IRM cardiaque dans le suivi des cardiopathies congénitales à l'âge adulte [Cardiac MRI in the follow-up of adult congenital cardiomyopathy patients].


Autoria(s): Monney P.; Stalder N.; Clair M.; Vogt P.; Schwitter J.; Meijboom E.J.; Bouchardy J.
Data(s)

2011

Resumo

Magnetic resonance imaging is a rapidly developing modality in cardiology. It offers an excellent image definition and a large field of view, allowing a more accurate morphological assessment of cardiac malformations. Due to its unique versatility and its ability to provide myocardial tissue characterization, cardiac magnetic resonance (CMR) is now recognized as a central imaging modality for a wide range of congenital heart diseases, including assessment of post-surgical cardiac anatomy, quantification of valvular disease and detection of myocardial ischemia. CMR provides useful diagnostic information without any radiation exposure, and improves the global management of patients with congenital heart disease.

Identificador

http://serval.unil.ch/?id=serval:BIB_1AF5DAE4D485

isbn:1660-9379 (Print)

pmid:21717692

Idioma(s)

fr

Fonte

Revue Médicale Suisse, vol. 7, no. 297, pp. 1194-1199

Palavras-Chave #Adolescent; Adult; Coronary Vessel Anomalies/diagnosis; Female; Follow-Up Studies; Heart Defects, Congenital/diagnosis; Heart Defects, Congenital/surgery; Humans; Loeys-Dietz Syndrome/diagnosis; Magnetic Resonance Imaging; Male; Middle Aged; Predictive Value of Tests; Reproducibility of Results; Risk Assessment; Sensitivity and Specificity; Tetralogy of Fallot/diagnosis; Transposition of Great Vessels/diagnosis
Tipo

info:eu-repo/semantics/review

article