Evidence map›Paper›PMID 41575455›Full record

Trial reportKidney3602026

Impact of Loop Diuretics on Long-Term Kidney Outcome: A Post Hoc Analysis of the STOP-Angiotensin-Converting Enzyme Inhibitor Trial.

Sunil Bhandari, Samir Mehta, Natalie Ives, John G F Cleland, Paul Cockwell

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Kidney360, 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

5 authors.

Sunil BhandariDepartment of Renal Medicine, Hull University Teaching Hospitals NHS Trust, Hull York Medical School, Kingston Upon Hull, United Kingdom.ORCID 0000-0002-0996-9622
Samir MehtaBirmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0001-7096-513
Natalie IvesBirmingham Clinical Trials Unit, University of Birmingham, Birmingham, United Kingdom.ORCID 0000-0002-1664-7541
John G F ClelandBritish Heart Foundation Centre of Research Excellence, School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, United Kingdom.ORCID 0000-0002-1471-7016
Paul CockwellDepartment of Renal Medicine, Queen Elizabeth Hospital, Birmingham, United Kingdom.ORCID 0000-0003-1975-266

Funding

NIHR Bristol Biomedical Research Center NIHR-HTA 11/30/07. STOP ACEi
6 · The paper itself

Abstract

key pointsRenin-angiotensin system inhibitors have less effect on decline in eGFR and no greater effect on delaying ESKD/KRT in patients receiving loop diuretics compared with those who do. Although loop diuretic use was not associated with higher rates of ESKD/KRT, it might be associated with a higher mortality. The decline in eGFR was slower in those taking loop diuretics.

backgroundIn the STOP-Angiotensin-Converting Enzyme Inhibitor trial, patients with advanced CKD were randomized to continue or stop renin-angiotensin system inhibitors (RASi) and showed no difference in kidney outcomes. This post hoc analysis investigates interactions with loop diuretic use.

methodsPatients with eGFR <30 ml/min per 1.73 m 2 and progressive CKD were randomized to stop or continue RASi. Primary outcome was eGFR over 3 years using repeated-measures, mixed-effects linear regression, random-slope models. Cox models were used to calculate hazard ratios for time-to-event outcomes, including ESKD and KRT.

resultsAt baseline, eGFR, arterial pressure, and proteinuria were similar for 133 patients taking loop diuretics and 278 who were not. Those receiving loop diuretics at randomization, least-squares mean (±SE) eGFR at 3 years was 12.3 (±1.1) for those stopping compared with 10.1 (±1.2) for those continuing RASi, trend favoring stopping RASi (+2.2; 95% confidence interval [CI], -0.9 to 5.4), but eGFR slope over 3 years was similar (-7.2 versus -7.7 ml/min per 1.73 m 2 ). Those not receiving loop diuretics, eGFR at 3-years was 8.8 (±0.8) and 11.6 (±0.8; discontinue and continue RASi groups), a difference favoring continuing RASi (-2.8; 95% CI, -4.9 to -0.8), and a steeper eGFR slope for those discontinuing RASi (-9.9 versus -7.6 ml/min per 1.73 m 2 ). The interaction between loop diuretic use and the effect of RASi on eGFR at 3 years and the three-way interaction between diuretic subgroup, effect of RASi, and time were both statistically significant ( P = 0.01 and P = 0.04, respectively). Of patients taking loop diuretics, 73 (55%) developed ESKD/KRT and 23 (17%) died. Of patients not taking loop diuretics, 170 (61%) developed ESKD/KRT and 19 (7%) died.

conclusionsWithdrawal of RASi was associated with a steeper decline in eGFR over 3 years in those not receiving loop diuretics, but this was not observed in those who were taking loop diuretics. Patients receiving loop diuretics had a high mortality. These data support the need for randomized trials investigating the efficacy and safety of loop diuretics in patients with advanced CKD.

Indexed as

Angiotensin-Converting Enzyme InhibitorsGlomerular Filtration RateKidneyKidney Failure, ChronicRenal Insufficiency, ChronicSodium Potassium Chloride Symporter InhibitorsAgedDisease ProgressionFemaleHumansMaleMiddle AgedRenin-Angiotensin SystemTreatment OutcomeAngiotensin-Converting Enzyme InhibitorsSodium Potassium Chloride Symporter InhibitorsACE inhibitorschronic kidney diseaseCKDclinical trialdiureticsGFRmortalityprogression of renal failurerenal function declinerenin-angiotensin system

Identifiers

PMID41575455
PMCPMC13134784

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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.