Clinical characteristics of hospitalized patients with COVID-19 in Yueyang, Hunan, China

DOI: https://doi.org/10.21203/rs.3.rs-37583/v1

Abstract

The clinical characteristics of patients with novel coronavirus disease (COVID-19) in Hunan Province are less understood. We analyzed retrospectively the epidemiological, clinical characteristics, and risk factors associated with severity of 113 confirmed COVID-19 cases in Yueyang, Hunan Province, China, from January 20, 2020, to March 8, 2020, and followed until April 13, 2020. Of the 113 confirmed cases, 92 (81.4%) were from or infected by patients from Hubei province. More than half (63) of patients with COVID-19 had no fever in the early stages of disease. 23% patients had no symptoms at the onset. As of March 8, 2020, 113 (100%) of 113 patients had met the discharge criteria, 0 (0%) patients died. Compared with the non-severe cases, severe cases were associated with older age or patients with comorbidities, secondary bacterial infections, and higher levels of C-reactive protein. Longer duration of virus clearance was associated with a higher risk of progression to critical status. Older patients or patients with comorbidities such as diabetes were more likely to have severe condition. Prompt and effective treatment and sufficient medical resources may still significantly reduce hospital-related transmissions and mortality.

Introduction

In December 2019, a series of cases of pneumonia with unknown cause, now known as Corona Virus Disease 2019 (COVID-19), had been reported in Wuhan, China1. Soon after, other areas across the country reported outbreaks, and as of April 29, 2020, a total of 82,862 COVID-19 cases in China have been confirmed with 4633 deaths 2. Unfortunately, the number of infections and deaths is still increasing in the rest of the world 3-5.

At present, information regarding the epidemiological, clinical characteristics, and risk factors of COVID-19 in Hunan province is limited. Yueyang, adjacent to Wuhan, is the second largest prefecture-level city in Hunan province with a population of 5.77 million. There are a large number of people working and studying in Wuhan. Therefore, Yueyang has become one of the main epidemic areas of imported cases. In a retrospective study from Wuhan, the estimated mortality rate was 1.1% for non-critical patients and 32.5% for critical patients6. Another report from the city analyzed the clinical characteristics of 138 hospitalized patients with COVID-19 in Wuhan. They reported 26% of patients received ICU care and the mortality rate was 4.3%7. However, these studies may not represent the realities in the cities outside of Wuhan.

This study describes the epidemiological, clinical characteristics, and risk factors associated with severity of 113 confirmed COVID-19 cases in Yueyang, Hunan Province.

Results

Demographic and clinical characteristics

A total of 113 patients with confirmed COVID-19 were included in the study. The demographic and clinical characteristics were summarized in Table 1. The median age of all patients was 48 years (IQR, 34-59). 49.6% of all patients were male. The median age of severe patients was older than that of non-severe patients (median, years, 63 vs 45, p = 0.001). The median weight was 60 kg (53-68). 32 (28.3%) patients were imported cases from Hubei province, 60 (53.1%) had not been to Hubei Province but were infected by patients form Hubei, and the remaining 21 (18.6%) had no clear contact history. A small number of patients had preexisting comorbidities including diabetes (8.8%), hypertension (10.6%), cardiovascular disease (3.5%), COPD (2.7%), Chronic kidney disease (3.5), Chronic liver disease (7.1%) or HIV infection (0.9%). The most common symptom at onset of illness was cough (68 [60.2%]) and fever (50 [44.2%]), but 23% patients had no symptoms at the onset. For the 26 people with no symptoms, 10 cases had early mild lung lesions, and 16 cases had a normal CT. Compared with non-severe cases, severe cases exhibited more diabetes (45.5% vs 4.9%, p=0.001) and symptoms, including fever (90.9% vs 39.2%, p=0.003), chest Congestion (54.5% vs 8.8%, p<0.001), dyspnea (54.5% vs 2.9%, p<0.001). There are different epidemiological histories between severe and non-severe patients (p=0.009).

Table 1. Baseline Characteristics of Patients With COVID-19                        

Characteristics

Total

Non-severe

Severe

P value

(n=113)

(n=102, 90.3%)

(n=11, 9.7%)

Age (median [IQR])

48.00 [34.0, 59.0]

45.00 [31.3, 58.0]

63.00 [53.0, 68.5]

0.001

Sex, N (%)





   Female

57 (50.4)

52 (51.0)

5 (45.5)

0.975

   Male

56 (49.6)

50 (49.0)

6 (54.5)


Weight (kg, median [IQR])

60.0 [53.0, 68.0]

60.0 [53.0, 67.6]

67.0[57.0, 70.5]

0.149

Epidemiology information, N (%)





   Without any clear contact history

21 (18.6)

17 (16.7)

4 (36.4)

0.009

   Not been to Hubei, but infected by patients 

60 (53.1)

59 (57.8)

1 (9.1)


   From Hubei

32 (28.3)

26 (25.5)

6 (54.5)


Comorbidities, N (%)





   Diabetes 

10 (8.8)

5 (4.9)

5 (45.5)

0.001

   Hypertension 

12 (10.6)

11 (10.8)

1 (9.1)

1.000

   Cardiovascular disease 

4 (3.5)

3 (2.9)

1 (9.1)

0.340

   COPD 

3 (2.7)

2 (2.0)

1 (9.1)

0.267

   Chronic kidney disease 

4 (3.5)

3 (2.9)

1 (9.1)

0.340

   Chronic liver disease 

8 (7.1)

7 (6.9)

1 (9.1)

0.571

   HIV infection 

1 (0.9)

1 (1.0)

0 (0.0)

1.000

Signs and symptoms, N (%)





   Fever 

50 (44.2)

40 (39.2)

10 (90.9)

0.003

   Cough 

68 (60.2)

59 (57.8)

9 (81.8)

0.223

   Fatigue 

31 (27.4)

26 (25.5)

5 (45.5)

0.292

   Chest Congestion 

15 (13.3)

9 (8.8)

6 (54.5)

<0.001

   Dyspnea 

9 (8.0)

3 (2.9)

6 (54.5)

<0.001

   Sore throat 

15 (13.3)

13 (12.7)

2 (18.2)

0.639

   Diarrhea 

6 (5.3)

6 (5.9)

0 (0.0)

1.000

   Myalgia 

18 (15.9)

15 (14.7)

3 (27.3)

0.378

   Headache 

5 (4.4)

5 (4.9)

0 (0.0)

1.000

   Asymptomatic 

26 (23.0)

26 (25.5)

0 (0.0)

0.066


Laboratory and radiographic findings on admission

As shown in Table 2, lymphocytes (P = 0.001) and white blood cell (p = 0.041) were significantly decreased in severe patients. Compared with non-severe patients, the C-reactive protein (CRP, p < 0.001), procalcitonin (PCT, p = 0.001) and lactate dehydrogenase (LDH, p = 0.027) were significantly increased in severe patients. No significant differences in serum biochemical indexes of the liver (ALT and TBIL) and kidney (BUN and Cr), hemoglobin (HGB), platelet count (PLT), erythrocyte sedimentation rate (ESR) and D-dimer were observed between severe and non-severe patients at admission. Of the chest CT images of the 113 patients, 17 (15%) had no change, 75 (66.4%) were mild, 15 (13.3%) were in advanced stage, and 6 (5.3%) were severe on admission. Figure 1 is a typical patient's chest CT from mild to severe stages.

Table 2. Laboratory and Imaging Characteristics of Patients With COVID-19 on Admission to Hospital.

Characteristics

Normal 

Range

Overall

Non-severe

Severe

P value

(n = 113)

(n = 102)

(n = 11)

Laboratory, Median [IQR]






  WBC, ×10^9/L

3.5 - 9.5

4.8 [3.6, 6.1]

4.9 [3.8, 6.2]

3.3 [2.7, 4.8]

0.041

  N, ×10^9/L

1.8 - 6.3

2.8 [2.1, 3.6]

2.8 [2.1, 3.6]

2.1 [1.9, 3.2]

0.245

  L, ×10^9/L

1.1 - 3.2

1.2 [0.9, 1.7]

1.3 [0.9, 1.9]

0.7 [0.5, 1.1]

0.001

  HGB, g/L

115 - 150

130.0 [119.0, 140.0]

130.0 [120.2, 140.0]

125.0 [115.0, 137.5]

0.444

  PLT, ×10^9/L

125 - 350

178.0 [128.0, 240.0]

181.5 [139.3, 241.5]

129.0 [106.5, 208.0]

0.243

  CRP, mg/L

0 - 10

12.0 [1.7, 33.7]

9.4 [1.6, 24.4]

52.2 [39.2, 58.6]

<0.001

  PCT, ng/mL

< 0.05

0.05 [0.04, 0.08]

0.05 [0.04, 0.07]

0.09 [0.08, 0.11]

0.001

  ESR, mm/h

10.0 - 20.0

34.0 [16.0, 45.0]

34.0 [15.0, 45.0]

42.0 [31.0, 64.5]

0.058

  AST, U/L

13 - 35

25.7 [19.4, 31.2]

25.1 [19.2, 30.3]

29.8 [26.5, 41.1]

0.035

  ALT, U/L

7 - 40

20.8 [14.4, 30.8]

20.3 [14.4, 30.0]

30.5 [15.5, 51.0]

0.257

  TBIL, µmol/L

1.7 - 25.0

14.3 [10.0, 20.0]

14.2 [10.6, 19.3]

14.9 [9.6, 22.6]

0.892

  CK, U/L

40 - 200

81.1 [54.2, 128.7]

79.3 [51.2, 124.5]

109.7 [69.7, 205.9]

0.145

  CK-MB, U/L 

0 - 24

13.1 [10.2, 17.1]

13.1 [10.1, 17.1]

11.6 [11.2, 15.3]

0.907

  LDH, U/L

120 - 250

203.9 [167.7, 250.8]

195.2 [167.0, 243.5]

269.2 [219.6, 333.2]

0.027

  BUN, mmol/L

2.6 - 7.5

4.2 [3.5, 5.4]

4.0 [3.4, 5.0]

4.7 [4.4, 6.4]

0.043

  CR, µmol/L

41 - 73

63.7 [53.8, 76.0]

63.7 [53.5, 74.6]

78.6 [57.3, 99.2]

0.104

  D-dimer, mg/L

0 - 500

230.0 [160.0, 367.0]

230.0 [160.0, 350.0]

340.0 [185.0, 630.0]

0.167

Imaging diagnosis, N (%)






  Normal


17 (15.0)

17 (16.7)

0 (0.0)

<0.001

  Early


75 (66.4)

75 (73.5)

0 (0.0)


  Advanced


15 (13.3)

10 (9.8)

5 (45.5)


  Severe

 

6 (5.3)

0 (0.0)

6 (54.5)

 

Abbreviations: WBC, white blood cell; N, neutrophil count; L, lymphocyte count; HGB, hemoglobin; PLT, platelet count; CRP, C-reactive protein; PCT, procalcitonin; ESR, erythrocyte sedimentation rate; AST, glutamic oxaloacetic transaminase; ALT, aspartate aminotransferase; TBIL, total bilirubin abnormal; CK, creatine kinase; CK-MB, creatine kinase-MB; LDH, lactate dehydrogenase; BUN, Blood Urea Nitrogen; CR, creatinine.


Disease progression, complications, treatment and clinical outcomes

As shown in Table 3, the duration of fever (7 vs 2, p = 0.02), days from symptom onset to virus clearance (24 vs 15.5, p < 0.001), days from symptom onset to pneumonia resolution (28 vs 17, p <0.001) and length of hospital stay (21 vs 11, p < 0.001) were longer among severe patients than non-severe patients. In the hospitalization and follow-up period, the complications of COVID-19 were assessed, including secondary bacterial infections (8%), pulmonary fibrosis (2.7%) and acute respiratory distress syndrome (ARDS) (8%). All the above-mentioned complications were more common in 11 severe cases, compared with non-severe cases (all P<0.05). Antiviral drugs were used specifically to treat COVID-19 during hospitalization, including lopinavir/ritonavir (77.9%), arbidol (90.3%), oseltamivir (39.8%) and chloroquine (10%). For severe cases, methylprednisolone (1-2 mg/kg/d) for 3-5 days combined with human gamma-globulin (10-20 g/d) was prescribed. Seven patients received ICU care, and 3 cases received invasive mechanical ventilation. Interferon inhalation was used in almost all patients. As of March 8, 2020, 113 (100%) of 113 patients had met the discharge criteria. 0 (0%) patients died.

Table 3. Disease Progression, Complications, Treatments and Outcome of Patients With COVID-19   

Characteristics

Overall

Non-severe

Severe

P value

(n = 113)

n = (102)

n = (11)

Disease progression, median [IQR]





  Duration of fever 

3.0 [0.0, 4.0]

2 [0.0, 4.0]

7.0 [4.0, 8.0]

0.02

  Peak temperature 

37.3 [36.8, 38.4]

37.0 [36.8, 38.0]

38.5 [38.2, 39.0]

0.001

  From onset to hospitalization 

6.0 [3.0, 9.0]

5.0 [3.0, 9.8]

6.0 [4.5, 7.0]

0.946

  From onset to viral clearance 

16.0 [12.0, 22.0]

15.5 [11.0, 20.8]

24.0 [20.5, 28.5]

<0.001

  From onset to pneumonia resolution 

18.0 [12.0, 24.0]

17.0 [11.3, 22.0]

28.0 [25.0, 40.5]

<0.001

  Length of hospital stay 

12.0 [9.0, 18.0]

11.0 [9.0, 16.0]

21.0 [18.0, 32.5]

<0.001

Complications, N (%)





  Secondary bacterial infections 

9 (8.0)

2 (2.0)

7 (63.6)

<0.001

  Pulmonary fibrosis 

3 (2.7)

0 (0.0)

3 (27.3)

0.001

  ARDS 

9 (8.0)

2 (2.0)

7 (63.6)

<0.001

  Shock 

1 (0.9)

0 (0.0)

1 (9.1)

0.097

Treatment, N (%)





  Lopinavir/ritonavir 

88 (77.9)

78 (76.5)

10 (90.9)

0.475

  Arbidol 

102 (90.3)

92 (90.2)

10 (90.9)

1

  Oseltamivir 

45 (39.8)

37 (36.3)

8 (72.7)

0.043

  Chloroquine 

10 (8.8)

10 (9.8)

0 (0.0)

0.597

  Gamma-globulin 

23 (20.4)

13 (12.7)

10 (90.9)

<0.001

  Corticosteroid 

10 (8.8)

1 (1.0)

9 (81.8)

<0.001

  Need ICU care 

7 (6.2)

0 (0.0)

7 (63.6)

<0.001

  Invasive mechanical ventilation 

3 (2.7)

0 (0.0)

3 (27.3)

0.001

Outcome, N (%)





  Discharge 

113 (100)

102 (90.3)

11 (9.7)

0.172


Risk factors for severe cases

In the multivariable binary stepwise logistic regression model, variables such as secondary bacterial infections (OR 3.43; 95% CI 3.69-6.53), duration of virus clearance (OR 1.16; 95% CI 1.04-1.34), CRP (OR 1.04; 95% CI 1.01-1.08) were significantly associated with severe cases with COVID-19 (Table 4).

Table 4. Risk factors associated with progression to severity

Variables

OR (95% CI)

P value

Secondary bacterial infections 

3.43 (3.69-6.53)

0.005

From onset to viral clearance (d)

1.16 (1.04-1.34)

0.018

Fever 

4.00 (1.70-5.95)

0.071

CRP

1.04 (1.01-1.08)

0.032

 Note: Multivariable binary stepwise logistic regression analysis was used to assess risk factors associated with progression to severity, with factors included age, gender, weight, epidemiology information, comorbidity, fever, lymphocyte count (L), C-reactive protein (CRP), lactate dehydrogenase (LDH), duration of virus clearance, secondary bacterial infections.


Factors affecting virus clearance

In order to assess factors affecting virus clearance, duration of virus clearance is converted into an ordered variable: ≤15d, 15-30d, >30d. The Kruskal-Wallis test found that the rate of patient progress to severe clinical condition was correlated with the duration of virus clearance (P = 0.0025), as shown in Figure 2. In ordered logistic regression model, comorbidity was the only independent prognostic factor of viral clearance (OR 4.85; 95% CI 1.11-22.07, P = 0.037) (Table 5).

Table 5. Factors Associated with Viral Clearance in Ordered Logistic Regression Analysis.

Variables

OR (95% CI)

P value

Age

1.01 (0.99-1.04)

0.335 

Gender (Male)

0.46 (0.20-1.03)

0.060 

Epidemiology information



  Not been to Hubei vs Without any clear contact history

2.12 (0.63-7.44)

0.231 

  From Hubei vs Not been to Hubei

0.84 (0.24-2.95)

0.781 

Comorbidity

4.85 (1.11-22.07)

0.037 

Fever

1.49 (0.64-3.52)

0.354 

Secondary bacterial infections

0.94 (0.14-6.72)

0.954 

Imaging diagnosis



  Early vs Normal

1.53 (0.40-5.93)

0.529 

  Advanced vs Early

2.05 (0.30-14.38)

0.465 

  Severe vs Advanced

4.17 (0.28-62.31)

0.296 

L

1.13 (0.85-1.50)

0.380 

CRP

1.01 (0.99-1.03)

0.356 

LDH

0.99 (0.99,1.00)

0.275 

Weight

0.99 (0.96-1.02)

0.582 

  Note: Duration of virus clearance is converted into an ordered variable: ≤15d, 15-30d, >30d.

Abbreviations: L, lymphocyte count; CRP, C-reactive protein; LDH, lactate dehydrogenase.

Discussion

Data on COVID-19 in Hunan province are very limited. This study provided a comprehensive data on the demographic, epidemiological, laboratory, and radiological characteristics as well as the comorbidities, treatment, and outcomes of inpatients with non-severe and severe COVID-19 in Yueyang, Hunan province. 11 (9.7%) patients in this study were identified as severe cases and mortality was 0%, which differ from the results of Wuhan1,6,7.

Of the 113 confirmed cases, 92 (81.4%) were from or infected by patients from Hubei province, which indicate the importance of disease control measures, especially in the case of peak numbers in areas such as Wuhan, in order to prevent ongoing transmission and contact with close contacts. Severe patients were older and had comorbidities such as diabetes more often than non-severe patients. Therefore, high-quality medical treatment should be given priority to older patient. As shown in the previous studies7, there were no gender difference between severe and non-severe patients in our study. For SARS patients, fever was almost always the first clinical symptom commonly13. However, our data showed more than half (63) of COVID-19 patients had no fever in the early stages of disease. This means that screening a population using a thermometer alone is not enough, and that screening criteria should include other indications.

In previous retrospective study of COVID-19 in Wuhan City1, nearly 1/3 of patients were admitted to the intensive care unit (ICU). In our study, the patients presenting to the hospital were mostly non-severe (90.3%) cases. Although the rate of progression from non-severe to severe cases is not as high as that of SARS or MERS (ranging from 70% to 90%)14,15, prompt and effective treatment may still significantly reduce hospital-related transmissions and mortality.

According to the suggestion of Diagnosis and Treatment of COVID-19 (version 7) 10, all of the patients in this study received antiviral therapy (lopinavir/ritonavir or arbidol), aerosol inhalation of interferon-alpha and traditional Chinese medicine treatment. Until now, all treatments have relied on meticulous supportive care and improved immunity. Specific antiviral drugs for COVID-19 are being developed, but this process may take time. In addition, among our cohort of 113 confirmed patients with COVID-19, glucocorticoid was used in 1% of non-severe patients and 81.8% of severe patients. However, the use of glucocorticoid remains controversial. One study showed that clinical evidence did not support glucocorticoid therapy for COVID-19, nor did the benefits of glucocorticoid-supported therapy be observed 16. Risk factors for severity identified in this study included secondary bacterial infections, duration of virus clearance and CRP, consistent with those in previous reports6,17,18. However, different from previous studies19, our logistic regression analysis results showed comorbidity was identified as an independent risk factor for viral clearance.

Our study had several notable limitations. First, since this was a single-center retrospective study, the results could not be generalized. Second, because some severe patients were directly transferred to provincial medical institutions for treatment, only a few severe patients were monitored in this study. Additionally, the long-term complications of COVID-19 could not be fully assessed due to limited study time.

Methods

Study Design and Participants

Since January 20, 2020, most patients diagnosed with COVID-19 in Yueyang City have been transferred to the Frist People's Hospital of Yueyang. All patients with COVID-19 enrolled in this study were diagnosed according to the interim guidance from the World Health Organization8. The clinical outcomes (discharges, mortality, length of stay) were monitored until April 13, 2020, the final date of follow-up. Acute respiratory distress syndrome (ARDS) was defined according to the Berlin definition9. For severe and non-severe cases, refer to Diagnosis and Treatment of COVID-19 (version 7) issued by National Health Commission of the People’s Republic of China10. Severe cases is defined according to one of the following: (1) Respiratory distress and the respiratory rate (RR)≥30 times/min; (2) In a resting state, transcutaneous oxygen saturation (SaO2) ≤ 93%; (3) Oxygenation index(PaO2/FiO2) ≤ 300 mmHg; (4) Pulmonary imaging showed that the lesion progressed more than 50% at 24-48 hours.

Image assessment method

Images were assessed according to Imaging of Coronavirus Disease 2019: A Chinese expert consensus statement11. Typical CT findings included bilateral pulmonary parenchymal ground-glass opacity (GGO) and consolidative pulmonary opacities, sometimes with a rounded morphology and a peripheral lung distribution12. The computed tomography (CT) scans were divided into four stages: (1) Early-stage: CT showed lung focal single or multiple GGO, mainly distributed in the foreign lung field, and the lower leaf is more common; (2) Advanced stage: Disease progression mostly occurs in a course of 7-10 days, with enlarged and increased density of GGO, and consolidated lesions with air bronchogram sign. GGOs from the early stage expand, and the density increases gradually; (3) Severe stage: Pulmonary imaging may show further expansion of consolidations and diffuse distribution, involving the center and periphery of the lung. More than 2/3 of the lung field was timely affected by lesions, a so-called "white lung". Some studies have shown that the lesion significantly progresses to more than 50% within 24 to 48 hours, indicating that the patients were severe. (4) Recovery stage: The lesion area is reduced and absorbed, or only residual fibrous lesions are seen. These four stages in a 56-year-old male patient are shown in Figure 1.

Data collection

In this retrospective study, we collected data of all the hospitalized patients with COVID-19 from January 20, 2020, to March 8, 2020, and all confirmed cases were followed up to April 13, 2020. The medical records of patients were collected and analyzed from electronic medical records by the research team of the Department of Critical Care Medicine, Xiangya Hospital Centre South University. Demographic information, epidemiological history, laboratory findings, clinical characteristics, chest computed tomographic (CT) scans, treatment and outcomes data were obtained with data collection forms.

Statistical analysis

The median for continuous variables were compared by using Mann-Whitney test. Unordered categorical variables were compared using the chi square test, and the Fisher exact test was used when the sample was limited. Kruskal-Wallis test was used to compare ordered categorical variables across groups.

Multivariable binary stepwise logistic regression analysis was used to assess risk factors associated with progression to severity. Ordered logistic regression analysis was applied to evaluate the factors affecting virus clearance (duration of virus clearance is converted into an ordered variable: ≤15d, 15-30d, >30d). All statistical analyses were performed using R (version 3.6.3). The ggplot2 package was used to plot. A two-tailed p value of less than 0.05 was considered to be statistically significant.

Data Availability

All data generated or analyzed during this study are included in this published article.

Declarations

Author contributions CG performed the literature search, reviewed articles, completed the data analysis using the R (version 3.6.3) and wrote the manuscript. LW and KD collected clinical information of patients with COVID-19. YJ and QP reviewed the articles and provided secondary reviews during the manuscript preparation. JY designed the analysis and revised the manuscript.

Competing interests There is no conflict of interest.

Informed consent Because of the retrospective nature of the study, the Ethics Committee of the Frist People’s Hospital of Yueyang determined that no patient consent was required.

Ethics approval All experimental protocols were approved by the Ethics Committee of the Frist People’s Hospital of Yueyang. All methods were carried out in accordance with relevant guidelines and regulations.

References

1          Huang, C. et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet (London, England) 395, 497-506, doi:10.1016/s0140-6736(20)30183-5 (2020).

2          Update on COVID-19 Outbreak as of 24:00 on 29 April.National Health Commission of the People’s republic of China. http://www.nhc.gov.cn/xcs/yqfkdt/202004/ce78f5575e0d4ef0b4543eb072acebc3.shtml.

3          Richardson, S. et al. Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area. Jama, doi:10.1001/jama.2020.6775 (2020).

4          Onder, G., Rezza, G. & Brusaferro, S. Case-Fatality Rate and Characteristics of Patients Dying in Relation to COVID-19 in Italy. Jama, doi:10.1001/jama.2020.4683 (2020).

5          Livingston, E. & Bucher, K. Coronavirus Disease 2019 (COVID-19) in Italy. Jama, doi:10.1001/jama.2020.4344 (2020).

6          Li, X. et al. Risk factors for severity and mortality in adult COVID-19 inpatients in Wuhan. The Journal of allergy and clinical immunology, doi:10.1016/j.jaci.2020.04.006 (2020).

7          Wang, D. et al. Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus-Infected Pneumonia in Wuhan, China. Jama 323, 1061-1069, doi:10.1001/jama.2020.1585 (2020).

8          World Health Organization.Clinical management of severe acute respiratory infection when COVID-19 is suspected.Published March 13, 2020. Accessed April 1, 2020. https://www.who.int/publications-detail/clinical-management-of-severe-acute-respiratory-infection-when-novel-coronavirus-(ncov)-infection-is-suspected.

9          Ranieri, V. M. et al. Acute respiratory distress syndrome: the Berlin Definition. Jama 307, 2526-2533, doi:10.1001/jama.2012.5669 (2012).

10         Diagnosis and Treatment of COVID-19 (version 7). National Health Commission of the People’s Republic of China. Accessed April 1th 2020., http://www.nhc.gov.cn/yzygj/s7653p/202003/46c9294a7dfe4cef80dc7f5912eb1989.shtml.

11         Yang, Q. et al. Imaging of coronavirus disease 2019: A Chinese expert consensus statement. European journal of radiology 127, 109008, doi:10.1016/j.ejrad.2020.109008 (2020).

12         Chung, M. et al. CT Imaging Features of 2019 Novel Coronavirus (2019-nCoV). Radiology 295, 202-207, doi:10.1148/radiol.2020200230 (2020).

13         Jernigan, J. A., Low, D. E. & Hefland, R. F. Combining clinical and epidemiologic features for early recognition of SARS. Emerging infectious diseases 10, 327-333, doi:10.3201/eid1002.030741 (2004).

14         Vu, H. T. et al. Clinical description of a completed outbreak of SARS in Vietnam, February-May 2003. Emerging infectious diseases 10, 334-338, doi:10.3201/eid1002.030761 (2004).

15         Zumla, A., Hui, D. S. & Perlman, S. Middle East respiratory syndrome. Lancet (London, England) 386, 995-1007, doi:10.1016/s0140-6736(15)60454-8 (2015).

16         Russell, C. D., Millar, J. E. & Baillie, J. K. Clinical evidence does not support corticosteroid treatment for 2019-nCoV lung injury. Lancet (London, England) 395, 473-475, doi:10.1016/s0140-6736(20)30317-2 (2020).

17         Zhang, J. J. et al. Clinical characteristics of 140 patients infected with SARS-CoV-2 in Wuhan, China. Allergy, doi:10.1111/all.14238 (2020).

18         Wu, C. et al. Risk Factors Associated With Acute Respiratory Distress Syndrome and Death in Patients With Coronavirus Disease 2019 Pneumonia in Wuhan, China. JAMA internal medicine, doi:10.1001/jamainternmed.2020.0994 (2020).

19         Cai, Q. et al. COVID-19 in a Designated Infectious Diseases Hospital Outside Hubei Province, China. Allergy, doi:10.1111/all.14309 (2020).