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Treatment persistence to tolvaptan in patients with autosomal dominant polycystic kidney disease: A secondary use of data analysis of patients in the IMADJIN dataset

BMC Nephrology Dec 10, 2021

Thomas M, Gois PHF, Butcher BE, et al. - Analysis of the real-world IMADJIN dataset revealed a 76% persistence to tolvaptan. Discontinuation attributable to hepatic events was low.

  • Before October 2020 access to tolvaptan in Australia was restricted by a controlled monitoring and distribution program called IMADJIN.

  • In this retrospective, secondary data analysis of the IMADJIN dataset, experts focused on the time to all-cause discontinuation of tolvaptan in Australia.

  • Of 479 autosomal dominant polycystic kidney disease patients included, the Kaplan-Meier estimation of 12-month persistence was 76.7%, and 23.8% discontinued treatment.

  • Younger patients were more likely to discontinue tolvaptan than older ones therefore prescribers are advised to take extra care when initiating treatment in the former group.

  • Aquaretic tolerability (4.2%), hepatic adverse events (abnormal liver function tests) (2.1%), disease progression (1.5%), and acute kidney injury (0.2%) were noted to be the reasons for discontinuation.

  • A shorter time to discontinuation was observed in patients exhibiting a lack of aquaretic tolerance.

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