- Workshop presentation
- Open Access
Flow-sensitive four-dimensional magnetic resonance imaging facilitates the quantitative analysis of systemic-to-pulmonary collateral flow in patients with univentricular hearts
© Nordmeyer et al; licensee BioMed Central Ltd. 2012
Published: 1 February 2012
Systemic-to-pulmonary collateral flow (SPCF) may constitute a risk factor for increased morbidity and mortality in patients with single-ventricle physiology (SV). However, clinical research is limited by the complexity of multi-site two-dimensional (2D) cardiovascular magnetic resonance (CMR) flow assessment. We sought to validate four-dimensional flow (4D-flow) for concise quantification of SPCF in patients with SV.
29 patients with SV physiology prospectively underwent CMR (1.5T) to quantify SPCF (n=14 bidirectional cavopulmonary connection [BCPC], age 2.9±1.3 years; and n=15 Fontan, 14.4±5.9 years) and 20 healthy volunteers (age, 28.7±13.1 years) served as controls. Five 2D-flow measurements (ascending aorta, superior/inferior caval veins, right/left pulmonary arteries) were performed and SPCF (=aortic minus caval flows) was calculated and compared with 4D-flow measurements and calculations. Additionally, 4D-flow measurements were used to calculate SPCF as pulmonary venous minus pulmonary arterial flow.
The comparison between 4D-flow and 2D-flow showed good Bland-Altman agreement for all individual vessels (mean bias, 0.05±0.24 l/min/m2), calculated SPCF (-0.02±0.18 l/min/m2), low intra and inter-observer variance (ICC>0.95[0.91-0.97]) and significantly shorter 4D-flow acquisition-time (12:34min/17:28min,p<0.01). 4D-flow in patients versus controls revealed (1) good agreement between systemic versus pulmonary estimator for SPFC; (2) significant SPCF in patients (BCPC 0.79±0.45 l/min/m2; Fontan 0.62±0.82 l/min/m2) and not in controls (0.01+0.16 l/min/m2) and (3) inverse relation of right/left pulmonary artery perfusion and right/left SPCF (Pearson=-0.47,p=0.01).
4D-flow is reliable, operator-independent and more time-efficient than 2D-flow to quantify SPCF. There is considerable SPCF in BCPC and Fontan patients. SPCF was more pronounced towards the respective lung with less pulmonary arterial flow suggesting more collateral flow where less anterograde branch pulmonary artery perfusion.
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