Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2018) 59 EP53 | DOI: 10.1530/endoabs.59.EP53

SFEBES2018 ePoster Presentations Clinical practice, governance & case reports (22 abstracts)

Case Report: The experience of using Etomidate in the management of severe Cushing’s disease and MRSA bacteraemia in a district general hospital in the United Kingdom

Stephanie Wong 1 , Yew Wen Yap 1 , Prakash Narayanan 2 , Christina Daousi 1 , Mohammad Al-Jubouri 2 & Yahya Mahgoub 2


1Aintree University Hospital, Liverpool, UK; 2Whiston Hospital, Liverpool, UK.


Background: The management of Cushing’s disease can be challenging especially when patients can present with sepsis and severely immunocompromised with limited oral medications to achieve cortisol control. We review a case of Cushing’s disease and the medical management of Cushing’s disease.

Case Report: A 54 year old female presented with symptomatic hyperglycaemia with truncal obesity, proximal muscle weakness, right posterior thorax haematoma and hypertension. Her glycated haemoglobin was 115 mmol/mol, consistent with newly diagnosed Type II diabetes mellitus. She had refractory hypokalaemia and elevated cortisol levels on overnight, low and high dose dexamethasone suppression tests. Pituitary magnetic resonance imaging revealed a 16X 16X 18 mm hypoenhancing lesion on the right pituitary gland with stalk deviation consistent with Cushing’s disease secondary to a pituitary macroadenoma. This was complicated by severe cellulitis from her infected haematoma. Treatment for Cushing’s syndrome was initiated with Metyrapone with cortisol levels improving to nadir of 900 nmol/L. A week later, she developed hospital-acquired pneumonia and acute respiratory distress syndrome with hypoxia requiring intubation and ventilation in the intensive care unit. Due to suboptimal administration of Metyrapone capsules and under-dosing of crushed Ketoconazole tablets through a nasogastric tube, her cortisol levels rose to a peak of 3319 nmol/l. The alternative option of a bilateral adrenalectomy was unsafe given the degree of metabolic decompensation and severe sepsis. Therefore, parental Etomidate was trialled to achieve target cortisol levels of between 600–800 nmol/L. The accumulation of 11b-deoxycortisol interfered with the laboratory assay and a mass spectrometry from another tertiary hospital was utilised to accurately quantify cortisol levels instead. Once stable, she was transferred for a transsphenoidal hypophysectomy at the tertiary centre where she made a good recovery.

Conclusion: This case reviews the treatment options for Cushing’s disease and recommends the use of Etomidate use in challenging cases such as this one.

Volume 59

Society for Endocrinology BES 2018

Glasgow, UK
19 Nov 2018 - 21 Nov 2018

Society for Endocrinology 

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