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2013 Annual Report highlights and new directions for the Registry

2013 Annual Report highlights and new directions for the Registry . UK Renal Registry 2014 Annual Audit Meeting. Dr Fergus Caskey Medical Director , UK Renal Registry. Annual Report 2013. Published December 2013 Data up to 31 st December 2012 April: extract 1 st quarter

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2013 Annual Report highlights and new directions for the Registry

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  1. 2013 Annual Report highlightsand new directions for the Registry UK Renal Registry2014 Annual Audit Meeting Dr Fergus Caskey Medical Director, UK Renal Registry

  2. Annual Report 2013 • Published December 2013 • Data up to 31st December 2012 • April: extract 1st quarter • April-June: data extracts obtained & validated • July: database closed • July-August: dataset cleaned; stats performed • Sept-Nov: chapters written, edited & formatted • December: published • Second report in 2013

  3. Annual Report 2013 • Informatics, data management and programming • Fiona Braddon, Shaun Mannings, Fran Benoy-Deeney, Lynsey Billett, Paul Dawson, Jo Wilson, Matthew Brealey, George Swinnerton • Authors and editors† • Anna Casula, Julie Gilg, David Pitcher, Rishi Pruthi, Ani Rao, Catriona Shaw, Retha Steenkamp • Victoria Briggs, Fergus Caskey, Lisa Crowley, Andrew Davenport, Anne Dawnay, Ken Farrington, Terry Feest, Richard Fluck, Damian Fogarty, Iain McPhee, Rommel Ravanan, Paul Roderick, Manish Sinah, Martin Wilkie, Andrew Williams • Business • Ron Cullen, Hilary Doxford, Steph Shearn, Laura Woodward † First authors and last authors

  4. Terry Feest Award Dr Andrew Williams Swansea Involved in Registry from very start (including pilot) Helped set up the Welsh data validation exercise Contribution to Registry Committee and Study Groups Editorial support for annual report Championing local high quality data

  5. RRT incidence1980-2012, by age Gilg J. Chapter 1. UKRR Annual Report 2013

  6. RRT incidence1990-2012, by country Gilg J. Chapter 1. UKRR Annual Report 2013

  7. eGFR at start of RRT Restricted to centres reporting since 2003 Gilg J. Chapter 1. UKRR Annual Report 2013

  8. Trends in late presentation Restricted to centres with 75+ completeness Gilg J. Chapter 1. UKRR Annual Report 2013

  9. Late presentation in 2011/2012 32% 7% Late presentation < 90 days Restricted to centres with 75+ completeness Gilg J. Chapter 1. UKRR Annual Report 2013

  10. Transplant wait listingprevalence by age by country Pruthi R. Chapter 4. UKRR Annual Report 2013

  11. Ethnicity Access to transplant (adjusted HR) waiting list transplant living donor transplant White ref ref ref S Asian 1.10 (0.97-1.24) 0.74 (0.65-0.85) 0.66 (0.45-0.96) Black 0.95 (0.79-1.14) 0.66 (0.49-0.87) 0.40 (0.21-0.73) Udayaraj U. Chapter 6. UKRR Annual Report 2013

  12. SurvivalTrends in 1 year after 90 day survival Pruthi, R. Chapter 8. UKRR Annual Report 2013

  13. SurvivalAdjusting for comorbidity with HES data 6 outliers 4 outliers 1 outliers “The addition of a combination of 16 comorbid conditions present at the start of RRT reduced the number of centres with worse than expected survival to one.” Fotheringham NDT 2014

  14. SurvivalMonthly hazard of death

  15. Survival Monthly hazard of death

  16. Survival "The Registry now asks all nephrologists to complete the timeline as accurately as possible, recording the date of first dialysis or haemofiltration and, separately, the date on which the patient was deemed to be chronic. This will allow us to distinguish between patients who have an acute start and those whose start on RRT was planned.“ UKRR 2009

  17. Dialysis Access AuditEngland, Wales and Northern Ireland % PD catheter failures in 1 year by centre Referred < 90 days Briggs, V. Chapter 14. UKRR Annual Report 2013

  18. Reported infectionsEngland only Trends in MRSA Funnel plot of MRSA rates Crowley L. Chapter 15. UKRR Annual Report 2013

  19. Current and new directions

  20. Core work • Data timeliness • 2013 database closed end June 2014 for report published December 2014 • Three sites significantly behind schedule • Data quality • Plans for fixed term appointment to establish source data verification • Sensitivity and specificity for core data items • Benchmarking • Research • Renal Data Collaboration • Proof of concept completed, contract signed with InterSystems, training begun

  21. Core work • Dataset • Version 3.30 end July 2014 • PD dataset • Then vascular access dataset • Patient Council • Fiona Loud agreed to chair, advertised for potential members, interviews May 2014, first meeting July 2014 • Beyond ESRD • Obtained Section 251 exemption for CKD2+ and dialysis dependent AKI, June 2013 • Applying for Section 251 exemption for any AKI

  22. Core work • Specialist Commissioning Dashboard • Asked by Specialist Commissioners to take over quarterly Dashboard data collection • Four indicators • PD peritonitis rate • Adequacy of Haemodialysis Dose • Rate of Staph Aureus bacteraemia in patients treated with chronic HD • Access to Transplant listing

  23. UKRR accountability NHS England Commissioners National Clinical Director Patients

  24. Major projects • Acute Kidney Injury • Partnership with NHS England over 2 years • Six workstreams – risk, education, detection, intervention, implementation, measurement • Registry leading on measurement • Launch meeting 8th April 2014 • Inclusion of Wales, Scotland and Northern Ireland

  25. Major projects • Patient participation • Funding awarded by NHS England (Patient Experience) Feb-March 2014 • Board to be establish to oversee work around: • Patient reported outcome measures (HRQoL) • Patient reported experience measures • Patient activation measures • Quality of shared decision making • Inclusion of Wales, Scotland and Northern Ireland

  26. The PROMs Pilot - DRAFT Translation Qualitative evaluation Health economic evaluation • 10 sites • All dialysis patients – HD (in centre/ satellite/ home), PD • PROM/ PREM collected quarterly for 12 months • Paper vs electronic • Local versus central • PROM: • EQ-5D • POS-s renal (symptoms) • ? Recovery time question (for HD) • PREM: • Scottish Renal Patient Experience Questionnaire

  27. PROMs – a European consensus “Consensus meeting on collecting quality of life and patient experience data in renal registries in Europe” • ERA-EDTA Registry QUEST funded • Bristol 23rd June 2014 • Delegates invited from all interested renal registries in Europe

  28. UKRRpast present and future work Haemodialysis Peritoneal dialysis Demographics Case-mix Laboratory data PROMs & PREMs Activation & QSDM Kidney transplantation AKI dialysis dependent AKI in 1y & 2y care CKD 2-4 in 2y care CKD 2-4 in 1y & 2 care

  29. Research • Research methods Study Group • First meeting March 2014 • Solve analytical problems from dialysis and transplant study groups • Plan high impact analyses • Appointment of Tony Wing Fellow • BKPA funded fellow appointed March 2014 to start August 2014 • Data linkage opportunities • Revised work proposal forms soon on UKRR website • Now three levels (including no analysis input from UKRR)

  30. Research • Current PhD Students • Dr Claire Castledine • Explaining regional variation in renal service provision in the UK • PhD awarded • Retha Steenkamp • Multiple imputation and prognostic survival modelling • Submitted • Dr Catriona Shaw • CKD outcomes with MINAP / NICOR linkage (London) • Dr Rishi Pruthi • Qualitative research in the ATTOM Study (Southampton) • Dr Ani Rao • Mixed methods alongside EQUAL (pre dialysis CKD in the elderly) (Bristol) • A different model in the future?

  31. Any questions?

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