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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