Evidence map›Paper›PMID 42519496›Full record

ReviewWorld journal of pediatric surgery2026

Postoperative hyperinflammation and recovery challenges in necrotizingenterocolitis.

Christopher John Luschen, Catherine J Hunter

Abstract readReview
In one paragraph

Review in World journal of pediatric surgery, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Christopher John LuschenDepartment of Surgery, University of Oklahoma, Oklahoma City, Oklahoma, USA.ORCID https://orcid.org/0009-0001-2701-212X
Catherine J HunterDepartment of Surgery, University of Oklahoma, Oklahoma City, Oklahoma, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Necrotizing enterocolitis (NEC) remains one of the most devastating gastrointestinal emergencies in neonates, particularly affecting premature infants with immature intestinal, immune and microvascular systems. While surgical intervention is often lifesaving in severe NEC, the postoperative period introduces distinct challenges that critically influence survival and long-term outcomes. This review examines postoperative hyperinflammation as a central driver of morbidity following surgical NEC. Despite resection of necrotic bowel, many infants experience persistent systemic inflammation characterized by dysregulated innate immune activation, excessive cytokine release and sustained gut barrier dysfunction. Key mediators including tumor necrosis factor-alpha (TNF-α), interleukin (IL)-6, IL-1β and IL-8 contribute to endothelial injury, capillary leak, hemodynamic instability and multiorgan dysfunction. Ongoing intestinal permeability and microbial translocation perpetuate inflammatory signaling, delaying mucosal healing and predisposing infants to recurrent NEC, sepsis and short bowel syndrome. Clinically, postoperative hyperinflammation manifests as systemic inflammatory response syndrome, coagulopathy, feeding intolerance, impaired wound healing and neurodevelopmental injury. Recovery is frequently prolonged by nutritional compromise, dependence on parenteral nutrition and recurrent infections, which further amplify inflammatory stress. Current management remains largely supportive, focusing on optimization of nutrition, infection prevention and multidisciplinary care. Emerging immunomodulatory and microbiome-based therapies remain investigational. Postoperative hyperinflammation remains a difficult and complex sequelae of NEC and future investigation is needed to improve long-term outcomes.

Indexed as

NeonatologyPediatricsPhysiology

Identifiers

PMID42519496
PMCPMC13384141

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.