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Cardiorespiratory Optimisation By Arteriovenous fistula Ligation after renal Transplantation (COBALT): study protocol for a multicentre randomised interventional feasibility trial

Authors :
Veena Surendrakumar
Emma Aitken
Patrick Mark
Reza Motallebzadeh
James Hunter
Aimen Amer
Dominic Summers
Kirsten Rennie
Leila Rooshenas
Madalina Garbi
Karl Sylvester
Cara Hudson
Jennifer Banks
Anna Sidders
Andrew Norton
Matthew Slater
Matthew Bartlett
Simon Knight
Gavin Pettigrew
Surendrakumar, Veena [0000-0003-2272-1143]
Mark, Patrick [0000-0003-3387-2123]
Knight, Simon [0000-0003-4837-9446]
Apollo - University of Cambridge Repository
Publication Year :
2023
Publisher :
BMJ Journals, 2023.

Abstract

Peer reviewed: True<br />Acknowledgements: We thank Lewis Griffiths (MRC Epidemiology Unit) for their support for the physical activity measurement collection. We also give special thanks to Andrew Norton, our patient representative, who was instrumental in helping us develop this study proposal and securing support and funding from our local kidney patient association.<br />IntroductionCardiovascular events are a major cause of mortality following successful kidney transplantation.Arteriovenous fistulas (AVFs) are considered the best option for haemodialysis, but may contribute to this excess mortality because they promote adverse cardiac remodelling and ventricular hypertrophy. This raises the question whether recipients with a well-functioning kidney transplant should undergo elective AVF ligation.Methods and analysisThe COBALT feasibility study is a multicentre interventional randomised controlled trial (RCT) that will randomise renal transplant patients with stable graft function and a working AVF on a 1:1 basis to standard care (continued conservative management) or to AVF ligation. All patients will perform cardiopulmonary exercise testing (CPET) on recruitment and 6 months later. Daily functioning and quality of life will be additionally assessed by questionnaire completion and objective measure of physical activity. The primary outcome—the proportion of approached patients who complete the study (incorporating rates of consent, receipt of allocated intervention and completion of both CPETs without withdrawal)—will determine progression to a full-scale RCT. Design of the proposed RCT will be informed by an embedded qualitative assessment of participant and healthcare professional involvement.Ethics and disseminationThis study has been approved by the East Midlands—Derby Research Ethics Committee (22/EM/0002) and the Health Research Authority. The results of this work will be disseminated academically through presentation at national and international renal meetings and via open access, peer-reviewed outputs. Existing networks of renal patient groups will also be used to disseminate the study findings to other key stakeholders.Trial registration numberISRCTN49033491.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....5130d57f837e7506e66d8e105d6e4e31