Evidence map›Paper›PMID 41962874›Full record

ArticleClinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association2026

The Impact of Diet and Enteral Tube Type on Gastric Bile Acid Concentrations and Pulmonary Outcomes.

Rachel Rosen, Kenneth D R Setchell, Monica Narvaez-Rivas, Toni Solari, Lauren Jalali, Jasper Brezsny-Feldman, Elise Delaney, Christopher Chalmers, Michael Kim, Jada Lee and 5 more

Abstract read
In one paragraph

Article in Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Rachel RosenDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Kenneth D R SetchellDivision of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Monica Narvaez-RivasDivision of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
Toni SolariDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Lauren JalaliDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Jasper Brezsny-FeldmanDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Elise DelaneyDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Christopher ChalmersDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Michael KimDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Jada LeeDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Dagny ScannellDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Nicole ZunoDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Sahil PatelDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Samuel NurkoDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Bridget M HronDivision of Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts. Electronic address: bridget.hron@childrens.harvard.edu.

Funding

The impact of upper gastrointestinal dysmotility on aspiration-associated aerodigestive disorders in childrenR01DK097112 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI Rachel L Rosen · 2015 to 2026
$4.9M
A Novel N-of-1 Randomized, Controlled, Clinical Trial to Assess the Effect of Blenderized Tube Feeds on Esophagogastric PhysiologyK23DK133679 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI Bridget Mary Hron · 2022 to 2026
$1.0M
NIDDK NIH HHS K23 DK133679NIDDK NIH HHS R01 DK097112
6 · The paper itself

Abstract

BACKGROUND &

aimsBile acid reflux has been implicated as a cause for esophagitis, pulmonary fibrosis, and other aerodigestive disorders. The goal of this study was to determine the relationship between gastric and lung bile acid concentrations and if diet was a modifiable risk factor to reduce bile acid reflux.

methodsWe prospectively recruited children with oropharyngeal dysphagia and respiratory symptoms undergoing aerodigestive testing. Gastric and, when available, lung bile acid concentrations were quantified using liquid chromatography-mass spectrometry. In a subgroup of enterally fed patients, serum 7α-hydroxy-4-cholesten-3-one (C4) levels were measured.

resultsIn this prospective cohort of 141 participants, gastric bile acids concentrations were highest in those fed orally compared with enteral tubes (P = .008). Gastric bile acid was a strong predictor of lung bile acids in children receiving blenderized tube feeds (r = 0.57; P = .03), but not formula (r = 0.34; P = .09), or oral feeds (r = -0.02; P = .89). Low lung bile acid concentration predicted low neutrophil counts in the lung (r = 0.39; P = .003), as did use of blenderized tube feeds (oral, 5 [interquartile range (IQR), 26]; formula, 7.5 [IQR, 37.5]; blenderized, 0 [IQR, 0]; P = .008). Quartile gastric and lung bile acids were strong predictors of hospitalization rates (P< .001 for both). Serum C4 levels, a surrogate for bile acid synthesis rate, did not support evidence of excessive bile acid loss with blenderized tube feeds (blenderized, 2.3 [IQR, 11.3] vs formula, 18.1 [IQR, 34.8] ng/mL; P = .03).

conclusionsFor patients at high risk for bile acid-related aerodigestive complications, tube and diet type may affect gastric bile acid concentrations, in turn impacting important clinical outcomes of hospitalization rates and airway inflammation.

Indexed as

AspirationBile AcidsBlenderized Tube FeedsGastroesophageal RefluxGastrostomy Tube

Identifiers

PMID41962874
PMCPMC13382878

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.