Evidence map›Paper›PMID 41951879›Full record

ArticleCommunications medicine2026

Association of pharmacotherapy with all-cause mortality among patients with irritable bowel syndrome.

Sepideh Mehravar, Yee Hui Yeo, Mark Pimentel, Parnian Naji, Wee Han Ng, Nils Burger, Will Takakura, Ali Rezaie

Abstract read
In one paragraph

Article in Communications medicine, 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

8 authors.

Sepideh MehravarKarsh Division of Gastroenterology and Hepatology, Department of Medicine, Cedars-Sinai, Los Angeles, CA, USA.
Yee Hui YeoKarsh Division of Gastroenterology and Hepatology, Department of Medicine, Cedars-Sinai, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-2703-5954
Mark PimentelKarsh Division of Gastroenterology and Hepatology, Department of Medicine, Cedars-Sinai, Los Angeles, CA, USA.
Parnian NajiDepartment of Surgery, University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
Wee Han NgDepartment of Public Health and Primary Care, University of Cambridge, Cambridge, UK.
Nils BurgerDepartment of Cancer Biology, Dana-Farber Cancer Institute, Boston, MA, USA.
Will TakakuraDepartment of Medicine, Division of Gastroenterology and Hepatology, Kaiser Permanente Panorama City, Panorama City, CA, USA.
Ali RezaieKarsh Division of Gastroenterology and Hepatology, Department of Medicine, Cedars-Sinai, Los Angeles, CA, USA. ali.rezaie@cshs.org.ORCID http://orcid.org/0000-0002-0106-372X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIrritable bowel syndrome (IBS) is a common disorder associated with high healthcare costs and reduced quality of life. The long-term safety of its pharmacotherapies remains unclear. This study aims to assess the association between long-term pharmacotherapies and all-cause mortality in this population.

methodWe performed a retrospective cohort study using a nationwide U.S. electronic health record database (January 1, 2005, to January 1, 2023). A 1:1 propensity score-matched cohort included 669,083 adults (aged 18-65) with IBS. Patients were grouped by pharmacotherapy use, with subgroup analyses for IBS with diarrhea (IBS-D) and IBS with constipation (IBS-C). Follow-up started at the time of medication prescription after diagnosis. Exposures included guideline-recommended therapies for IBS, IBS-D, or IBS-C. The primary outcome was all-cause mortality, assessed using Cox proportional hazards models and target trial emulation.

resultsAntidepressant use is associated with an increased risk of all-cause mortality (hazard ratio [HR], 1.35; 95% CI, 1.26-1.45; mortality rate, 1.6% vs. 1.0%). This association remains consistent across antidepressant subclasses and demographic subgroups. Antispasmodic use is not linked to increased mortality (HR, 0.95; 95% CI, 0.89-1.00). For IBS-D, cholestyramine/colestipol, eluxadoline, and rifaximin are not associated with mortality. However, diphenoxylate (HR, 1.89; 95% CI, 1.02-3.51) and loperamide (HR, 2.39; 95% CI, 1.48-3.90) show increased mortality risk. For IBS-C, polyethylene glycol-3350 and secretagogues have no significant association with mortality.

conclusionsThese findings raise concerns regarding the safety of antidepressants and mu receptor agonists in IBS treatment and underscore the need for cautious prescribing and further research.

Identifiers

PMID41951879
PMCPMC13061985

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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.