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September 10, 2026Implementation Science CommunicationsOpen Access

Understanding variation between kidney centres in implementation of tolvaptan in the management of autosomal dominant polycystic kidney disease: a multiple case study

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Authors

MGMatthew GittusUniversity of SheffieldJFJames FotheringhamUniversity of SheffieldAOAlbert OngUniversity of Sheffield

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Overview

Multiple case study shows that centralised specialist care standardises tolvaptan delivery in polycystic kidney disease, highlighting that pathway design dictates access to targeted therapy.

Key Points

  • To identify the organisational, individual, and contextual factors driving variation in tolvaptan implementation across UK kidney centres managing autosomal dominant polycystic kidney disease.
  • Conducted a multiple case study across three National Health Service kidney centres in the UK selected for divergent prescribing practices between December 2024 and September 2025.
  • Collected and analysed data from 12 healthcare professional interviews, 23 patient consultation observations, and 8 clinical documents using framework analysis mapped to the Consolidated Framework for Implementation Research (CFIR).
  • Prior trial involvement and professional networks enabled two centres to rapidly launch tolvaptan pathways without additional funding, unlike the trial-naive centre.
  • A centralised, specialist-led model allowed systematic eligibility assessments and prompt initiation, whereas distributed and hybrid models introduced application discrepancies, capacity bottlenecks, or off-guideline prescribing.
  • Active consultant nephrologist champions improved access to therapy, while less experienced teams and high patient volumes limited timely treatment.

Cite This Study

Gittus et al. (2026) studied this question.

synapsesocial.com/papers/6aa27b6f58559d80afc74afehttps://doi.org/10.1186/s43058-026-01087-7
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