BMJ Open (Jul 2023)

Quality assurance in surgical trials of arteriovenous grafts for haemodialysis: protocol for a systematic review

  • Mike Stephens,
  • Karen Stevenson,
  • Andrew Jackson,
  • Rajesh Sivaprakasam,
  • Peter Thomson,
  • Ram Kasthuri,
  • Richard D White,
  • Colin Geddes,
  • Francis Calder,
  • Nikolaos Karydis,
  • Emma Aitken,
  • Ben Edgar,
  • David B Kingsmore,
  • Marco Franchin,
  • Nick Inston,
  • Rob G Jones,
  • Gaspar Mestres,
  • Georgios Papadakis,
  • Callum Stove,
  • Lazslo Szabo,
  • Matteo Tozzi

DOI
https://doi.org/10.1136/bmjopen-2023-071646
Journal volume & issue
Vol. 13, no. 7

Abstract

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Introduction Decisions regarding the optimal vascular access for haemodialysis patients are becoming increasingly complex, and the provision of vascular access is open to variations in systems of care as well as surgical experience and practice. Two main surgical options are recognised: arteriovenous fistula and arteriovenous graft (AVG). All recommendations regarding AVG are based on a limited number of randomised controlled trials (RCTs). It is essential that when considering an RCT of a surgical procedure, an appropriate definition of quality assurance (QA) is made for both the new approach and the comparator, otherwise replication of results or implementation into clinical practice may differ from published results. The aim of this systematic review will be to assess the methodological quality of RCT involving AVG, and the QA measures implemented in delivering interventions in these trials.Methods and analysis The Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines will be followed. A systematic search will be performed of the MEDLINE, Embase and Cochrane databases to identify relevant literature. Studies will be selected by title and abstract review, followed by a full-text review using inclusion and exclusion criteria. Data collected will pertain to generic measures of QA, credentialing of investigators, procedural standardisation and performance monitoring. Trial methodology will be compared against a standardised template developed by a multinational, multispecialty review body with experience in vascular access. A narrative approach will be taken to synthesise and report data.Ethics and dissemination Ethical approval is not required as it is a protocol for a systematic review. Findings will be disseminated through peer-reviewed publications and conference presentations, with the ultimate aim of providing recommendations for future RCT of AVG design.