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Dive into the research topics where Rod Jones is active.

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Featured researches published by Rod Jones.


Circulation | 2006

Physiological and Clinical Consequences of Relief of Right Ventricular Outflow Tract Obstruction Late After Repair of Congenital Heart Defects

Louise Coats; Sachin Khambadkone; Graham Derrick; Shankar Sridharan; Silvia Schievano; Bryan Mist; Rod Jones; John Deanfield; Denis Pellerin; Philipp Bonhoeffer; Andrew M. Taylor

Background— Right ventricular outflow tract obstruction (RVOTO) is a common problem after repair of congenital heart disease. Percutaneous pulmonary valve implantation (PPVI) can treat this condition without consequent pulmonary regurgitation or cardiopulmonary bypass. Our aim was to investigate the clinical and physiological response to relieving RVOTO. Methods and Results— We studied 18 patients who underwent PPVI for RVOTO (72% male, median age 20 years) from a total of 93 who had this procedure for various indications. All had a right ventricular outflow tract (RVOT) gradient >50 mm Hg on echocardiography without important pulmonary regurgitation (less than mild or regurgitant fraction <10% on magnetic resonance imaging [MRI]). Cardiopulmonary exercise testing, tissue Doppler echocardiography, and MRI were performed before and within 50 days of PPVI. PPVI reduced RVOT gradient (51.4 to 21.7 mm Hg, P<0.001) and right ventricular systolic pressure (72.8 to 47.3 mm Hg, P<0.001) at catheterization. Symptoms and aerobic (25.7 to 28.9 mL · kg−1 · min−1, P=0.002) and anaerobic (14.4 to 16.2 mL · kg−1 · min−1, P=0.002) exercise capacity improved. Myocardial systolic velocity improved acutely (tricuspid 4.8 to 5.3 cm/s, P=0.05; mitral 4.7 to 5.5 cm/s, P=0.01), whereas isovolumic acceleration was unchanged. The tricuspid annular velocity was not maintained on intermediate follow-up. Right ventricular end-diastolic volume (99.9 to 89.7 mL/m2, P<0.001) fell, whereas effective stroke volume (43.7 to 48.3 mL/m2, P=0.06) and ejection fraction (48.0% to 56.8%, P=0.01) increased. Left ventricular end-diastolic volume (72.5 to 77.4 mL/m2, P=0.145), stroke volume (45.3 to 50.6 mL/m2, P=0.02), and ejection fraction (62.6% to 65.8%, P=0.03) increased. Conclusions— PPVI relieves RVOTO, which leads to an early improvement in biventricular performance. Furthermore, it reduces symptoms and improves exercise tolerance. These findings have important implications for the management of this increasingly common condition.


Pediatric Radiology | 2007

Magnetic resonance imaging protocols for paediatric neuroradiology

Dawn E. Saunders; Clare Thompson; R Gunny; Rod Jones; Tim Cox; Wui Khean Chong

Increasingly, radiologists are encouraged to have protocols for all imaging studies and to include imaging guidelines in care pathways set up by the referring clinicians. This is particularly advantageous in MRI where magnet time is limited and a radiologist’s review of each patient’s images often results in additional sequences and longer scanning times without the advantage of improvement in diagnostic ability. The difficulties of imaging small children and the challenges presented to the radiologist as the brain develops are discussed. We present our protocols for imaging the brain and spine of children based on 20xa0years experience of paediatric neurological MRI. The protocols are adapted to suit children under the age of 2xa0years, small body parts and paediatric clinical scenarios.


British Journal of Radiology | 2016

Perinatal and paediatric post-mortem magnetic resonance imaging (PMMR): sequences and technique

Wendy Norman; Noorulhuda Jawad; Rod Jones; Andrew M. Taylor; Owen J. Arthurs

As post-mortem MRI (PMMR) becomes more widely used for investigation following perinatal and paediatric deaths, the best possible images should be acquired. In this article, we review the most widely used published PMMR sequences, together with outlining our acquisition protocol and sequence parameters for foetal, perinatal and paediatric PMMR. We give examples of both normal and abnormal appearances, so that the reader can understand the logic behind each acquisition step before interpretation, as a useful day-to-day reference guide to performing PMMR.


Journal of Biomechanics | 2016

Can finite element models of ballooning procedures yield mechanical response of the cardiovascular site to overexpansion

Giorgia M. Bosi; Benedetta Biffi; Giovanni Biglino; Valentina Lintas; Rod Jones; Spyros Tzamtzis; Gaetano Burriesci; Francesco Migliavacca; Sachin Khambadkone; Andrew M. Taylor; Silvia Schievano

Patient-specific numerical models could aid the decision-making process for percutaneous valve selection; in order to be fully informative, they should include patient-specific data of both anatomy and mechanics of the implantation site. This information can be derived from routine clinical imaging during the cardiac cycle, but data on the implantation site mechanical response to device expansion are not routinely available. We aim to derive the implantation site response to overexpansion by monitoring pressure/dimensional changes during balloon sizing procedures and by applying a reverse engineering approach using a validated computational balloon model. This study presents the proof of concept for such computational framework tested in-vitro. A finite element (FE) model of a PTS-X405 sizing balloon (NuMed, Inc., USA) was created and validated against bench tests carried out on an ad hoc experimental apparatus: first on the balloon alone to replicate free expansion; second on the inflation of the balloon in a rapid prototyped cylinder with material deemed suitable for replicating pulmonary arteries in order to validate balloon/implantation site interaction algorithm. Finally, the balloon was inflated inside a compliant rapid prototyped patient-specific right ventricular outflow tract to test the validity of the approach. The corresponding FE simulation was set up to iteratively infer the mechanical response of the anatomical model. The test in this simplified condition confirmed the feasibility of the proposed approach and the potential for this methodology to provide patient-specific information on mechanical response of the implantation site when overexpanded, ultimately for more realistic computational simulations in patient-specific settings.


Biomedical Engineering Online | 2016

Numerical model of a valvuloplasty balloon: in vitro validation in a rapid-prototyped phantom

Benedetta Biffi; Giorgia M. Bosi; Valentina Lintas; Rod Jones; Spyros Tzamtzis; Gaetano Burriesci; Francesco Migliavacca; Andrew M. Taylor; Silvia Schievano; Giovanni Biglino

BackgroundPatient-specific simulations can provide insight into the mechanics of cardiovascular procedures. Amongst cardiovascular devices, non-compliant balloons are used in several minimally invasive procedures, such as balloon aortic valvuloplasty. Although these balloons are often included in the computer simulations of these procedures, validation of the balloon behaviour is often lacking. We therefore aim to create and validate a computational model of a valvuloplasty balloon.MethodsA finite element (FE) model of a valvuloplasty balloon (Edwards 9350BC23) was designed, including balloon geometry and material properties from tensile testing. Young’s Modulus and distensibility of different rapid prototyping (RP) rubber-like materials were evaluated to identify the most suitable compound to reproduce the mechanical properties of calcified arteries in which such balloons are likely to be employed clinically. A cylindrical, simplified implantation site was 3D printed using the selected material and the balloon was inflated inside it. The FE model of balloon inflation alone and its interaction with the cylinder were validated by comparison with experimental Pressure–Volume (P–V) and diameter–Volume (d–V) curves.ResultsRoot mean square errors (RMSE) of pressure and diameter were RMSEPxa0=xa0161.98xa0mmHg (3.8xa0% of the maximum pressure) and RMSEdxa0=xa00.12xa0mm (<0.5xa0mm, within the acquisition system resolution) for the balloon alone, and RMSEPxa0=xa094.87xa0mmHg (1.9xa0% of the maximum pressure) and RMSEdxa0=xa00.49xa0mm for the balloon inflated inside the simplified implantation site, respectively.ConclusionsThis validated computational model could be used to virtually simulate more realistic valvuloplasty interventions.


Ultrasound in Obstetrics & Gynecology | 2006

Postmortem magnetic resonance imaging as an adjunct to the diagnosis of skeletal dysplasias: short‐rib polydactyly syndrome

Andrew M. Taylor; Rod Jones; Amaka C. Offiah; Øystein E. Olsen; Nj Sebire

1. Orioli IM, Castilla EE, Barbosa-Neto JG. The birth prevalence rates for the skeletal dysplasias. J Med Genet 1986; 23: 328–332. 2. Gorlin RJ, Cohen MM, Levin LS. Syndromes of the head and neck. Oxford: Oxford University Press: 1990; 158–227. 3. McKusick V. Online Mendelian Inheritance in Man. 2004. http://www.ncbi.nlm.nih.gov/ (Accessed February 2005). 4. Foster JW, Dominguez-Steglich MA, Guioli S, Kowk G, Weller PA, Stevanovic M, Weissenbach J, Mansour S, Young ID, Goodfellow PN. Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene. Nature 1994; 372: 525–530. 5. Parilla BV, Leeth EA, Kambich MP, Chilis P, MacGregor SN. Antenatal detection of skeletal dysplasias. J Ultrasound Med 2003; 22: 255–558; Quiz 259–261. 6. Tongsong T, Wanapirak C, Pongsatha S. Prenatal diagnosis of campomelic dysplasia. Ultrasound Obstet Gynecol 2000; 15: 428–430. 7. Krakow D, Williams J, 3rd, Poehl M, Rimoin DL, Platt LD. Use of three-dimensional ultrasound imaging in the diagnosis of prenatal-onset skeletal dysplasias. Ultrasound Obstet Gynecol 2003; 21: 467–472. 8. Ruano R, Molho M, Roume J, Ville Y. Prenatal diagnosis of fetal skeletal dysplasias by combining two-dimensional and three-dimensional ultrasound and intrauterine threedimensional helical computer tomography. Ultrasound Obstet Gynecol 2004; 24: 134–140. 9. Seow KM, Huang LW, Lin YH, Pan HS, Tsai YL, Hwang JL. Prenatal three-dimensional ultrasound diagnosis of a camptomelic dysplasia. Arch Gynecol Obstet 2004; 269: 142–144. 10. Garjian KV, Pretorius DH, Budorick NE, Cantrell CJ, Johnson DD, Nelson TR. Fetal skeletal dysplasia: three-dimensional US–initial experience. Radiology 2000; 214: 717–723.


Cardiology in The Young | 2006

Post-mortem magnetic resonance imaging provides the diagnosis following aortic rupture in an infant with treated aortic interruption.

Andrew M. Taylor; Rod Jones; Graham Derrick

In the United Kingdom, there has been a steady decline in the number of conventional autopsies performed in children. For cardiovascular disease, structural and not pathological considerations are often more important in defining the cause of death. Magnetic resonance imaging is now often used in the assessment of congenital cardiac malformations during life. In this case report, we demonstrate how post-mortem magnetic resonance imaging was able to establish the diagnosis of aortic rupture in a patient who had undergone surgical repair of aortic interruption. In this patient, the parents had declined conventional histopathological autopsy, but were happy to consent to magnetic resonance post-mortem assessment.


Journal of Cardiovascular Magnetic Resonance | 2011

Atrial septal defect: hemodynamic changes before and after closure assessed with magnetic resonance exercise imaging

Pia Schuler; Philipp Lurz; Vivek Muthurangu; Rod Jones; Andrew M. Taylor

ASDs are among the most common congenital cardiac anomalies seen in the adult population and closure leads to a significant improvement in cardiopulmonary function.


European Heart Journal | 2007

Physiological consequences of percutaneous pulmonary valve implantation: the different behaviour of volume- and pressure-overloaded ventricles

Louise Coats; Sachin Khambadkone; Graham Derrick; Marina Hughes; Rod Jones; Bryan Mist; Denis Pellerin; Jan Marek; John Deanfield; Philipp Bonhoeffer; Andrew M. Taylor


Clinical Radiology | 2016

Diagnostic accuracy of perinatal post-mortem MRI: single reporter experience

Clare Ashwin; Ciaran Hutchinson; Wendy Norman; Rod Jones; Nj Sebire; Owen J. Arthurs

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Andrew M. Taylor

Great Ormond Street Hospital

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Graham Derrick

Great Ormond Street Hospital

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Sachin Khambadkone

Great Ormond Street Hospital

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Bryan Mist

University College London

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Louise Coats

UCL Institute of Child Health

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Philipp Bonhoeffer

UCL Institute of Child Health

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Silvia Schievano

Great Ormond Street Hospital

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Benedetta Biffi

Great Ormond Street Hospital

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Denis Pellerin

Great Ormond Street Hospital

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