Hypoxic-ischemic enterocolitis in extremely low birth weight infants: diagnostic insights from a pilot study

Tainá Cristina Ferrari1, Rafael Simone Saia2, Cristina Helena Faleiros Ferreira1

  • 1Department of Pediatrics, Ribeirão, Preto Medical School, University of São Paulo, Bandeirantes Avenue 3900, Ribeirão Preto, São Paulo, Brazil.

Insights

Hypoxic-ischemic enterocolitis (HIEnt) in extremely low birth weight (ELBW) infants is often missed due to vague symptoms. Lower birth weight, abnormal prenatal Doppler, and early platelet decrease may signal HIEnt, necessitating multimodal diagnostic approaches.

Area of Science:

  • Neonatal Medicine
  • Pediatric Gastroenterology
  • Perinatal Research

Background:

  • Hypoxic-ischemic enterocolitis (HIEnt) is a severe condition in extremely low birth weight (ELBW) infants, often presenting within the first week of life.
  • Underdiagnosis is common due to non-specific clinical signs and limitations of current diagnostic tools.

Purpose of the Study:

  • To evaluate early diagnostic tools for HIEnt in ELBW infants.
  • To characterize HIEnt during the first week of life.
  • To identify potential early markers for future large-scale studies.

Main Methods:

  • Prospective, single-center pilot study of 23 ELBW infants (<1000g).
  • Systematic collection of clinical, perinatal, and neonatal variables, including serum biomarkers (sodium, platelets, bicarbonate, I-FABP) on days 2, 4, and 6.
  • Diagnosis of HIEnt based on modified Bell's criteria.

Main Results:

  • Three infants (13%) were diagnosed with HIEnt.
  • HIEnt cases had significantly lower birth weight and higher incidence of abnormal antenatal Doppler findings.
  • Lower platelet counts on day 4 and delayed diet initiation were observed in the HIEnt group.
  • Serum I-FABP and common clinical symptoms did not differentiate between groups.

Conclusions:

  • Prenatal risk factors, low birth weight, feeding intolerance, and decreased platelet levels may indicate HIEnt in ELBW infants.
  • Findings suggest distinct pathophysiological origins for HIEnt.
  • Integrated, multimodal diagnostic strategies are needed, along with larger validation studies.