care unit (NICU). Acetaminophen has been shown to reduce post-operative opiate burden and may provide similar efficacy for closure of the patent ductus arteriosus (PDA) as nonsteroidal anti-inflammatory drugs (NSAIDs). However, while APAP exposures have spread to a highly vulnerable population of increasingly less mature infants, robust pharmacokinetic and pharmacodynamic data for APAP are lacking. Concerningly, preclinical studies suggest that perinatal APAP exposures may result in unanticipated adverse effects that are unique to the developing lung. I will discuss the clinical observations linking APAP exposures to adverse respiratory outcomes and the preclinical data demonstrating a developmental susceptibility to APAP-induced lung injury. I will discuss how clinical observations linking perinatal APAP exposures to pulmonary injury have been taken to the bench to produce important insights into the potential mechanisms underlying these findings.

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Publication Details

Journal
Journal of Animal Science
Published
2025-12-19
DOI
https://doi.org/10.1093/jas/skaf398.055
Primary Topic
Pregnancy and Medication Impact
Type
article
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article

65 Is the developing lung susceptible to acetaminophen toxicity?

Clyde J Wright*
Journal of Animal Science
Pregnancy and Medication Impact
article

65 Is the developing lung susceptible to acetaminophen toxicity?

Clyde J Wright*
article en

Abstract

Abstract Acetaminophen exposures in the perinatal period are ubiquitous. In addition to being the most commonly used drug during pregnancy, clinicians have increasingly prescribed acetaminophen (APAP) for patients in the neonatal intensive care unit (NICU). Acetaminophen has been shown to reduce post-operative opiate burden and may provide similar efficacy for closure of the patent ductus arteriosus (PDA) as nonsteroidal anti-inflammatory drugs (NSAIDs). However, while APAP exposures have spread to a highly vulnerable population of increasingly less mature infants, robust pharmacokinetic and pharmacodynamic data for APAP are lacking. Concerningly, preclinical studies suggest that perinatal APAP exposures may result in unanticipated adverse effects that are unique to the developing lung. I will discuss the clinical observations linking APAP exposures to adverse respiratory outcomes and the preclinical data demonstrating a developmental susceptibility to APAP-induced lung injury. I will discuss how clinical observations linking perinatal APAP exposures to pulmonary injury have been taken to the bench to produce important insights into the potential mechanisms underlying these findings.

Journal of Animal ScienceVol. 104(Supplement_1)
Children's Hospital Colorado (US), University of Colorado Denver (US)
Good health and well-being
Openalex Percentile: Top 26%
Pregnancy and Medication Impact
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