Searchable abstracts of presentations at key conferences in endocrinology

ea0077p244 | Reproductive Endocrinology | SFEBES2021

Service evaluation of patients referred for PCOS - Are we doing enough to diagnose and manage them well?

Soman Sooriya , Abidoye Omolade , Mohammed Ismail Haji Saliha , Davison Andrew , Sharma Dushyant , Hegde Pallavi

Introduction: Polycystic ovary syndrome (PCOS) is a complex endocrine disorder of uncertain aetiology, affects 1 in 10 reproductive women and has broad spectrum risks related to reproductive, cardiometabolic and psychosocial health. The wide overlap with other hyperandrogenemic conditions, complexity of PCOS spectrum, and inconsistencies in investigation and management potentially can result in risks of delay in diagnosis and management.Aim: To evaluate ...

ea0077p130 | Nursing Practice | SFEBES2021

Assessing the effectiveness of the endocrine specialist nurses (ESN) hydrocortisone education video created during covid-19 pandemic

Grounds Kerrie , Lewin Michelle , Hamilton Amanda , Jones Karen , Beeharry Deepa , Sharma Dushyant

Background: During Covid-19 pandemic, we recognised the importance of optimising adrenal insufficient patients’ ability to manage adrenal crisis and seek medical intervention thereby reducing the need for more intensive support. Evidence suggests omission of steroids during an adrenal crisis is a medical emergency and can be fatal. Research by National Reporting Learning System (2020) identified 4 deaths, 4 admissions to critical care, 320 incidents relating to steroid re...

ea0081p505 | Late-Breaking | ECE2022

Primary hyperparathyroidism, familial hypocalciuric hypercalcaemia or both?

Kapoor Ashutosh , Sharma Bhavna , Sriranganathan Danujan , Tolley Neil , Dimarco Aimee , Rahman Mushtaqur

Introduction: Primary hyperparathyroidism (PHPT) is an endocrine condition in which autonomous excessive secretion of parathyroid hormone (PTH) results in hypercalcaemia. In approximately 80% of cases the aetiology is due to a single parathyroid adenoma, the remainder are due to hyperplasia of more than one gland. Familial Hypocalciuric Hypercalcaemia (FHH) is an autosomal dominant, inactivating mutation of the calcium-sensing receptor, causing a right-shift in the concentrati...

ea0081ep70 | Adrenal and Cardiovascular Endocrinology | ECE2022

Adverse events associated with supraphysiological glucocorticoid dosing in congenital adrenal hyperplasia (CAH): results of a structured literature review

Sharma Vijay , Coope Helen , Maskin Kamran , Parviainen Lotta , Porter John , Withe Michael , Barnes Anne-Marie

Objectives: Congenital adrenal hyperplasia (CAH) is a rare condition caused by enzyme deficiency in cortisol biosynthesis. Patients with CAH require lifelong therapy, with the aim of replacing deficient hormones (cortisol +/− aldosterone) and reducing excess androgen production. Guidelines state that the lowest effective glucocorticoid (GC dose) should be used; however, current GC therapy is suboptimal, and supraphysiological GC doses are used to reduce excess androgens....

ea0081ep351 | Diabetes, Obesity, Metabolism and Nutrition | ECE2022

Double Trouble. Metformin and empagliflozin induced lactic acidosis - A case report

Sharma Bhavna , Mantega Michele , Deore Mahesh , Seetho Ian , Seechurn Shivashankar , Hui Elaine , Rahman Mushtaqur , Qureshi Asjid

63 years old with sarcoidosis since 2018 and type 2 diabetes was referred by GP for hypercalcemia related to likely dehydration and sarcoidosis. She was started on a weaning dose of prednisolone and empagliflozin. She had already been on metformin for several years. She was discharged after calcium improved from 2.97 mmol/l to 2.83 mmol/l. She was advised to follow up in Ambulatory care in 1 week for repeat calcium levels. On follow up, noted to have calcium levels of 2.67 mmo...

ea0081ep599 | Endocrine-Related Cancer | ECE2022

Co-secretory ACTH & Calcitonin tumor presented with refractory hypokalemia

Sharma Bhavna , Joshi Pratichi , Fatima Anees , Lakha Meena , Hamdulay Shahir , Hui Elaine

81-year-old ex-smoker presented to emergency with transient facial droop, slurring of speech and generalized weakness. He had a background of ischemic heart disease, hypertension, and previous bladder cancer (treated 5 years ago). Examination revealed clinical signs of hypocalcaemia with no cushingoid features. Bloods revealed refractory severe hypokalemia, severe hypocalcaemia with normal phosphate, and metabolic alkalosis requiring High dependency Unit.<p class="abstext"...

ea0082wa7 | Workshop A: Disorders of the hypothalamus and pituitary | SFEEU2022

Non-functioning granulomatous pituitary adenoma: Common pathology in an unlikely site

ZM Lim Jonathan , Purewal Tejpal , K Sinha Ajay , Grounds Kerrie , Sharma Dushyant

Background: Tuberculosis (TB) is an important cause of mortality and morbidity globally. Only a small proportion cases of systemic TB present with lesions spreading to meninges, sella, or ventricles. Cases of intra-sellar pituitary adenoma secondary to TB have been rarely identified, often with uncertainty on medical management as opposed to more aggressive surgical therapy. We report an interesting case of pituitary adenoma presenting with pan-hypopituitarism and posterior pi...

ea0082oc6 | Oral Communications | SFEEU2022

Treatment with Selective RET inhibitors in Medullary Thyroid Cancer – A Case series

Sharma Aditi , Sairam Shwetha , Narula Kavita , Newbold Kate , Di Marco Aimee , Wernig Florian

Case history: A 54-year-old lady was diagnosed with primary hypoparathyroidism in 2005, after being referred by her Rheumatologist as her father and brother had familial hypoparathyroidism and sensorineural deafness. She was followed up in endocrine clinic for management of primary hypoparathyroidism. Her hypocalcaemia is well managed with calcium supplementation, with no specific symptoms of hypocalcaemia. She has recurrent urinary tract infections with known borderline chron...

ea0086oc6.3 | Thyroid | SFEBES2022

Long-Term effectiveness of ethanol ablation in controlling selected postoperative neck nodal metastases in fourteen patients presenting with ATA pediatric intermediate or high-risk papillary thyroid carcinoma

Hay Ian , Lee Robert , Pittock Siobhan , Sharma Animesh , Thompson Geoffrey , Charboneau Bill

Introduction: Childhood papillary thyroid carcinoma (CPTC), despite bilateral thyroidectomy (BT), nodal resection and radioiodine remnant ablation (RRA), recurs within neck nodal metastases (NNM) in >30% within 20 postoperative years. However, these NNM are usually treated with re-operation or further radioiodine; US-guided ethanol ablation (EA) may be considered (j.sempedsurg.2020.150920) for patients with limited numbers of NNMMethods: We studied l...

ea0086p265 | Neuroendocrinology and Pituitary | SFEBES2022

Not just a prolactinoma- Conservative management of co-secretory macroadenoma

Sharma Bhavna , Vanieri Erika , Deore Mahesh , Rahman Mushtaqur , Qureshi Asjid , Garg Ranjna

45 years old male of Romanian origin presented with shortness of breath and reduced exercise tolerance over 3 months with increased sweating and weight gain from 90 kgs to 118 kgs over 2 years. Also reported hands/fingers/feet size increase. He also complained that his breathlessness worse by as tongue and lips were ‘large’. Denied any visual disturbance, especially peripheral vision. On examination, coarse features, prognathism and possible macroglossia noted. Photo...