Evidence map›Paper›PMID 40720490›Full record

ArticlePloS one2025

Effect of cystic fibrosis transmembrane conductance regulator modulators and dedicated cystic fibrosis gastrointestinal clinic visits on the incidence of distal intestinal obstructive syndrome in persons with cystic fibrosis.

Nicha Wongjarupong, Malique F Delbrune, Jameel Alp, Daphne M Moutsoglou, Talia Wiggen, Ashley Benner, Joanne L Billings, Jordan M Dunitz, Sarah J Schwarzenberg, Baharak Moshiree and 1 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

11 authors.

Nicha WongjarupongDepartment of Gastroenterology, Hepatology, and Nutrition, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID https://orcid.org/0000-0001-8676-413X
Malique F DelbruneUniversity of Minnesota Medical School, Minneapolis, Minnesota, United States of America.
Jameel AlpDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota, United States of America.
Daphne M MoutsoglouDepartment of Medicine, University of Minnesota, Minneapolis, Minnesota, United States of America.
Talia WiggenClinical and Translational Science Institute, University of Minnesota, Minneapolis, Minnesota, United States of America.
Ashley BennerClinical and Translational Science Institute, University of Minnesota, Minneapolis, Minnesota, United States of America.ORCID https://orcid.org/0000-0002-2833-5772
Joanne L BillingsDepartment of Medicine, Division of Pulmonology and Critical Care, University of Minnesota, Minneapolis, Minnesota, United States of America.
Jordan M DunitzDepartment of Medicine, Division of Pulmonology and Critical Care, University of Minnesota, Minneapolis, Minnesota, United States of America.
Sarah J SchwarzenbergDepartment of Pediatrics, Division of Pediatric Gastroenterology, and Hepatology and Nutrition, University of Minnesota, Minneapolis, Minnesota, United States of America.
Baharak MoshireeDivision of Gastroenterology, Hepatology, and Nutrition, Atrium Health, Wake Forest University, Charlotte, North Carolina, United States of America.
Shahnaz SultanDepartment of Gastroenterology, Hepatology, and Nutrition, University of Minnesota, Minneapolis, Minnesota, United States of America.

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UM1TR004405 · NCATS · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar, Damien A Fair · 2023 to 2026
$30.8M
NCATS NIH HHS UM1 TR004405
6 · The paper itself

Abstract

backgroundGastrointestinal (GI) complications are the second most common disorders in persons with cystic fibrosis (PwCF). There is limited data on how having a dedicated CF-GI clinic and cystic fibrosis transmembrane conductance regulator (CFTR) modulators may affect rates of GI complications. Our aim was to assess the effect of the CF-GI clinic and CFTR modulators on GI complications with incidence of distal intestinal obstructive syndrome (DIOS).

methodsThis was a retrospective study of adult PwCF who were seen in a CF-GI clinic from 2000-2023. Comparisons were made between the numbers of admissions and emergency department (ED) visits for DIOS at three years before and after CFTR modulator use and the first CF-GI clinic visit.

resultsOf the 1,076 PwCF identified, 242 were seen in CF-GI clinic. Of this, 126 (52.1%) were female, with a median age of 40 (IQR: 30-47) years. There were 146 (60.3%) with regular use of laxatives. Of the 59 PwCF with CF-GI clinic visits for constipation, hospital admissions decreased in 16, were unchanged in 32, and increased in 11 (p = 0.402) while ED visits decreased in 9, remained the same in 40, and increased in 10 (p = 0.862). Of the 125 PwCF with CFTR modulator use, DIOS-related hospital admissions decreased in 15 patients, remained unchanged in 89, and increased in 21 (p = 0.021) while ED visits were fewer in 8, unchanged in 97, and increased in 20 (p = 0.587).

conclusionPwCF had high burden of constipation with a majority of patients regularly using laxatives, and almost half had a history of DIOS. CFTR modulator use and CF-GI clinic were not associated with a decrease of DIOS incidence.

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorIntestinal ObstructionAdultConstipationEmergency Service, HospitalFemaleHospitalizationHumansIncidenceLaxativesMaleMiddle AgedRetrospective StudiesCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorLaxatives

Identifiers

PMID40720490
PMCPMC12303333

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Registered trials

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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 OpenQuestion graph.