Searchable abstracts of presentations at key conferences in endocrinology

ea0033oc2.8 | Oral Communications 2 | BSPED2013

Establishing a national audit of paediatric GH prescribing

Gault Emma-Jane , Shepherd Sheila , Shaw Nick

Introduction: GH therapy is prescribed to UK children for a variety of indications. However, no central record exists, making follow-up studies difficult.Aim: To establish an ongoing audit of UK children and adolescents newly-prescribed GH in order to i) monitor trends in prescribing practice and ii) facilitate future long-term follow-up.Patient population: UK children aged ≤16.0 years newly starting GH therapy.<p class="...

ea0033p57 | (1) | BSPED2013

Middle ear disease in Turner syndrome: prevalence and risk factors

Lupton Kenneth , Gault Emma-Jane , Al-Hassani Sarah , Kubba Haytham , Donaldson Malcolm

Introduction: Middle ear disease in Turner syndrome (TS) is common, often resulting in troublesome temporary hearing loss, and more rarely to serious suppurative disease with cholesteatoma formation. We have examined the prevalence and pattern of middle ear disease in our TS clinic in relation to age and karyotype.Methods: Case note review of all girls with TS attending clinic 1989–2012, scoring the most serious middle ear problem for each as: none ...

ea0030p43 | (1) | BSPED2012

Prevalence and diagnosis of cholesteatoma in Turner syndrome

Lim David , Gault Emma Jane , Kubba Haytham , Morrissey Simon , Donaldson Malcolm

Background: Cholesteatoma, a serious suppurative middle ear condition, has an increased prevalence in Turner syndrome (TS).Aims: To estimate its incidence in our TS population; identify risk factors; highlight distinctive operative findings; and suggest strategies for earlier detection.Methods: Retrospective casenote review for patients attending a TS clinic to identify those with cholesteatoma; each age-matched with three unaffect...

ea0030p42 | (1) | BSPED2012

Feasibility of measuring birth length and parental height for small babies and following-up short children at 2 years

Sardar Colette Montgomery , Kinmond Sheena , Siddique Jamila , McGowan Sheena , Paterson Wendy , Donnelly Sharon , Gault Emma Jane , Donaldson Malcolm

Background: Small for gestational age (SGA) and short stature at birth can be defined as birth weight (BW) and birth length (BL) ≤−2 S.D.. Affected neonates can be classified as: i) SGA, ii) Short, iii) SGA + Short. Catch-up growth occurs by age 6 months in 90–95% of Short and SGA + Short infants. A minority remain short after age 2–4 years when the lack of data on BL and parental height (PH) renders assessment difficult.<p class="abste...

ea0023oc2.1 | Oral Communications 2 | BSPED2009

Final height in Turner syndrome after Oxandrolone and delayed pubertal induction: results of a UK randomised, double-blind, placebo-controlled trial

Gault Emma-Jane , Perry Rebecca , Casey Sarah , Cole Tim , Paterson Wendy , Hindmarsh Peter , Betts Peter , Dunger David , Donaldson Malcolm

The UK Turner Study examined in girls with Turner syndrome (TS) the impact on final height (FH) of Oxandrolone (Ox) and/or delayed pubertal induction (14y).Methods: Girls with TS aged 7–13y receiving GH were randomised to Ox (0.05 mg/kg per day, max. dose 2.5 mg/day) or placebo from 9y (or from enrolment if >9y). Girls requiring oestrogen were further randomised to begin oral Ethinylestradiol (E2) (Y1:2 μg/day; Y2:4 μg/day; ...