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      Effect of Intravenous or Perivascular Injection of Synthetic Adrenocorticotropic Hormone on Stimulation Test Results in Dogs

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          Abstract

          Background

          Standard protocols for adrenocorticotropic hormone ( ACTH) stimulation testing ( ACTHst) often involve intravenous ( IV) injection of corticotropin. ACTH might be unintentionally injected into the perivascular ( PV) space.

          Objective

          To compare stimulation test results after IV and PV injections of ACTH.

          Animals

          Twenty privately owned dogs were studied: 10 healthy and 10 with trilostane‐treated naturally occurring hyperadrenocorticism ( HAC).

          Methods

          Prospective study. Each of 20 dogs underwent 2 ACTHst not <4 nor more than 14 days apart. Five healthy and 5 HAC dogs had an IV ACTHst first and PV second; 5 healthy and 5 HAC dogs had a PV ACTHst first and IV second. Blood samples for measurement of serum cortisol concentration were collected before and 1 hour after ACTH administration.

          Results

          No significant difference in results was demonstrated when comparing serum cortisol concentrations after IV and PV ACTH administration in all 20 dogs (median μg/ dL; interval μg/ dL: 8.2; 1.4–17.4 versus 7.8; 0.9–16.9; P = .23). No significant difference in results was demonstrated when comparing serum cortisol concentrations after IV and PV ACTH administration in the 10 healthy dogs (median μg/ dL; interval μg/ dL: 10.9; 7.3–17.4 versus 10.6; 7.1–16.9; P = .54) or in the 10 HAC dogs (median μg/ dL; interval μg/ dL: 6.3; 1.4–8.6 versus 5.2; 0.9–8.7; P = .061).

          Conclusions and Clinical Importance

          Perivascular administration of ACTH does not significantly alter stimulation test results in healthy dogs or in dogs with HAC undergoing therapy with trilostane.

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          Most cited references21

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          Diagnosis of spontaneous canine hyperadrenocorticism: 2012 ACVIM consensus statement (small animal).

          This report offers a consensus opinion on the diagnosis of spontaneous canine hyperadrenocorticism. The possibility that a patient has hyperadrenocorticism is based on the history and physical examination. Endocrine tests should be performed only when clinical signs consistent with HAC are present. None of the biochemical screening or differentiating tests for hyperadrenocorticism are perfect. Imaging can also play a role. Awareness of hyperadrenocorticism has heightened over time. Thus, case presentation is more subtle. Due to the changes in manifestations as well as test technology the Panel believes that references ranges should be reestablished. The role of cortisol precursors and sex hormones in causing a syndrome of occult hyperadrenocorticism remains unclear.
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            Trilostane treatment of 78 dogs with pituitary-dependent hyperadrenocorticism.

            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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              Evaluation of Basal Serum or Plasma Cortisol Concentrations for the Diagnosis of Hypoadrenocorticism in Dogs

              Background Previous studies that included limited numbers of affected dogs have suggested basal cortisol concentrations ≤55 nmol/L (2 μg/dL) are sensitive, but nonspecific, for a diagnosis of hypoadrenocorticism. A detailed assessment of the diagnostic utility of basal cortisol concentrations is warranted. Hypothesis/Objectives To evaluate the utility of basal cortisol concentrations for the diagnosis of hypoadrenocorticism in a large number of dogs, including those with and without serum electrolyte abnormalities. Animals Five hundred and twenty‐two dogs, including 163 dogs with hypoadrenocorticism, 351 dogs with nonadrenal gland illness, and 8 dogs with equivocal results. Methods Retrospective study. Basal and post‐ACTH cortisol concentrations and sodium and potassium concentrations were collected from medical records. A receiver operating characteristic (ROC) curve was constructed for basal cortisol concentrations by standard methodologies. Sensitivity, specificity, and predictive values were determined for various cut‐points. Results The area under the ROC curve was 0.988 and was similarly excellent regardless of serum electrolyte concentrations. At the most discriminatory cut‐point of 22 nmol/L (0.8 μg/dL), sensitivity and specificity were 96.9 and 95.7%, respectively. A basal cortisol concentration of ≤55 nmol/L (2 μg/dL) resulted in a sensitivity of 99.4%. Conversely, a basal cortisol concentration of ≤5.5 nmol/L (0.19 μg/dL) resulted in a specificity of 99.1%. Conclusions and Clinical Importance Similar to findings in previous studies, basal cortisol concentrations >55 nmol/L (2 μg/dL) are useful in excluding a diagnosis of hypoadrenocorticism. Interestingly, excellent specificities and positive predictive values were observed at lower cut‐point cortisol concentrations.
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                Author and article information

                Contributors
                johnson.4407@osu.edu
                Journal
                J Vet Intern Med
                J. Vet. Intern. Med
                10.1111/(ISSN)1939-1676
                JVIM
                Journal of Veterinary Internal Medicine
                John Wiley and Sons Inc. (Hoboken )
                0891-6640
                1939-1676
                13 April 2017
                May-Jun 2017
                : 31
                : 3 ( doiID: 10.1111/jvim.2017.31.issue-3 )
                : 730-733
                Affiliations
                [ 1 ] Department of Small Animal Internal MedicineAnimal Specialty and Emergency Center Los Angeles CA
                [ 2 ] Department of Population Health and Reproduction School of Veterinary Medicine and School of MedicineUniversity of California Davis CA
                [ 3 ] Department of Medicine and Epidemiology School of Veterinary MedicineUniversity of California DavisCA
                Author notes
                [*] [* ]Corresponding author: C.M. Johnson, College of Veterinary Medicine, 601 Vernon L. Tharp St, Columbus, OH 43210; e‐mail: johnson.4407@ 123456osu.edu .
                Author information
                http://orcid.org/0000-0001-9954-6238
                Article
                JVIM14708
                10.1111/jvim.14708
                5435047
                28407319
                17eed9b4-edbb-4475-b9ea-ae661f93e459
                Copyright © 2017 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 23 December 2016
                : 22 February 2017
                : 02 March 2017
                Page count
                Figures: 0, Tables: 0, Pages: 4, Words: 3677
                Funding
                Funded by: UC Davis School of Veterinary Medicine clinical laboratory services
                Categories
                Standard Article
                SMALL ANIMAL
                Standard Articles
                Endocrinology
                Custom metadata
                2.0
                jvim14708
                May/June 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.0.9 mode:remove_FC converted:17.05.2017

                Veterinary medicine
                hyperadrenocorticism,endocrinology,adrenal,pituitary,trilostane
                Veterinary medicine
                hyperadrenocorticism, endocrinology, adrenal, pituitary, trilostane

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