AI Article Synopsis

  • Infants with necrotizing enterocolitis (NEC) can develop intestinal gangrene, which is a severe form of the disease characterized by intestinal tissue death due to lack of blood flow.
  • A study conducted from 1998 to 2006 reviewed cases of infants who underwent surgery for NEC, focusing on the serum enzyme levels in those with and without intestinal gangrene.
  • Results showed that infants with gangrene had significantly higher levels of lactate dehydrogenase (LDH), suggesting that measuring LDH could help doctors make better surgical decisions for NEC patients.

Article Abstract

In infants with necrotizing enterocolitis (NEC), intestinal gangrene defines advanced disease. Since intestinal ischemia is considered a pathogenetic factor for intestinal gangrene, serum activity of mucosal and seromuscular enzymes may be elevated in these patients. Our aim was to evaluate if serum enzymes activity is increased in infants with NEC associated with intestinal gangrene. We performed a retrospective review of the case notes of infants operated on for NEC between 1998 and 2006. Patients with preoperative determination of serum enzymes were included in the study, and were divided into Group A and Group B based on the presence or absence of intestinal gangrene, respectively. Serum activities of alkaline phosphatase (ALP), glutamic oxaloacetic transaminase (GOT), creatine kinase (CK), and lactate dehydrogenase (LDH) were compared in the two Groups. Values are medians (interquartile range). Thirty-five infants were operated on for NEC in the study period. Eighteen patients fulfilled the inclusion criteria: 12 in Group A and six in Group B. Group A patients had significantly higher LDH activity [1131.0 (1092.0-1300.0) vs. 482.0 (440.0-624.5) IU/L; P < 0.005]. Our findings suggest that LDH activity may be increased in infants with NEC and intestinal gangrene. Its evaluation could be a further tool in the surgical decision making process in infants with NEC.

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Source
http://dx.doi.org/10.1007/s00383-008-2156-2DOI Listing

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