IDEXX > Companion Animal > Laboratory Services > Small Animal Protocols > ACTH Stimulation Test
 

ACTH Stimulation Test

Indications:

Diagnostic test for the differentiation of normal dogs from those with hypo- or hyperadrenocorticism.

Test of choice for the assessment of:

i) adrenocortical reserve in dogs on treatment for hyperadrenocorticism.

ii) the presence of concurrent hyperadrenocorticism in diabetic dogs.

iii) diagnosis of suspected hypercortisolism in dogs that have a history of steroid therapy.

Notes:

ACTH is not licensed for use in the dog. ACTH stimulation testing in many published surveys has a slightly lower sensitivity than the low dose dexamethasone suppression test which, except in the circumstances outlined above, would be our recommended screening test for hyperadrenocorticism.

Results of ACTH stimulation can be affected by prior glucocorticoid administration, stress, anticonvulsant therapy and chronic disease. As a result, final interpretation of the results must be made in the context of the history and clinical findings. ACTH stimulation tests, in common with other endocrine tests, can be associated with occasional false positive and negative results.

Where there has been prolonged (greater than 2 weeks) administration of glucocorticoids at anti-inflammatory or higher doses, ACTH testing should be delayed for at least 14 days after the withdrawal of therapy to allow normalisation of the pituitary-adrenal axis. Chronic anticonvulsant medication can be associated with abnormal cortisol concentrations and test results must be interpreted with caution in such cases.

Injectable drugs, including betamethasone, dexamethasone, depomedrone, delmadinone (Tardak) and proligestone, may all affect ACTH test results for variable periods of time. Please contact the laboratory to discuss the diagnostic approach to cases where these drugs have been administered.

As the results of iatrogenic hypercortisolism and spontaneous hypoadrenocorticism can be similar on ACTH testing, a history of prior drug therapy is helpful in interpreting the test.

Protocol:

To minimise diurnal variation, it is preferable to commence this test as early as possible in the morning.

  • Collect 1-2 ml blood in plain/gel tube.
  • Administer 0.25 mg (250 µg) Synacthen (intravenously).
  • Collect 1-2 ml blood sample at 120 minutes post-injection.
  • Label tubes with name and time of sample.
  • Submit tubes and request form to the laboratory.

October 2001

 
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