Evidence map›Paper›PMID 42105307›Full record

Trial reportESC heart failure2026

Renal replacement therapy in type 2 severe cardiorenal syndrome: a randomized controlled trial.

Maxime Schleef, Florence Sens, Laurent Magaud, Julie Haesebaert, Carole Langlois-Jacques, Laurent Sebbag, Laurent Juillard, Eric Bonnefoy, Guillaume Baudry, UF-CARE Study Group

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in ESC heart failure, 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

10 authors.

Maxime SchleefService de Néphrologie Dialyse Explorations Fonctionnelles Rénales, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon 69003, France.ORCID 0000-0002-3711-7259
Florence SensService de Néphrologie Dialyse Explorations Fonctionnelles Rénales, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon 69003, France.
Laurent MagaudService Recherche et Epidémiologie Cliniques, Pôle de Santé Publique, Hospices Civils de Lyon, Lyon, France.
Julie HaesebaertService Recherche et Epidémiologie Cliniques, Pôle de Santé Publique, Hospices Civils de Lyon, Lyon, France.
Carole Langlois-JacquesService de Biostatistiques, Hospices Civils de Lyon, Lyon, France.
Laurent SebbagService d'insuffisance cardiaque, Hôpital Louis Pradel, Hospices Civils de Lyon, Bron, France.
Laurent JuillardService de Néphrologie Dialyse Explorations Fonctionnelles Rénales, Hôpital Edouard Herriot, Hospices Civils de Lyon, Lyon 69003, France.
Eric BonnefoyUniversité Lyon 1 Claude Bernard, INSERM U1060, INRAE, Laboratoire CarMeN, Bron 69500, France.
Guillaume BaudryUniversité de Lorraine, INSERM, Centre d'Investigation Clinique Plurithématique 1433, Inserm U1116, CHRU de Nancy, Nancy, France.ORCID 0000-0002-9200-2729
UF-CARE Study Group

Funding

French Ministry of Health PHRC-14-004Hospices Civils de Lyon
6 · The paper itself

Abstract

introductionType 2 cardiorenal syndrome (CRS), characterized by chronic heart failure (HF) leading to chronic kidney disease (CKD), is associated with high morbidity and mortality. In patients with refractory congestive HF, extrarenal fluid removal techniques can be proposed. We aimed to evaluate whether adding ultrafiltration through peritoneal dialysis (PD), haemodialysis (HD), or isolated ultrafiltration (IUF) improves clinical outcomes compared with optimized medical therapy alone.

methodsUltrafiltration Versus Medical Therapies in the Management of the Cardio Renal Syndrome (UF-CARE) was a multicentre, randomized, controlled, open-label trial conducted in 15 French centres. Adults with severe HF, persistent or recurrent congestion despite high-dose diuretics and guideline-directed medical therapy, and mild to severe CKD were randomized to optimized medical therapy alone (Control group) or optimized medical therapy plus ultrafiltration (Ultrafiltration group), through PD, HD, or IUF, according to clinical judgement, patient characteristics and preferences, and availability in each centre. The primary outcome was a composite of all-cause mortality or unplanned hospitalization for acute HF within 12 months.

resultsAmong 108 screened patients, 46 were randomized (24 Control group, 22 Ultrafiltration group). After a median follow-up of 262 days, the primary outcome occurred in 63% of patients in the Ultrafiltration group and 87% in the Control group (P = .144). Quality-of-life scores seemed to improve over time in both groups, with a slightly more sustained improvement in the ultrafiltration group. One death related to the technique was reported.

conclusionIn patients with type 2 CRS and refractory congestive HF, adding ultrafiltration through PD, HD, or IUF did not significantly reduce mortality or HF-related hospitalizations at 12 months compared with optimized medical therapy and close multidisciplinary follow-up, although the trial was underpowered.

Indexed as

Cardio-Renal SyndromeRenal Replacement TherapyAgedFemaleFollow-Up StudiesFranceHumansMaleMiddle AgedSeverity of Illness IndexTreatment OutcomeCardiorenal syndromeDiureticsHeart failureRenal dialysisRenal insufficiencyUltrafiltration

Identifiers

PMID42105307
PMCPMC13559848

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.