Luke Starling | International and Private Care

Luke Starling is a Consultant Paediatric Cardiologist, specialising in Inherited Cardiovascular Diseases and arrhythmia. He leads the Inherited Arrhythmia Service at Great Ormond Street Hospital and has a particular interest in ion channel disease (including long QT syndrome, Brugada syndrome, and CPVT) and sudden cardiac death. He has established a novel neurocardiac channelopathies Service and a left cardiac sympathetic denervation (LCSD) programme, whilst combining his role in inherited cardiovascular diseases with general paediatric and congenital cardiology. Dr Starling studied medicine at University College London and undertook training in Paediatric Cardiology at GOSH and The Royal Brompton Hospital. He is a Fellow of the Royal College of Paediatrics and Child Health (FRCPCH) and is the paediatric representative on the Council of the Association of Inherited Cardiac Conditions.

Inherited Cardiovascular Diseases/Inherited Cardiac Conditions
Ion channel disease
Arrhythmogenic cardiomyopathy
Sudden death
Syncope
Paediatric arrhythmias
Congenital heart disease

Inherited arrhythmias - particularly the ion channel diseases: long QT syndrome, CPVT, Brugada syndrome, and short QT syndrome
Sudden death and family screening
Paediatric arrhythmia

Fellow of Royal College of Paediatrics and Child Health (FRCPCH)
Certificate of Completion of Training (CCT) in Paediatric Cardiology
Association of Inherited Cardiac Conditions (AICC) council member
MB BS
BSc (Hons)

Cardiac ion channel diseases: long QT syndrome, CPVT, Brugada syndrome, calcium release deficiency syndrome (CRDS)
Sudden cardiac death
Neurocardiac channelopathies and sudden unexpected death in epilepsy (SUDEP)

Публикации и статьи

• Lawley CM, Tester M, Sanatani S, Prendiville T, Beach CM, Vinocur JM, Horie M, Uhm JS, Khongphatthanayothin A, Ayers MD, Starling L, Yoshida Y, Shah MJ, Skinner JR, Turner C. Life-threatening cardiac arrhythmia and sudden death during electronic gaming: An international case series and systematic review. Heart Rhythm. 2022 Nov;19(11):1826-1833.

• Silksmith B, Munot P, Starling L, Pujar S, Matthews E, Accelerating the genetic diagnosis of neurological disorders presenting with episodic apnoea in infancy, Lancet Child Adolesc Health, 2022; Jul;6(7):495-508.

• Brunet-Garcia L, Odori A, Fell H, Field E, Roberts A, Starling L, Kaski JP, Cervi E, Non-compaction cardiomyopathy, sick sinus disease, and aortic dilatation: too much for a single diagnosis?, JACC Case Rep, 2022; 4(5):287-293.

• Brunet-Garcia L, Johnson J, Field E, Norrish G, Tollit J, Shoshan J, French N, Addis A, Cervi E, Starling L, Kaski JP, Prevalence of inherited cardiac conditions in pediatric first-degree relatives of patients with idiopathic ventricular fibrillation, Pediatr Cardiol, 2022; 43(5):1114-1121.

• Elston S, Kaski JP, Starling LD, Long QT syndrome with a functional 2:1 block and multilevel conduction disease; Progress in Pediatric Cardiology, 2018; 50: 46-49.

• Starling LD & Till J, A T-Wave Tight Spot (Chapter 18 of: Magee AG, Till JA, Seale AN (Eds.), Practical Pediatric Cardiology: Case-based management of potential pitfalls), Nov 2015; Springer, ISBN 978-1-4471-4183-9.