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The CONVINCE randomized trial found positive effects on quality of life for patients with chronic kidney disease treated with hemodiafiltration.
Rose, Matthias; Fischer, Felix H; Liegl, Gregor; Strippoli, Giovanni F M; Hockham, Carina; Vernooij, Robin W M; Barth, Claudia; Canaud, Bernard; Covic, Adrian; Cromm, Krister; Cucui, Andrea M; Davenport, Andrew; Fischer, Kathrin I; Hegbrant, Jörgen; Jaha, Hanna; Schappert, Anna; Török, Marietta; Woodward, Mark; Bots, Michiel L; Blankestijn, Peter J.
Affiliation
  • 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
  • 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
  • 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
  • Strippoli GFM; Department of Precision and Regenerative Medicine and Ionian Area (DIMEPRE-J), University of Bari, Bari, Italy; School of Public Health, University of Sydney, Sydney, Australia.
  • Hockham C; The George Institute for Global Health, School of Public Health, Imperial College London, London, UK.
  • Vernooij RWM; Department of Nephrology and 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.
  • Barth C; B. Braun Avitum AG, Medical Scientific Affairs, Melsungen, Germany.
  • Canaud B; Montpellier University, School of Medicine, Montpellier, France.
  • Covic A; Department of Nephrology, University of Medicine "Grigore T. Popa", Iasi, Romania; Fresenius Nephrocare, Iasi, Romania.
  • 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
  • Cucui AM; Fresenius Nephrocare Dialysis Center, Bucharest, Romania.
  • Davenport A; Department of Renal Medicine, Royal Free Hospital, Division of Medicine, University College London, London, UK.
  • 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
  • Hegbrant J; Division of Nephrology, Department of Clinical Sciences, Lund University, Lund, Sweden.
  • 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
  • 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
  • Török M; Corporate Medical Office Diaverum, Malmö, Sweden.
  • Woodward M; School of Public Health, University of Sydney, Sydney, Australia; The George Institute for Global Health, University of New South Wales, Sydney, Australia.
  • Bots ML; Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Blankestijn PJ; Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
Kidney Int ; 106(5): 961-971, 2024 Nov.
Article in En | MEDLINE | ID: mdl-39089577
ABSTRACT
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 (11); 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. REGISTRATION NTR7138 on the International Clinical Trials Registry Platform.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Cognition / Hemodiafiltration / Renal Insufficiency, Chronic Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Kidney Int Year: 2024 Document type: Article Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Cognition / Hemodiafiltration / Renal Insufficiency, Chronic Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Kidney Int Year: 2024 Document type: Article Country of publication: United States