Minseong Kwon1, Juyeon Lee2, Sungho Park3,4, and Hyungkyu Huh1
1Medical Device Development Center, Daegu-Gyeongbuk Medical Innovation Foundation, Daegu, Korea, Republic of, 2Ulsan university, Ulsan, Korea, Republic of, 3Department of Radiology, Children's Hospital Colorado, University-Campus, Aurora, CO, United States, 4Institute of Medical Devices, Kangwon National University, Chuncheon, Korea, Republic of
Synopsis
Keywords: Flow, Cardiovascular
Motivation: Mitral valve regurgitation (MVR) is the most common heart valve diseases, but accurate quantification of MVR has been limited due to the dynamic motion of valves.
Goal(s): We hypothesize that volumetric flow information by 4D flow MRI with the compensation of MV motion could address this challenge.
Approach: MVR was measured using a simulated-in vitro model by comparing with actual flow from pump, ultrasound, and 4D flow MRI with/without a mitral registration algorithm.
Results: PISA method overestimated MVR. 4D flow MRI without algorithm seems to have similar the amount of actual MVR, while it decreased with employing algorithm.
Impact: Accurate quantification of regurgitation
plays an important role for diagnosing patients with valvular diseases. This
study would have a chance to measure accurate MVR quantification and quantify complex
intracardiac blood flow using 4D flow MRI.
Introduction
Mitral valve regurgitation (MVR),
generating backflow from left ventricle (LV) to left atrium (LA) by MV
dysfunction, has been closely associated with various cardiovascular complications
such as ventricular fibrillation and heart failure1. Thus, early diagnosis plays
an important role to determine severity of diseases and treatment timing. Many
studies have investigated non-invasive diagnostic techniques such as ultrasound
and magnetic resonance imaging (MRI) to diagnose MVR2,3. In addition, time-resolved
three-dimensional phase-contrast MRI (4D flow MRI) technique has emerged as a
promising tool to obtain volumetric intracardiac flow information, which
enables accurate quantification for complex blood flow4. However, the static placement
of measurement planes during 4D flow MRI analysis is not capable of precisely quantifying
flow when accompanied by dynamic motions of MV5. Our overarching hypothesis is that tracking
dynamic MV motion would potentially compensate flow quantification compared
with fixed-plane quantification method. Thus, this study aims to investigate the
performance of MVR assessment using an in-house pulsatile pump with a given
actual flow, gold-standard ultrasound measurement, and 4D flow MRI with/without
a motion correction algorithm through a MVR-simulated in vitro phantom model. Methods
MVR-simulated in vitro phantom model,
composing of artificial LV and LA, was fabricated to compare the performance of
MVR assessment by both ultrasound and 4D flow MRI (Fig.1a,b). A silicon
partition with a tiny hole was placed at the center of the model to replicate
MVR.
Valve annulus tracking (VAT) algorithm was
developed using cardiac MR (CMR) images of a porcine model (Fig. 1c). Spatial
orientation and resolution of 4D flow MRI and CMR data were matched in
2-chamber and 4-chamber views. MV plane was extracted from three points, and time-sequential
MV planes were obtained at each cardiac cycle.
4D flow MRI images were acquired using a 3T
clinical MR scanner (Skyra, Siemens AG, Munich, Germany). Potential actual MVR
flow (Qpump) was summarized in Table 1. MVR by ultrasound was quantified
using the Proximal Isovelocity Surface Area (PISA) method, while fixed plane
and VAT-corrected MVR quantification by 4D flow MRI was also performed using
maximum flow rate and time-dependent flow rate, respectively (Fig. 1d). Result
Fixed plane 4D
flow MRI had consistent MVR flow over time, while VAT-4D flow MRI is capable of
changing MVR over time (Fig. 3). However, we observed that systematic underestimation
of MVR quantification by 4D flow MRI with both fixed plane and VAT methods,
while the PISA method overestimate MVR quantification (Table 1). This is mainly
attributed to the differences in velocity measurement: Fixed plane 4D flow MRI –
peak jet velocity, VAT 4D flow MRI – time-dependent flow, ultrasound – maximum
velocity (Fig 4).Discussion
We have
successfully developed the in vitro analysis platform compatible with both
ultrasound and MRI, enabling MVR assessment. However, we observed a discrepancy
in the MVR flow measured by the VAT-4D flow MRI, which theoretically should
provide precise measurements, compared to Qpump. We speculate that
there might be two potential challenges: (1) underestimation of velocity due to
the limitations of the MRI system's low spatiotemporal resolution and (2) flow
resistance along an extended tube length, resulting in a lower inlet flow within
the tube compared to the actual flow generated by the pump. A detailed
examination is required for an accurate assessment of MVR and different
scenarios of mitral valve dysfunction will be further investigated.Conclusion
The fixed
plane and VAT plane 4D flow MRI showed that MVR was underestimated, but most
similar to the actual value in the fixed plane and was overestimated in PISA.Acknowledgements
This research was
supported by National Research Foundation of Korea (NRF) grant funded by the
Korea government (MSIP) (NRF-2021R1C1C1003481)References
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