Evidence map›Paper›PMID 40826036›Full record

ArticleBMC nephrology2025

Diagnostic value of the urea-to-creatinine ratio for gastrointestinal bleeding source: influence of renal function.

Philipp Russ, Julian M Koppenhöfer, Simon Bedenbender, Thomas S Tarawneh, Ulrike W Denzer, Ivica Grgic, Martin Rußwurm, Christian S Haas

Abstract read
In one paragraph

Article in BMC nephrology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

8 authors.

Philipp RussDivision of Nephrology, Centre for Internal Medicine, Marburg University, University Hospital Giessen and Marburg, Marburg, Germany. russp@staff.uni-marburg.de.ORCID 0009-0007-2799-5449
Julian M KoppenhöferDivision of Nephrology, Centre for Internal Medicine, Marburg University, University Hospital Giessen and Marburg, Marburg, Germany.
Simon BedenbenderDivision of Nephrology, Centre for Internal Medicine, Marburg University, University Hospital Giessen and Marburg, Marburg, Germany.
Thomas S TarawnehDivision of Hematology and Oncology, Centre for Internal Medicine, Marburg University, University Hospital Giessen and Marburg, Marburg, Germany.
Ulrike W DenzerDivision of Gastroenterology and Endocrinology, Centre for Internal Medicine, Marburg University, University Hospital Giessen and Marburg, Marburg, Germany.
Ivica GrgicDivision of Nephrology, Centre for Internal Medicine, Marburg University, University Hospital Giessen and Marburg, Marburg, Germany.
Martin Rußwurm *Division of Nephrology, Centre for Internal Medicine, Marburg University, University Hospital Giessen and Marburg, Marburg, Germany.
Christian S Haas *Division of Nephrology, Centre for Internal Medicine, University Medicine Rostock, Rostock, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastrointestinal (GI) bleeding is frequent and clinically critical, especially in patients with renal dysfunction. Localization of the source is relevant for treatment and outcomes. The urea-to-creatinine ratio (UCR) has been proposed as a tool to differentiate between upper and lower GI bleeding. However, its diagnostic utility across varying degrees of renal impairment remains unclear.

methodsFrom January 2021 to October 2023, all patients with suspected GI bleeding who underwent endoscopy were retrospectively analyzed in a single center. Patients without confirmed bleeding were excluded. Patients were stratified by renal function: normal renal function, chronic kidney disease (CKD), acute kidney injury (AKI), and AKI with pre-existing CKD (acute-on-chronic). We assessed the discriminatory power of the UCR to distinguish upper from lower GI bleeding within each group.

resultsA total of 849 patients (mean age 66.9 ± 18.2 years) were included. Approximately two-thirds of the patients (n = 544; 64.1%) were male. CKD was present in 321 (37.8%) and AKI in 354 (41.7%) patients; 199 (56.2%) of those with AKI had pre-existing CKD. Upper GI bleeding occurred more frequently in patients with AKI (75.1%) and CKD (72.9%) than in those with normal renal function (p < 0.0001 and p = 0.0003, respectively); both groups also required transfusions more frequently (p < 0.0001 for both). UCR values were significantly higher in upper vs. lower GI bleeding in patients with normal renal function (67.5 vs. 42.5; p < 0.0001), but this difference was reduced in CKD (49.3 vs. 41.0; p = 0.0103) and not significant in AKI (53.1 vs. 47.7; p = 0.09). The diagnostic performance of UCR was best in patients with normal renal function (AUROC 0.69) and markedly impaired in CKD (AUROC 0.56) and AKI (AUROC 0.54).

conclusionThe diagnostic value of UCR to localize GI bleeding depends strongly on renal function. While the UCR may help to identify the bleeding site in patients with normal kidney function, impaired renal function hampers the reliability of the UCR, especially in patients with AKI. As renal dysfunction is common in patients with GI bleeding, kidney function must be taken into account when interpreting UCR values.

Indexed as

Acute Kidney InjuryCreatinineGastrointestinal HemorrhageRenal Insufficiency, ChronicUreaAgedFemaleHumansMaleMiddle AgedRetrospective StudiesCreatinineUreaAcute kidney injury (AKI)Chronic kidney disease (CKD)EndoscopyGastrointestinal (GI) bleedingRenal dysfunctionUrea-to-creatinine ratio (UCR)

Identifiers

PMID40826036
PMCPMC12359887

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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.