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Immune function and infectious complications in children with jejunoileal atresia
Sittichoke Prachuapthunyachart1, Shaheed Merani2, Madeline Cloonan2
1Pediatric Gastroenterology, Hepatology and Nutrition, University of Nebraska Medical Center and Children's Hospital & Medical Center, Omaha, NE, United States.
Insights
Children with isolated intestinal atresia (IA) may experience immunodeficiency and infections. Early immune screening in IA and multiple intestinal atresia (MIA) patients can improve outcomes.
Area of Science:
- Pediatric Surgery
- Immunology
- Gastroenterology
Background:
- Immune function differences between isolated intestinal atresia (IA) and multiple intestinal atresia (MIA) in children are not well understood.
- Such differences may impact infectious complications and patient outcomes.
Purpose of the Study:
- To investigate and compare immune function in children with IA and MIA.
- To determine the impact of immune function on infectious complications and patient outcomes in these pediatric populations.
Main Methods:
- A retrospective cohort study of children (0-19 years) with intestinal atresia from 2000-2016.
- Data collected included patient characteristics, surgical history, immunologic work-up, and infection-related hospitalizations.
- Comparison between IA and MIA groups using appropriate statistical tests (chi-square, Fisher's exact, Mann-Whitney).
Main Results:
- Over half of patients in both IA and MIA groups exhibited low CD counts for age.
- Hypogammaglobulinemia was observed in 6/12 IA and 3/8 MIA children.
- Frequent bacteremia occurred in 3/10 IA and 3/5 MIA children; MIA patients had worse post-transplant outcomes.
Conclusions:
- Children with IA may present with immunodeficiency and associated infectious complications.
- Immunologic evaluation is recommended for both IA and MIA children in intestinal rehabilitation programs.
- Early screening for immunodeficiency can guide interventions and improve patient outcomes.
Objective:
Little is known about differences in immune function among children with multiple intestinal atresia (MIA) and those with isolated intestinal atresia (IA), and how such differences may manifest as infectious complications and patient outcomes. This study aimed to investigate the immune function and its impact on patient outcomes in IA and MIA children.
Methods:
A single-center retrospective cohort study included children aged 0-19 years with intestinal atresia who were referred to a multidisciplinary intestinal rehabilitation program from 1/2000 to 12/2016. Data were collected for patient characteristics, surgical history, immunologic work-up, and infection-related hospitalizations. Groups of IA and MIA children were compared using chi-square test or Fisher's exact test for categorical variables and using Mann-Whitney test for continuous variables, as appropriate.
Results:
Twenty-seven children (18 IA, 9 MIA) were included. More than half of the patients had low CD counts for age in IA and MIA groups: CD3 58.3% vs. 66.7% (p = 1.0), CD4 50.0% vs. 66.7% (p = 0.7), CD8 67.7% vs. 88.9% (p = 0.3), respectively. Six out of 12 IA children and 3 out of 8 MIA children had hypogammaglobulinemia (p = 0.7). Three out of 10 IA patients and 3 out of 5 MIA children had frequent bacteremia (≥5/year). Eight children (6 IA and 2 MIA) underwent intestinal and/or liver transplant; MIA children had a worse posttransplant outcome.
Conclusions:
IA children may have an immunodeficiency and associated infectious complications requiring hospitalization. We suggest performing immunologic evaluation not only in MIA but also in IA children presenting to an intestinal rehabilitation program to identify immunodeficiency. Early immunodeficiency screening may help initiate appropriate intervention and improve patient outcomes.
Level Of Evidence:
Level III.
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