Value and prognostic impact of a deep learning segmentation model of COVID-19 lung lesions on low-dose chest CT.

ACE, angiotensin-converting enzyme Artificial intelligence BMI, body mass index CNN, convolutional neural network COVID-19 COVID-19, coronavirus disease 2019 CT-SS, chest tomography severity score Cons, consolidation DL, deep learning DSC, Dice similarity coefficient Deep learning Diagnostic imaging GGO, ground-glass opacity ICU, intensive care unit LDCT, low-dose computed tomography MAE, mean absolute error MVSF, mean volume similarity fraction Multidetector computed tomography ROC, receiver operating characteristic

Journal

Research in diagnostic and interventional imaging
ISSN: 2772-6525
Titre abrégé: Res Diagn Interv Imaging
Pays: France
ID NLM: 9918574385706676

Informations de publication

Date de publication:
Mar 2022
Historique:
received: 04 11 2021
revised: 02 03 2022
accepted: 09 03 2022
medline: 1 3 2022
pubmed: 1 3 2022
entrez: 31 7 2023
Statut: ppublish

Résumé

1) To develop a deep learning (DL) pipeline allowing quantification of COVID-19 pulmonary lesions on low-dose computed tomography (LDCT). 2) To assess the prognostic value of DL-driven lesion quantification. This monocentric retrospective study included training and test datasets taken from 144 and 30 patients, respectively. The reference was the manual segmentation of 3 labels: normal lung, ground-glass opacity(GGO) and consolidation(Cons). Model performance was evaluated with technical metrics, disease volume and extent. Intra- and interobserver agreement were recorded. The prognostic value of DL-driven disease extent was assessed in 1621 distinct patients using C-statistics. The end point was a combined outcome defined as death, hospitalization>10 days, intensive care unit hospitalization or oxygen therapy. The Dice coefficients for lesion (GGO+Cons) segmentations were 0.75±0.08, exceeding the values for human interobserver (0.70±0.08; 0.70±0.10) and intraobserver measures (0.72±0.09). DL-driven lesion quantification had a stronger correlation with the reference than inter- or intraobserver measures. After stepwise selection and adjustment for clinical characteristics, quantification significantly increased the prognostic accuracy of the model (0.82 vs. 0.90; A DL-driven model can provide reproducible and accurate segmentation of COVID-19 lesions on LDCT. Automatic lesion quantification has independent prognostic value for the identification of high-risk patients.

Identifiants

pubmed: 37520010
doi: 10.1016/j.redii.2022.100003
pii: S2772-6525(22)00003-5
pmc: PMC8939894
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100003

Informations de copyright

© 2022 The Authors.

Déclaration de conflit d'intérêts

The authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article.

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Auteurs

Axel Bartoli (A)

Department of Radiology, Hôpital de la Timone Adultes, AP-HM. 264, rue Saint-Pierre, 13385 Marseille Cedex 05, France.
CRMBM - UMR CNRS 7339, Medical Faculty, Aix-Marseille University, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.

Joris Fournel (J)

Department of Radiology, Hôpital de la Timone Adultes, AP-HM. 264, rue Saint-Pierre, 13385 Marseille Cedex 05, France.
CRMBM - UMR CNRS 7339, Medical Faculty, Aix-Marseille University, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.

Arnaud Maurin (A)

Department of Radiology, Hôpital de la Timone Adultes, AP-HM. 264, rue Saint-Pierre, 13385 Marseille Cedex 05, France.

Baptiste Marchi (B)

Department of Radiology, Hôpital de la Timone Adultes, AP-HM. 264, rue Saint-Pierre, 13385 Marseille Cedex 05, France.

Paul Habert (P)

Department of Radiology, Hôpital de la Timone Adultes, AP-HM. 264, rue Saint-Pierre, 13385 Marseille Cedex 05, France.
LIEE, Medical Faculty, Aix-Marseille University, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.
CERIMED, Medical Faculty, Aix-Marseille University, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.

Maxime Castelli (M)

Department of Radiology, Hôpital de la Timone Adultes, AP-HM. 264, rue Saint-Pierre, 13385 Marseille Cedex 05, France.

Jean-Yves Gaubert (JY)

Department of Radiology, Hôpital de la Timone Adultes, AP-HM. 264, rue Saint-Pierre, 13385 Marseille Cedex 05, France.
LIEE, Medical Faculty, Aix-Marseille University, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.
CERIMED, Medical Faculty, Aix-Marseille University, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.

Sebastien Cortaredona (S)

Institut Hospitalo-Universitaire Méditerannée Infection, 19-21 boulevard Jean Moulin, 13005, Marseille, France.
IRD, VITROME, Institut Hospitalo-Universitaire Méditerannée Infection, 19-21 boulevard Jean Moulin, 13005, Marseille, France.

Jean-Christophe Lagier (JC)

Institut Hospitalo-Universitaire Méditerannée Infection, 19-21 boulevard Jean Moulin, 13005, Marseille, France.
IRD, MEPHI, Institut Hospitalo-Universitaire Méditerannée Infection, 19-21 boulevard Jean Moulin, 13005, Marseille, France.

Matthieu Million (M)

Institut Hospitalo-Universitaire Méditerannée Infection, 19-21 boulevard Jean Moulin, 13005, Marseille, France.
IRD, MEPHI, Institut Hospitalo-Universitaire Méditerannée Infection, 19-21 boulevard Jean Moulin, 13005, Marseille, France.

Didier Raoult (D)

Institut Hospitalo-Universitaire Méditerannée Infection, 19-21 boulevard Jean Moulin, 13005, Marseille, France.
IRD, MEPHI, Institut Hospitalo-Universitaire Méditerannée Infection, 19-21 boulevard Jean Moulin, 13005, Marseille, France.

Badih Ghattas (B)

I2M - UMR CNRS 7373, Aix-Marseille University. CNRS, Centrale Marseille, 13453 Marseille, France.

Alexis Jacquier (A)

Department of Radiology, Hôpital de la Timone Adultes, AP-HM. 264, rue Saint-Pierre, 13385 Marseille Cedex 05, France.
CRMBM - UMR CNRS 7339, Medical Faculty, Aix-Marseille University, 27, Boulevard Jean Moulin, 13385 Marseille Cedex 05, France.

Classifications MeSH