[Who are these patients on dialysis and not on the kidney transplant waiting list?]

Elsa Vabret1, Cécile Vigneau2, Sahar Bayat3

  • 1Université Rennes 1, 2, avenue du Pr Léon-Bernard, 35000 Rennes, France; Service de néphrologie, CHU de Rennes, 2, rue Henri-le-Guilloux, 35033 Rennes, France.

Nephrologie & Therapeutique
|May 16, 2020
PubMed

Insights

Medical contraindications prevent most dialysis patients from joining the kidney transplant waiting list in France. A significant number also refuse transplantation, highlighting the need for further patient-centered analysis.

Area of Science:

  • Nephrology
  • Transplantation Medicine
  • Public Health Policy

Background:

  • Access to kidney transplantation is a significant challenge for end-stage chronic renal disease patients in France.
  • Registration on the national waiting list is a prerequisite for receiving a transplant.
  • The Haute Autorité de santé (HAS) revised contraindications for transplant listing in 2015.

Purpose of the Study:

  • To inventory reasons for non-registration on the renal transplant waiting list.
  • To analyze patients on dialysis for at least one year and under 80 years old in France.
  • To identify barriers to kidney transplant access.

Main Methods:

  • Analysis of patients from the Epidemiology and Nephrology Information Register (REIN).
  • Inclusion of patients with annual monitoring between August 1 and November 30, 2016.
  • Data collection via a dedicated questionnaire completed by dialysis centers.

Main Results:

  • 3172 patients were analyzed.
  • Medical contraindications were the primary reason for non-registration (73%), often vascular.
  • Patient refusal accounted for 14%, with a higher proportion of women; 13% had no recorded reason, but 65% of these had initiated assessment.

Conclusions:

  • Medical contraindication is the leading cause for non-registration on the French renal transplant list.
  • The rate of patient refusal for transplantation warrants further investigation, particularly from the patient's perspective.
  • A very small percentage of patients (4.5%) lacked an informed reason or ongoing assessment for non-registration.

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