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Trilostane treatment of 78 dogs with pituitary-dependent hyperadrenocorticism
  1. R. Neiger, DrMedVet, PhD, DACVIM, DECVIM-CA1,
  2. K. J. Hurley, DVM, DACVIM, DECVIM-CA1,
  3. I. Ramsey, BVSc, PhD, DSAM, DECVIM-CA, MRCVS2,
  4. J. O'Connor, MVB3 and
  5. C. T. Mooney, MVB, MPhil, PhD, DECVIM-CA, MRCVS3
  1. 1 Department of Veterinary Clinical Sciences, Royal Veterinary College, Hawkshead Lane, Hatfield AL9 7TA
  2. 2 Department of Veterinary Clinical Studies, University of Glasgow, Bearsden Road, Bearsden, Glasgow G61 1QH
  3. 3 Department of Small Animal Clinical Studies, Faculty of Veterinary Medicine, University College Dublin, Ballsbridge, Dublin 4, Ireland
  1. Waltham Centre for Pet Nutrition, Waltham-on-the-Wolds, Melton Mowbray, Leicestershire LE14 4RT


The efficacy of trilostane in the treatment of canine pituitary-dependent hyperadrenocorticism (PDH) was evaluated in 78 dogs with the condition which were treated for up to three years. The drug appeared to be well tolerated by almost all the dogs, and only two developed clinical signs and biochemical evidence of hypoadrenocorticism. Polyuria and polydipsia completely resolved in 70 per cent of the dogs that had these problems, and skin changes resolved in 62 per cent of the dogs that had skin abnormalities. There was a significant reduction (P<0.001 in each case) in both the mean basal and post-adrenocorticotrophic hormone (ACTH) cortisol concentrations after a mean of 12.3 days of treatment. The post-ACTH cortisol concentration decreased to less than 250 nmol/litre in 81 per cent of the dogs within one month of the start of treatment and in another 15 per cent at some later time. The median survival time of the 26 dogs which died was 549 days, and 51 of the dogs were alive at the completion of the study. One was lost to follow up after 241 days treatment.

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