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Aust Vet J. 2003 Oct;81(10):600-7.

Trilostane treatment in dogs with pituitary-dependent hyperadrenocorticism.

Author information

1
Faculty of Veterinary Science, The University of Sydney, New South Wales, 2006.

Abstract

OBJECTIVE:

To evaluate the efficacy of trilostane in treating dogs with pituitary-dependent hyperadrenocorticism.

DESIGN:

Prospective clinical trial using client-owned dogs with pituitary-dependent hyperadrenocorticism treated at University Veterinary Centre, Sydney from September 1999 to July 2001.

PROCEDURE:

Thirty dogs with pituitary-dependent hyperadrenocorticism treated with trilostane, a competitive inhibitor of 3beta-HSD, were monitored at days 10, 30 and 90 then 3-monthly by clinical examination, tetracosactrin stimulation testing, urinary corticoid:creatinine ratio measurement and by client questionnaire.

RESULTS:

Twenty-nine of 30 dogs were successfully treated with trilostane (median dose 16.7 mg/kg; range 5.3 to 50 mg/kg, administered once daily); one responded favourably but died of unrelated disease before full control was achieved.

CONCLUSION:

Trilostane administration controlled pituitary-dependent hyperadrenocorticism in these dogs. It was safe, effective and free of side-effects at the doses used. Most dogs were initially quite sensitive to the drug for 10 to 30 days, then required higher doses until a prolonged phase of stable dose requirements occurred. Urinary corticoid:creatinine ratio was useful in assessing duration of drug effect. Some dogs treated for more than 2 years required reduction or temporary cessation of drug because of iatrogenic hypoadrenocorticism.

PMID:
15080470
[Indexed for MEDLINE]

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