Evidence map›Paper›PMID 38863856›Full record

ArticleThe journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG2024

Enteral Feedings Do Not Increase the Risk of NEC in ELBW Infants Undergoing Treatment of Patent Ductus Arteriosus With Acetaminophen.

Katherine V Katsivalis, Jessica L Jacobson, Rakhee Bowker, Andrew Berenz, Sara Hovey, Kristen W Click

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Article in The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Katherine V KatsivalisDepartment of Pharmacy (KVK, JLJ, SH, KMW), Rush University Medical Center, Chicago, IL.
Jessica L JacobsonDepartment of Pharmacy (KVK, JLJ, SH, KMW), Rush University Medical Center, Chicago, IL.
Rakhee BowkerDepartment of Pediatrics (RB, AB), Rush University Medical Center, Chicago, IL.
Andrew BerenzDepartment of Pediatrics (RB, AB), Rush University Medical Center, Chicago, IL.
Sara HoveyDepartment of Pharmacy (KVK, JLJ, SH, KMW), Rush University Medical Center, Chicago, IL.
Kristen W ClickDepartment of Pharmacy (KVK, JLJ, SH, KMW), Rush University Medical Center, Chicago, IL.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAcetaminophen (APAP) is an alternative to indomethacin and ibuprofen for treatment of patent ductus arteriosus (PDA). The side effect profile of non-steroidal anti-inflammatory drugs (NSAIDs) presents enteral feeding safety concerns; however, the safety of enteral feeding on APAP is largely unknown. Optimal feeding strategies during pharmacological PDA treatment are unknown, leading to practice variation. This study aims to assess the incidence of adverse gastrointestinal (GI) outcomes in neonates treated with APAP for PDA closure while receiving enteral feedings.

methodsSingle-center retrospective cohort study of 59 extremely low birth weight (ELBW), premature neonates who received APAP for PDA treatment divided into Low Volume (LV; ≤ 20 mL/kg/day) and High Volume (HV; > 20 mL/kg/day) enteral feeding groups. The primary outcome was the incidence of any suspected or confirmed necrotizing enterocolitis (NEC). Timing of nutrition milestones, parenteral nutrition (PN) days, and adverse outcomes (feeding intolerance, liver dysfunction, death prior to discharge) were evaluated.

resultsThe incidence of suspected or confirmed NEC was 19.5% in the LV group and 13.3% in the HV group (p = 0.593). The HV group reached full feeds 6 days sooner (18 vs 24 days, p = 0.024) and had fewer PN days (17 vs 23.5 days, p = 0.044) with no difference in adverse outcomes.

conclusionsProvision of > 20 mL/kg/day of enteral feeds during APAP treatment of PDA decreased time to full feeds and PN days compared to trophic feedings (≤ 20 mL/kg/day) with no difference in adverse GI outcomes. Continuing enteral feeding during APAP PDA treatment appears safe while improving achievement of nutritional milestones.

Indexed as

acetaminophenextremely low birth weightfeeding strategiesnecrotizing enterocolitis­patent ductus arteriosuspreterm

Identifiers

PMID38863856
PMCPMC11163909

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.