Autosomal dominant polycystic kidney disease
ICD-10 Q61.2 · ICD-11 GB81

Treatment of ADPKD in Adults with eGFR ≥25 ml/min per 1.73 m² at Risk of Rapid Disease Progression

Clinical Scenario

This protocol addresses adults with autosomal dominant polycystic kidney disease (ADPKD) who have an eGFR ≥25 ml/min per 1.73 m² and evidence of rapid progression risk — identified by a Mayo Imaging Classification of class 1C, 1D, or 1E, or a documented historical eGFR decline rate of ≥3 ml/min per 1.73 m² per year.

Treatment Approach

In this population, management involves tolvaptan, initiated under a structured dose titration schedule with progressive escalation toward a defined target dose. The complete dosing sequence, titration intervals, and full clinical guidance are contained in the protocol below.

Full regimen, escalation steps, and decision logic are available via the link below.

Instant Access to Structured Evidence-Based Regimens

References

DOI: 10.1016/j.kint.2024.07.010

We recommend initiating tolvaptan treatment in adults with ADPKD with an estimated glomerular filtration rate (eGFR) ≥25 ml/min per 1.73 m2 who are at risk for rapidly progressive disease (Figure 25).

Tolvaptan should be initiated with a daily dose of 45 mg upon waking and 15 mg 8 hours later (Figure 28).

Uptitrating to a target daily dose of 90 mg upon waking and 30 mg 8 hours later should generally be the goal of therapy in all people with ADPKD unless this becomes intolerable or is contraindicated by drug interactions (Figure 28).