Publications
165 results found
Weintraub RQ, Chondros P, Nugent A, et al., 2004, Thromboembolic events among children with cardiomyopathy: Results from the National Australian Childhood Cardiomyopathy Study, 54th Annual Scientific Session of the American-College-of-Cardiology, Publisher: ELSEVIER SCIENCE INC, Pages: 391A-391A, ISSN: 0735-1097
Sidwell RU, Daubeney PEF, Porter W, et al., 2004, Neonatal hemangiomatosis and atrial septal defect: A rare cause of right heart failure in infancy, PEDIATRIC DERMATOLOGY, Vol: 21, Pages: 66-69, ISSN: 0736-8046
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- Citations: 3
Kinali M, Olpin SE, Clayton PT, et al., 2004, Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathy, EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, Vol: 8, Pages: 217-219, ISSN: 1090-3798
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- Citations: 1
Gardiner HM, Franklin RC, Loughna PV, et al., 2003, Percutaneous fetal valvuloplasty - Case selection and outcome, 76th Annual Scientific Session of the American-Heart-Association, Publisher: LIPPINCOTT WILLIAMS & WILKINS, Pages: 495-495, ISSN: 0009-7322
Nugent AW, Daubeney PEF, Chondros P, et al., 2003, The epidemiology of childhood cardiomyopathy in Australia, NEW ENGLAND JOURNAL OF MEDICINE, Vol: 348, Pages: 1639-1646, ISSN: 0028-4793
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- Citations: 490
Abrams DJR, Rigby ML, Daubeney PEF, 2003, Membranous pulmonary atresia treated by radiofrequency-assisted balloon pulmonary valvotomy, CIRCULATION, Vol: 107, Pages: E98-E99, ISSN: 0009-7322
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- Citations: 2
Daubeney PE, Nugent AW, Chondros P, et al., 2003, Presenting features and outcomes for children with dilated cardiomyopathy who develop persisting cardiac dysfunction, 52nd Annual Scientific Session of the American-College-of-Cardiology, Publisher: ELSEVIER SCIENCE INC, Pages: 491A-491A, ISSN: 0735-1097
One-hundred authors, 2003, Diagnosis and Management of Adult Congenital Heart Disease (1st edition), Publisher: Elsevier Health Sciences, ISBN: 9780443071034
This practical resource provides essential guidance on the anatomic issues, clinical presentation, diagnosis, and clinical management of adults with congenital ...
Abrams D, Gerlis L, Daubeney PEF, 2003, Tracheoesophageal Compression in Congenital Heart Disease: Vascular Rings, Pulmonary Slings and Other Vascular Abnormalities, Diagnosis and Management of Adult Congenital Heart Disease (1st edition), Editors: Gatzoulis, Webb, Daubeney, Publisher: Elsevier Health Sciences, Pages: 273-282, ISBN: 9780443071034
Rowlinson G, Daubeney PEF, 2003, Review of 'Paediatric Cardiology' edited Anderson 2002, Europace, Vol: 5
Daubeney PEF, 2003, Pulmonary Atresia With Intact Ventricular Septum, Diagnosis and Management of Adult Congenital Heart Disease (1st edition), Editors: Gatzoulis, Webb, Daubeney, Publisher: Elsevier Health Sciences, Pages: 339-348, ISBN: 9780443071034
Daubeney PEF, Delany DJ, Anderson RH, et al., 2002, Pulmonary atresia with intact ventricular septum - Range of morphology in a population-based study, JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol: 39, Pages: 1670-1679, ISSN: 0735-1097
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- Citations: 102
Daubeney PEF, Delany DJ, Anderson RH, et al., 2002, Pulmonary atresia with intact ventricular septum: range of morphology in a population-based study., J Am Coll Cardiol, Vol: 39, Pages: 1670-1679, ISSN: 0735-1097
OBJECTIVES: We describe the morphologic variability in pulmonary atresia with intact ventricular septum (PAIVS) within a population-based study. BACKGROUND: An uncommon disease, PAIVS shows considerable morphologic heterogeneity. Clinical reports, based mostly on small samples of patients, may not reflect the true spectrum of pathology of this condition. We have studied the entire range of morphology in a prospective population-based study of patients over a five-year period (1991 to 1995). METHODS; As part of the United Kingdom and Ireland Collaborative Study of PAIVS, all 18 pediatric cardiac centers were visited by a single investigator. Morphologic features of each case were determined by direct review of the echocardiograms and angiocardiograms, from surgical and autopsy reports, and by review of pathology specimens where available. RESULTS: Among 183 live-born infants, atresia was valvar (membranous) in 74.7% and muscular in 25.3%. Muscular obliteration of the apical trabecular cavity, and in some cases its infundibulum, resulted in "bipartite" right ventricle (RV) in 33.6%, and a "unipartite" chamber in 7.7%. The remaining 58.7% had "tripartite" morphology. Coronary arterial abnormalities were identified in 45.8%, including arterial stenoses, interruptions and ectasia in 7.6%. Ebstein's malformation coexisted in 18 patients. Median tricuspid valvar size and RV inlet Z-scores were -5.2 and -5.1, respectively. CONCLUSIONS: This study provides unique data on the diverse pathology of PAIVS in an unselected population. This will help determine if published reports reflect the true spectrum of pathology of the condition.
Daubeney PE, Nugent A, Chondros P, et al., 2002, Outcome for children with lymphocytic myocarditis enrolled in the National Australian Childhood Cardiomyopathy Study, JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol: 39, Pages: 161A-161A, ISSN: 0735-1097
Nugent A, Daubeney P, Chondros P, et al., 2002, The natural history of restrictive cardiomyopathy presenting during childhood, JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol: 39, Pages: 144A-144A, ISSN: 0735-1097
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- Citations: 4
Daubeney PE, Nugent A, Chondros P, et al., 2002, Presenting features and clinical outcomes for children with metabolic cardiomyopathies, JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol: 39, Pages: 402A-402A, ISSN: 0735-1097
Daubeney P, Nugent A, Colan S, et al., 2001, The natural history of dilated cardiomyopathy presenting during childhood, JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol: 37, Pages: 462A-462A, ISSN: 0735-1097
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- Citations: 2
Nugent A, Daubeney P, Chondros P, et al., 2001, The natural history of hypertrophic cardiomyopathy presenting during childhood, JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol: 37, Pages: 465A-465A, ISSN: 0735-1097
Daubeney P, Nugent A, Cheung M, et al., 2001, The natural history of left ventricular noncompaction presenting during childhood, JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, Vol: 37, Pages: 462A-462A, ISSN: 0735-1097
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- Citations: 2
Abrams DJR, Radley-Smith R, Daubeney PEF, et al., 2000, Survival in children presenting to a cardiac intensive care unit with acute inflammatory or idiopathic ventricular dysfunction., CRITICAL CARE MEDICINE, Vol: 28, Pages: A156-A156, ISSN: 0090-3493
Daubeney PEF, Blackstone EH, Weintraub RG, et al., 1999, Relationship of the dimension of cardiac structures to body size: an echocardiographic study in normal infants and children, CARDIOLOGY IN THE YOUNG, Vol: 9, Pages: 402-410, ISSN: 1047-9511
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- Citations: 198
Scott JS, Boyle GJ, Daubeney PE, et al., 1999, Tacrolimus: A cause of hypertrophic cardiomyopathy in pediatric heart transplant recipients?, TRANSPLANTATION PROCEEDINGS, Vol: 31, Pages: 82-83, ISSN: 0041-1345
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- Citations: 8
Daubeney PE, Sharland GK, Cook AC, et al., 1998, Pulmonary atresia with intact ventricular septum: impact of fetal echocardiography on incidence at birth and postnatal outcome. UK and Eire Collaborative Study of Pulmonary Atresia with Intact Ventricular Septum., Circulation, Vol: 98, Pages: 562-566, ISSN: 0009-7322
BACKGROUND: Fetal echocardiography is widely established in the United Kingdom for prenatal diagnosis of congenital heart disease. This may result in a substantial reduction in incidence at birth because of selected termination of pregnancy. The objective of this population-based study was to determine the incidence of pulmonary atresia with intact ventricular septum (PAIVS) at birth, the impact of fetal echocardiography on this incidence, and to compare the outcome of cases with and those without prenatal diagnosis. METHODS AND RESULTS: From 1991 to 1995, all infants born with PAIVS and all fetal diagnoses in the United Kingdom and Eire were studied. There were 183 live births (incidence 4.5/100,000 live births). The incidence was 4.1 cases per 100,000 live births in England and Wales, 4.7 in Scotland, 6.8 in Eire, and 9.6 in Northern Ireland (P=0.01). There were 86 fetal diagnoses made at a mean of 22.0 weeks of gestation leading to 53 terminations of pregnancy (61%), 4 intrauterine deaths (5%), and 29 live births (34%). The incidence at birth would be 5.6 per 100,000 births in England and Wales, 5.3 in Scotland, and unchanged in Eire and Northern Ireland, if there were no terminations of pregnancy and assuming no further spontaneous fetal deaths (P=0.28). An initial diagnosis of critical pulmonary stenosis was made in 6 cases, at a mean of 22.3 weeks of gestation with progression to PAIVS by 31.4 weeks. Probability of survival at 1 year was 65% and was the same for live-born infants whether or not a fetal diagnosis had been made. CONCLUSIONS: PAIVS is rare, occurring in 1 in 22,000 live births in the United Kingdom and Eire. Termination of pregnancy has resulted in an important reduction in the live-born incidence in mainland Britain.
Daubeney PEF, Sharland GK, Cook AC, et al., 1998, Pulmonary atresia with intact ventricular septum - Impact of fetal echocardiography on incidence at birth and postnatal outcome, CIRCULATION, Vol: 98, Pages: 562-566, ISSN: 0009-7322
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- Citations: 119
Daubeney PEF, Smith DC, Pilkington SN, et al., 1998, Cerebral oxygenation during paediatric cardiac surgery: identification of vulnerable periods using near infrared spectroscopy, EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, Vol: 13, Pages: 370-377, ISSN: 1010-7940
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- Citations: 64
Monro JL, Tolan MJ, Daubeney PE, et al., 1997, Aortic valve repair in children - Reply, ANNALS OF THORACIC SURGERY, Vol: 64, Pages: 1223-1223, ISSN: 0003-4975
Tolan MJ, Daubeney PE, Slavik Z, et al., 1997, Aortic valve repair of congenital stenosis with bovine pericardium, ANNALS OF THORACIC SURGERY, Vol: 63, Pages: 465-469, ISSN: 0003-4975
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- Citations: 22
Daubeney PEF, Webber SA, 1997, Cerebral oxygenation measured by near-infrared spectroscopy - Reply, ANNALS OF THORACIC SURGERY, Vol: 63, Pages: 292-293, ISSN: 0003-4975
Daubeney PEF, Taylor C, McGaw J, et al., 1997, Immunogenicity and tolerability of a trivalent influenza subunit vaccine (Influvac) in high-risk children aged 6 months to 4 years., Br J Clin Pract, Vol: 51, Pages: 87-90
Webber SA, Hatchwell E, Barber JCK, et al., 1996, Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: A three-year prospective study, JOURNAL OF PEDIATRICS, Vol: 129, Pages: 26-32, ISSN: 0022-3476
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- Citations: 85
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