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Access to Transplantation and Transplant Outcome Measures (ATTOM): study protocol of a UK wide, in-depth, prospective cohort analysis
  1. Gabriel C Oniscu1,
  2. Rommel Ravanan2,
  3. Diana Wu1,
  4. Andrea Gibbons3,
  5. Bernadette Li4,
  6. Charles Tomson5,
  7. John L Forsythe1,
  8. Clare Bradley3,
  9. John Cairns4,
  10. Christopher Dudley2,
  11. Christopher J E Watson6,
  12. Eleanor M Bolton6,
  13. Heather Draper7,
  14. Matthew Robb8,
  15. Lisa Bradbury8,
  16. Rishi Pruthi9,
  17. Wendy Metcalfe1,
  18. Damian Fogarty9,
  19. Paul Roderick10,
  20. J Andrew Bradley6
  21. on behalf of the ATTOM investigators
  1. 1Transplant Unit, Royal Infirmary of Edinburgh, Edinburgh, UK
  2. 2Richard Bright Renal Unit, Southmead Hospital, Bristol, UK
  3. 3Health Psychology Research Unit, Royal Holloway, University of London, London, UK
  4. 4Department of Health Services Research and Policy, London School of Hygiene and Tropical Medicine, London, UK
  5. 5Department of Renal Medicine, Freeman Hospital, Newcastle upon Tyne, UK
  6. 6Department of Surgery, University of Cambridge and the NIHR Cambridge Biomedical Research Centre, Cambridge, UK
  7. 7School of Health and Population Sciences, University of Birmingham, Birmingham, UK
  8. 8NHS Blood and Transplant, Bristol, UK
  9. 9UK Renal Registry, Bristol, UK
  10. 10Primary Care and Population Sciences, Faculty of Medicine, University of Southampton, Southampton, UK
  1. Correspondence to Gabriel C Oniscu; gabriel.oniscu{at}ed.ac.uk

Abstract

Introduction There is significant intercentre variability in access to renal transplantation in the UK due to poorly understood factors. The overarching aims of this study are to improve equity of access to kidney and kidney–pancreas transplantation across the UK and to optimise organ allocation to maximise the benefit and cost-effectiveness of transplantation.

Methods and analysis 6844 patients aged 18–75 years starting dialysis and/or receiving a transplant together with matched patients active on the transplant list from all 72 UK renal units were recruited between November 2011 and March 2013 and will be followed for at least 3 years. The outcomes of interest include patient survival, access to the transplant list, receipt of a transplant, patient-reported outcome measures (PROMs) including quality of life, treatment satisfaction, well-being and health status on different forms of renal replacement therapy. Sociodemographic and clinical data were prospectively collected from case notes and from interviews with patients and local clinical teams. Qualitative process exploration with clinical staff will help identify unit-specific factors that influence access to renal transplantation. A health economic analysis will explore costs and outcomes associated with alternative approaches to organ allocation. The study will deliver: (1) an understanding of patient and unit-specific factors influencing access to renal transplantation in the UK, informing potential changes to practices and policies to optimise outcomes and reduce intercentre variability; (2) a patient-survival probability model to standardise access to the renal transplant list and (3) an understanding of PROMs and health economic impact of kidney and kidney–pancreas transplantation to inform the development of a more sophisticated and fairer organ allocation algorithm.

Ethics and dissemination The protocol has been independently peer reviewed by National Institute for Health Research (NIHR) and approved by the East of England Research Ethics Committee. The results will be published in peer-reviewed journals and presented at conferences.

  • TRANSPLANT SURGERY
  • QUALITATIVE RESEARCH
  • HEALTH ECONOMICS
  • EPIDEMIOLOGY

This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/

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