Ashifa Hudani1, David Patton 2, James A White3, Steven Greenway2, and Julio Garcia3
1University of Calgary, Calgary, AB, Canada, 2Alberta Children's Hospital Research Institute, Calgary, AB, Canada, 3Libin Cardiovascular Institute, Calgary, AB, Canada
Synopsis
Tetralogy of Fallot (TOF) occurs
in 1 in 3,500 births and is the most common cyanotic congenital heart defect.
Patients with repaired TOF (rTOF) require constant monitoring to prevent
life-threatening adverse effects. Hence, this study used 4D Flow MRI to assess
pulmonary flow hemodynamics in patients with rTOF. All hemodynamic parameters
calculated along the main pulmonary were shown to be higher in patients
compared to controls.
Background
Tetralogy of Fallot
(TOF) is the most common form of cyanotic (“blue baby”) Congenital Heart
Disease (CHD), occurring in 4 of every 10,000 live births and accounts for ~10%
of all CHD1. Current surgical techniques allow patients with TOF to survive
until adulthood1. However, these patients require multiple repeat surgeries and
procedures over their lifetime but the hemodynamic factors contributing to the
optimal quality of life and outcomes are understudied and poorly understood2. Hence, the objective of this study was to use 4D Flow MRI
to assess pulmonary flow hemodynamics in patients with repaired TOF (rTOF) to
better identify and characterize altered hemodynamic patterns to assist with
future interventions. We hypothesize patients with rTOF and those with main
pulmonary artery (mPA) dilation will have higher Peak Velocity (PV), Wall Shear
Stress (WSS), Energy Loss (EL), and Pressure drop as compared to non-dilated
and controls. Methods
A total of 17
rTOF patients (29 ± 9 years, 35% women) and 20 controls (36 ± 12 years, 25% women) were
enrolled in this study. Both controls and patients underwent standard cardiac
MRI followed by 4D Flow MRI acquisition. 4D Flow MRI acquisition
parameters included the following: temporal resolution 44.0-48.0 ms, spatial
resolution 2.5-3.9×2.0–3.1×3.0–3.5 mm3, echo time = 2.85-3.24 ms, flip
angle = 15°, Venc = 150-450 cm/s, matrix 130-160×110–160, pulse repetition time
= 5.50-6.00 ms, bandwidth 490 pixel/MHz, FOV 240-400×320–400 mm2, and time frames per cardiac cycle = 12-20. Figure 1 demonstrates the workflow
of the analysis that was performed using CVI42 (Circle Cardiovascular Imaging, Calgary,
AB, Canada). First, the main pulmonary artery along with the left and right
bifurcations were segmented. Followed by placing analysis planes perpendicular
to the flow of interest. Flow visualization and quantitative
flow analysis was performed at each plane shown in Figure 1 as well. Hemodynamic
parameters that were calculated included PV, WSS, EL, and Pressure drop3. Diameters of the mPA for both cohorts were calculated using RadiAnt DICOM
Viewer (Medixant, Poznan, Poland). This data was
compared to a standard mPA diameter of 25.7 mm and both cohorts were categorized into two groups including dilated mPA diameters and non-dilated mPA diameters4. Statistics on the data collected were calculated using SPSS (IBM,
Chicago, IL). First, an independent-samples t-test was used to compare the
hemodynamic parameter along with identifying significant differences between
controls and patients. Values of p < 0.05 were considered significant. This was followed by computing the Pearson correlation for each hemodynamic parameter along the mPA and mPA diameter. Values of p < 0.01
were considered significant.Results
The hemodynamic parameters that were calculated in
this study at the mid-pulmonary were shown to be higher in patients compared to controls (p<0.05)
as shown in Table 1. However, the correlation between the mPA diameter and abnormal
hemodynamics present along the mPA in patients with rTOF was not shown to be statistically significant
as shown in Table 2. Maximum pressure along the mPA was shown to be highly
correlated with pulmonary diameter in patients with rTOF (R = 0.443, P = 0.0075) as demonstrated in
Table 2. While average WSS along the mPA was shown to be negatively correlated
with pulmonary diameter in patients (R = -0.119, P = 0.650) as seen in Table 2 as well. Lastly, patients demonstrated a higher mPA diameter compared
to controls (Average Mean = 34.11mm vs. Average Mean = 23.95 mm, p<0.05). Conclusion
In conclusion, this
study unveiled abnormal pulmonary blood flow in patients with rTOF demonstrating increased PV, WSS,
EL, and Pressure drop along the mPA. However, a high correlation was not
observed between the diameter of the mPA and pulmonary hemodynamic parameters observed in patients with rTOF. This may be due to the small sample size available along with mild
to moderate cases of obstruction along the right ventricular outflow tract demonstrated
in the patient cohort. Future studies will focus on collecting more data as
well as assessing the hemodynamic parameters present in the right ventricle. Acknowledgements
No acknowledgement found.References
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