Faecal calprotectin concentrations in neonates with CHD: pilot study

Cardiol Young. 2020 May;30(5):624-628. doi: 10.1017/S1047951120000645. Epub 2020 Apr 3.

Abstract

Neonates with CHD are at increased risk of developing necrotising enterocolitis due to mesenteric hypoperfusion. Necrotising enterocolitis results in repeated feed interruptions contributing to poor growth during the early post-operative phase. Poor weight gain and longer hospital stay are risk factors for death in neonates with CHD. Abdominal radiography is used as a diagnostic tool for necrotising enterocolitis; however, its utility is limited in the early stages of necrotising enterocolitis when pneumatosis intestinalis is absent. Calprotectin is a neutrophil activation biomarker, and elevated levels are evident in inflammatory diseases such as necrotising enterocolitis. The aim of this study was to determine whether there is a correlation between faecal calprotectin concentration and gut inflammation in neonates with CHD. This prospective single-centre study recruited newly diagnosed term patients with duct-dependent CHD between March 2018 and March 2019. Faecal calprotectin concentrations were measured in post-surgical patients using enzyme-linked immunosorbent assay methods. A total of 30 patients were included in the analysis. Calprotectin concentration for patients who developed necrotising enterocolitis was 3528 µg/g compared with 390 µg/g without, compared with 1339 µg/g in patients with suspected necrotising enterocolitis (p = 0.0001). Patients with suspected necrotising enterocolitis had a significantly longer length of hospital stay, on average 18 days longer compared to patients without necrotising enterocolitis (p = 0.03). Faecal calprotectin concentrations may reflect severity of gut inflammation in neonates with CHD. Suspected necrotising enterocolitis contributes to longer days nil by mouth and an increase in length of hospital stay.

Keywords: CHD; faecal calprotectin; feeding; necrotising enterocolitis; suspected necrotising enterocolitis.

MeSH terms

  • Biomarkers / analysis
  • Enteral Nutrition / methods
  • Enterocolitis, Necrotizing / diagnosis*
  • Enterocolitis, Necrotizing / metabolism
  • Feces / chemistry*
  • Female
  • Heart Defects, Congenital / complications*
  • Humans
  • Infant, Newborn
  • Infant, Premature
  • Length of Stay / statistics & numerical data*
  • Leukocyte L1 Antigen Complex / metabolism*
  • Male
  • Pilot Projects
  • Prospective Studies

Substances

  • Biomarkers
  • Leukocyte L1 Antigen Complex