Skip to main content
Wiley - PMC COVID-19 Collection logoLink to Wiley - PMC COVID-19 Collection
. 2020 Nov 9;75(4):e13760. doi: 10.1111/ijcp.13760

Clinical differences in chest CT characteristics between the progression and remission stages of patients with COVID‐19 pneumonia

Jie‐lan Liao 1, Yu Chen 1, Chong‐Quan Huang 1, Gui‐qing He 2,3, Ji‐Cheng Du 1,, Que‐Lu Chen 1,
PMCID: PMC7645958  PMID: 33068310

Abstract

Introduction

Computed tomography (CT) can be effective for the early screening and diagnosis of COVID‐19. This study aimed to investigate the distinctive CT characteristics of two stages of the disease (progression and remission).

Methods

We included all COVID‐19 patients admitted to Wenzhou Central Hospital from January to February, 2020. Patients underwent multiple chest CT scans at intervals of 3‐10 days. CT features were recorded, such as the lesion lobe, distribution characteristics (subpleural, scattered or diffused), shape of the lesion, maximum size of the lesion, lesion morphology (ground‐glass opacity, GGO) and consolidation features. When consolidation was positive, the boundary was identified to determine its clarity.

Results

The ratios of some representative features differed between the remission stage and the progression phase, such as round‐shape lesion (8.0% vs 34.4%), GGO (65.0% vs 87.5%), consolidation (62.0% vs 31.3%), large cable sign (59.0% vs 9.4%) and crazy‐paving sign (20.0% vs 50.0%). Using these features, we pooled all the CT data (n = 132) and established a logistic regression model to predict the current development stage. The variables consolidation, boundary feature, large cable sign and crazy‐paving sign were the most significant factors, based on a variable named “prediction of progression or remission” (PPR) that we constructed. The ROC curve showed that PPR had an AUC of 0.882 (cutoff value = 0.66, sensitivity = 0.75, specificity = 0.875).

Conclusion

CT characteristics, in particular, round shape, GGO, consolidation, large cable sign, and crazy‐paving sign, may increase the recognition of the intrapulmonary development of COVID‐19.


What’s known

Computed tomography (CT) characteristics, in particular the characteristics of round shape, GGO, consolidation, large cable sign and crazy‐paving sign, may help radiologists to distinguish the progression and remission phases of COVID‐19. Using CT characteristics, we established a regression model to predict the current development stage of COVID‐19.

What’s new

Consolidation does not necessarily indicate a worsening of COVID‐19 but can be an indicator of a sufficient immune reaction, as well as a sign of improvement.

1. INTRODUCTION

The highly infectious disease Coronavirus Disease 2019 (COVID‐19) has widely spread throughout the world since the beginning of 2020, and is caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2). Since emerging in Wuhan, it has rapidly spread to other cities in China, and multiple countries beyond China. On 28 February 2020, the World Health Organization (WHO) declared COVID‐19 a global public health emergency (World Health Organization 2020 COVID‐19 situation report). As of March 2020, ~800,000 individuals have had a positive diagnosis, and the number is still rising sharply. 1 , 2 , 3

Among the limited detection approaches, CT is effective for the early screening and diagnosis of COVID‐19. CT features have be used to distinguish community acquired pneumonia and COVID‐19 through artificial intelligence algorithms. 4 In addition, CT features may help to indicate severe/critical development, as the incidences of consolidation, linear opacities, crazy‐paving pattern and bronchial wall thickening in severe/critical patients were significantly higher than those in ordinary patients. 5 Previous studies have used the total severity score (TSS) according to CT visual quantitative evaluation for diagnosing severe/critical COVID‐19, which provides a high area under the curve (AUC) value. 6 Overall, different factors are related to the onset and severity of COVID‐19, which contribute to diagnosis and prognosis. 7 , 8 However, very few studies have focused on the different stages of development of COVID‐19, or have accurately distinguished between the progression stage and remission stage using CT data. In the present study, we analysed the CT images from 107 COVID‐19 cases, and examined the distinctive characteristics of both the progression and remission stages. Our findings provide a reference for assessing the clinical condition/stage of patients and will help in determining treatment strategies.

2. METHODS

2.1. Patients

This retrospective study included all COVID‐19 patients admitted to our hospital from 10 January 2020 to 20 February 2020. Each patient provided informed consent at admission. The inclusion criteria were as follow: (a) Positive SARS‐CoV‐2 nucleic acid throat swab test, and a diagnosis consistent with the Diagnostic Standards for COVID‐19 Pneumonia Diagnosis and Treatment Program (Trial Version 6). (b) A definite outcome (survival or death). (c) Clear blood routine test results. (d) Chest CT scans were undertaken and the appropriate features were acquired. Almost all patients underwent multiple chest CT scans during the treatment period, at intervals of 3‐10 days. Specifically, 32 patients received two scans at two time points (the progression stage and the remission stage), and 100 patients had complete data from a scan at only one stage (the remission stage). Herein, the two stages were defined as follows. If the scan was performed within 3 days before the severity category worsened (from ordinary to severe, or from severe to critical) or the total chest lesion was significantly enlarged, this time point was regarded as the progression stage. If the scan was performed within 3 days before the severity category was alleviated (from mild to cured, from ordinary to mild, from severe to ordinary or from critical to severe), this time point was regarded as the remission stage.

2.2. CT scanning

A GE OPTIMA 540 16‐row multilayer spiral scanner ( ) was used for CT scanning. Patients underwent scanning in the supine position. The continuous scan range was from the apex to the bottom of the lung. Scanning parameters were as follows: voltage, 120 kV; tube current, 200 mA; rotation speed, 27.5 mm/turn; pitch, 1.375; and layer pace and layer thickness, 5 mm. Later, the routine algorithm for thin‐layer reconstruction (layer thickness, 1.25 mm) was used to acquire the CT images. Subsequently, chest images were reviewed independently by two senior diagnostic radiologists (one with 15 years and the other with 32 years of experience). The radiologists were blinded to the pathological and clinical status of each patient. When their opinions differed, agreement was reached through discussion.

The lung window and mediastinum window were used to analyse the images, which were grouped according to the dynamic observation and the medical record. We recorded the following CT image characteristics: the lesion lobe, distribution characteristics (subpleural, scattered, or diffused), shape of the lesion (round, nodular or irregular patches), maximum size of the lesion (<3 cm, ≥3 cm and <5 cm, or ≥5 cm), lesion morphology (ground‐glass opacity [GGO] and consolidation features, and when consolidation was positive, the boundary was observed to distinguish whether it was clear), large cable sign (a clear large cable sign that usually appears in the late stages and also the similar linear opacities that are usually observed in the early stages; commonly, an early linear opacity can turn to a large cable sign after absorption; when this sign was positive, we further observed whether it was parallel to the pleura or bridged to the pleura. Figure 1C shows some typical large cable signs), crazy‐paving sign, air bronchogram signs, septal thickening, pleural effusion and mediastinal lymph node enlargement. Other important features are shown in Figure s1.

FIGURE 1.

FIGURE 1

Typical chest CT images. (A) A 43‐year‐old male patient with severe COVID‐19. Left: Scan on the third day after onset of symptoms (progression). Multiple patchy ground‐glass opacities (GGOs) were observed. Right: Scan on the 13th day after onset of symptoms (remission). Lesion volume was reduced, consolidation was significantly increased, and the linear consolidation sign parallel to the pleura appeared in the subpleural area (white arrow). (B) A 67‐year‐old male with severe COVID‐19. Left: Scan on the seventh day after onset of symptoms. Multiple patchy GGOs and some crazy‐paving signs can be seen. Right: Scan on the 25th day after onset of symptoms (remission). Lesions were significantly improved and absorbed, thin sheets of GGO and cable signs can be observed. (C) A 58‐year‐old male patient with ordinary‐type COVID‐19. Left: Scan on the eighth day after onset of symptoms (progression). Multiple patchy GGO shadows can be observed, ground glass with consolidation and stripe shadows in multiple areas. Right: Scan on the 15th day after onset of symptoms (remission). Lesion size was reduced, and consolidation and large cable signs can be seen (some cables parallel to the pleura, as indicated by the white arrow and some cables bridged to the pleura, as indicated by black arrow heads)

2.3. Statistical analysis

SPSS software (version 25.0) was used for statistical analyses. Categorical data were compared using Fisher's exact test. Continuous data were described as mean ± standard and compared using the Mann‐Whitney test or Wilcoxon matched‐pairs signed rank test. Logistic regression was used to predict the development stage. Receiver operating characteristic (ROC) curves were generated using SPSS to assess predictive power. All statistical tests were two‐sided, and a value of P < .05 was considered statistically significant.

3. RESULTS

3.1. Patient characteristics

Together, we enrolled 107 cases, including 58 males and 49 females, with an average age of 44.9 ± 12.7 years. Other demographic characteristics are listed in Table 1. Regarding severity levels, 89.7% were of the ordinary type and 10.3% were in severe stages (severe or critical). Baseline symptoms and signs, and laboratory examination results of enrolled patients were as follows. For symptoms and signs (Table 2), fever, dry cough, expectoration, diarrhoea, throat pain, fatigue and muscle aches were commonly seen signs. For laboratory examination results, elevated C‐reactive protein, lymphopenia and leukopenia were significant phenotypes (Table 2). After an average period of 22.7 days of treatment (22.7 ± 9.0 days, min = 5 days, max = 60 days), all patients were cured and no deaths occurred.

TABLE 1.

Demographic information of enrolled subjects

Index Value or number %
Age 44.88 ± 12.68 (2‐85)
Sex
Male 58 54.2
Female 49 45.8
Nationality
Han 107 100
Labour type
NA 54 50.5
Manual 22 20.6
Mental 31 29.0
Marital status
Unmarried 9 8.4
Married 95 88.8
Divorced 2 1.9
Widowed 1 0.9
Weight (kg) 66.29 ± 13.86 (11.0‐125.0)
Height (cm) 164.45 ± 14.05 (83‐1830)
Severe or not
No 96 89.7
Yes 11 10.3
Infected through family gathering
Unknown 67 62.6
Yes 12 11.2
No 28 26.2
From Wuhan
No 62 57.9
Yes 45 42.1

TABLE 2.

The baseline situation and laboratory examination of enrolled patients

Index Case number %
Symptoms and signs
Fever 68 63.6
Dry cough 32 29.9
Expectoration 6 5.6
Diarrhea 5 4.7
Throat pain 2 1.9
Fatigue 2 1.9
Muscle ache 2 1.9
Headache 1 0.9
Chest tightness 1 0.9
Runny 1 0.9
Conjunctival congestion 1 0.9
Constipation 0 0
Chilly 0 0
Dyspnoea 0 0
Laboratory examination
Total white blood cells
Normal 79 73.8
Declined 27 25.2
Increased 1 0.9
Lymphocyte absolute value
Normal 54 50.5
Declined 53 49.5
Increased 0 0.0
C‐reactive protein (CRP)
Normal 48 44.9
Increased 59 55.1

3.2. CT imaging differences between the two stages

Among all enrolled patients, we found 32 cases with CT images indicating the progression and 100 cases with images indicating the remission stage. Some features were different between the two stages, including round‐shape lesion (8.0% vs 34.4%), GGO (65.0% vs 87.5%), consolidation (62.0% vs 31.3%), large cable sign (59.0% vs 9.4%) and crazy‐paving sign (20.0% vs 50.0%) (Table 3). Fisher's exact test was performed to analyse these features in the 32 cases with CT scans at two time points. Here, a negative result meant that there was no longer an association between remission and progression, namely that large changes occurred when patients entered the remission stage. Consistently, the round‐shape lesion proportion, GGO ratio, consolidation ratio, large cable signs and crazy‐paving signs in the remission stage were no longer correlated with the progression stage (Table 4). In particular, consolidation does not necessarily mean a worsening of COVID‐19 but can be an indicator of a sufficient immune reaction, as well as a sign of improvement. Finally, remission of crazy‐paving sign (which disappeared in 11 individuals) was an obvious indicator of improvement. Some typical cases with consolidation and large cable sign changes are presented in Figure 1, which consistently implied that consolidation and large cable signs are more frequently seen in the remission stage rather than in the progression stage.

TABLE 3.

CT imaging characteristics in progression and remission stages

Progression % Remission %
Total N 32 100
Lobe involved
Right upper lobe 26 81.3% 70 70.0%
Right middle lobe 23 71.9% 66 66.0%
Right lower lobe 30 93.8% 94 94.0%
Left upper lobe 28 87.5% 79 79.0%
Left lower lobe 30 93.8% 94 94.0%
Distribution characteristics
Subpleural 29 90.6% 92 92.0%
Scattered 23 71.9% 72 72.0%
Diffused 8 25.0% 18 18.0%
Lesion shape
Round 11 34.4% 8 8.0%
Irregular patches 31 96.9% 91 91.0%
Max lesion size
<3 cm 7 21.9% 23 23.0%
3‐5 cm 5 15.6% 14 14.0%
≥5 cm 20 62.5% 63 63.0%
Lesion morphology
GGO 28 87.5% 65 65.0%
GGO and consolidation 17 53.1% 56 56.0%
Consolidation 10 31.3% 62 62.0%
Consolidation with clear boundary 9 28.1% 10 10%
Consolidation with blurred boundary 1 3.1% 52 52%
Large cables
Large cable sign 3 9.4% 59 59.0%
Cables parallel to the pleura 1 3.1% 52 52.0%
Cables bridging the pleura 1 3.1% 49 49.0%
Crazy‐paving sign 16 50.0% 20 20.0%
Air bronchogram 25 78.1% 68 68.0%
Septal thickening 25 78.1% 85 85.0%
Pleural effusion 0 0.0% 3 3.0%
Mediastinal lymph node enlargement 0 0.0% 0 0.0%

Abbreviation: GGO, ground‐glass opacity.

TABLE 4.

CT feature changes at the remission stage (using Fisher's exact test)

Features

Progression

No

Progression

Yes

P value
Round‐shape lesion .111
Remission‐No 21 9
Remission‐Yes 0 2
Ground‐glass opacity (GGO) .620
Remission‐No 2 10
Remission‐Yes 2 18
Consolidation .141
Remission‐No 11 2
Remission‐Yes 11 8
Large cable sign .253
Remission‐No 13 0
Remission‐Yes 16 3
Crazy‐paving sign .394
Remission‐No 14 11
Remission‐Yes 2 5

3.3. Features predicting COVID‐19 progression and remission

Using the above associated factors, we pooled all the CT data (n = 132) into one dataset and established a model to predict the current developing stage (remission or progression). Using logistic (two‐tailed) regression, we found the consolidation, boundary feature, large cable sign and crazy‐paving sign variables were the most significant factors distinguishing between progression and remission (Table 5). Next, we constructed a variable that we named “prediction of progression or remission” (PPR) based on the above four parameters (Table 6). The ROC curve showed that PPR had an AUC of 0.882 (cutoff value = 0.66, with a sensitivity of 0.75 and a specificity of 0.875) (Figure 2).

TABLE 5.

Logistics regression in prediction of progression or remission stage

B SE Wald P OR
Right upper lobe −20.440 7090.507 0.000 .998
Right middle lobe −23.063 7090.507 0.000 .997
Right lower lobe −18.572 7090.506 0.000 .998
Left upper lobe −21.436 7090.507 0.000 .998
Left lower lobe −16.321 7090.507 0.000 .998
Involved lobe number 5.418 .247
1 17.236 7090.507 0.000 .998
2 36.871 14 181.014 0.000 .998
3 57.971 21 271.520 0.000 .998
4 80.369 28 362.027 0.000 .998
Subpleural distribution −0.651 1.499 0.188 .664
Scattered distribution −2.685 2.079 1.667 .197
Diffused distribution −2.211 2.068 1.143 .285
GGO −0.025 1.097 0.001 .982
Consolidation 2.952 1.416 4.347 .037 19.149
Boundary feature 4.361 1.496 8.502 .004 78.352
Round lesion shape −1.269 0.805 2.486 .115
Irregular patches −1.201 2.147 0.313 .576
Large cable sign 3.420 0.986 12.027 .001 30.565
Crazy‐paving sign −1.486 0.753 3.895 .048 0.226
Air bronchogram −1.142 0.889 1.650 .199
Septal thickening 20.742 18 803.657 0.000 .999
Pleural effusion 0.975 0.918 1.129 .288
Constant 20.161 7090.507 0.000 .998

TABLE 6.

Logistics regression in prediction of progression or remission stage using four parameters

B SE Wald P OR
Consolidation 2.849 1.074 7.037 .008 17.273
Boundary feature 3.697 1.174 9.910 .002 40.326
Large cable sign 2.373 0.692 11.761 .001 10.729
Crazy‐paving sign −1.195 0.538 4.935 .026 0.303
Constant −3.201 1.221 6.876 .009 0.041

FIGURE 2.

FIGURE 2

A variable named “prediction of progression or remission” (PPR) was constructed to predict the progression and remission stage logistic (two‐tailed) regression based on four signs (consolidation, boundary feature, large cable sign and crazy‐paving sign). The ROC curve showed that PPR had an AUC of 0.882 (cutoff value = 0.66, with a sensitivity of 0.75 and a specificity of 0.875)

4. DISCUSSION

To date, this is the first report regarding unique CT features during progression and remission of COVID‐19. We revealed that the characteristics of round shape, GGO, consolidation, large cable sign and crazy‐paving sign significantly change between the progression and remission stages. Using four features (variable consolidation, boundary feature, large cable sign and crazy‐paving sign) can help to distinguish the development stage of COVID‐19.

Using CT examinations, the occurrence, development and prognosis of COVID‐19 can be comprehensively understood. CT has advantages over histological examination in that it can evaluate the whole lungs. Histological examination may be prone to sampling errors because of sample being obtained from localised regions. Since its emergence, the CT imaging characteristics of COVID‐19 have been studied by different research groups. Case reports have shown common trends during development, such as rapidly progressing peripheral consolidations and GGOs in both lungs. 9 In addition, patchy GGOs have been found in both adult and paediatric COVID‐19 patients., 10 Positive CT findings, including consolidation, greater total lung involvement, linear opacities, crazy‐paving signs and reversed halo signs, are usually more frequent a long time after the onset of symptoms. 11 After the accumulation of samples, typical manifestations of COVID‐19 were reported. Early radiological investigations consistently reported that bilateral GGOs and consolidation with a peripheral and posterior lung distribution were regarded as a cardinal hallmark of COVID‐19. Up to 98% of cases have presented GGO as the most common imaging finding. 12 In Zhejiang province of China, it was reported that the imaging pattern of multifocal peripheral ground‐glass or mixed opacity with predominance in the lower lung is highly indicative of COVID‐19 in the first week of symptom onset. 13 In Korea, the observation of pure to mixed GGO lesions with a patchy to confluent or nodular shape is frequent. 14 Some indirect evidence shows that when compared with the initial CT features, a progressive process may exhibit opacities, consolidation, interstitial thickening, fibrous strips and air bronchograms. 15 GGO with a peripheral distribution is the most widely reported manifestation of COVID‐19. 16 In summary, early CT findings are generally patchy GGO with or without consolidation involving multiple lobes, mainly in the peripheral zone, accompanied by halo sign, vascular thickening, crazy‐paving pattern or air bronchogram sign. 17 However, very few studies have investigated the differences in CT between severity stages, and even fewer studies have reported on the features of progression and remission. In contrast, several reports have described the typical trends of progression. A study published in Lancet Infectious Diseases described Wuhan patients grouped on the basis of the interval between symptom onset and the first CT scan. They showed a trend that as the disease developed, the prevalence of GGOs continued to decrease; meanwhile, consolidation and mixed patterns became more frequent. 18

In our study, the 32 progression cases were all included in the 100 remission cases, and as expected, they had some imaging features in common. Overall, the baseline imaging characteristics were as follow: multiple lesions, multiple lobe involvement, mostly subpleural distribution, lesions located in both lungs, irregular patches, air bronchogram and septal thickening, which are largely consistent with published reports. 19 , 20 , 21

When the disease enters the remission stage, there are no changes in lobe involvement, the distribution of lesions, the maximum lesion size and the shape of the lesion. However, some interesting changes warrant attention. In the remission stage, the frequency of GGO decreases and the frequency of consolidation significantly increases, especially consolidation with blurred boundary. Moreover, increased large cable sign and reduced crazy‐paving sign were indicators of remission in our study. As previously suggested, consolidation and cable sign are common signs of viral pneumonia. 22 , 23 Machine‐learning studies have also suggested that consolidation is one of the most discriminative features of COVID‐19. Theoretically, consolidation may be associated with the coagulopathy status 24 , 25 , 26 in pneumonia. Some researchers believe that an increase in consolidation indicates disease progression, and the degree of lung consolidation and fibrosis is closely related to the severity of the patient's condition. 27 However, the present study is the first work indicating that consolidation is more closely associated with an improvement rather than worsening, and this feature is diverse in the two stages. In our study, the consolidation feature in progression generally showed nodular consolidation or reversed halo sign changes, while the consolidation in remission frequently showed an increased GGO density but reduced volume, and subsequently many consolidations of the GGO areas were dissipated or absorbed accompanied by large cable signs. This is consistent with the observation from Pan et al’s work, 28 which shows that when the disease reaches the peak stage, consolidation usually becomes apparent, and then it enters the absorption phase followed by improvement. In addition, Jin et al claimed that there is a consolidation period after sufficient progression, and the consolidation volume decreases and enters the absorption period. 29 The dynamic observation of all patients showed no increase in consolidation volume. To date, most scholars believe that the consolidation change is an essential part of disease progression, and even a landmark of severe or critical stages. 11 , 30 , 31 However, in our study, we found that consolidation differed in the two stages; the remission stage had more frequent consolidation, and the boundary of consolidation in the remission stage was usually blurred, while that in the progression stage was much clearer. Moreover, the possible pathological mechanisms of consolidation in the two stages are different. Progressive consolidation includes the accumulation of a large amount of cell exudate in the alveolar cavity and vasodilation in the interstitial blood vessels, which cause oedema in alveolar and interstitial vessels, and this aggravates symptoms. Remissive consolidation may include the fibrous exudation of the alveolar cavity and the resolution of capillary congestion in the alveoli wall.

Another finding of our study was that the large cable sign was positively correlated with remission, which suggests that large cable sign indicates the gradual absorption of the lesion and that the patient is recovering. Similar changes were also observed in the study by Bernheim et al 11 but very few studies have drawn a conclusion about the implication to remission. Out of 53 large cable sign cases, 50 showed cable bridging the pleura, which may be because of the absorption speed in the oedema‐thickened interlobular septal being slower than in the exudative lesion. However, the definite mechanism requires further study.

Our study has some limitations. Based on a limited number of cases, we pooled the data of ordinary and severe patients together to form the progression and remission groups, which may have induced intra‐group differences. Our future studies will examine features in different subgroups separately. In addition, the follow‐up time of absorption was limited, and further recovery of lung function and CT remission features is unclear.

5. CONCLUSIONS

In conclusion, CT characteristics may strengthen the recognition of the intrapulmonary development of COVID‐19 and help radiologists distinguish progression and remission phases more accurately over time. In particular, these characteristics include round shape, GGO, consolidation, large cable sign and crazy‐paving sign. Understanding different CT characteristics will help us to better determine the clinical condition and formulate reasonable treatment plans, potentially avoiding over‐treatment.

AUTHOR CONTRIBUTIONS

JL collected data, drafted the initial manuscript, and reviewed and revised the manuscript. YC and CH collected data, and reviewed and revised the manuscript. GH reviewed and revised the manuscript. QC conceptualised and designed the study, collected data, carried out the analyses, critically reviewed the manuscript for important intellectual content, and reviewed and revised the manuscript. JD carried out the analyses, critically reviewed the manuscript for important intellectual content, and reviewed and revised the manuscript.

DISCLOSURE

The authors declare no potential conflicts of interest with respect to authorship, and/or publication of this study.

Supporting information

Fig S1

Liao J‐L, Chen Y, Huang C‐Q, He G‐Q, Du J‐C, Chen Q‐L. Clinical differences in chest CT characteristics between the progression and remission stages of patients with COVID‐19 pneumonia. Int J Clin Pract.2021;75:e13760. 10.1111/ijcp.13760

Jie‐lan Liao, Yu Chen, Chong‐Quan Huang and Gui‐qing He contributed equally as the co‐first authors.

Funding informationThe study was supported by the Major Project of Wenzhou Municipal Science and Technology Bureau (ZY202004), and Basic Public Welfare Research Project of Zhejiang Province (LGF20H010003)

Contributor Information

Ji‐Cheng Du, Email: wzdujicheng@163.com, Email: wzchenquelu@163.com.

Que‐Lu Chen, Email: wzdujicheng@163.com, Email: wzchenquelu@163.com.

DATA AVAILABILITY STATEMENT

The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.

REFERENCES

  • 1. Li T, Lu L, Zhang W, et al. Clinical characteristics of 312 hospitalized older patients with COVID‐19 in Wuhan, China. Arch Gerontol Geriatr. 2020;91:104185. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Hu Y, Chen Y, Zheng Y, et al. Factors related to mental health of inpatients with COVID‐19 in Wuhan, China. Brain Behav Immun. 2020;S0889. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Meehan MT, Rojas DP, Adekunle AI, et al. Modelling insights into the COVID‐19 pandemic. Paediatr Respir Rev. 2020;S1526–0542(20):30099–30103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Li L, Qin L, Xu Z, et al. Artificial intelligence distinguishes COVID‐19 from community acquired pneumonia on chest CT. Radiology. 2020;200905. [Google Scholar]
  • 5. Li K, Wu J, Wu F, et al. The clinical and chest CT features associated with severe and critical COVID‐19 pneumonia. Invest Radiol. 2020;55:327–331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Li K, Fang Y, Li W, et al. CT image visual quantitative evaluation and clinical classification of coronavirus disease (COVID‐19). Eur Radiol. 2020;1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Neri E, Miele V, Coppola F, et al. Use of CT and artificial intelligence in suspected or COVID‐19 positive patients: statement of the Italian Society of Medical and Interventional Radiology. Radiol Med. 2020;125:505–508. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Martino A, Fiore E, Mazza EM, et al. CT features of coronavirus disease 2019 (COVID‐19) pneumonia: experience of a single center in Southern Italy. Infez Med. 2020;28:104–110. [PubMed] [Google Scholar]
  • 9. Wei J, Xu H, Xiong J, et al. 2019 novel coronavirus (COVID‐19) pneumonia: serial computed tomography findings. Korean J Radiol. 2020;21:501–504. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Li W, Cui H, Li K, et al. Chest computed tomography in children with COVID‐19 respiratory infection. Pediatr Radiol. 2020;50:796–799. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Bernheim A, Mei X, Huang M, et al. Chest CT findings in coronavirus disease‐19 (COVID‐19): relationship to duration of infection. Radiology. 2020;295:200463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Ye Z, Zhang Y, Wang Y, et al. Chest CT manifestations of new coronavirus disease 2019 (COVID‐19): a pictorial review. Eur Radiol. 2019;2020:1–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Yang W, Cao Q, Qin L, et al. Clinical characteristics and imaging manifestations of the 2019 novel coronavirus disease (COVID‐19): a multi‐center study in Wenzhou city, Zhejiang, China. J Infect. 2020;80:388–393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Yoon SH, Lee KH, Kim JY, et al. Chest radiographic and CT findings of the 2019 novel coronavirus disease (COVID‐19): analysis of nine patients treated in Korea. Korean J Radiol. 2020;21:494–500. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Xiong Y, Sun D, Liu Y, et al. Clinical and high‐resolution CT Features of the COVID‐19 infection: comparison of the initial and follow‐up changes. Invest Radiol. 2020;55:332–339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Lu T, Pu H. Computed tomography manifestations of 5 cases of the novel coronavirus disease 2019 (COVID‐19) pneumonia from patients outside Wuhan. J Thorac Imag. 2020;35:W90–W93. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17. Han R, Huang L, Jiang H, et al. Early Clinical and CT Manifestations of Coronavirus Disease 2019 (COVID‐19) Pneumonia. AJR Am J Roentgenol. 2019;2020:1–6. [DOI] [PubMed] [Google Scholar]
  • 18. Shi H, Han X, Jiang N, et al. Radiological findings from 81 patients with COVID‐19 pneumonia in Wuhan, China: a descriptive study. Lancet Infect Dis. 2020;20:425–434. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Chen L, Liu HG, Liu W, et al. Analysis of clinical features of 29 patients with 2019 novel coronavirus pneumonia. Zhonghua Jie He He Hu Xi Za Zhi. 2020;43:203–208. [DOI] [PubMed] [Google Scholar]
  • 20. Fang Y, Zhang H, Xu Y, et al. CT Manifestations of two cases of 2019 novel coronavirus (2019‐nCoV) pneumonia. Radiology. 2020;295:208–209. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Kanne JP, Chest CT. Findings in 2019 novel coronavirus (2019‐nCoV) infections from Wuhan, China: key points for the radiologist. Radiology. 2020;295:16–17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Franquet T. Imaging of pulmonary viral pneumonia. Radiology. 2011;260:18–39. [DOI] [PubMed] [Google Scholar]
  • 23. Koo HJ, Lim S, Choe J, et al. Radiographic and CT features of viral pneumonia. Radiographics. 2018;38:719–739. [DOI] [PubMed] [Google Scholar]
  • 24. Georgescu B, Chaganti S, Aleman GB, et al. Machine learning automatically detects COVID‐19 using chest CTs in a large Multicenter Cohort. Elect Eng Syst Sci. 2020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Fu F, Lou J, Xi D, et al. Chest computed tomography findings of coronavirus disease 2019 (COVID‐19) pneumonia. Eur Radiol. 2019;2020:1–10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Okamura K, Kitajima K, Maeyama T, et al. Heparin‐induced thrombocytopenia and disseminated intravascular coagulation in a patient with drug‐induced pneumonia. Nihon Kokyuki Gakkai Zasshi. 2010;48:157–161. [PubMed] [Google Scholar]
  • 27. Shi J, Jiang X, Liu S, et al. Imaging features of COVID‐19: a series of 56 cases. Chin J Clin Infect Dis. 2020;13:E013. [Google Scholar]
  • 28. Pan F, Ye T, Sun P, et al. Time course of lung changes on chest CT during recovery from 2019 novel coronavirus (COVID‐19) pneumonia. Radiology. 2020;295:715–721. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Jin Y‐H, Cai L, Cheng Z‐S, et al. A rapid advice guideline for the diagnosis and treatment of 2019 novel coronavirus (2019‐nCoV) infected pneumonia (standard version). Mil Med Res. 2020;7:2–23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Song FX, Shi NN, Shan F, et al. Emerging coronavirus 2019‐nCoV pneumonia. Radiology. 2020;295:210–217. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Xu YH, Dong JH, An WM, et al. Clinical and computed tomographic imaging features of novel coronavirus pneumonia caused by SARS‐CoV‐2. J Infect. 2020;80:394–400. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Fig S1

Data Availability Statement

The datasets generated and/or analysed during the current study are available from the corresponding author on reasonable request.


Articles from International Journal of Clinical Practice are provided here courtesy of Wiley

RESOURCES