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About:
CT quantification of pneumonia lesions in early days predicts progression to severe illness in a cohort of COVID-19 patients
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
CT quantification of pneumonia lesions in early days predicts progression to severe illness in a cohort of COVID-19 patients
Creator
Shi, Lei
Zhang, Zhiyong
Wang, Lin
Zhang, Qi
Lu, Hongzhou
Shi, Jing
Huang, Chao
Shi, Nannan
Shi, Yuxin
Zhu, Tongyu
Shan, Fei
Song, Fengxiang
Fang, Cong
Ding, Zezhen
Liu, Fengjun
Mei, Xue
Shi, Chunzi
Su, Xiaoming
Yang, Zhongcheng
Source
Medline; PMC
abstract
Rationale: Some patients with coronavirus disease 2019 (COVID-19) rapidly develop respiratory failure or even die, underscoring the need for early identification of patients at elevated risk of severe illness. This study aims to quantify pneumonia lesions by computed tomography (CT) in the early days to predict progression to severe illness in a cohort of COVID-19 patients. Methods: This retrospective cohort study included confirmed COVID-19 patients. Three quantitative CT features of pneumonia lesions were automatically calculated using artificial intelligence algorithms, representing the percentages of ground-glass opacity volume (PGV), semi-consolidation volume (PSV), and consolidation volume (PCV) in both lungs. CT features, acute physiology and chronic health evaluation II (APACHE-II) score, neutrophil-to-lymphocyte ratio (NLR), and d-dimer, on day 0 (hospital admission) and day 4, were collected to predict the occurrence of severe illness within a 28-day follow-up using both logistic regression and Cox proportional hazard models. Results: We included 134 patients, of whom 19 (14.2%) developed any severe illness. CT features on day 0 and day 4, as well as their changes from day 0 to day 4, showed predictive capability. Changes in CT features from day 0 to day 4 performed the best in the prediction (area under the receiver operating characteristic curve = 0.93, 95% confidence interval [CI] 0.87~0.99; C-index=0.88, 95% CI 0.81~0.95). The hazard ratios of PGV and PCV were 1.39 (95% CI 1.05~1.84, P=0.023) and 1.67 (95% CI 1.17~2.38, P=0.005), respectively. CT features, adjusted for age and gender, on day 4 and in terms of changes from day 0 to day 4 outperformed APACHE-II, NLR, and d-dimer. Conclusions: CT quantification of pneumonia lesions can early and non-invasively predict the progression to severe illness, providing a promising prognostic indicator for clinical management of COVID-19.
has issue date
2020-04-27
(
xsd:dateTime
)
bibo:doi
10.7150/thno.45985
bibo:pmid
32373235
has license
cc-by
sha1sum (hex)
5e27a621e9d938f46d71cabbb2878723dbe0fe95
schema:url
https://doi.org/10.7150/thno.45985
resource representing a document's title
CT quantification of pneumonia lesions in early days predicts progression to severe illness in a cohort of COVID-19 patients
has PubMed Central identifier
PMC7196293
has PubMed identifier
32373235
schema:publication
Theranostics
resource representing a document's body
covid:5e27a621e9d938f46d71cabbb2878723dbe0fe95#body_text
is
schema:about
of
named entity 'algorithms'
named entity 'features'
named entity 'day'
named entity 'PCV'
named entity 'day 4'
named entity 'patients'
named entity 'UNDERSCORING'
named entity 'FOLLOW-UP'
named entity 'SEMI-CONSOLIDATION'
named entity '0.93'
named entity '134'
named entity 'DAYS'
named entity 'OPERATING'
named entity 'RISK OF'
named entity 'PREDICTION'
named entity 'CHARACTERISTIC'
named entity 'NON-'
named entity 'ALGORITHMS'
named entity 'PROGNOSTIC'
named entity 'non-invasively'
named entity 'terms'
named entity 'volume'
named entity 'gender'
named entity 'die'
named entity 'proportional'
named entity 'early'
named entity 'area'
named entity 'day'
named entity 'volume'
named entity 'severe'
named entity 'pneumonia'
named entity 'pneumonia'
named entity 'COVID-19'
named entity 'physiology'
named entity 'PSV'
named entity '95% CI'
named entity 'lymphocyte'
named entity 'lungs'
named entity 'chronic health'
named entity 'PCV'
named entity 'follow-up'
named entity 'receiver operating characteristic'
named entity 'ARDS'
named entity 'ground glass opacity'
named entity 'binary logistic regression'
named entity 'CDC'
named entity 'GGO'
named entity 'COVID-19'
named entity 'CT images'
named entity 'lactate'
named entity 'biomarkers'
named entity '10.0'
named entity 'individual effects'
named entity 'd-dimer'
named entity 'COVID-19'
named entity 'Japan'
named entity 'COVID'
named entity 'risk stratification'
named entity 'cardiovascular'
named entity 'd-dimer'
named entity 'COVID'
named entity 'd-dimer'
named entity 'Vienna'
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