Searchable abstracts of presentations at key conferences in endocrinology

ea0041ep742 | Neuroendocrinology | ECE2016

How frequently can we predict failure of fluid restriction in SIAD? Results of a multicenter prospective audit

Cuesta Martin , Ortola Ana , Slattery 2David , Garrahy Aoife , Pascual Alfonso Luis Calle , Tormey William , de la Vega Isabelle Runkle , Thompson Christopher J.

Context: Fluid restriction (FR) is recommended as first line therapy for SIAD by both the European1 and the American guidelines2 for management of SIAD. Not all patients respond to FR however, and the American guidelines have identified clinical predictors of failure to respond to FR. These include 1.Urine osmolality (UOsm) >500 mOsm/Kg 2. Furst formula (ratio UNa+UK/pNa) > 1, and 3. 24 hour-urine volume<1500 mlObjective...

ea0056p1063 | Thyroid (non-cancer) | ECE2018

The accuracy of diagnostic tests in amiodarone-induced thyrotoxicosis; a case-series

Cuesta Martin , Ruiz Cristina Gonzalez , Varas Ines Jimenez , Lapena Luis , Ganado Tomas , Merino Salome , Santiago Alejandro , Recio Lourdes , Pascual Alfonso Luis Calle , Vega Isabelle Runkle de la

Introduction: Amiodarone-induced thyrotoxicosis (AIT) can present a high morbi-mortality.Initial subtype identification facilitates appropriate management.We describe the utility of diagnostic tests in a cohort of patients with AIT.Material and methods: Retrospective, observational study of 59 patients attended from 2007 to 2018 in outpatient clinic. Differential diagnosis: type I if FT4 and FT3 (TH) were normalized following therapy with antithyroid dru...

ea0035p724 | Neuroendocrinology | ECE2014

Treatment of SIADH in a patient with fatal familial insomnia (FFI) and hypersomnia

Hoyos Emilia Gomez , Gracia Teresa Ruiz , Azorin David Garcia , Hernandez Martin Cuesta , Buigues Ana Ortola , Hernandez Irene Crespo , Orozco Francisco Martinez , Pascual Alfonso Luis Calle , Dolado Alberto Marco , Vega Isabelle Runkle de la

Introduction: Fatal insomnia is a neurodegenerative spongiform prion disease. Presentation can be sporadic or hereditary (autonomal dominant). The latter, FFI, is caused by a mutation in the human prion protein gene on chromosome 20. Affected individuals present a disorderd sleep-wake cycle, dysautonomia and motor signs, with a predominance of lesions in the thalamus. SIADH has been described in two affected patients.Case Study: A 70-year-old woman was r...