Precision measurement of cardiac structure and function in cardiovascular magnetic resonance using machine learning

Author:

Davies Rhodri H.,Augusto João B.,Bhuva Anish,Xue Hui,Treibel Thomas A.,Ye Yang,Hughes Rebecca K.,Bai Wenjia,Lau Clement,Shiwani Hunain,Fontana Marianna,Kozor Rebecca,Herrey Anna,Lopes Luis R.,Maestrini Viviana,Rosmini Stefania,Petersen Steffen E.,Kellman Peter,Rueckert Daniel,Greenwood John P.,Captur Gabriella,Manisty Charlotte,Schelbert Erik,Moon James C.ORCID

Abstract

Abstract Background Measurement of cardiac structure and function from images (e.g. volumes, mass and derived parameters such as left ventricular (LV) ejection fraction [LVEF]) guides care for millions. This is best assessed using cardiovascular magnetic resonance (CMR), but image analysis is currently performed by individual clinicians, which introduces error. We sought to develop a machine learning algorithm for volumetric analysis of CMR images with demonstrably better precision than human analysis. Methods A fully automated machine learning algorithm was trained on 1923 scans (10 scanner models, 13 institutions, 9 clinical conditions, 60,000 contours) and used to segment the LV blood volume and myocardium. Performance was quantified by measuring precision on an independent multi-site validation dataset with multiple pathologies with n = 109 patients, scanned twice. This dataset was augmented with a further 1277 patients scanned as part of routine clinical care to allow qualitative assessment of generalization ability by identifying mis-segmentations. Machine learning algorithm (‘machine’) performance was compared to three clinicians (‘human’) and a commercial tool (cvi42, Circle Cardiovascular Imaging). Findings Machine analysis was quicker (20 s per patient) than human (13 min). Overall machine mis-segmentation rate was 1 in 479 images for the combined dataset, occurring mostly in rare pathologies not encountered in training. Without correcting these mis-segmentations, machine analysis had superior precision to three clinicians (e.g. scan-rescan coefficients of variation of human vs machine: LVEF 6.0% vs 4.2%, LV mass 4.8% vs. 3.6%; both P < 0.05), translating to a 46% reduction in required trial sample size using an LVEF endpoint. Conclusion We present a fully automated algorithm for measuring LV structure and global systolic function that betters human performance for speed and precision.

Funder

British Heart Foundation

SBRI Healthcare Award

European Regional Development Fund

Engineering and Physical Sciences Research Council

Horizon 2020

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,Radiological and Ultrasound Technology

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