Recipient organisationKing's College LondonSource-published name: King's College London
Funding£243K
PeriodMay 2025 — May 2026
In plain English
AI plain-English summary
A Doppler ultrasound device now lets MRI scanners track a fetal heartbeat in real time, making it possible to capture sharp 3D movies of blood flow inside the unborn heart. Around 1% of babies are born with congenital heart disease, but current 2D ultrasound often misses the full 3D structure of complex defects. This means some newborns who need immediate surgery are not identified before birth, while others are wrongly flagged for urgent care. Fetal MRI could solve this, but the baby’s movements and a heart that beats three times faster than an adult’s have made it impractical. The team’s new approach combines a CE-marked Doppler gating device with their own motion-correction software to lock the MRI scans to each heartbeat, even as the fetus shifts. If successful, the technique will allow accurate 3D measurements of cardiac anatomy and blood flow in 300 fetal subjects. Clinicians could then diagnose severe congenital heart disease before birth with far greater confidence, ensuring babies who need surgery are delivered in the right hospital, and sparing families unnecessary worry and the NHS wasted resources. The tools will be designed to work with standard MRI scanners, so any centre with a fetal MRI programme could adopt them.
View original technical description
Congenital heart disease (CHD) affects approximately 1% of live births. Detection of CHD through routine fetal ultrasound screening continues to rise, however accurate identification of babies who require life-saving surgical intervention immediately after birth remains challenging for many complex cardiac anomalies. Prenatal diagnosis, reliant predominantly on 2D ultrasound, is often incomplete, even in expert hands, due to difficulties in visualising the 3D structure of the heart and vessels. Additionally, 2D Doppler ultrasound provides only a limited understanding of blood flow in fetal heart and vessels. In the postnatal life ultrasound limitations have been addressed by cardiac MRI, which provides 3D visualisation, volumetric and vascular flow measurements. Fetal MRI has seen a growing role in diagnosis of fetal anomalies, but it is susceptible to corruption by fetal motion and maternal breathing. To address this, we have developed motion corrected 3D MRI, by composing multiple fast 2D acquisitions into a consistent 3D volume for static structures. Imaging the beating fetal heart, however, presents additional challenges: not only does it beats three times faster than in adults, but until recently there was no practical method that could measure fetal heart rate during acquisition in real time. In our previous work we proposed motion-corrected 3D+time fetal cardiac MRI with the fetal heart rate estimated after acquisition directly from the imaging data, but this did not accurately capture beat-to-beat heart rate variation, resulting in errors which have so far prevented clinical adoption of these techniques. Recently, a CE-marked, MRI-compatible Doppler ultrasound gating device has become available. This device can accurately measure the fetal heart rate and provide an external gating signal directly to MRI scanner in real time. This recent technology provides new exciting opportunities for development of high temporal resolution imaging of the fetal heart. To date, due to lack of motion compensation, the Doppler gating has been limited mainly to 2D anatomy and flow imaging, which is still highly susceptible to fetal motion. In this project we propose to develop Doppler-gated motion-compensated 3D+time MRI of moving fetal cardiac anatomy and flow. This new technology will unlock opportunities for large clinical studies to enable accurate diagnosis, discovery of novel biomarkers and understanding of pathological in-utero development in different forms of CHD. We will close the current technological gap by combining new Doppler ultrasound gating device with our motion corrected fetal 3D MRI technique. Our preliminary results show that Doppler-gated 3D+time imaging of moving fetal cardiac anatomy is not only feasible and efficient, but also provides accurate measurements of fetal cardiac function superior to image-gated 3D+time MRI. We now intend to further develop this technique to generate motion corrected Doppler-gated 3D+time flow and evaluate 3D+time anatomical and flow imaging on a large dataset of 300 fetal subjects. We aim to develop a practical vendor independent acquisition and software tools for accurate volumetric measurements of fetal heart function, based on Doppler-gated “off-the-shelf” MRI sequences that can be easily deployed in any centre with an existing fetal MRI programme. The proposed technology has potential to improve clinical management of fetuses with suspicion of severe forms of CHD, by ensuring that babies who require urgent postnatal surgery are more accurately diagnosed before birth. Additionally, confident exclusion of severe lesions will reduce pressure on NHS resources and the emotional burden on affected families.
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