Automated postoperative muscle assessment of hip arthroplasty patients using multimodal imaging joint segmentation.


Journal

Computer methods and programs in biomedicine
ISSN: 1872-7565
Titre abrégé: Comput Methods Programs Biomed
Pays: Ireland
ID NLM: 8506513

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 05 07 2018
revised: 15 08 2019
accepted: 02 09 2019
pubmed: 16 9 2019
medline: 8 8 2020
entrez: 16 9 2019
Statut: ppublish

Résumé

In patients treated with hip arthroplasty, the muscular condition and presence of inflammatory reactions are assessed using magnetic resonance imaging (MRI). As MRI lacks contrast for bony structures, computed tomography (CT) is preferred for clinical evaluation of bone tissue and orthopaedic surgical planning. Combining the complementary information of MRI and CT could improve current clinical practice for diagnosis, monitoring and treatment planning. In particular, the different contrast of these modalities could help better quantify the presence of fatty infiltration to characterise muscular condition and assess implant failure. In this work, we combine CT and MRI for joint bone and muscle segmentation and we propose a novel Intramuscular Fat Fraction estimation method for the quantification of muscle atrophy. Our multimodal framework is able to segment healthy and pathological musculoskeletal structures as well as implants, and develops into three steps. First, input images are pre-processed to improve the low quality of clinically acquired images and to reduce the noise associated with metal artefact. Subsequently, CT and MRI are non-linearly aligned using a novel approach which imposes rigidity constraints on bony structures to ensure realistic deformation. Finally, taking advantage of a multimodal atlas we created for this task, a multi-atlas based segmentation delineates pelvic bones, abductor muscles and implants on both modalities jointly. From the obtained segmentation, a multimodal estimation of the Intramuscular Fat Fraction can be automatically derived. Evaluation of the segmentation in a leave-one-out cross-validation study on 22 hip sides resulted in an average Dice score of 0.90 for skeletal and 0.84 for muscular structures. Our multimodal Intramuscular Fat Fraction was benchmarked on 27 different cases against a standard radiological score, showing stronger association than a single modality approach in a one-way ANOVA F-test analysis. The proposed framework represents a promising tool to support image analysis in hip arthroplasty, being robust to the presence of implants and associated image artefacts. By allowing for the automated extraction of a muscle atrophy imaging biomarker, it could quantitatively inform the decision-making process about patient's management.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
In patients treated with hip arthroplasty, the muscular condition and presence of inflammatory reactions are assessed using magnetic resonance imaging (MRI). As MRI lacks contrast for bony structures, computed tomography (CT) is preferred for clinical evaluation of bone tissue and orthopaedic surgical planning. Combining the complementary information of MRI and CT could improve current clinical practice for diagnosis, monitoring and treatment planning. In particular, the different contrast of these modalities could help better quantify the presence of fatty infiltration to characterise muscular condition and assess implant failure. In this work, we combine CT and MRI for joint bone and muscle segmentation and we propose a novel Intramuscular Fat Fraction estimation method for the quantification of muscle atrophy.
METHODS METHODS
Our multimodal framework is able to segment healthy and pathological musculoskeletal structures as well as implants, and develops into three steps. First, input images are pre-processed to improve the low quality of clinically acquired images and to reduce the noise associated with metal artefact. Subsequently, CT and MRI are non-linearly aligned using a novel approach which imposes rigidity constraints on bony structures to ensure realistic deformation. Finally, taking advantage of a multimodal atlas we created for this task, a multi-atlas based segmentation delineates pelvic bones, abductor muscles and implants on both modalities jointly. From the obtained segmentation, a multimodal estimation of the Intramuscular Fat Fraction can be automatically derived.
RESULTS RESULTS
Evaluation of the segmentation in a leave-one-out cross-validation study on 22 hip sides resulted in an average Dice score of 0.90 for skeletal and 0.84 for muscular structures. Our multimodal Intramuscular Fat Fraction was benchmarked on 27 different cases against a standard radiological score, showing stronger association than a single modality approach in a one-way ANOVA F-test analysis.
CONCLUSIONS CONCLUSIONS
The proposed framework represents a promising tool to support image analysis in hip arthroplasty, being robust to the presence of implants and associated image artefacts. By allowing for the automated extraction of a muscle atrophy imaging biomarker, it could quantitatively inform the decision-making process about patient's management.

Identifiants

pubmed: 31522089
pii: S0169-2607(19)30325-6
doi: 10.1016/j.cmpb.2019.105062
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105062

Informations de copyright

Copyright © 2019. Published by Elsevier B.V.

Auteurs

Marta B M Ranzini (MBM)

Centre for Medical Imaging Computing, University College London, London, UK; School of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, United Kingdom; Medical Physics and Biomedical Engineering Department, University College London, London WC1E 6BT, United Kingdom. Electronic address: marta.ranzini.15@ucl.ac.uk.

Johann Henckel (J)

Royal National Orthopaedic Hospital NHS Foundation Trust, London, UK.

Michael Ebner (M)

Centre for Medical Imaging Computing, University College London, London, UK; School of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, United Kingdom; Medical Physics and Biomedical Engineering Department, University College London, London WC1E 6BT, United Kingdom.

M Jorge Cardoso (MJ)

School of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, United Kingdom; Medical Physics and Biomedical Engineering Department, University College London, London WC1E 6BT, United Kingdom.

Amanda Isaac (A)

School of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, United Kingdom; Radiology Department, Guys & St Thomas Hospitals NHS Foundation Trust, London SE1 7EH, UK.

Tom Vercauteren (T)

School of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, United Kingdom; Medical Physics and Biomedical Engineering Department, University College London, London WC1E 6BT, United Kingdom.

Sébastien Ourselin (S)

School of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, United Kingdom; Medical Physics and Biomedical Engineering Department, University College London, London WC1E 6BT, United Kingdom.

Alister Hart (A)

Royal National Orthopaedic Hospital NHS Foundation Trust, London, UK.

Marc Modat (M)

School of Biomedical Engineering & Imaging Sciences, King's College London, King's Health Partners, St Thomas' Hospital, London SE1 7EH, United Kingdom; Medical Physics and Biomedical Engineering Department, University College London, London WC1E 6BT, United Kingdom.

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Classifications MeSH