Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Carla Favoccia"'
Publikováno v:
Italian Journal of Medicine, Vol 12, Iss 3 (2018)
Pulmonary hypertension (PH) is a hemodynamic and pathophysiological condition defined as an increase in mean pulmonary arterial pressure of 25 mmHg or more at rest assessed by right heart catheterisation. It is a progressive disease characterized by
Externí odkaz:
https://doaj.org/article/6c1897310434429cad321aac3243ba2e
Autor:
Massimo Stefano Silvetti, Carla Favoccia, Fabio Anselmo Saputo, Ilaria Tamburri, Chiara Mizzon, Marta Campisi, Fabrizio Gimigliano, Gabriele Rinelli, Lucilla Rava, Fabrizio Drago
Publikováno v:
EP Europace. 25:1482-1490
Aims In congenitally corrected transposition of the great arteries (CCTGA) the right ventricle (RV) is systemic. Atrioventricular block (AVB) and systolic dysfunction are frequently observed. Permanent pacing of the subpulmonary left ventricle (LV) m
Autor:
Carla Favoccia, Neerod Kumar Jha, Magdi Tofeig, Massimo Chessa, Mohammad Daud Khan, Andreas Eicken, Gianfranco Butera, José Diogo Ferreira Martins, Luis Fernandez Gonzalez, Fátima Pinto, Mario Carminati
Publikováno v:
EuroIntervention. 16:e1274-e1280
AIMS Aortic arch atresia (AAA) is one of the rarest obstructive defects. The presence of this anomaly in adult age is uncommon. The typical anatomic feature consists of a complete occlusion of the membranous obstruction resulting in an acquired atres
Publikováno v:
Journal of Congenital Cardiology, Vol 4, Iss S1, Pp 1-9 (2020)
Pulmonary hypertension is not uncommon in adult patients with congenital heart disease and can significantly affect their exercise capacity, quality of life and prognosis. Timely identification and management of pulmonary hypertension in these patien
Publikováno v:
Progress in Pediatric Cardiology. 51:62-66
Transition, the planned passage of adolescents and young adults with chronic disease from paediatric to adult care, has a significant role in preparing individuals to take charge over their health and lives as adults. Transition is a process that spa
Publikováno v:
Journal of Congenital Cardiology, Vol 4, Iss S1, Pp 1-4 (2020)
Background An increasing number of patients with previously repaired congenital heart disease (CHD) present with pulmonary arterial hypertension (PAH). This can occur immediately after repair (residual PAH) or years later. Case presentation We presen
Autor:
Laura C. Price, Stephen J. Wort, Colm McCabe, Carla Favoccia, Carl Harries, Iain Armstrong, Janelle Yorke, Konstantinos Dimopoulos, Aleksander Kempny
Publikováno v:
European Journal of Preventive Cardiology. 26:1338-1340
Publikováno v:
Expert review of cardiovascular therapy. 17(6)
Introduction: Eisenmenger syndrome (ES) is the most advanced form of pulmonary arterial hypertension (PAH) in patients with congenital heart disease (CHD). It is characterised by a severe rise in pulmonary vascular resistance resulting in shunt rever
Autor:
Alexander Kempny, Laura C. Price, Stephen J. Wort, Kostantinos Dimopoulos, Carla Favoccia, Colm McCabe
Publikováno v:
Pulmonary hypertension.
Background: Pulmonary Hypertension (PH) is associated with significant morbidity and mortality, greatly affecting patients’ quality of life (QoL). The emPHasis-10 (E10) questionnaire has recently been proposed as a short yet effective means of rout
Publikováno v:
Italian Journal of Medicine, Vol 12, Iss 3 (2018)
Pulmonary hypertension (PH) is a hemodynamic and pathophysiological condition defined as an increase in mean pulmonary arterial pressure of 25 mmHg or more at rest assessed by right heart catheterisation. It is a progressive disease characterized by