Literature DB >> 34295769

Early recognition of necrotizing pneumonia in children based on non-contrast-enhanced computed tomography radiomics signatures.

Xin Chen1,2, Weiguo Li2,3, Fang Wang4, Ling He1,2, Enmei Liu2,3.   

Abstract

BACKGROUND: Necrotizing pneumonia (NP) is an infrequent but severe complication of pneumonia in children. In the early stages of NP, CT imaging shows lung consolidation, which cannot be detected in time. This study aimed to explore the ability of non-contrast-enhanced CT radiomics features to recognize NP in early stage.
METHODS: This was a retrospective study, and 250 patients who presented with lung consolidation on initial CT images were included in this study. After a follow-up period of 1-3 weeks, 116 patients developed NP, whose CT or X-ray shows cavitation or liquefied necrosis. Manual segmentation of lesion sites in the initial non-contrast-enhanced CT scans was performed with RadCloud (Huiying Medical Technology Co., Ltd., China), and 1,409 radiomics features were extracted. We used Variance threshold (0.8), SelectKBest, and the least absolute shrinkage and selection operator (LASSO) methods for feature dimension reduction. Three machine learning algorithms, k-nearest neighbor (KNN), support vector machine (SVM), and logistic regression (LR) models, were established to recognize NP early. To assess the recognition performance, the area under the receiver operating characteristic curve (AUC), sensitivity, specificity, and other indicators were used in the validation cohort.
RESULTS: Radiomics features helped to recognize NP in early stage in both the training and validation cohorts. The AUC (sensitivity, specificity) for the training and validation cohorts were 0.81 (0.73, 0.68) and 0.71 (0.61, 0.65) for KNN, respectively; 0.81 (0.72, 0.70) and 0.77 (0.66, 0.65) for SVM, respectively; and 0.82 (0.73, 0.73) and 0.76 (0.63, 0.70) for LR, respectively. Recall and F1-scores determined that LR performed better at diagnosing early NP, with the values of the above two indexes being 0.70 and 0.67, respectively.
CONCLUSIONS: Non-contrast-enhanced CT-based radiomics models may be helpful for recognizing NP in early stage. 2021 Translational Pediatrics. All rights reserved.

Entities:  

Keywords:  Necrotizing pneumonia (NP); children; machine learning; radiomics

Year:  2021        PMID: 34295769      PMCID: PMC8261593          DOI: 10.21037/tp-20-241

Source DB:  PubMed          Journal:  Transl Pediatr        ISSN: 2224-4336


Introduction

Necrotizing pneumonia (NP) is a serious complication of community-acquired pneumonia and may cause necrosis and destruction of the lung parenchyma in children (1). While NP in children is a rare complication, its incidence is increasing (2). In the United States, 0.8–7% of children develop NP in tertiary centers (3). Although the condition is serious, a full recovery and good prognosis can be achieved if NP is detected and treated early. As the clinical features of NP are similar to those of simple pneumonia (SP) (2), routine tests do not provide an accurate diagnosis. Currently, chest computed tomography (CT) is the most sensitive method for the diagnosis of NP, and is characterized by destruction of lung parenchyma, loss of parenchymal enhancement, and multiple thin-walled cavities (1,3). In the early stage of lung necrosis, the density shown in plain scan images is similar to the real lung lesions, so it cannot be detected in time (4). If the consolidation area of the lung is loss of parenchymal enhancement after injection of iodine in contrast-enhanced CT, which can help for recognizing NP in early stage, but this increases the radiation dose required (1). If plain CT data can be used to recognize lung necrosis in early stage in children, this will allow for timely clinical decisions to be made regarding therapeutic options without increasing a child’s exposure to radiation. Radiomics is a field of medicine that utilizes characterization algorithms to allow analysis of many quantitative image features from medical images (5). Radiomics signatures have been proven to reflect tissue heterogeneity (6-9). Radiology has been widely used in the diagnosis of tumors and the prediction of tumor grades, metastasis, and prognosis (10-13). CT-based radiomics have been used for predicting the spread through air spaces in lung adenocarcinoma and response to immunotherapy (14,15). Machine-learning radiomics have been used for predicting early recurrence in perihilar cholangiocarcinoma after curative resection (16). The purpose of this study was to recognize pulmonary necrosis in early stage in children with pulmonary consolidation based on radiographic features observed on non-enhanced CT scans. We present the following article in accordance with the TRIPOD reporting checklist (available at http://dx.doi.org/10.21037/tp-20-241).

Methods

Patients

The study was conducted in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by the Ethics Committee of the Children’s Hospital Affiliated with Chongqing Medical University (NO.: 20190218) and individual consent for this retrospective analysis was waived. In total, 303 patients with histologically confirmed pneumonia consolidation between April 2009 and December 2019 were involved. Patients were deemed eligible for in this study if their initial CT scans showed consolidation range larger than 1 pulmonary segment and if they were followed up over a 1–3-week period to monitor for necrosis with CT or X ray (). The diagnosis of NP include the loss of normal parenchymal architecture, decreased parenchymal enhancement, air filled cavities (2). Patients who had incomplete CT scan data or poor-quality images were excluded from the study. Two hundred and fifty patients were finally enrolled in this study. There were 116 cases of NP and 134 cases of SP. The clinical and histopathological characteristics of the patients included are shown in .
Figure 1

The flowchart of the inclusion of study subjects.

Table 1

The clinical and histopathological characteristics of the patients

GroupNecrotizing pneumoniaSimple pneumoniaP value
Number116134
Age (mean ± SD)1.47±0.501.46±0.500.83
Sex0.86
   M6172
   F5562

SD, standard deviation.

The flowchart of the inclusion of study subjects. SD, standard deviation.

CT acquisition

The CT scan was performed using a 64-detector CT scanner (GE Lightspeed VCT 64, Philips Medical Systems, Amsterdam, the Netherlands) or a 128-detector CT scanner (Brilliance ICT, Philips Medical Systems). A tube voltage of 80–120 kV was applied with the tube current being automatically regulated. A collimation of 0.6 mm was used, and images with a slice thickness of 5 mm with a gap of 1 mm were reconstructed using a standard reconstruction algorithm. Digital Imaging and Communications in Medicine (DICOME) images were downloaded from the picture archiving and communication system (PACS). Data were randomly divided into training and validation cohorts at a ratio of 3.3:6.7, and 74 random seeds were used.

Image pre-processing, segmentation, and extraction of radiomics features

Radiomics was adopted to acquire knowledge from high-dimensional data. Radiomics features of each patient were extracted from plain CT images using the Pyradiomics v.2.1.2 package. Preprocessing of the images before feature extraction by a radiologist. The normalization of the images was centered on the mean standard deviation. The radiomics workflow was presented in . CT images were centrally managed in Radcloud software. A radiologist (with 9-year experience). The regions of interest (ROIs) for each slice, covering the whole lesion, were manually delineated by a radiologist (with 9-year experience in thoracic radiology), Which were supervised by a radiologist (with 23-year experience). A sample of the manual voxel of interest (VOI) drawing is presented in .
Figure 2

Radiomics workflow and study flowchart.

Figure 3

A sample of manually segmenting and contouring ROIs. (A) An original image showing lung consolidation. (B) The region of interest (ROI) of a manual sketch in the lung consolidation image.

Radiomics workflow and study flowchart. A sample of manually segmenting and contouring ROIs. (A) An original image showing lung consolidation. (B) The region of interest (ROI) of a manual sketch in the lung consolidation image. Based on the delineated ROIs in CT images, 1,409 features were automatically extracted which could be divided into 4 categories: (I) first-order statistics, which mainly describe the distribution of voxel intensity in CT images; (II) shape-and size-based features; (III) texture features, which including gray-level dependence matrix (GLDM) features, gray-level run-length matrix (GLRLM) features, neighborhood gray difference matrix features, gray-level size zone matrix (GLSZM) features, and textural features that could quantify regional heterogeneity differences; (IV) higher-order statistics features, which were obtained by filter transformation of the original image. The filters used in this study include exponential, square, square root, logarithm, gradient, Ibp-2D, and wavelet.

Feature selection

As described above, thousands of image features were obtained. However, the inclusion of too many features would have affected the recognition performance of the model, as the complexity of the model would be increased and multicollinearity would occur. Therefore, it was necessary to select the best feature set for the subsequent data analysis process. In our study, using the variance threshold, SelectKBest, and the least absolute shrinkage and selection operator (LASSO) methods were used to reduce redundant features. The variance threshold method removed the feature of variances of less than 0.8, while SelectKBest retained the features with P values of less than 0.05 in the univariate test. Finally, features with non-zero coefficients are selected using Lasso, which used an L1 regularizer as the cost function, 10 cross-validations, and a maximum of 1,000 iterations. Finally, the 15 indicators most relevant to NP were selected as shown in .
Table 2

Table of selected radiomics features, including feature name, feature category and filter

Radiomic featureRadiomic classFilter
DependenceEntropyGLDMExponential
DependenceEntropyGLDMGradient
DependenceEntropyGLDMlbp-2D
DependenceVarianceGLDMWavelet-HHL
LargeDependenceHighGrayLevelEmphasisGLDMWavelet-LHL
EnergyFirstorderSquare
TotalEnergyFirstorderSquare
ZoneEntropyGLSZMWavelet-LLH
LongRunLowGrayLevelEmphasisGLRLMWavelet-LLL
EnergyFirstorderWavelet-LLH
TotalEnergyFirstorderWavelet-LLH
RangeFirstorderWavelet-LLL
SizeZoneNonUniformityGLSZMWavelet-HHH
LargeDependenceHighGrayLevelEmphasisGLDMWavelet-LHH
SkewnessFirstorderWavelet-LLH

GLDM, gray-level dependence matrix; GLSZM, gray-level size zone matrix; GLRLM, gray-level run-length matrix.

GLDM, gray-level dependence matrix; GLSZM, gray-level size zone matrix; GLRLM, gray-level run-length matrix.

Statistical analysis

Continuous variables (such as age) were compared by t-test, while qualitative variables (such as gender) were analyzed by Chi-square test. A P value less than 0.05 indicated statistical significance. In machine learning, the training cohort (67%) was used to develop the radiomics models [k-nearest neighbor (KNN), support vector machine (SVM), and logistic regression (LR)] to recognize NP in early stage and SP. The validation cohort (33%) was only used to evaluate the model’s generalization ability. To assess the diagnosis performance, the receiver operating characteristic (ROC) curve method, namely, the AUC, was used both in the training and validation cohorts. Five indicators including area under the ROC curve (AUC), recall, specificity, accuracy, and F1-score were used to evaluate the performance of the classifier in this study. Among them, with recall (R) = true positive / (true positive + false negative), precision (P) = true positive / (true positive + false positive), F1-score = P × R × 2 / (P + R). All statistical analyses were performed in software R (version 4.0.3).

Results

Clinical characteristics

The patient clinical characteristics are shown in . The NP and SP groups showed no significant differences in clinical characteristics (P>0.05).

Extraction and selection of features

For feature selection, 453 out of 1,409 features were initially selected using the variance threshold method. Subsequently 297 features were identified with the SelectKBest method. Ultimately, 15 optimal features () were selected with the LASSO algorithm ().
Figure 4

LASSO algorithm on feature selection. (A) The LASSO path describes the relationship between the regression coefficient of the independent variable and the LASSO penalty coefficient α. The best α value selected by model was 0.37. (B) The MSE path for LASSO training process. The dotted vertical line was plotted on the value selected in (A). (C) The optimal coefficients of 15 features selected by LASSO. LASSO parameters: cv [10] and max_iter [1000]. LASSO, least absolute shrinkage and selection operator.

LASSO algorithm on feature selection. (A) The LASSO path describes the relationship between the regression coefficient of the independent variable and the LASSO penalty coefficient α. The best α value selected by model was 0.37. (B) The MSE path for LASSO training process. The dotted vertical line was plotted on the value selected in (A). (C) The optimal coefficients of 15 features selected by LASSO. LASSO parameters: cv [10] and max_iter [1000]. LASSO, least absolute shrinkage and selection operator.

Recognition performance of the 3 classification models

In the training cohort, the AUC (95% confidence interval [CI]), recall, and specificity of the KNN, SVM, and LR classifiers were 0.81 (0.74 to 0.88), 0.73, and 0.68; 0.81 (0.74 to 0.88), 0.72, and 0.70; and 0.82 (0.75 to 0.89), 0.73, and 0.73, respectively. Accordingly, in the validation cohort, the above evaluation indicators of these 3 classifiers were 0.71 (0.61 to 0.82), 0.61, and 0.65; 0.77 (0.67 to 0.88), 0.66, and 0.65; and 0.76 (0.65 to 0.86), 0.63, and 0.70, respectively. Combining the recall and F1-scores revealed that LR outperformed the other 2 classifiers in the recognition of NP in patients. Detailed evaluation indicator information is shown in , and the ROC curves of the 3 classifiers are shown in .
Table 3

The ROC results with KNN, SVM, and LR classifiers of the training and validation cohorts

Evaluation indicatorTraining cohortValidation cohort
KNNSVMLRKNNSVMLR
AUC0.810.810.820.710.770.76
95% CI0.74–0.880.74–0.880.75–0.890.61–0.820.67–0.880.65–0.86
Recall0.730.720.730.610.660.63
Specificity0.680.700.730.650.650.70
Precision0.690.690.710.600.630.63
F1-score0.680.700.720.620.640.67

ROC, receiver operating characteristics; KNN, k-nearest neighbour; SVM, support vector machine; LR, logistic regression.

Figure 5

ROC curves of KNN (A-T), SVM (B-T), and LR (C-T) classifiers in the training cohort, with, A-V, B-V, and C-V being the respective ROC results in the validation cohort. ROC, receiver operating characteristics; KNN, k-nearest neighbor; SVM, support vector machine; LR, logistic regression.

ROC, receiver operating characteristics; KNN, k-nearest neighbour; SVM, support vector machine; LR, logistic regression. ROC curves of KNN (A-T), SVM (B-T), and LR (C-T) classifiers in the training cohort, with, A-V, B-V, and C-V being the respective ROC results in the validation cohort. ROC, receiver operating characteristics; KNN, k-nearest neighbor; SVM, support vector machine; LR, logistic regression.

Discussion

NP has increasingly been identified as a complication of pediatric pneumonia (1). Staphylococcus aureus and Streptococcus pneumoniae are the most common biological factors contributing to the of emergence of NP (2). Due to the short-term severe morbidity of childhood NP, treatment usually involves pediatric intensive care unit hospitalization and a lengthy course of antibiotics. Severe cases may involve invasive surgery, including thoracic duct video-assisted thoracoscopic surgery or segmental pneumonectomy, or even the use of extracorporeal membrane oxygenation (ECMO) (1,17). Insufficient recognition of NP can lead to misdiagnosis and serious errors in clinical management (18). Thus, early identification is important for guiding appropriate clinical treatment and reducing the incidence and mortality rates associated with this disease (19). In the early stage of NP, diagnostic radiographs may show lung consolidation; However, chest CT scans are needed for a more definitive diagnosis (1). If the consolidation area of the lung shows decreased parenchymal enhancement after injection of iodine, the possibility of pulmonary necrosis is higher, but this results in exposure to an increased radiation dose (1,4). Enhanced CT is also associated with a higher radiation dose, and children are more sensitive to the risk of radiation-induced cancer than adults (20,21). Enhanced CT also increases the contrast agent load and increases the possibility of contrast agent-associated nephropathy (22). Therefore, if plain CT data can be used to recognize lung necrosis in early stage in children, this will allow for timely clinical decisions to be made regarding therapeutic options without increasing a child’s exposure to radiation. In this study, we described the recognition of NP in lung consolidation by using a CT-based radiomics machine learning model. Our preliminary results indicated that 15 radiomics features were associated with NP. The AUC, recall, and f1-score values of the LR model in the validation cohort were 0.76, 0.70, and 0.67, respectively, outperforming both KNN and SVM. Therefore, this radiomics model has the potential to serve as a promising imaging biomarker for recognition NP, contributing to early detection, risk assessment, and treatment decisions. Radiomics is an emerging field of study that utilizes a series of qualitative and quantitative analyses of high-throughput image features to obtain heterogeneity information from medical images. This method is different from the traditional method, which only interprets the image visually (23). Radiomics has been widely used in the diagnosis, prediction, and classification of cancers in many systems of the body (24-27). Several reports have described the use of radiomics for pulmonary infectious diseases. Some recent studies used this approach to distinguish pneumonia from paraquat poisoning, and to discriminate focal organizing pneumonia from peripheral lung adenocarcinoma (28,29). Kloth et al. noted differences in texture analysis parameters between active alveolitis and lung fibrosis in chest CT scans of patients with systemic sclerosis (30). Feng et al. reported that radiomics-based predictive models reliably identified patients with glucocorticoid-sensitive connective tissue disease-associated interstitial lung disease (31). Another study showed that these models could be used to differentiate primary progressive pulmonary tuberculosis from community-acquired pneumonia in children (32). This present study aimed to recognize the occurrence of NP by choosing an optimum machine learning model based on the Radiomics features of the lung consolidation. In comparison with the SVM and KNN classifiers, plain CT images based on the strongest LR results showed the best classification effect. The results demonstrated that LR and radiomics can be used as novel methods for recognition of lung necrosis in early stage and can guide the planning of further clinical treatments. This method avoids the use of excessive radiation and its related complications. Therefore, it can serve as a tool to assist clinicians in determining a suitable treatment method for patients and has wide applications in clinical practice. Radiomics features can reveal subtle changes in lesions that are difficult to quantitatively recognize by the naked eye. The report used plain CT scan images to extract the radiomics features associated with lung necrosis and these features can be used to build artificial intelligence models. Fifteen radiomics features were extracted in this study, including first-order statistics, texture feature classes, and higher-order GLSZM, GLRLM, and other parameters. The texture features describe the texture characteristics of the image. Among the feature parameters selected in this study, ZoneEntropy measures the uncertainty or randomness in the area size and the gray-level distribution. The first-order characteristics GLDM and GLRLM were correlated with the intensity, gray-length, and distribution heterogeneity of the lesion voxel. In summary, this study cited the performance of the VOIs on CT scan images of the lung to demonstrate the feasibility of combining artificial intelligence with CT scan radiomics to recognize lung necrosis in early stage. This method is a non-invasive, high-precision approach for diagnosing lung necrosis in early stage that allows for improved guidance in treatment planning, prevention of radiation-related complications, and avoidance of the high costs associated with enhanced scanning. There are several limitations in the current study. First, due the retrospective design of the study, the quality of the images could not be strictly controlled. Second, the number of NP cases was limited, although the results are promising. Third, our research is single-centered and further verification from multi-center research is required. Therefore, we aim to conduct further studies to verify these results with larger, more comprehensive, and more uniform samples. Patients with NP can become seriously ill, and early recognition is vital for timely clinical management and the reduction of sequelae linked to this disease. The article’s supplementary files as
  32 in total

1.  Radiomics analysis of lung CT image for the early detection of metastases in patients with breast cancer: preliminary findings from a retrospective cohort study.

Authors:  Yana Qi; Xiaoxiao Cui; Meng Han; Ranran Li; Tiehong Zhang; Baocheng Geng; Jianjun Xiu; Jing Liu; Zhi Liu; Mingyong Han
Journal:  Eur Radiol       Date:  2020-03-12       Impact factor: 5.315

2.  Radiomics to predict response to immunotherapy, bridging the gap from proof of concept to clinical applicability?

Authors:  E Deutsch; N Paragios
Journal:  Ann Oncol       Date:  2019-06-01       Impact factor: 32.976

Review 3.  Pediatric Necrotizing Pneumonia: A Case Report and Review of the Literature.

Authors:  Sriram Ramgopal; Yaron Ivan; Avinash Medsinge; Richard A Saladino
Journal:  Pediatr Emerg Care       Date:  2017-02       Impact factor: 1.454

Review 4.  Radiomics: the process and the challenges.

Authors:  Virendra Kumar; Yuhua Gu; Satrajit Basu; Anders Berglund; Steven A Eschrich; Matthew B Schabath; Kenneth Forster; Hugo J W L Aerts; Andre Dekker; David Fenstermacher; Dmitry B Goldgof; Lawrence O Hall; Philippe Lambin; Yoganand Balagurunathan; Robert A Gatenby; Robert J Gillies
Journal:  Magn Reson Imaging       Date:  2012-08-13       Impact factor: 2.546

5.  Assessment of primary colorectal cancer heterogeneity by using whole-tumor texture analysis: contrast-enhanced CT texture as a biomarker of 5-year survival.

Authors:  Francesca Ng; Balaji Ganeshan; Robert Kozarski; Kenneth A Miles; Vicky Goh
Journal:  Radiology       Date:  2012-11-14       Impact factor: 11.105

6.  Necrotising pneumonia is an increasingly detected complication of pneumonia in children.

Authors:  G S Sawicki; F L Lu; C Valim; R H Cleveland; A A Colin
Journal:  Eur Respir J       Date:  2008-01-23       Impact factor: 16.671

7.  Differentiation of focal organising pneumonia and peripheral adenocarcinoma in solid lung lesions using thin-section CT-based radiomics.

Authors:  T Zhang; M Yuan; Y Zhong; Y-D Zhang; H Li; J-F Wu; T-F Yu
Journal:  Clin Radiol       Date:  2018-10-04       Impact factor: 2.350

Review 8.  Necrotizing pneumonia: an emerging problem in children?

Authors:  I Brent Masters; Alan F Isles; Keith Grimwood
Journal:  Pneumonia (Nathan)       Date:  2017-07-25

9.  Pneumonectomy in a Child with Multilobar Pneumatocele Secondary to Necrotizing Pneumonia: Case Report and Review of the Literature.

Authors:  Christopher A Gerdung; B Catherine Ross; Bryan J Dicken; Candice L Bjornson
Journal:  Case Rep Pediatr       Date:  2019-07-17

10.  Radiomics Nomogram Analyses for Differentiating Pneumonia and Acute Paraquat Lung Injury.

Authors:  Wang Yanling; Gao Duo; Geng Zuojun; Shi Zhongqiang; Wu Yankai; Lu Shan; Cui Hongying
Journal:  Sci Rep       Date:  2019-10-21       Impact factor: 4.379

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.