MED-PHCVIVDec 5, 2024

Multi-dynamic deep image prior for cardiac MRI

arXiv:2412.04639v26 citationsh-index: 5Magn Reson Med
Originality Incremental advance
AI Analysis

This work addresses the need for improved diagnostic imaging in cardiac MRI for patients with breathing difficulties, offering an unsupervised method that does not require external training data, though it appears incremental as it builds on prior DIP-based approaches.

The paper tackled the problem of high-quality cardiac MRI reconstruction in free-breathing conditions, which is challenging for patients with arrhythmias or limited breath-holding capacity, by introducing the Multi-Dynamic Deep Image Prior (M-DIP) framework. It achieved better image quality metrics on phantom data and higher reader scores on in-vivo cine and LGE data compared to state-of-the-art methods.

Cardiovascular magnetic resonance imaging is a powerful diagnostic tool for assessing cardiac structure and function. However, traditional breath-held imaging protocols pose challenges for patients with arrhythmias or limited breath-holding capacity. This work aims to overcome these limitations by developing a reconstruction framework that enables high-quality imaging in free-breathing conditions for various dynamic cardiac MRI protocols. Multi-Dynamic Deep Image Prior (M-DIP), a novel unsupervised reconstruction framework for accelerated real-time cardiac MRI, is introduced. To capture contrast or content variation, M-DIP first employs a spatial dictionary to synthesize a time-dependent intermediate image. Then, this intermediate image is further refined using time-dependent deformation fields that model cardiac and respiratory motion. Unlike prior DIP-based methods, M-DIP simultaneously captures physiological motion and frame-to-frame content variations, making it applicable to a wide range of dynamic applications. We validate M-DIP using simulated MRXCAT cine phantom data as well as free-breathing real-time cine, single-shot late gadolinium enhancement (LGE), and first-pass perfusion data from clinical patients. Comparative analyses against state-of-the-art supervised and unsupervised approaches demonstrate M-DIP's performance and versatility. M-DIP achieved better image quality metrics on phantom data, higher reader scores on in-vivo cine and LGE data, and comparable scores on in-vivo perfusion data relative to another DIP-based approach. M-DIP enables high-quality reconstructions of real-time free-breathing cardiac MRI without requiring external training data. Its ability to model physiological motion and content variations makes it a promising approach for various dynamic imaging applications.

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