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OP0061 (2020)
FEASIBILITY STUDY ON AN AUTOMATED QUANTITATIVE SYSTEM FOR ULTRASOUND JOINT INFLAMMATION ASSESSMENT IN RHEUMATOID ARTHRITIS USING DEEP LEARNING
Y. K. Tan1, S. Suriyanto2, P. H. Yeung3, S. Xu4,5
1Department of Rheumatology and Immunology, Singapore General Hospital, Singapore, Singapore
2Diagnostics Development Hub, Accelerate Technologies, Singapore, Singapore
3Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Oxford, United Kingdom
4Department of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou, China
5Voxel Imaging Pte Ltd, Singapore, Singapore

Background: The most widely accepted ultrasound (US) joint inflammation scoring system in rheumatoid arthritis (RA) is semi-quantitative in nature. This process involves manual image acquisition followed by image interpretation. The subjectivity inherent in manual scoring may be overcome by the development of an automated quantitative system to measure joint inflammation.


Objectives: To develop an automated quantitative system to measure US detected power Doppler (PD) joint inflammation in patients with RA.


Methods: The synovial region of interest (sROI) on US images at the metacarpophalangeal joints (MCPJs) and the metatarsophalangeal joint (MTPJs) within the Doppler box is manually segmented by a clinician experienced in musculoskeletal US (figure 1). PD joint inflammation was scored manually semi-quantitatively (0-3). Deep learning based image segmentation was applied to the US images to automatically identify sROI and quantify the amount of PD signals within the sROI (figure 1) to obtain a computer derived PD reading reflecting the extent of PD vascularity within the sROI. The performance of computer derived PD reading was evaluated in comparison with the clinician’s manual scoring.


Results: 820 joints from bilateral 1 st to 5 th MCPJs and MTPJs in 41 adult RA patients (baseline characteristics: 75.6% Chinese; 73.2% female; mean (SD) DAS28, 4.23 (1.25); mean (SD) disease duration, 73.3 (57.8) months) were evaluated in this cross-sectional study. The respective mean (SD)/ median (IQR) computer derived PD readings were 0.13 (0.75)/0.04 (0.08), 1.62 (1.77)/1.21 (1.19) and 10.12 (6.86)/7.51 (5.24) for manual score 0, 1 and 2 (no joints had manual score 3), with statistically significant differences found among the different manual score classes (for non-normally distributed data, Kruskal-Wallis H-test, p=1.69 x 10 -92 , Mann-Whitney Test: manual score 0 versus 1, p=1.04 x 10 -62 ; manual score 0 versus 2, p=3.28 x 10 -43 ; manual score 1 versus 2, p=1.53 x 10 -28 ). Area under the ROC curve (AUC) based on computer derived PD reading cut-off of 0.26 to identify manual score 0 versus 1 was 0.98, while AUC based on computer derived PD reading cut-off of 3.37 to identify manual score 1 versus 2 was 0.98. The overall agreement of the score classes (0, 1 and 2) based on computer prediction using the above cut-offs versus manual scores of 0, 1 and 2 is 791/820=96.46%. Table 1 summarizes the performance of computer prediction using the above cut-offs when compared to clinician evaluation (i.e. score 0 versus 1, comparing computer prediction with clinician evaluation, sensitivity=99.14% and specificity=97.00%; score 1 versus 2, comparing computer prediction with clinician evaluation, sensitivity=97.14% and specificity=93.97%).

Performance of computer prediction versus clinician evaluation

Score 0 vs. 1
Assessor Clinician Evaluation: Score 0 Clinician Evaluation: Score 1
Computer Prediction: Score 0 615 1
Computer Prediction: Score 1 19 115
Sensitivity=99.14%, Specificity=97.00%
Score 1 vs. 2
Assessor Clinician Evaluation: Score 1 Clinician Evaluation: Score 2
Computer Prediction: Score 1 109 2
Computer Prediction: Score 2 7 68
Sensitivity=97.14%, Specificity=93.97%

Conclusion: An automated quantitative system for US PD joint inflammation assessment using deep learning showed high sensitivity and specificity when results from computer prediction were compared to clinician evaluation. Further validation in a larger RA cohort with a longitudinal study design would be required.


REFERENCES:

Nil


Disclosure of Interests: None declared


Citation: Ann Rheum Dis, volume 79, supplement 1, year 2020, page 41
Session: Artificial intelligence and machine learning in imaging of rheumatology: Are we ready? (Oral Presentations)