MA Thesis: Deep Learning based detection model of the temporal and axillary artery in suspected giant cell arteritis in ultrasound images -- Not available

Abstract. Giant cell arteritis (GCA) is a systemic autoimmune disease marked by inflammation of blood vessels (“vasculitis”) that can cause impairment and damage to organs [1]. GCA typically affects large and medium size arteries, such as the aorta and the temporal and axillary arteries [2–4]. It is considered the most common form of systemic vasculitis in adults [5–8], older than 50 years, in Europe [5,9,10] and the USA. Every week, we diagnose one to two new patients with GCA in our department. A diagnosis of GCA must be made as soon as possible through ultrasound verification or falsification as it is a severe rheumatologic and ophthalmologic emergency that can cause permanent vision loss in up to 50% of patients [11,12]. One way to early diagnose GCA is by observing whether hypoechoic wall thickening of the superficial temporal artery is present and measurable in Ultrasound (US) imaging (Fig.1). US devices are widely available and easily accessible because they are noninvasive, patient-friendly, and cost-effective [13]. Moreover, they offer a superior image resolution of less than 0.1mm when used in modern transducers [14]. Although the US can be used to detect GCA [15], expertise in the interpretation of the resulting images is still lacking, and ultrasound specialists are not readily available for the GCA diagnosis.

Aim. To this end, we aim to develop a deep learning-based model which detects the temporal and axillary artery wall thickening in suspected GCA in US images, basically classifying the images whether abnormal or not. Such a model would have an impact on the throughput and precision of the US diagnosis of GCA.

Research Questions:

• Would unsupervised learning, e.g, anomaly detection models, deliver acceptable performance compared to the supervised models, trained on a few amount of annotated data, which is prone to overfitting?

• Do the results of the off-the-shelves Interpretability tools; e.g., uncertainty quantification, and visualization methods, e.g., class activation maps (CAMs), correlate with the findings/annotations reported by the US specialists?

Dataset:

• We expect to deliver an amount of 1000 GCA ultrasound images of the temporal artery and 1000 GCA-negative ultrasound images of healthy individuals at a minimum. Starting from an already pre-existing stock of hundreds (> 500 patients) of ultrasound images on GCA and healthy controls and being equipped with three high-end ultrasound machines (GE Logiq S8 and E10) at our site and five to ten ultrasound examinations on patients suspected of having GCA alone each week will help the fulfillment of our goal. In addition, US images would also be retrievable from an international GCA expert group we are part of (the “OMERACT ultrasound subgroup on large vessel vasculitis”). Saving videos instead of just motionless images during future artery ultrasound examinations at our site would generate additional “leverage”, by allowing for later video footage decomposition into single ‘frames per second’ (thereby yielding up to 30 images per second from an ultrasound video), aside from commonly used data augmentation techniques.

Roadmap:

• Familiarize yourself with the current literature [15-20]
• Build the baseline supervised model and develop the anomaly detection model.
• Run the necessary comparisons.
• Equip the models with the Monte-Carlo Dropout [21] for uncertainty estimation.
• Equip the models with the visualization methods, e.g., INNvitstigate [22-23]
• Run extensive experiments and analysis
• Write up your thesis

Requirements:

• Solid background in Machine/Deep Learning
• Familiar with discriminative deep learning models and SOTA architectures
• Sufficient knowledge of Python programming language and libraries (Scikit-learn)
• Experience with a mainstream deep learning framework such as PyTorch.
• Machine/Deep learning hands-on experience

References:

Interested, please contact Prof. Dr. Shadi Albarqouni