Searchable abstracts of presentations at key conferences in endocrinology
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48th Meeting of the British Society for Paediatric Endocrinology and Diabetes

Online, Virtual
24 Nov 2021 - 26 Nov 2021

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Poster Presentations

Miscellaneous

ea0078p40 | Miscellaneous | BSPED2021

Can playing a computer game assess muscle function? Using ability captured through interactive video evaluation (ACTIVE) in duchenne muscular dystrophy

McElvaney Joseph , Wood Claire , Hollingsworth Kieren G , Hughes Eric , Muni Lofra Robert , Mayhew Anna , Sodhi Jassi , James Meredith , Cheetham Tim , Straub Volker

Introduction: Duchenne muscular dystrophy (DMD) is associated with progressive decline in muscle function and loss of ambulation in the teenage years. Objective assessments of upper limb performance are required but functional assessments and magnetic resonance imaging (MRI) are time consuming and costly. ACTIVE-seated (Ability Captured Through Interactive Video Evaluation) is a fun, inexpensive, movement tracking video game that can measure Functional Reaching Volume (FRV). <...

ea0078p41 | Miscellaneous | BSPED2021

Paediatric society calls for a review of access to funding for continuous glucose monitoring systems for patients with recurrent hypoglycaemia

May Ng Sze , Mushtaq Talat , Randell Tabitha

Continuous glucose monitoring (CGM) allows continuous real-time blood glucose monitoring and informs users of blood glucose trend data and alarms which warn users of high or low blood glucose readings. Current evidence suggests that CGM can reduce episodes of hypoglycaemia in conditions such as congenital hyperinsulinism and metabolic disorders. Hypoglycaemia secondary to these conditions is serious with almost 50% of children demonstrating neurological impairments as a result...

ea0078p42 | Miscellaneous | BSPED2021

A rare case of steroid cell tumor, not otherwise specified (NOS) of the ovary presenting with cushing syndrome and hyperandrogenism

Rani Rai Versha , Noor Ibrahim Mohsina , Raza Jamal , Muhammad Laghari Taj , Khoso Zubair , Riaz Maira

Background: Steroid cell tumour of ovaries comes under sex cord stromal tumour that accounts less than 0.1% of all ovarian tumour. Majority are benign in childhood age group. It may produce steroids and testosterone resulting in virilisation and Cushing’s syndrome. Histology remains the gold standard for diagnosis of NOS. The gross appearance of NOS generally is well circumscribed, solid and noncalcifed with a lobulated appearance Till date only 10 cases has been reported...

ea0078p43 | Miscellaneous | BSPED2021

Hypoglycaemia in paediatrics – Re-Audit post introduction of “Hypo Packs”

Longley Catherine , Bruce Marnie , Patel Harsita , Rangasami Jayanti

Introduction: Hypoglycaemia is a common paediatric medical emergency, hence prompt treatment with appropriate investigations of causes is essential.Aims: 1) Re-audit investigations sent for children with hypoglycaemia after introduction of “Hypo-packs” from previous audit; (2) To improve awareness of local guidelines to unify clinical practice; (3) Review “Hypo-packs” and consider other improvements.Methods: A r...

ea0078p44 | Miscellaneous | BSPED2021

Interpretation of CGM-measured nocturnal hypoglycaemia in congenital hyperinsulinism

Yang Leyi , Worth Chris , Salomon Estebanez Maria , O‘Shea Elaine , Banerjee Indi

Background: Congenital Hyperinsulinism (CHI) is characterised by dysregulated and excess secretion of insulin leading to severe hypoglycaemia. Monitoring of glucose levels is essential in this condition as prolonged hypoglycaemia can cause life-threatening complications such as permanent neurological impairment. Interstitial glucose monitoring by continuous glucose monitoring (CGM) devices can identify nocturnal hypoglycaemia retrospectively through data analysis. Analysis can...

ea0078p45 | Miscellaneous | BSPED2021

Heterozygous mutations in ATP-sensitive potassium channel (KATP) genes associated with transient and mild hyperinsulinaemic hypoglycaemia

Siese Thomas , Alins-Sahun Yolanda , Crowne Elizabeth , Giri Dinesh

Introduction: Congenital hyperinsulinism (CHI) is a rare disease, characterized by an unregulated insulin release, leading to hypoglycaemia. It is the most frequent cause of persistent and severe hypoglycaemia during the neonatal period and early childhood. Mutations in KATP < genes (ABCC8 and KCNJ11), together account for up to 70% of CHI. CHI can either be transient or persistent. Transient CHI tends to resolve spontaneously and is n...