Gastrointestinal Factors Associated With Hospitalization in Infants With Cystic Fibrosis: Results From the Baby Observational and Nutrition Study

Meghana Sathe, Rong Huang, Sonya Heltshe, Alexander Eng, Elhanan Borenstein, Samuel I Miller, Lucas Hoffman, Daniel Gelfond, Daniel H Leung, Drucy Borowitz, Bonnie Ramsey, A Jay Freeman, Meghana Sathe, Rong Huang, Sonya Heltshe, Alexander Eng, Elhanan Borenstein, Samuel I Miller, Lucas Hoffman, Daniel Gelfond, Daniel H Leung, Drucy Borowitz, Bonnie Ramsey, A Jay Freeman

Abstract

Objectives: To identify factors that increase the risk of gastrointestinal-related (GI-related) hospitalization of infants with cystic fibrosis (CF) during the first year of life.

Methods: The Baby Observational and Nutrition Study was a longitudinal, observational cohort of 231 infants diagnosed with CF by newborn screening. We performed a post-hoc assessment of the frequency and indications for GI-related admissions during the first year of life.

Results: Sixty-five participants had at least one admission in the first 12 months of life. High pancreatic enzyme replacement therapy (PERT) dosing (>2000 lipase units/kg per meal; hazard ratio [HR] = 14.75, P = 0.0005) and use of acid suppressive medications (HR = 4.94, P = 0.01) during the study period were positively associated with subsequent GI-related admissions. High levels of fecal calprotectin (fCP) (>200 μg/g) and higher relative abundance of fecal Klebsiella pneumoniae were also positively associated with subsequent GI-related admissions (HR = 2.64, P = 0.033 and HR = 4.49, P = 0.002, respectively). During the first 12 months of life, participants with any admission had lower weight-for-length z scores (WLZ) (P = 0.01). The impact of admission on WLZ was particularly evident in participants with a GI-related admission (P < 0.0001).

Conclusions: Factors associated with a higher risk for GI-related admission during the first 12 months include high PERT dosing, exposure to acid suppressive medications, higher fCP levels, and/or relative abundance of fecal K pneumoniae early in life. Infants with CF requiring GI-related hospitalization had lower WLZ at 12 months of age than those not admitted as well as those admitted for non-GI-related indications.

Trial registration: ClinicalTrials.gov NCT01424696.

Copyright © 2021 by European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition.

Figures

Figure 1:
Figure 1:
Impact of hospitalization on growth of infants in the first year of life.
Figure 2:
Figure 2:
The relationship of GI admission and baseline measurements of fecal calprotectin, relative abundance of fecal K. pneumoniae and PERT dose

Source: PubMed

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