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Benefits and harms of high-dose haemodiafiltration versus high-flux haemodialysis: the comparison of high-dose haemodiafiltration with high-flux haemodialysis (CONVINCE) trial protocol

Authors :
Blankestijn, P.J.
Fischer, K.I.
Barth, C.
Cromm, K.
Canaud, B.
Davenport, A.
Grobbee, D.E.
Hegbrant, J.
Roes, K.C.B.
Rose, M.
Strippoli, G.F.
Vernooij, R.W.M.
Woodward, M.
Wit, G.A. de
Bots, M.L.
Blankestijn, P.J.
Fischer, K.I.
Barth, C.
Cromm, K.
Canaud, B.
Davenport, A.
Grobbee, D.E.
Hegbrant, J.
Roes, K.C.B.
Rose, M.
Strippoli, G.F.
Vernooij, R.W.M.
Woodward, M.
Wit, G.A. de
Bots, M.L.
Source :
BMJ Open; 2044-6055; 2; vol. 10; e033228; ~BMJ Open~~~~~2044-6055~2~10~~e033228
Publication Year :
2020

Abstract

Contains fulltext : 229369.pdf (publisher's version ) (Open Access)<br />INTRODUCTION: End-stage kidney disease (ESKD) is a major public health problem affecting more than 2 million people worldwide. It is one of the most severe chronic non-communicable diseases. Haemodialysis (HD) is the most common therapeutic option but is also associated with a risk of cardiovascular events, hospitalisation and suboptimal quality of life. Over the past decades, haemodiafiltration (HDF) has become available. Although high-dose HDF has shown some promising survival advantage compared to conventional HD, the evidence remains controversial. A Cochrane systematic review found, in low-quality trials, with various convective forms of dialysis, a reduction in cardiovascular, but not all-cause mortality and the effects on non-fatal cardiovascular events and hospitalisation were uncertain. In contrast, an individual patient data analysis suggested that high-dose HDF reduced both all-cause and cardiovascular mortality compared to HD. In view of these discrepant results, a definitive trial is required to determine whether high-dose HDF is preferable to high-flux HD. The comparison of high-dose HDF with high-flux HD (CONVINCE) study will assess the benefits and harms of high-dose HDF versus a conventional high-flux HD in adults with ESKD. METHODS AND ANALYSIS: This international, prospective, open label, randomised controlled trial aims to recruit 1800 ESKD adults treated with HD in nine European countries. Patients will be randomised 1:1 to high-dose HDF versus continuation of conventional high-flux HD. The primary outcome will be all-cause mortality at 3 years' follow-up. Secondary outcomes will include cause-specific mortality, cardiovascular events, all-cause and infection-related hospitalisations, patient-reported outcomes (eg, health-related quality of life) and cost-effectiveness. ETHICS AND DISSEMINATION: The CONVINCE study will address the question of benefits and harms of high-dose HDF compared to high-flux HD for kidney replacement therapy in patients

Details

Database :
OAIster
Journal :
BMJ Open; 2044-6055; 2; vol. 10; e033228; ~BMJ Open~~~~~2044-6055~2~10~~e033228
Publication Type :
Electronic Resource
Accession number :
edsoai.on1284020079
Document Type :
Electronic Resource