The CONVINCE randomized trial found positive effects on quality of life for patients with chronic kidney disease treated with hemodiafiltration.

health-related quality of life HRQoL hemodiafiltration hemodialysis patient-reported outcomes PRO quality of life QoL randomized controlled trial RCT

Journal

Kidney international
ISSN: 1523-1755
Titre abrégé: Kidney Int
Pays: United States
ID NLM: 0323470

Informations de publication

Date de publication:
30 Jul 2024
Historique:
received: 25 01 2024
revised: 18 06 2024
accepted: 02 07 2024
medline: 2 8 2024
pubmed: 2 8 2024
entrez: 1 8 2024
Statut: aheadofprint

Résumé

In the CONVINCE trial, the primary analysis demonstrated a survival benefit for patients receiving high-dose hemodiafiltration (HDF) as compared with high-flux hemodialysis (HD). A secondary objective was to evaluate effects on health-related quality of life (HRQoL); assessed in eight domains (physical function, cognitive function, fatigue, sleep disturbance, anxiety, depression, pain interference, social participation) applying instruments from the Patient-Reported Outcome Measurement Information System (PROMIS) before randomization and every three months thereafter. In total 1360 adults with dialysis-dependent chronic kidney disease, eligible to receive high-flux HDF (23 liters or more), were randomized (1:1); 84% response rate to all questionnaires. Both groups reported a continuous deterioration in all HRQoL domains. Overall, raw score changes from baseline were more favorable in the HDF group, resulting in a significant omnibus test after a median observation period of 30 months. Most relevant single raw score differences were reported for cognitive function. Patients receiving HDF reported a decline of -0.95 units (95% confidence interval - 2.23 to +0.34) whereas HD treated patients declined by -3.90 units (-5.28 to - 2.52). A joint model, adjusted for mortality differences, utilizing all quarterly assessments, identified a significantly slower HRQoL decline in physical function, cognitive function, pain interference, and social participation for the HDF group. Their physical health summary score declined -0.46 units/year slower compared to the HD group. Thus, the CONVINCE trial showed a beneficial effect of high-dose hemodiafiltration for survival as well as a moderate positive effect on patients' quality of life, most pronounced with respect to their cognitive function.

Identifiants

pubmed: 39089577
pii: S0085-2538(24)00534-9
doi: 10.1016/j.kint.2024.07.014
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Matthias Rose (M)

Department of Psychosomatic Medicine, Center of Internal Medicine and Dermatology, Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany; Center for Patient Centered Outcomes Research, Charité Universitätsmedizin Berlin (CPCOR), Germany; German Center for Mental Health (DZPG), Germany.

Felix H Fischer (FH)

Department of Psychosomatic Medicine, Center of Internal Medicine and Dermatology, Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany; Center for Patient Centered Outcomes Research, Charité Universitätsmedizin Berlin (CPCOR), Germany; German Center for Mental Health (DZPG), Germany. Electronic address: felix.fischer@charite.de.

Gregor Liegl (G)

Department of Psychosomatic Medicine, Center of Internal Medicine and Dermatology, Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany; Center for Patient Centered Outcomes Research, Charité Universitätsmedizin Berlin (CPCOR), Germany.

Giovanni Fm Strippoli (GF)

Department of Precision and Regenerative Medicine and Ionian Area (DIMEPRE-J), University of Bari, Italy; School of Public Health, University of Sydney, Australia.

Carina Hockham (C)

The George Institute for Global Health, School of Public Health, Imperial College London, London, UK.

Robin Wm Vernooij (RW)

Department of Nephrology & Hypertension, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Claudia Barth (C)

B. Braun Avitum AG, Medical Scientific Affairs, Melsungen, Germany.

Bernard Canaud (B)

Montpellier University, School of Medicine, Montpellier, France.

Adrian Covic (A)

Department of Nephrology, University of Medicine "Grigore T. Popa" Iasi and Fresenius Nephrocare, Romania.

Krister Cromm (K)

Department of Psychosomatic Medicine, Center of Internal Medicine and Dermatology, Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany; Center for Patient Centered Outcomes Research, Charité Universitätsmedizin Berlin (CPCOR), Germany; Fresenius Medical Care Deutschland GmbH, Global Medical Office, Bad Homburg, Germany.

Andrea M Cucui (AM)

Fresenius Nephrocare Dialysis Center, Bucharest, Romania.

Andrew Davenport (A)

UCL Department of Renal Medicine, Royal Free Hospital, Division of Medicine, University College London, London, UK.

Kathrin I Fischer (KI)

Department of Psychosomatic Medicine, Center of Internal Medicine and Dermatology, Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany; Center for Patient Centered Outcomes Research, Charité Universitätsmedizin Berlin (CPCOR), Germany.

Jörgen Hegbrant (J)

Division of Nephrology, Department of Clinical Sciences, Lund University, Lund, Sweden.

Hanna Jaha (H)

Department of Psychosomatic Medicine, Center of Internal Medicine and Dermatology, Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany; Center for Patient Centered Outcomes Research, Charité Universitätsmedizin Berlin (CPCOR), Germany.

Anna Schappert (A)

Department of Psychosomatic Medicine, Center of Internal Medicine and Dermatology, Charité Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany; Center for Patient Centered Outcomes Research, Charité Universitätsmedizin Berlin (CPCOR), Germany; German Center for Mental Health (DZPG), Germany.

Marietta Török (M)

Corporate Medical Office Diaverum, Malmö, Sweden.

Mark Woodward (M)

School of Public Health, University of Sydney, Australia; The George Institute for Global Health, University of New South Wales, Sydney, Australia.

Michiel L Bots (ML)

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Peter J Blankestijn (PJ)

Department of Nephrology & Hypertension, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Classifications MeSH