Evidence map›Paper›PMID 39103605›Full record

ArticleJournal of general internal medicine2025

Risk of Serious Adverse Gastrointestinal Events with Potassium Binders in Hospitalized Patients: A National Study.

Jürgen L Holleck, Ling Han, Melissa Skanderson, Lori A Bastian, Craig G Gunderson, Cynthia A Brandt, Melissa Perkal, John J Chang, Kathleen M Akgün

Abstract read
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Article in Journal of general internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

9 authors.

Jürgen L HolleckDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, USA. Jurgen.Holleck@yale.edu.ORCID 0000-0001-7701-4345
Ling HanDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Melissa SkandersonDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, West Haven, CT, USA.
Lori A BastianDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Craig G GundersonDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Cynthia A BrandtDepartment of Medicine, Veterans Affairs Connecticut Healthcare System, West Haven, CT, USA.
Melissa PerkalDepartment of Surgery, Yale School of Medicine, New Haven, CT, USA.
John J ChangDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.
Kathleen M AkgünDepartment of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.

Funding

VA Health Services Research and Development CIN 13-407
6 · The paper itself

Abstract

backgroundConcerns about serious adverse gastrointestinal (GI) events with sodium polystyrene sulfonate (SPS) led to development of two new potassium binders, patiromer and sodium zirconium cyclosilicate (SZC), for treatment of hyperkalemia.

objectiveTo compare risk of intestinal ischemia/thrombosis or other serious GI events associated with SPS, patiromer, or SZC in hospitalized patients.

designRetrospective cohort study.

participantsNational sample of 3,144,960 veterans hospitalized 2016-2022 in the U.S. Department of Veterans Affairs Healthcare System. MAIN MEASURES: Demographics, comorbidities, medications and outcomes were ascertained from the VA Corporate Data Warehouse. Exposures were SPS, patiromer, SZC. Outcomes were 30-day intestinal ischemia/thrombosis, and a composite of intestinal ischemia/thrombosis, peptic ulcer/perforation or bowel resection/ostomy. KEY

resultsPotassium binders were used during 39,270 (1.3%) hospitalizations: SPS = 30,040 (1.0%), patiromer = 3,750 (0.1%), and SZC = 5,520 (0.2%). Intestinal ischemia/thrombosis occurred with 106/30,040 (0.4%) SPS, 12/3750 (0.3%) patiromer and 24/5520 (0.4%) SZC, vs. 6998/3,105,650 (0.2%) without potassium binder. Adjusted odds ratios (aOR) were 1.40 [95% CI, 1.16 to 1.69] with SPS, 1.36 [CI, 0.79 to 2.36] with patiromer, and 1.78 [CI, 1.21 to 2.63] with SZC exposures. Composite GI adverse events occurred with 754/30,040 (2.5%) SPS, 96/3750 (2.6%) patiromer, 2.6% SZC, vs. 144/5520 (2.4%) without binder; aOR were 1.00 [CI, 0.94 to 1.08] with SPS, 1.08 [CI, 0.89 to 1.32] with patiromer, and 1.08 [CI, 0.93 to 1.27] with SZC exposures. No statistical difference in intestinal ischemia/thrombosis between each new agent and SPS was seen (p = 0.274 for SPS vs. SZC; p = 0.916 for SPS vs. patiromer).

conclusionRisk of intestinal ischemia/thrombosis or other serious adverse GI events was low and did not differ across three potassium-binding drugs.

Indexed as

Chelating AgentsGastrointestinal DiseasesHospitalizationHyperkalemiaPolymersPolystyrenesPotassiumSilicatesAgedAged, 80 and overCohort StudiesFemaleHumansMaleMiddle AgedRetrospective StudiesChelating AgentspatiromerPolymersPolystyrenespolystyrene sulfonic acidPotassiumSilicatessodium zirconium cyclosilicatecation exchange resinsgastrointestinal diseasemedication adverse events

Identifiers

PMID39103605
PMCPMC11861845

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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.