Literature DB >> 2158760

Continuous dexamethasone infusion for seven hours in patients with the Cushing syndrome. A superior differential diagnostic test.

P Biemond1, F H de Jong, S W Lamberts.   

Abstract

STUDY
OBJECTIVE: To determine the usefulness of the continuous intravenous dexamethasone suppression test in the differential diagnosis of patients with the Cushing syndrome.
DESIGN: Comparison of the results of this test with those of other tests in the study population and with data from the literature.
SETTING: Referral-based endocrine division in a university hospital. PATIENTS: One hundred and twenty-one patients with the Cushing syndrome were evaluated: corticotropin (ACTH)-secreting pituitary tumors, 90 cases; adrenal adenoma, 13; adrenal carcinoma, 9; ectopic ACTH-secreting tumors, 6; corticotropin-releasing-hormone (CRH)-secreting tumors, 2; and autonomous bilateral micronodular adrenal hyperplasia, 1. The continuous intravenous dexamethasone suppression test was done in 101 patients.
MEASUREMENTS AND MAIN RESULTS: Dexamethasone (1 mg/h) was administered intravenously for 7 hours. A cortisol decrease of at least 190 nmol/L was defined as a positive response. In identification of patients with ACTH-secreting pituitary adenomas, this test had a sensitivity of 100% (95% CI, 95% to 100%), a specificity of 90% (CI, 70% to 99%), and a diagnostic accuracy of 98% (CI, 93% to 100%). Only two patients had false test results. They both had CRH-secreting tumors. Cortisol secretion was also shown to be sensitive for feedback control in other tests, however.
CONCLUSION: The continuous intravenous dexamethasone suppression test has better diagnostic accuracy than other tests that are currently used in the differential diagnosis of the Cushing syndrome, and this test is very convenient. The only false test results were found in patients with CRH-secreting tumors.

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Year:  1990        PMID: 2158760     DOI: 10.7326/0003-4819-112-10-738

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  6 in total

1.  A patient with recurrent hypercortisolism after removal of an ACTH-secreting pituitary adenoma due to an adrenal macronodule.

Authors:  H J L M Timmers; E M van Ginneken; P Wesseling; C G J Sweep; A R M M Hermus
Journal:  J Endocrinol Invest       Date:  2006-11       Impact factor: 4.256

2.  Endogenous ACTH concentration-cortisol secretion dose analysis unmasks decreased ACTH potency in Cushing's disease with restoration after successful pituitary adenomectomy.

Authors:  Ferdinand Roelfsema; Daniel M Keenan; Johannes D Veldhuis
Journal:  J Clin Endocrinol Metab       Date:  2011-09-14       Impact factor: 5.958

3.  Irregular and frequent cortisol secretory episodes with preserved diurnal rhythmicity in primary adrenal Cushing's syndrome.

Authors:  M O van Aken; A M Pereira; S W van Thiel; G van den Berg; M Frölich; J D Veldhuis; J A Romijn; F Roelfsema
Journal:  J Clin Endocrinol Metab       Date:  2004-12-14       Impact factor: 5.958

4.  Corticotropin-releasing hormone production by a small cell carcinoma in a patient with ACTH-dependent Cushing's syndrome.

Authors:  R J Auchus; G Mastorakos; T C Friedman; G P Chrousos
Journal:  J Endocrinol Invest       Date:  1994-06       Impact factor: 4.256

5.  Failure of functional imaging with gallium-68-DOTA-D-Phe1-Tyr3-octreotide positron emission tomography to localize the site of ectopic adrenocorticotropic hormone secretion: a case report.

Authors:  Linsey U Gani; Emily J Gianatti; Ada S Cheung; George Jerums; Richard J Macisaac
Journal:  J Med Case Rep       Date:  2011-08-23

6.  Cushing's syndrome complicated by multiple opportunistic infections.

Authors:  R C Bakker; P R Gallas; J A Romijn; W M Wiersinga
Journal:  J Endocrinol Invest       Date:  1998-05       Impact factor: 4.256

  6 in total

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