Key result
A 7.5 mg tolvaptan starting dose fails to eliminate rapid sodium correction risk in SIADH.
Why the study?
Post-approval reports indicate increasing use of 7.5 mg tolvaptan as a starting dose for SIADH-related hyponatremia, but its pharmacokinetics and pharmacodynamics compared to the approved 15 mg dose are unclear.
Does low-dose tolvaptan affect pharmacodynamics and serum sodium correction differently in SIADH patients compared to healthy adults?
RCT (n=44)
Double-blind
Randomized
Yes
Does low-dose tolvaptan affect pharmacodynamics and serum sodium correction differently in SIADH patients compared to healthy adults?
Starting tolvaptan at a lower dose of 7.5 mg does not eliminate the risk of overly rapid serum sodium correction in patients with SIADH, and monitoring fluid balance may help identify patients at risk.
Caution against 7.5 mg tolvaptan start in SIADH to avoid overcorrection; extends RCT evidence of absent thirst response versus healthy adults.
PURPOSE: Tolvaptan (TLV) is indicated to treat hyponatremia due to syndrome of inappropriate diuretic hormone (SIADH) in Europe. Treatment is to be initiated at 15 mg QD but post-approval reporting indicates increasing use of 7.5 mg as the starting dose. Physicians believe 7.5 mg is effective and has a lower incidence of overly rapid correction of serum sodium. METHODS: Single TLV doses of 3.75, 7.5, and 15 mg were administered to 14 healthy adults in a crossover design and to 29 subjects ≥18 years with SIADH and serum sodium between 120 and 133 mmol/L in a parallel-group design. Pharmacodynamics and TLV plasma concentrations were assessed for 24 h post-dose. RESULTS: = 0.37) with maximum increases in serum sodium; subjects with large corrections had large (~1 L) negative FB. Compared to healthy adults, subjects with SIADH did not drink in response to their negative FB and had larger increases in serum sodium at 24 h. Median time of maximum increase in healthy adults was 6 h, with no rapid corrections, and FB was near 0 mL by 24 h. CONCLUSION: Starting titration with 7.5 mg TLV will not eliminate the risk of rapid corrections in serum sodium. Monitoring FB may indicate that a subject is at risk for over correction.
No takes yet. Share an insight, caveat, or question.
Shoaf et al. (2017) conducted an RCT in Hyponatremia due to SIADH (n=44). Tolvaptan vs. Healthy adults and dose comparison was evaluated on Maximal increase and time of maximal increase in serum sodium concentrations. Single doses of 3.75, 7.5, and 15 mg tolvaptan in SIADH patients resulted in overly rapid correction of serum sodium in 1, 1, and 2 subjects respectively, indicating that a 7.5 mg starting dose does not eliminate the risk of rapid correction.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: