| Literature DB >> 22347958 |
Bjoern Stinn, Paul Stolzmann, Juergen Fornaro, Dennis Hibbeln, Hatem Alkadhi, Simon Wildermuth, Sebastian Leschka.
Abstract
Cardiac magnetic resonance imaging and echocardiography are often the primary imaging techniques for many patients with congenital heart disease (CHD). However, with modern generations of CT systems and recent advances in temporal and spatial resolution, cardiac CT has been gaining an increasing reputation in the field of cardiac imaging and in the evaluation of patients with congenital heart disease. The CT imaging protocol depends on the suspected cardiac defect, the type of previous surgical repair, and the patient's age and level of cooperation. Various strategies are available for reducing radiation exposure, which is of utmost importance particularly in paediatric patients. A sequential segmental analysis is a commonly used approach to analysing congenital heart defects. Familiarity of the performing radiologist with dedicated CT protocols, the complex anatomy, morphology and terminology of CHD, as well as with the surgical procedures used to correct congenital abnormalities is a prerequisite for correct diagnosis.Entities:
Year: 2011 PMID: 22347958 PMCID: PMC3259356 DOI: 10.1007/s13244-011-0088-1
Source DB: PubMed Journal: Insights Imaging ISSN: 1869-4101
Recommended imaging range and ECG synchronisation depending on the congenital heart disease type
| Congenital heart disease type | Imaging range | ECG synchronisation required? | Comment |
|---|---|---|---|
| Aortic coarctation | Aortic arch to diaphragm | No | Thin collimation is recommended for identification of collateral pathways |
| Anomalous pulmonary venous return | Aortic arch to diaphragm | No | Imaging range should be extended to the level of the kidneys in the infracardiac type |
| Patent ductus arteriosus | Aortic arch to diaphragm | No | Thin collimation is recommended for identification of small ductus arteriosus |
| Persistent superior left vena cava | Aortic arch to diaphragm | No | — |
| Atrial septal defect | Below tracheal bifurcation to diaphragm | Yes | ECG synchronisation may be beneficial for small intracardiac shunts |
| Ventricular septal defect | Below tracheal bifurcation to diaphragm | Yes | ECG synchronisation may be beneficial for small intracardiac shunts |
| Tetralogy of Fallot | Above the pulmonary bifurcation to diaphragm | No | — |
| Common aortic-pulmonary trunk | Above the pulmonary bifurcation to diaphragm | No | — |
| Transposition of the great arteries | Above the pulmonary bifurcation to diaphragm | No | — |
| Univentricular heart | Below tracheal bifurcation to diaphragm | No | No saline chasing bolus should be used to avoid wash-out |
| Double outlet ventricle | Above pulmonary bifurcation to diaphragm | No | No saline chasing bolus should be used to avoid wash-out |
| Isomerism | Below tracheal bifurcation to diaphragm | Yes | ECG synchronisation is recommended for morphological identification of the atrial appendages to determine sideness; the imaging range must include the thorax and spleen for identification of extracardiac abnormalities |
| Coronary artery anomaly | Below tracheal bifurcation to diaphragm | Yes | Thin collimation and ECG synchronisation are mandatory |
Relevant CT parameters for imaging patients with congenital heart disease using a dual-source CT system
| Paediatric patients | Adult patients | |
|---|---|---|
| Slice collimation | Thin collimation: 2 × 64 × 0.6 mm | |
| Thick collimation: 2 × 24 × 1.2 mm | ||
| Tube voltage / tube current | <20 kg: 80 kVp/50 mAs | BMI ≤25 kg/m2: 100 kVp/150 mAs |
| 20–30 kg: 80 kVp/80 mAs | (ECG-synchronised: 100 kVp/220 mAs) | |
| 30–50 kg: 80 kVp/150 mAs | BMI >25 kg/m2: 120 kVp/180 mAs | |
| 50–60 kg: 80 kVp/250 mAs | (ECG-synchronised: 120 kVp/330 mAs) | |
| Gantry rotation time | 330 ms | |
| Pitch | 1 (non-ECG-synchronised CT) | |
| 0.2–0.5 (retrospective ECG-gated CT; pitch depending on the heart rate) | ||
Fig. 1Non-ECG-synchronised CT in a 24-year-old man demonstrating a large atrial septal defect (arrow)
Fig. 2Retrospective ECG-gated CT in a 14-year-old girl in a transverse (a) and short-axis reconstruction (b) performed for follow-up evaluation after surgical correction of a tetralogy of Fallot. The patch completely closes the ventricular septal defect (arrow). Note the overriding position of the aorta and the right ventricular hypertrophy
Fig. 3a–cProspective ECG-gated CT in a 20-year-old man. Transverse sections at the level of the pulmonary trunk (a), the origin of the coronary arteries (arrows in b) and the ventricles (c) demonstrate levo-transposition of the great arteries. The aorta (Ao) and the pulmonary trunk (PT) are transposed with the aorta anterior and to the left of the pulmonary artery. Note the superior cava vein draining into the left-sided atrium (arrow) and the pulmonary veins draining into the right-sided atrium (arrowheads)
Examples of descriptions of common congenital heart disease in the segmental sequential nomenclature
| CHD type | Sequential segmental analysis |
|---|---|
| Ventricular septal defect | Normal atrial arrangement, concordant atrioventricular and ventriculo-arterial connections, levocardia |
| + VSD | |
| Aortic coarctation | Normal atrial arrangement, concordant atrioventricular and ventriculo-arterial connections, levocardia |
| + Aortic coarctation | |
| Tetralogy of Fallot | Normal atrial arrangement, concordant atrioventricular and ventriculo-arterial connections, levocardia |
| + VSD with pulmonary stenosis, overriding aorta, right ventricular hypertrophy | |
| Transposition of the great arteries with associated VSD | Normal atrial arrangement, concordant atrioventricular and discordant ventriculo-arterial connections, levocardia |
| + VSD | |
| Congenitally corrected transposition of the great arteries | Normal atrial arrangement, discordant atrioventricular and discordant ventriculo-arterial connections, levocardia |
| Double-outlet right ventricle | Normal atrial arrangement, concordant atrioventricular and double-outlet ventriculo-arterial connections from the right ventricle, levocardia |
| + VSD | |
| Left isomerism | Ambiguous atrial arrangement, ambiguous atrioventricular and ambiguous ventriculo-arterial connections, levocardia |
| + Bilateral bilobed lungs with hyparterial bronchus on both sides, polysplenia, interrupted inferior vena cava with azygos continuation |
VSD Ventricular septal defect