TY - GEN
T1 - Fast multiple landmark localisation using a patch-based iterative network
AU - Li, Yuanwei
AU - Alansary, Amir
AU - Cerrolaza, Juan J.
AU - Khanal, Bishesh
AU - Sinclair, Matthew
AU - Matthew, Jacqueline
AU - Gupta, Chandni
AU - Knight, Caroline
AU - Kainz, Bernhard
AU - Rueckert, Daniel
N1 - Publisher Copyright:
© Springer Nature Switzerland AG 2018.
PY - 2018
Y1 - 2018
N2 - We propose a new Patch-based Iterative Network (PIN) for fast and accurate landmark localisation in 3D medical volumes. PIN utilises a Convolutional Neural Network (CNN) to learn the spatial relationship between an image patch and anatomical landmark positions. During inference, patches are repeatedly passed to the CNN until the estimated landmark position converges to the true landmark location. PIN is computationally efficient since the inference stage only selectively samples a small number of patches in an iterative fashion rather than a dense sampling at every location in the volume. Our approach adopts a multi-task learning framework that combines regression and classification to improve localisation accuracy. We extend PIN to localise multiple landmarks by using principal component analysis, which models the global anatomical relationships between landmarks. We have evaluated PIN using 72 3D ultrasound images from fetal screening examinations. PIN achieves quantitatively an average landmark localisation error of 5.59 mm and a runtime of 0.44 s to predict 10 landmarks per volume. Qualitatively, anatomical 2D standard scan planes derived from the predicted landmark locations are visually similar to the clinical ground truth.
AB - We propose a new Patch-based Iterative Network (PIN) for fast and accurate landmark localisation in 3D medical volumes. PIN utilises a Convolutional Neural Network (CNN) to learn the spatial relationship between an image patch and anatomical landmark positions. During inference, patches are repeatedly passed to the CNN until the estimated landmark position converges to the true landmark location. PIN is computationally efficient since the inference stage only selectively samples a small number of patches in an iterative fashion rather than a dense sampling at every location in the volume. Our approach adopts a multi-task learning framework that combines regression and classification to improve localisation accuracy. We extend PIN to localise multiple landmarks by using principal component analysis, which models the global anatomical relationships between landmarks. We have evaluated PIN using 72 3D ultrasound images from fetal screening examinations. PIN achieves quantitatively an average landmark localisation error of 5.59 mm and a runtime of 0.44 s to predict 10 landmarks per volume. Qualitatively, anatomical 2D standard scan planes derived from the predicted landmark locations are visually similar to the clinical ground truth.
UR - http://www.scopus.com/inward/record.url?scp=85054102833&partnerID=8YFLogxK
U2 - 10.1007/978-3-030-00928-1_64
DO - 10.1007/978-3-030-00928-1_64
M3 - Conference contribution
AN - SCOPUS:85054102833
SN - 9783030009274
T3 - Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
SP - 563
EP - 571
BT - Medical Image Computing and Computer Assisted Intervention – MICCAI 2018 - 21st International Conference, 2018, Proceedings
A2 - Schnabel, Julia A.
A2 - Davatzikos, Christos
A2 - Alberola-López, Carlos
A2 - Fichtinger, Gabor
A2 - Frangi, Alejandro F.
PB - Springer Verlag
T2 - 21st International Conference on Medical Image Computing and Computer Assisted Intervention, MICCAI 2018
Y2 - 16 September 2018 through 20 September 2018
ER -