Searchable abstracts of presentations at key conferences in endocrinology

ea0051p081 | Diabetes | BSPED2017

Acute treatment induced diabetic neuropathy in a 15 year old boy

Mathews Claire , Rayman Gerry , Buck Jackie , Wadham Claire , Perkins Emma

Acute Treatment-Induced Diabetic Neuropathy (ATDN) is a reversible small nerve fibre neuropathy involving pain and autonomic nerves precipitated by a rapid improvement in glycaemia. It is well described in adults with type 1 and 2 diabetes, but not in children. A 15 year old boy developed ATDN shortly after starting treatment for type 1 diabetes. He presented with polyuria and polydipsia and a blood glucose of 51.4 mmol/L. He was started on a basal bolus regime. Eight weeks la...

ea0033oc2.5 | Oral Communications 2 | BSPED2013

Continuous s.c. infusion of parathyroid hormone reduces PTH requirement in patient with activating mutation of the calcium sensing receptor

Cheung Moira , Buck Jackie , Brain Caroline , Allgrove Jeremy

Background: Activating mutations in the calcium sensing receptor can result in severe hypoparathyroidism with symptomatic hypocalcaemia. Complications of treatment with calcitriol or alfacacidol include hypercalciuria, nephrocalcinosis and renal failure. The use of synthetic parathyroid hormone (PTH 1–34, teriparatide) provides a more physiological treatment option and reduces the risk of hypercalciuria. Intermittent injections of PTH have been used with some success but ...

ea0027p60 | (1) | BSPED2011

Reducing the risk of serious infections for children with diabetes mellitus: an audit of immunisation practice

Chong Jiehan , Bailey Shivani , Kent Alison , Buck Jackie

Introduction: Patients with diabetes mellitus are known to have increased mortality and morbidity from influenza and pneumococcal disease. The Department of Health recommends that these children, along with other high risk patients, receive yearly influenza vaccination and additional immunisations against invasive pneumococcal disease. We audited the uptake of these additional immunisations in our patients.Method: Retrospective audit of all patients with...

ea0027p17 | (1) | BSPED2011

GH stimulation tests before and after the introduction of a new GH assay; are we finding a similar proportion of abnormal results ?

Buck Jackie , Vrajananda Kishore , Herath Darsheka , Olafimihan Shola , Yasmeen Ghazala , Twomey Patrick

Introduction: We previously used an assay measuring GH levels in microgram per litre. Peak GH levels >20, 10–20 and <10 μ/l representing sufficiency, partial deficiency and deficiency of GH respectively. With a new assay introduced in 2008 peak GH levels >8, 4–8 and <4 μg/l were quoted as normal, partial deficiency and deficiency. Although the patient groups tested were different we would have expected to have approximately similar rates o...

ea0023p37 | (1) | BSPED2009

Pitfalls of the four hour wait: keeping alert to potential endocrine presentations in Accident and Emergency

Cattaneo Elena , Hockings Catherine Ann , Foley Eleanor , James Matthew , Buck Jackie

Background: Emergency staff are under pressure to assess and refer within tight targets. Two adolescents presented to A&E with psychiatric symptoms, were referred to Child and Adolescent Mental Health (CAMH), but fortunately came to our attention and were diagnosed with thyroid disorders.Case 1: Fifteen-year-old boy presented with a two week history of disturbing auditory hallucinations and was referred to CAMH. He was commenced on antipsychotic medi...

ea0078oc4.2 | Oral Communications 4 | BSPED2021

Pseudohypoparathyroidism type 1A and 1B: presentation, phenotypes and phenotype-genotype associations

Prentice Philippa , Wilson Louise , Gevers Evelien , Buck Jackie , Raine Joseph , Rangasami Jayanti , McGloin Helen , Peters Catherine , Amin Rakesh , Wei Gan Hoong , Hughes Claire , Brain Caroline , Dattani Mehul , Allgrove Jeremy

Background & Objective: Pseudohypoparathyroidism (PHP), a heterogeneous condition, classically causes parathyroid hormone (PTH) resistance. PHP1a is caused by heterozygous inactivating mutations on the maternally derived GNAS allele. PHP1b results from methylation defects at the GNAS imprinted gene cluster, which are either sporadic, or familial, normally associated with maternally inherited intragenic STX16 deletions. We investigated the presentation, phenotype, ...