Dr Piers Daubeney is Reader in Paediatric Cardiology at NHLI, Imperial College London and Consultant Paediatric and Fetal Cardiologist at the Royal Brompton Hospital, Chelsea and Westminster Hospital and 3 district hospitals in the South-East.
He trained at Oxford and St Thomas' Hospitals with postgraduate training at the Wessex Cardiovascular Centre in Southampton, Royal Children's Hospital, Melbourne and the Hospital for Sick Children, Toronto.
Dr Daubeney has a research team and particular interests in the epidemiology and management of congenital heart disease, childhood cardiomyopathy, and drug studies in paediatric heart disease. He has jointly founded the following ongoing international multi-centre studies:
- UK and Ireland Study of Pulmonary Atresia with Intact Ventricular Septum
- National Australian Childhood Cardiomyopathy Study
- UK, Ireland and Sweden Study of Total Anomalous Pulmonary Venous Connection
- UK, Ireland and Sweden Study of Pulmonary Vein Stenosis.
He is also interested in the mechanisms of congenital heart disease and in particular connexin expression. He participates in a number of paediatric multi-centre drug trials in congenital heart disease.
Dr Daubeney has published widely in the field of congenital heart disease and his textbook ‘Diagnosis and Management of Adult Congenital Heart Disease' jointly edited with Professors Gatzoulis and Webb, is now in its third edition having been translated into several different languages.
Dr Daubeney is the lead clinician for paediatric cardiomyopathy at the Royal Brompton Hospital and has an active research programme. He welcomes postgraduate research fellows intending to attain higher qualifications.
et al., 2019, Complicated coarctation repair: The importance of three-dimensional cross-sectional imaging in late postoperative assessment, Annals of Pediatric Cardiology, Vol:12, ISSN:0974-2069, Pages:178-181
et al., 2019, Left Ventricular Twist Mechanics to Identify Left Ventricular Noncompaction in Childhood, Circulation-cardiovascular Imaging, Vol:12, ISSN:1941-9651
et al., A case series on cardiac and skeletal involvement in two families with PRKAG2 mutations, Case Reports in Pediatrics, Vol:2019, ISSN:2090-6803
et al., 2019, NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses, Brain, Vol:142, ISSN:0006-8950, Pages:50-58
et al., 2018, Clinical presentation and survival of childhood hypertrophic cardiomyopathy: a retrospective study in United Kingdom, European Heart Journal, ISSN:1522-9645