Evidence map›Paper›PMID 40600695›Full record

ArticleEuropean journal of heart failure2025

Exploring safety of down-titrating diuretics in heart failure management.

Chrit B G Geraeds, Anke Bruninx, Andre L A J Dekker, Arantxa Barandiarán Aizpurua, Inigo Bermejo, Hans-Peter Brunner-La Rocca

Abstract readControlled Clinical TrialMulticenter Study
In one paragraph

Article in European journal of heart failure, 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. Review
  2. Decongestion in chronic heart failure.JRSM cardiovascular disease
    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

6 authors.

Chrit B G GeraedsDepartment of Cardiology, CARIM, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID https://orcid.org/0009-0000-8804-8700
Anke BruninxDepartment of Radiation Oncology (MAASTRO), GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID https://orcid.org/0000-0002-5916-8735
Andre L A J DekkerDepartment of Radiation Oncology (MAASTRO), GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID https://orcid.org/0000-0002-0422-7996
Arantxa Barandiarán AizpuruaDepartment of Cardiology, CARIM, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID https://orcid.org/0000-0002-3448-5531
Inigo BermejoDepartment of Radiation Oncology (MAASTRO), GROW Research Institute for Oncology and Reproduction, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID https://orcid.org/0000-0001-9105-8088
Hans-Peter Brunner-La RoccaDepartment of Cardiology, CARIM, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID https://orcid.org/0000-0002-4356-8566

Funding

ZonMw
6 · The paper itself

Abstract

aimsLoop diuretics are widely used in heart failure (HF) for symptom relief. Guidelines advise treating patients with the lowest possible dose of loop diuretics to maintain euvolaemia, based on expert opinion only. However, data on the safety of this practice are scarce. This analysis aims to investigate the clinical course after changing loop diuretics in stable HF patients. METHODS AND

resultsA post-hoc analysis from the TIME-CHF study was conducted in 622 patients. Daily loop diuretic doses were meticulously recorded, resulting in 11 035 dose evaluations assessed. The frequency of relevant events within 30 days (hospitalization, death, dose change) following an up-titration, down-titration, or no change in diuretic therapy was calculated. Risk of hospitalization and deaths 30 days after down-titration was estimated after adjusting for congestion level. At baseline the cohort consisted mostly of males (59%), with a mean age of 77 years. Patients were highly symptomatic with 76% classified as New York Heart Association class III or IV. Within 30 days after a down-titration, diuretic dose necessitated an increase in 30.4% of cases, compared with 20.7% following up-titration and 8.0% on a stable dose. Hospitalization and death were significantly more frequent following down-titration (3.4% and 2% within 30 days, respectively) than with a stable dose (1% and 0.6%, p < 0.001). Similar hospitalization rates were observed after up-titration. The risk of hospitalization doubled and of death tripled after down-titration in patients with similar congestion levels.

conclusionsThere is a significant risk that reduction in diuretic dose requires restart or increase of diuretics within a short period. Additionally, there may be a significant risk associated with diuretic dose reduction. Therefore, HF patients need to be closely monitored after down-titration of loop diuretic therapy.

Indexed as

Heart FailureSodium Potassium Chloride Symporter InhibitorsAgedAged, 80 and overDose-Response Relationship, DrugFemaleHospitalizationHumansMaleMiddle AgedTreatment OutcomeSodium Potassium Chloride Symporter InhibitorsDiureticsHeart failureSafetyTherapy

Identifiers

PMID40600695
PMCPMC12482844

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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.