Randomized Trial to Compare Nasoduodenal Tube and Nasogastric Tube Feeding in Infants with Bronchiolitis on High-Flow Nasal Cannula

Abstract

Objectives In this article, we aimed to determine if there is a difference in length of respiratory support between nasoduodenal (NDT) and nasogastric tube (NGT) feedings in patients with bronchiolitis on high-flow nasal cannula (HFNC).

Methods A single-center nonblinded parallel randomized control trial at a tertiary care hospital was designed. Pediatric patients ≤ 12 months old with bronchiolitis, on HFNC, requiring nutrition via a feeding tube were eligible. Patients were randomized to NGT or NDT and stratified into low- and high-risk groups. Length of respiratory support was the primary outcome. Secondary outcomes included length of stay, number of emesis events, maximum level of respiratory support, number of X-rays to confirm tube placement, number of attempts to place the tube by staff, adverse events during placement, instances of pediatric intensive care unit admission, and emergency room visits and hospital readmissions within 7 and 30 days after discharge.

Results Forty patients were randomized, 20 in each arm. There were no significant differences in baseline characteristics. We found no significant difference in length of respiratory support between the two groups (NGT 0.84 incidence rate ratio [0.58, 1.2], p = 0.34). None of the secondary outcomes showed significant differences. Each arm reported one adverse event: nasal trauma in the NGT group and pneumothorax in the NDT group.

Conclusion For infants with bronchiolitis on HFNC that need enteric tube feedings, we find no difference in duration of respiratory support or other clinically relevant outcomes for those with NGT or NDT. These results should be interpreted in the context of a limited sample size and an indirect primary outcome of length of respiratory support that may be influenced by other factors besides aspiration events.

Keywords

nasogastric feeding tube - nasoduodenal feeding tube - bronchiolitis - high-flow nasal cannula - aspiration - enteral feeding

Authors' Contributions

Each author participated sufficiently in the work and take public responsibility for the content.

R.L.P.-C. and A.G. conceptualized and designed the study, collected data, analyzed the data, drafted the initial manuscript, reviewed and revised the manuscript, and approved the final manuscript as submitted.

M.L.-P., V.M.G., H.S.H., G.H.D., M.S.E., S.G., and S.K. collected data, reviewed and revised the manuscript, and approved the final manuscript.

Note:

This study was conducted at the Children's Memorial Hermann, Houston, TX, United States.

Publikationsverlauf

Eingereicht: 05. Dezember 2021

Angenommen: 01. März 2022

Artikel online veröffentlicht:
10. Juni 2022

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