Searchable abstracts of presentations at key conferences in endocrinology

ea0031p368 | Thyroid | SFEBES2013

Managing Graves' disease: management involving endocrine nurse led service: experience from DGH

Aziz Aftab , Cox Sue , Dyer Rob G.

Graves’ disease is an autoimmune condition predominantly affecting middle aged women. It can be difficult to manage and consumes a lot of medical time and resources.In Torbay Hospital, we introduced endocrine nurse specialist (ENS) follow up service to reduce medical burden. This has shifted the work-load of patient care but on the other hand, has resulted in identification of great need for support and increased nurse time.We...

ea0065p299 | Neuroendocrinology | SFEBES2019

Use of serial Short Synacthen tests (SST) in determining failure of hypothalamic–pituitary−adrenal (HPA) axis in patients with pituitary disorders

Koutroukas Vaios , Twine Gina , Flanagan Daniel , Aziz Aftab

Introduction: The study aim was to compare serial Short Synacthen test (SST) results to diagnose secondary Adrenal Insufficiency (AI) in patients with confirmed pituitary diseases.Methods: Serial SST results of patients, tested between 2006 and 2018 in the department of Diabetes and Endocrinology, at a tertiary centre, were reviewed retrospectively. Patient details were obtained from local dynamic test database, maintained by Endocrine Nurse Specialist. ...

ea0044p248 | Thyroid | SFEBES2016

One third of thyroid radionuclide uptake scans is deferentially interpreted leading to potentially differential treatment for patients with thyrotoxicosis

Aziz Aftab , Avades Tamar , Poyner Richard , Vaidya Bijay , Patel Kashyap

Background: Accurate diagnosis of an underlying cause of thyrotoxicosis is critical for targeted therapy. Thyroid radionuclide uptake scan is a useful second line investigation in patients who lack TSH receptor antibody. The uptake scan patterns identify patients who can be preferentially treated with anti-thyroid drugs (diffuse pattern - Graves’ disease) or radio-iodine treatment (patchy uptake - multinodular or localised uptake – toxic adenoma) or simple monitoring...

ea0034p149 | Clinical practice/governance and case reports | SFEBES2014

Adrenocortical carcinoma, where's the delay?

Aziz Aftab , Dyer Rob , Dunn Julie , Goodman Andy , Brooke Antonia

Adrenocortical carcinomas are rare malignancies (incidence 1–2/one million). They present in a variety of ways and carry a poor prognosis. Prompt diagnosis and early intervention offers better outcome.We describe 5 cases of adrenocortical carcinoma to help identify and improve delays in their pathway of care. Five patients (four females and one male), age range 38–76 years, presented between September 2011 and April 2013. Three patients referre...

ea0065p306 | Neuroendocrinology | SFEBES2019

Long term effects of cranial radiotherapy on hypothalamic–pituitary–adrenal axis in patients with established pituitary diseases

Koutroukas Vaios , Bond Hannah , Lim Elizabeth , Twine Gina , Flanagan Daniel , Aziz Aftab

Introduction: Radiotherapy is an important adjuvant treatment for pituitary and cranial diseases. The aim of the study was to observe response of Radiotherapy (RTX) on Hypothalamic–Pituitary–Adrenal (HPA) axis determined by serial Short Synacthen tests (SSTs). Methods: Patients treated with adjuvant Cranial Radiotherapy between the years 2000 and 2018 in the department of Radiation Oncology and who also underwent serial Short Synacthen tests, i...

ea0050p400 | Thyroid | SFEBES2017

Activating germline TSHR mutations are rare in adult hyperthyroid patients without autoimmunity and showing diffuse uptake on radionuclide thyroid scintigraphy

Patel Kashyap , Knight Bridget , Aziz Aftab , Avades Tamar , Ward Rebecca , Babiker Taz , Tysoe Carolyn , Dimitropoulos Ioannis , Panicker Vijay , Vaidya Bijay

Background: Sporadic and familial autosomal dominant non-autoimmune hyperthyroidism (S/FANH) is caused by activating germline mutations in the TSH Receptor (TSHR) gene. These patients lack TSHR-Ab, show diffuse uptake on radionuclide thyroid scan and often lack positive family history due to variable penetrance. Because of these overlapping features, S/FANH is difficult to distinguished from Graves’ disease without autoimmune features. Ther...

ea0050p400 | Thyroid | SFEBES2017

Activating germline TSHR mutations are rare in adult hyperthyroid patients without autoimmunity and showing diffuse uptake on radionuclide thyroid scintigraphy

Patel Kashyap , Knight Bridget , Aziz Aftab , Avades Tamar , Ward Rebecca , Babiker Taz , Tysoe Carolyn , Dimitropoulos Ioannis , Panicker Vijay , Vaidya Bijay

Background: Sporadic and familial autosomal dominant non-autoimmune hyperthyroidism (S/FANH) is caused by activating germline mutations in the TSH Receptor (TSHR) gene. These patients lack TSHR-Ab, show diffuse uptake on radionuclide thyroid scan and often lack positive family history due to variable penetrance. Because of these overlapping features, S/FANH is difficult to distinguished from Graves’ disease without autoimmune features. Ther...