Society for Cardiovascular Magnetic Resonance/European Society of Cardiovascular Imaging/American Society of Echocardiography/Society for Pediatric Radiology/North American Society for Cardiovascular Imaging Guidelines for the Use of Cardiac Magnetic Resonance in Pediatric Congenital and Acquired Heart Disease: Endorsed by The American Heart Association

Vaiyani, Danish; Anwar, Shaftkat; Broberg, Craig S.; Browne, Lorna P.; Chung, Taylor; Johnson, Tiffanie R.; Muthurangu, Vivek; Taylor, Michael D.; Valsangiacomo-Buechel, Emanuela; Wilhelm, Carolyn

doi:10.1161/circimaging.122.014415

Cited by 20 publications

(18 citation statements)

References 623 publications

(977 reference statements)

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“…The adults who have a late diagnosis may add the potential for the coexistence of ischemic heart disease related to atherosclerosis, and they must be evaluated by invasive coronary angiography. A complete picture of the patient evolution up to that age can be provided by adding angioMRI for all patients, including children [ 23 , 24 , 25 ].…”

Section: Discussionmentioning

confidence: 99%

Challenging Diagnosis of Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery

et al. 2022

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Anomalous origin of the right coronary artery (RCA) from the pulmonary artery, ARCAPA, is an extremely rare congenital heart disease. Only 200 cases were reported from 1885 to the present. Patients diagnosed with ARCAPA can be either asymptomatic or can experience symptoms, such as heart murmur, dyspnea, or angina, shortly after birth or around 40–60 years of life. Usually, those with isolated ARCAPA are diagnosed later in life compared to those who associate other structural cardiac defects. We report two cases of anomalous origin of the right coronary artery at the level of the pulmonary artery trunk (ARCAPA) that were diagnosed by invasive coronary angiography. Although asymptomatic, general recommendations suggest an early corrective intervention to prevent complications such as myocardial ischemia and cardiac dysfunction, which can lead to sudden cardiac death.

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Section: Discussionmentioning

confidence: 99%

Challenging Diagnosis of Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery

et al. 2022

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“…Since this first description, the technique has been extensively modified to lead to the contemporary TCPC [ 62 ]. These technical evolutions reflect parallel improvements in the understanding of univentricular heart circulation, and cardiovascular imaging plays a role in this sense [ 63 ].…”

Section: Discussionmentioning

confidence: 99%

Role of Cardiovascular Imaging in the Follow-Up of Patients with Fontan Circulation

et al. 2022

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Since its first description in 1971, the Fontan procedure and its modifications have led to a substantial improvement in the survival rates of patients with a variety of types of complex Congenital Heart Disease (CHD) characterised by the presence of a single, dominant ventricle. However, despite the significant improvement of the prognosis over the years, Fontan patients are still exposed to several cardiovascular and systemic complications. It is, therefore, important to fully understand the pitfalls hidden behind a Fontan anatomy and the potential predictors of ventricular failure. Cardiovascular imaging plays a key role in this context, allowing for the early identification of complications with important prognostic implications. Echocardiography remains the first-line imaging modality for serial evaluation of Fontan patients. However, there is a growing role of cardiovascular magnetic resonance and cardiac computed tomography from pre-operative assessment to longitudinal follow-up. The aim of this paper will be to provide a comprehensive overview of the role, strengths, and weaknesses of each imaging modality in the assessment of congenital cardiac conditions palliated with the Fontan procedure.

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“…The anatomy and function of the RV with CMR can be obtained using balanced SSFP cine images in four-chamber, RV two-chamber and short axis views [ 34 ]. Another possible acquisition is performed via imaging in the axial plane of multiple axially rotated long-axis slices.…”

Section: Role Of Cardiac Magnetic Resonance In Pulmonary Stenosis And...mentioning

confidence: 99%

Multimodality Imaging of the Neglected Valve: Role of Echocardiography, Cardiac Magnetic Resonance and Cardiac Computed Tomography in Pulmonary Stenosis and Regurgitation

Costantini

Perone²,

Siani³

et al. 2022

J. Imaging

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The pulmonary valve (PV) is the least imaged among the heart valves. However, pulmonary regurgitation (PR) and pulmonary stenosis (PS) can occur in a variety of patients ranging from fetuses, newborns (e.g., tetralogy of Fallot) to adults (e.g., endocarditis, carcinoid syndrome, complications of operated tetralogy of Fallot). Due to their complexity, PR and PS are studied using multimodality imaging to assess their mechanism, severity, and hemodynamic consequences. Multimodality imaging is crucial to plan the correct management and to follow up patients with pulmonary valvulopathy. Echocardiography remains the first line methodology to assess patients with PR and PS, but the information obtained with this technique are often integrated with cardiac magnetic resonance (CMR) and computed tomography (CT). This state-of-the-art review aims to provide an updated overview of the usefulness, strengths, and limits of multimodality imaging in patients with PR and PS.

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Cited by 20 publications

References 623 publications

Challenging Diagnosis of Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery

Challenging Diagnosis of Anomalous Origin of the Right Coronary Artery from the Pulmonary Artery

Role of Cardiovascular Imaging in the Follow-Up of Patients with Fontan Circulation

Multimodality Imaging of the Neglected Valve: Role of Echocardiography, Cardiac Magnetic Resonance and Cardiac Computed Tomography in Pulmonary Stenosis and Regurgitation

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