Abstract
Objective
The purpose of this article was to perform a systematic review and meta-analysis regarding the diagnostic test accuracy of chest CT for detecting coronavirus disease 2019 (COVID-19).
Methods
PubMed, Embase, Web of Science, and CNKI were searched up to March 12, 2020. We included studies providing information regarding diagnostic test accuracy of chest CT for COVID-19 detection. The methodological quality was assessed using the Quality Assessment of Diagnostic Accuracy Studies-2 tool. Sensitivity and specificity were pooled.
Results
Sixteen studies (n = 3186 patients) were included. The risks of bias in all studies were moderate in general. Pooled sensitivity was 92% (95% CI = 86–96%), and two studies reported specificity (25% [95% CI = 22–30%] and 33% [95% CI = 23–44%], respectively). There was substantial heterogeneity according to Cochran’s Q test (p < 0.01) and Higgins I2 heterogeneity index (96% for sensitivity). After dividing the studies into two groups based on the study site, we found that the sensitivity of chest CT was great in Wuhan (the most affected city by the epidemic) and the sensitivity values were very close to each other (97%, 96%, and 99%, respectively). In the regions other than Wuhan, the sensitivity varied from 61 to 98%.
Conclusion
Chest CT offers the great sensitivity for detecting COVID-19, especially in a region with severe epidemic situation. However, the specificity is low. In the context of emergency disease control, chest CT provides a fast, convenient, and effective method to early recognize suspicious cases and might contribute to confine epidemic.
Key Points
• Chest CT has a high sensitivity for detecting COVID-19, especially in a region with severe epidemic, which is helpful to early recognize suspicious cases and might contribute to confine epidemic.
Keywords: X-ray computed tomography, Coronaviruses, Pneumonias
Introduction
In December 2019, an outbreak of pneumonia associated with a novel coronavirus called severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was reported in Wuhan, Hubei Province, China [1]. Thereafter, the WHO named the disease as coronavirus disease 2019 (COVID-19). With virus spreading globally, the WHO characterizes COVID-19 as a pandemic.
The keys to control COVID-19 are early discovery, early isolation, and early treatment. At present, the real-time reverse transcription polymerase chain reaction (RT-PCR) assay remains the standard of reference, but it was reported that false-negative RT-PCR was not rare and, in these patients, initial chest CT might present abnormal findings indicating COVID-19 [2]. Moreover, shortage of laboratory test kits limited the use of RT-PCR with the spread of the epidemic, especially in regions severely affected by the epidemic. Therefore, some experts suggested that chest CT could be regarded as a diagnosis standard of COVID-19. The guideline of Diagnosis and Treatment of Pneumonitis Caused by 2019-nCoV (trial sixth version) published by the China government recommended chest CT as an effective method to screen suspicious cases [3]. The addition of chest CT for diagnosis of COVID-19 resulted in tens of thousands of clinically diagnosed cases in China which played an important role in controlling epidemic situation in China [4]. Therefore, comprehensive and timely evaluation of the effectiveness of chest CT for COVID-19 diagnosis remains urgent and mandatory. In the present study, we validated the effectiveness of chest CT for COVID-19 diagnosis through a systematical meta-analysis.
Material and methods
Search strategy and eligibility criteria
PubMed, Embase, Web of Science, and CNKI (until March 31, 2020) were searched for articles that focused on the role of chest CT in diagnosis of COVID-19; there were no language restrictions. The keywords were “COVID-19” or “SARS-CoV-2” or “novel coronavirus” or “2019 nCov.” We also checked the reference lists of all key articles for any additional eligible articles. Studies were included if they met the following criteria: (1) reported the performance of chest CT in diagnosing COVID-19, (2) participants were diagnosed as COVID-19 based on the results of multiple RT-PCR, (3) studies directly or indirectly provided enough information to extract 2 × 2 table information of diagnostic test of chest CT for COVID-19, and (4) study sample was larger than 30. We excluded duplicate reports, abstracts from meeting proceedings. The selection of eligible articles was performed by 2 investigators independently. Disparities between investigators were resolved by discussion between them.
Data extraction and quality assessment
The following data were extracted from each study: study site, sample size, characteristics of participants, chest CT findings, the results of multiple RT-PCR, and 2 × 2 table information. The methodological quality was evaluated by using the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) tool. QUADAS-2 entries include 4 domains: patient selection, index test, reference standard, and flow and timing. Definitions and judgment criteria for each domain are available in Cochrane Handbook. Data extraction and quality assessment were conducted by two independent authors. Disparities between investigators were resolved by discussion between them.
Statistical analysis
A bivariate random-effects model was used to analyze and pool diagnostic performance (sensitivity and specificity) measurements across studies. The chi square–based Q test was performed to test heterogeneity among studies. And, the I2 value was used to evaluate the percentage of interstudy variation in the total variation. When p < 0.05 and/or I2 > 50%, significant heterogeneity was presumed. The meta-analysis was conducted using the “midas” and “metandi” modules in Stata 12.0 software.
Results
Characteristics of studies and quality assessment
The study selection process is presented in Fig. 1. Briefly, 663 references were identified after searching databases. Eight references were removed due to duplication. After scanning the titles and abstracts, 623 records were excluded and 32 full-text articles were assessed for eligibility. Finally, 16 studies were included in our meta-analysis involving 3186 patients [5–20]. Of these patients, 2689 patients had positive RT-PCR results. Fourteen studies only enrolled patients diagnosed as COVID-19 by RT-PCR [6–14, 16–20]. Therefore, we could only calculate sensitivity from the information provided in these studies. Three studies were conducted in Wuhan [5, 8, 12]; 12 studies were conducted in the other regions, and the remaining one collected data throughout China [6, 7, 9–11, 14–20]. The mean or median age of patients ranged from 37 to 62. Seven studies reported the proportion of severe illness which ranged from 3.8 to 41% [6, 10–12, 14, 17, 19]. The characteristics of eligible studies are summarized in Table 1.
Fig. 1.

Flow diagram showing the study selection process for meta-analysis
Table 1.
Characteristics of enrolled studies
| Author | Sample size | Site | Gender (male, %) | Age | Severity (severe, %) | Median interval between CT and RT-PCR (days) |
|---|---|---|---|---|---|---|
| Ai et al [5] | 1014 | Wuhan, China | 46 | Mean age, 51 | NA | 1 |
| Guan et al [6] | 1099a | Throughout China | 58.1 | Median age, 47 | 15.7 | NA |
| Xu et al [7] | 62 | Not Wuhan, China | 56 | Median age, 47 | NA | NA |
| Li and Xia [8] | 51 | Wuhan, China | 55 | Mean age, 58 | NA | 3 |
| Fang et al [9] | 51 | Not Wuhan, China | 57 | Median age, 45 | NA | 3 |
| Yang et al [10] | 149 | Not Wuhan, China | 54 | Mean age, 45 | 8.7 | NA |
| Wu et al [11] | 80 | Not Wuhan, China | 51 | Mean age, 46 | 3.8 | NA |
| Zhang et al [12] | 140a | Wuhan, China | 49 | Median age, 57 | 41 | NA |
| Xu et al [13] | 90 | Not Wuhan, China | 43 | Mean age, 50 | NA | NA |
| Xu et al [14] | 50 | Not Wuhan, China | 58 | Median age, 45 | 26.0 | NA |
| Zhu et al [15] | 116 | Not Wuhan, China | 46 | Median age, 40 | NA | < 1 |
| Long et al [16] | 36 | Not Wuhan, China | 56 | Mean age, 45 | NA | NA |
| Li et al [17] | 78 | Not Wuhan, China | 49 | Mean age, 45 | 10.3 | NA |
| Wang et al [18] | 114 | Not Wuhan, China | 51 | Mean age, 53 | NA | NA |
| Liu et al [19] | 73 | Not Wuhan, China | 56 | Mean age, 37 | 33 | < 2 in 88% of patients |
| Inui et al [20] | 112 | Japan | 53 | Mean age, 62 | NA | NA |
NA not available
aNot all patients received chest CT
The risk of bias and applicability concerns for included studies are shown in Fig. 2. Overall, none of the studies was considered to be seriously flawed according to the QUADAS-2 assessment. At least 4 of 7 items of the QUADAS-2 tool were met in all studies. All studies were considered to have a low risk of bias in the patient selection and reference standard domain. Only two studies reported that the radiologists reading the chest CT images were blinded to the results of RT-PCR which was classified as low risk of bias in the index test domain [5, 20]. The remaining studies were considered to have an unclear risk of bias regarding the index test domain. With regard to the flow and timing domain, we noted that 11 studies had an ambiguous risk of bias due to the absence of mean interval data between chest CT and the RT-PCR assay [6, 7, 10–14]. And, the remaining studies reported a reasonable interval between chest CT and the RT-PCR assay (1–3 days) [5, 8, 9, 15, 19].
Fig. 2.
Grouped bar charts of risk of bias (left) and concerns for applicability (right) of 10 included studies using the Quality Assessment of Diagnostic Accuracy Studies-2 (QUADAS-2) tool
Diagnostic performance of chest CT for diagnosing COVID-19
Sensitivity was available in all studies ranging from 0.61 to 0.99 [5–20]. However, only two studies reported the specificity of chest CT for diagnosing COVID-19 about 25% (95% CI = 21–30%) and 33% (95% CI = 23–44%), respectively (due to the significant heterogeneity and small number of studies, it was inappropriate to pool the data). We pooled the sensitivity values (92%, 95% CI = 86–96%) (Fig. 3). Cochran’s Q test revealed a significant heterogeneity (Q = 419, p < 0.01; I2 = 96.4). Given that the severity of illness, experience of radiologists, and severity of epidemic might contribute to the heterogeneity, we classified the studies into two categories according to whether or not the study site was located in Wuhan where the epidemic was the most severe, patients suffered more severe illness and the radiologists might have more experience. Three studies were conducted in Wuhan which reported sensitivity values about 97% (95% CI = 95–98%) [5], 96% (0.87–100%) [8], and 99% (95% CI = 96–100%) [12], respectively. Due to the small number of enrolled studies, it was inappropriate to pool sensitivity among these three studies, but the sensitivity values were very close to each other. After excluding these three studies, we pooled the sensitivity values of the remaining studies. Nevertheless, the heterogeneity was still so significant that it was inappropriate to pool the sensitivity (Q = 212, p < 0.01; I2 = 94.5). The sensitivity value of the individual study ranged from 0.61 to 0.98 and is summarized in Fig. 3.
Fig. 3.
Coupled forest plots of pooled sensitivity and specificity. Numbers are pooled estimates (dots within squares) with 95% CIs (horizontal lines). Corresponding heterogeneity statistics are provided at the bottom
Due to the specificity only reported in two studies [5, 15], it was inappropriate to plot hierarchical summary receiver operating characteristic (HSROC) curves.
In addition to the significant heterogeneity of the value of chest CT in diagnosing COVID-19, the CT findings in COVID-19 were also varied across enrolled studies. The characteristics of chest CT findings in COVID-19 patients with abnormal CT images are summarized in Table 2. Although the reported proportion might vary across different studies, ground-glass opacity (GGO) and consolidative opacities were some of the most common CT findings, with reporting rates about 49–94% and 11–73%, respectively. Besides, interlobular septal thickening, pleural thickening, and bronchiectasis were also reported with various rates across the studies. With regard to lesion distribution, almost all studies reported that involvement of multiple lobes of both lungs was most common (65–97%). Peripheral zone and lower lobes were more predisposed to be affected.
Table 2.
CT findings in COVID-19 patients with positive chest CT from included studies
| Author | No. of COVID-19 patients with abnormal chest CT | Chest CT finding | Distribution or location | Chest CT manifestation in patients with initial false-negative RT-PCR |
|---|---|---|---|---|
| Ai et al [5] | 580 | GGO (49%); consolidation (55%) | 94% of patients had bilateral chest findings | 15 COVID-19 patients had initial negative RT-PCR. 10/15 patients have positive initial CT findings suggesting COVID-19, and 14/15 patients had positive CT findings prior or parallel to the initial positive results |
| Guan et al [6] | 975 | GGO (56%); local patchy shadowing (42%); bilateral patchy shadowing (52%); interstitial abnormalities (15%) | NA | NA |
| Xu et al [7] | 61 | Most patients showed bilateral or multiple lobular or subsegmental areas of consolidation or bilateral GGO | 84% of patients had bilateral involvement on chest CT | NA |
| Li and Xia [8] | 51 | GGO (90%); consolidation (62%); vascular enlargement (82%); thickened interlobular septa (71%); air bronchogram sign (69%); bronchus deformation due to fibrosis and strip-like lesions (20%); pleural effusion (2%) | 75% of patients had all five lobes affected; 16% of patients had both lower lobes affected; 6% of patients had the right lobe affected; 2% of patients had the left upper lobe and right lower lobe affected; 2% of patients had the left upper lobe and right middle lobe affected; | NA |
| Fang et al [9] | 50 | Most patients had GGO | 72% of patients had peripheral and subpleural lesions. Often in the lower lobes. | 15 patients had negative initial RT-PCR results. All these patients had positive chest CT prior initial positive RT-PCR |
| Yang et al [10] | 132 | GGO and consolidation were the most common presentation | By median, each patient had 3 involved lobes; 35.9% lesions located in the periphery | NA |
| Wu et al [11] | 55 | GGO was the most common presentation | 65% of patients had bilateral chest findings | NA |
| Zhang et al [12] | 134 | Most patients had bilateral multiple GGOs and consolidation | 90% of patients had bilateral chest findings | NA |
| Xu et al [13] | 69 | GGO (94%); consolidation (17%); crazy-paving pattern (12%); interlobular thickening (48%); combined linear opacities (80%); air bronchogram (10%); adjacent pleura thickening (72%) | 77% of patients had more than 2 lobes involved, more than half of the patients presented bilateral, multifocal lung lesions, with peripheral distribution. Lesions were inclined to distribute in the lower lobes. | NA |
| Xu et al [14] | 41 | GGO (73%); consolidation (37%); thickened intralocular septa (73%); thickened interlobular septa (80%); air bronchogram (54%) | Right upper lobe (73%); right middle lobe (54%); right lower lobe (95%); left upper lobe (80%); left lower lobe (88%). 95% of patients have more than 2 lobes involved | NA |
| Zhu et al [15] | 30 | GGO (50%); consolidation (13%); spider web sign (13%); crazy-paving pattern (3%); pleural effusion (7%) | 97% of patients had bilateral chest findings | NA |
| Long et al [16] | 35 | GGO (86%); consolidation (71%); pleural effusion (6%); lymphadenopathy (3%) | Right upper lobe (53%); right middle lobe (56%); right lower lobe (72%); left upper lobe (56%); left lower lobe (67%). 72% of patients had peripheral distribution pattern of lesions. | 6 patients had initial negative RT-PCR, and all these patients had initial positive CT findings |
| Li et al [17] | 56 | GGO (80%); consolidation (21%); thickened interlobular septa (45%); fibrotic lesion (54%); pleural effusion (9%) | 88% of patients had peripheral distribution and 83% of patients had both lungs involved; right upper lobe (57%); right middle lobe (54%); right lower lobe (86%); left upper lobe (75%); left lower lobe (86%) | NA |
| Wang et al [18] | 110 | GGO (73%); consolidation (73%) | 44% of patients had lesions only located in peripheral zone, and 56% of patients had patients located in both peripheral and central zone. 73% of patients had lesions distributing multiple lobes of both lungs | NA |
| Liu et al [19] | 70 | GGO (89%); paving stone sign (40%); consolidation (11%); thickened interlobular septa (93%); pleural effusion (4%) | 74% of patients had bilateral chest findings | NA |
| Inui et al [20] | 68 | GGO and/or consolidation (100%); airway abnormalities (44%) | 82% of patients had bilateral lung involvement; 56% of patients had a peripheral distribution pattern of lesions; right upper lobe (49%); right middle lobe (38%); right lower lobe (49%); left upper lobe (56%); left lower lobe (69%) | NA |
GGO ground-glass opacity, NA not available
In the present review, we also summarized the performance of chest CT in patients with initial false-negative RT-PCR (Table 2). Three studies reported related information [5, 9, 16]. After combining data among these studies, 36 patients had initial false-negative RT-PCR, but 31/36 patients had positive initial chest CT.
Discussion
The main results of this meta-analysis are as follows: (1) the sensitivity of chest CT for COVID-19 was great in Wuhan but varied among other regions, (2) few studies reported the specificity of chest CT which was about 25–33%, (3) typical chest CT findings of COVID-19 were GGO and consolidative opacities which involved multiple lobes of both lungs, and (4) chest CT had a high sensitivity in patients with initial false-negative RT-PCR.
Chest CT plays an important role in detection of COVID-19, especially in the initial and peak periods of epidemic, in China. Although the RT-PCR assay remains the standard of reference, it has been reported that false-negative result after the initial test was not rare and shortage of laboratory kit in the early stage of the outbreak restricted the early detection of COVID-19. As our findings, chest CT had great sensitivity for early detection of COVID-19, especially in regions more affected by epidemic such as Wuhan. Therefore, a clinical diagnosis criterion based on typical CT imaging features was temporarily adopted in the guideline of diagnosis and treatment, which was only applicable in Hubei Province, China [3]. This move allowed to early detect a large number of clinical diagnoses of COVID-19 under the background of shortage of RT-PCR assay which contributed to effective control of epidemic situation in China. Nevertheless, as mentioned above, among regions other than Wuhan, the reported sensitivity of chest CT varied and was generally lower than that in Wuhan. Several reasons might underlie this phenomenon, such as heterogeneity of experience of radiologists, severity of illness, and epidemic. However, unfortunately, most included studies did not provide related data to further confirm this hypothesis. Wu et al [11] reported a relatively low sensitivity of chest CT (69%), and in their study, the proportion of severe patients was only about 3.8% far less than the average level of China which was about 15% [6]. The reported sensitivity of chest CT by Inui et al [20] was particularly low among enrolled studies, about 61%. Although the authors did not report the severity of enrolled patients directly, 73% of patients were asymptomatic and the remaining patients only had mild symptoms [20]. Li et al [17] and Liu et al [19] analyzed the CT results according to the severity of illness and found that almost all mild patients had normal CT images. In addition to severity of illness, Bai et al [21] investigated the performance of radiologists in reading chest CT images of COVID-19 which found the experience of radiologists had a great impact on the diagnosis accuracy of chest CT. Overall, chest CT has a great sensitivity for detecting COVID-19, especially in regions with severe epidemic situation, and is helpful to early detect suspicious cases, which is vital to control epidemic.
In contrast to the great sensitivity of chest CT, the specificity was relatively low with reporting about 25–33%. According to our review, the typical chest CT findings of COVID-19 included GGOs, consolidations, and interlobular thickening, which were usually multifocal and involved bilateral lungs, which was consistent with the results by Salehi et al [22]. In mild patients or early period of COVID-19, chest CT could be negative or pure GGO lesions. The CT imaging features might overlap between COVID-19 and other viral pneumonias, which could reduce the specificity of chest COVID-19. Due to the low specificity of chest CT which might overwhelm available recourses, especially during an influenza epidemic, the American College of Radiology discourages systemic use for diagnosing COVID-19 [23]. Nevertheless, with further investigation and more experienced radiologist, more and more features have been found to be helpful in distinguishing COVID-19 from other pneumonias, such as multifocal or bilateral involvement. So, the specificity of chest CT might improve in the future. In addition, considering the rapidly spreading epidemic of COVID-19, it was a priority to identify any suspicious case in order to isolate the patients and avoid cross infection. Therefore, in the context of emergency disease control, sensitivity was more important than specificity. On the other hand, as mentioned above, although RT-PCR was still regarded as standard reference, false-negative results were not rare. In our review, more than 5% of patients had initial false-negative RT-PCR results and turned positive after multiple tests. However, 86% of these patients presented positive chest CT before the initial negative RT-PCR results. And, more and more cases with initial false-negative RT-PCR but initial positive chest CT have been reported [24]. Last but not the least, chest CT alone could not diagnose COVID-19. According to the guideline of Diagnosis and Treatment of Pneumonitis Caused by 2019-nCoV (trial sixth version) published by the China government, typical chest CT findings could be a diagnostic criterion to screen suspected cases when combined with epidemiology history, clinical manifestations, and laboratory results [3]. Given the concerns over false-negative result and limited availability of RT-PCR and a continuing increase in global cases, the British Society of Thoracic Imaging also underscores the importance of radiographic assessment, especially when there is diagnostic uncertainty [25].
In addition to detection, chest CT also plays an important role in the management of COVID-19. As other pneumonias, the severity of COVID-19 is also positively related to chest CT findings. Intensive care unit (ICU) patients on admission often presented with bilateral multiple lobular and subsegmental consolidations, while non-ICU patients presented with bilateral GGOs and subsegmental consolidation [26]. Moreover, chest CT is helpful to monitor disease progression of COVID-19. Pan et al [27] investigated 21 confirmed patients and summarized four stages of COVID-19: early, progressive, peak, and absorption. Growth of GGOs and expansion of consolidation are indicators of disease progression and, otherwise, might indicate the improvement [28–31].
In conclusion, on the basis of limited and heterogeneous data, chest CT offers the great sensitivity for detecting COVID-19, especially in a region with severe epidemic situation. The specificity is low. In the context of emergency disease control, chest CT provides a fast, convenient, and effective method to early recognize suspicious cases and contributes to reduction of cross infection.
Abbreviations
- COVID-19
Coronavirus disease 19
- GGO
Ground-glass opacity
- RT-PCR
Reverse transcription polymerase chain reaction
- SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2
Funding Information
The authors state that this work has not received any funding.
Compliance with ethical standards
Guarantor
The scientific guarantor of this publication is Fang Peng.
Conflict of interest
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.
Statistics and biometry
One of the authors has significant statistical expertise.
Informed consent
Written informed consent was not required for this study because this is a meta-analysis.
Ethical approval
Institutional review board approval was not required because this is a meta-analysis.
Methodology
• Meta-analysis
Footnotes
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Buyun Xu and Yangbo Xing contributed equally to this work.
References
- 1.Wang DW, Hu B, Hu C et al (2020) Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan, China. JAMA. 10.1001/jama.2020.1585 [DOI] [PMC free article] [PubMed]
- 2.Chan JF, Yuan SF, Kok KH et al (2020) A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster. Lancet. 10.1016/S0140-6736(20)30154-9 [DOI] [PMC free article] [PubMed]
- 3.General Office of National Health Committee. Notice on the issuance of a program for the diagnosis and treatment of novel coronavirus (2019-nCoV) infected pneumonia (trial sixth edition). Available via http://www.nhc.gov.cn/yzygj/s7653p/202002/8334a8326dd94d329df351d7da8aefc2. Accessed 18 Feb 2020
- 4.Zu ZY, Jiang MD, Xu PP et al (2020) Coronavirus disease 2019 (COVID-19): a perspective from China. Radiology. 10.1148/radiol.2020200490 [DOI] [PMC free article] [PubMed]
- 5.Ai T, Yang ZL, Hou HY et al (2020) Correlation of chest CT and RT-PCR testing in coronavirus disease 2019 (COVID-19) in China: a report of 1014 cases. Radiology. 10.1148/radiol.2020200642 [DOI] [PMC free article] [PubMed]
- 6.Guan WJ, Ni ZY, Hu Y et al (2020) Clinical characteristics of coronavirus disease 2019 in China. N Engl J Med. 10.1056/NEJMoa2002032 [DOI] [PMC free article] [PubMed]
- 7.Xu XW, Wu XX, Jiang XG et al (2020) Clinical findings in a group of patients infected with the 2019 novel coronavirus (SARS-Cov-2) outside of Wuhan, China: retrospective case series. BMJ. 10.1136/bmj.m606 [DOI] [PMC free article] [PubMed]
- 8.Li Y, Xia LM (2020) Coronavirus disease 2019 (COVID-19): role of chest CT in diagnosis and management. AJR Am J Roentgenol. 10.2214/AJR.20.22954 [DOI] [PubMed]
- 9.Fang YC, Zhang HQ, Xie JC et al (2020) Sensitivity of chest CT for COVID-19: comparison to RT-PCR. Radiology. 10.1148/radiol.2020200432 [DOI] [PMC free article] [PubMed]
- 10.Yang WJ, Cao QQ, Qin L et al (2020) Clinical characteristics and imaging manifestations of the 2019 novel coronavirus disease (COVID-19): a multi-center study in Wenzhou city, Zhejiang, China. J Infect. 10.1016/j.jinf.2020.02.016 [DOI] [PMC free article] [PubMed]
- 11.Wu J, Liu J, Zhao XG et al (2020) Clinical characteristics of imported cases of COVID-19 in Jiangsu Province: a multicenter descriptive study. Clin Infect Dis. 10.1093/cid/ciaa199 [DOI] [PMC free article] [PubMed]
- 12.Zhang JJ, Dong X, Cao YY et al (2020) Clinical characteristics of 140 patients infected with SARS-CoV-2 in Wuhan, China. Allergy. 10.1111/all.14238 [DOI] [PubMed]
- 13.Xu X, Yu CC, Qu J et al (2020) Imaging and clinical features of patients with 2019 novel coronavirus SARS-CoV-2. Eur J Nucl Med Mol Imaging. 10.1007/s00259-020-04735-9 [DOI] [PMC free article] [PubMed]
- 14.Xu YH, Dong JH, An WM et al (2020) Clinical and computed tomographic imaging features of novel coronavirus pneumonia caused by SARS-CoV-2. J Infect. 10.1016/j.jinf.2020.02.017 [DOI] [PMC free article] [PubMed]
- 15.Zhu W, Xie K, Lu H, Xu L, Zhou S, Fang S (2020) Initial clinical features of suspected coronavirus disease 2019 in two emergency departments outside of Hubei, China. J Med Virol. 10.1002/jmv.25763 [DOI] [PMC free article] [PubMed]
- 16.Long C, Xu H, Shen Q et al (2020) Diagnosis of the coronavirus disease (COVID-19): rRT-PCR or CT? Eur J Radiol. 10.1016/j.ejrad.2020.108961 [DOI] [PMC free article] [PubMed]
- 17.Li K, Fang Y, Li W et al (2020) CT image visual quantitative evaluation and clinical classification of coronavirus disease (COVID-19). Eur Radiol. 10.1007/s00330-020-06817-6 [DOI] [PMC free article] [PubMed]
- 18.Wang K, Kang S, Tian R, Zhang X, Zhang X, Wang Y (2020) Imaging manifestations and diagnostic value of chest CT of coronavirus disease 2019 (COVID-19) in the Xiaogan area. Clin Radiol. 10.1016/j.crad.2020.03.004 [DOI] [PMC free article] [PubMed]
- 19.Liu KC, Xu P, Lv WF et al (2020) CT manifestations of coronavirus disease-2019: a retrospective analysis of 73 cases by disease severity. Eur J Radiol. 10.1016/j.ejrad.2020.108941 [DOI] [PMC free article] [PubMed]
- 20.Inui S, Fujikawa A, Jitsu M et al (2020) Chest CT findings in cases from the cruise ship “Diamond Princess” with coronavirus disease 2019 (COVID-19). Radiology: Cardiothoracic Imaging. 10.1148/ryct.2020200110 [DOI] [PMC free article] [PubMed]
- 21.Bai HX, Hsieh B, Xiong Z et al (2020) Performance of radiologists in differentiating COVID-19 from viral pneumonia on chest CT. Radiology. 10.1148/radiol.2020200823 [DOI] [PMC free article] [PubMed]
- 22.Salehi S, Abedi A, Balakrishnan S, Gholamrezanezhad A (2020) Coronavirus disease 2019 (COVID-19): a systematic review of imaging findings in 919 patients. AJR Am J Roentgenol. 10.2214/AJR.20.23034 [DOI] [PubMed]
- 23.American College of Radiology. ACR recommendations for the use of chest radiography and computed tomography (CT) for suspected COVID-19 infection. Available via https://www.acr.org/Advocacy-and-Economics/ACR-PositionStatements/Recommendations-for-ChestRadiography-and-CT-for-Suspected-COVID19-Infection. Accessed 22 March 2020
- 24.Xie X, Zhong Z, Zhao W, Zheng C, Wang F, Liu J (2020) Chest CT for typical 2019-nCoV pneumonia: relationship to negative RT-PCR testing. Radiology. 10.1148/radiol.2020200343 [DOI] [PMC free article] [PubMed]
- 25.British Society of Thoracic Imaging. Radiology decision tool for suspected COVID-19. Available via https://www.bsti.org.uk/media/resources/files/NHSE_BSTI_APPROVED_Radiology_on_CoVid19_v6_ucQ1tNv. Accessed 16 March 2020
- 26.Huang CL, Wang YM, Li XW et al (2020) Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet. 10.1016/S0140-6736(20)30183-5 [DOI] [PMC free article] [PubMed]
- 27.Pan F, Ye TH, Sun P et al (2020) Time course of lung changes on chest CT during recovery from 2019 novel coronavirus (COVID-19) pneumonia. Radiology. 10.1148/radiol.2020200370
- 28.Song FX, Shi NN, Shan F et al (2020) Emerging 2019 novel coronavirus (2019-nCoV) pneumonia. Radiology. 10.1148/radiol.2020200274
- 29.Shi H, Han X, Zheng C (2020) Evolution of CT manifestations in a patient recovered from 2019 novel coronavirus (2019-nCoV) pneumonia in Wuhan, China. Radiology. 10.1148/radiol.2020200269 [DOI] [PMC free article] [PubMed]
- 30.Duan YN, Qin J (2020) Pre- and posttreatment chest CT findings: 2019 novel coronavirus (2019-nCoV) pneumonia. Radiology. 10.1148/radiol.2020200323 [DOI] [PMC free article] [PubMed]
- 31.Wu Y, Xie Y, Wang X (2020) Longitudinal CT findings in COVID-19 pneumonia: case presenting organizing pneumonia pattern. Radiology: Cardiothoracic Imaging. 10.1148/ryct.2020200031 [DOI] [PMC free article] [PubMed]


