key: cord-0964203-ox03vnpw
authors: Cao, Yukun; Han, Xiaoyu; Gu, Jin; Li, Yumin; Liu, Jia; Alwalid, Osamah; Cui, Yue; Zhang, Xin; Zheng, Chuansheng; Fan, Yanqing; Wu, Hanping; Shi, Heshui
title: Prognostic value of baseline clinical and HRCT findings in 101 patients with severe COVID-19 in Wuhan, China
date: 2020-10-16
journal: Sci Rep
DOI: 10.1038/s41598-020-74497-9
sha: ef1da581ad94a79d576b42162b005ff62623f8a7
doc_id: 964203
cord_uid: ox03vnpw

The aim of this study was to assess the prognostic value of baseline clinical and high resolution CT (HRCT) findings in patients with severe COVID-19. In this retrospective, two-center study, we included two groups of inpatients with severe COVID-19 who had been discharged or died in Jin Yin-tan hospital and Wuhan union hospital between January 5, 2020, and February 22, 2020. Cases were confirmed by real-time polymerase chain reaction. Demographic, clinical, and laboratory data, and HRCT imaging were collected and compared between discharged and deceased patients. Univariable and multivariable logistic regression models were used to assess predictors of mortality risk in these patients. 101 patients were included in this study, of whom 66 were discharged and 35 died in the hospital. The mean age was 56.6 ± 15.1 years and 67 (66.3%) were men. Of the 101 patients, hypertension (38, 37.6%), cardiovascular disease (21,20.8%), diabetes (18,17.8%), and chronic pulmonary disease (16,15.8%) were the most common coexisting conditions. The multivariable regression analysis showed older age (OR: 1.142, 95% CI 1.059–1.231, p < 0.001), acute respiratory distress syndrome (ARDS) (OR: 10.142, 95% CI 1.611–63.853, p = 0.014), reduced lymphocyte count (OR: 0.004, 95% CI 0.001–0.306, p = 0.013), and elevated HRCT score (OR: 1.276, 95% CI 1.002–1.625, p = 0.049) to be independent predictors of mortality risk on admission in severe COVID-19 patients. These findings may have important clinical implications for decision-making based on risk stratification of severe COVID-19 patients.

Baseline laboratory findings in severe COVID-19 patients. The laboratory findings showed the levels of hyper-sensitive C-reactive protein, Serum amyloid A protein, and erythrocyte sedimentation rate were markedly increased in almost all patients ( Table 2 ). The lymphocyte count, hemoglobin, albumin level on admission and oxygen saturation on room air were significantly lower in deceased patients than discharged patients (p < 0.05). Lactate dehydrogenase (LDH), creatinine, D-dimer and hypersensitive troponin I level on admission were higher in deceased patients than discharged patients (p < 0.05) ( Table 2 ).

Baseline HRCT findings in severe COVID-19 patients. The median time interval from admission to baseline CT scan in all patients were 4 days (IQR 1-9), with no difference between discharged and deceased patients ( Table 3 ). The typical chest CT findings of severe COVID-19 on admission were diffuse bilateral GGO and consolidation in peripheral areas (Figs. 2, 3, 4, 5, 6, 7) . GGO (90, 89.1%) is main diffusion lesion characteristics in all patients, and consolidation proportion (8 [22.9] vs 3 [4.5] , p = 0.005) was comparatively higher in deceased patients than discharged patients ( Table 3 ). The mean total CT scores in all patients was 17.4 ± 5.1. Deceased patients had higher CT scores than discharged patients (20.9 ± 3.0 vs 15.6 ± 5.0, p < 0.001) (Fig. 1) .

The other common CT findings were interlobular septal thickening (72/101, 71.3%), crazy paving (48/101, 47.5%) and air bronchograms (75/101, 74.3%). The relatively less common CT findings were pleural effusion (28/101, 28%), emphysema (15/101, 14 .9%), hydropericardium (10/101, 9.9%) and pneumomediastinum (3/101, 3.0%) ( Table 3) .

Interlobular septal thickening, crazy-paving, air bronchogram, and pleural effusion were significantly more common in deceased patients than discharged patients (p < 0.05) ( Table 3) .

Univariate and multivariable analysis of predictors of mortality risk. By univariate regression analysis in severe COVID-19 patients, the following baseline characteristics were predictors of mortality risk: older age, faster respiratory rate, ARDS, history of diabetes, history of hypertension; the following laboratory findings were predictors of mortality risk: reduced lymphocyte count, reduced albumin, elevated lactate dehydrogenase, elevated D-dimer, reduced SpO2 at room air; the following baseline HRCT findings were predictors of mortality risk: elevated total HRCT score, higher consolidation proportion, pleural effusion ( Table 4) .

The multivariable regression analysis showed older age www.nature.com/scientificreports/ www.nature.com/scientificreports/ p = 0.013), and elevated HRCT score (OR: 1.276, 95% CI 1.002-1.625, p = 0.049) independent predictors of mortality risk on admission in severe COVID-19 patients (Table 5 ).

In this study, we have investigated the prognostic value of baseline clinical and HRCT findings in severe patients with COVID-19. In two previously published prognostic studies 11, 12 , included groups were not all severe patients and HRCT findings associated with poor clinical outcomes have not been specified. The main finding of our study was that older age, developed ARDS, lymphocytopenia, and high CT score were the independent predictors of mortality risk in severe patients with COVID-19. In our study, the mean age of severe patients with COVID-19 was 56.6 ± 15.1 years old, and more than 60% of patients were men. As described in previous studies 2, 3, 9, 10 , elderly male patients are more susceptible to SARS-CoV-2 infection, which were supported by our severe patient cohort. But there was no sexual distinction between deceased and discharged patients in our study, which indicated gender is not a risk factor of death. In concert with a recent study 10 , we observed that deceased group was significantly older than the discharged group in severe COVID-19. And in the multivariable regression analysis, we have demonstrated the older age was an independent predictor of mortality risk in severe COVID-19 patients. Therefore, the clinical imperatively management for severe elderly patients requires further attention. Fever is the most common clinical symptom in severe patients with COVID-19, but 5% patients had no fever at the onset of disease, which is also in line with previous studies 8, 16 . If patients are asymptomatic SARS-CoV-2 carriers, early diagnosis is relatively difficult for areas with less medical specialties 1 . Absence of typical initial symptoms for few patients may delay the optimal quarantine and treatment time and lead to poor outcome. However, in our present study, no significant differences were found between the initial symptoms of deceased patients and discharged patients.

ARDS characterized by an acute, diffuse, inflammatory lung damage is one of the most common causes of respiratory failure in critically ill patients with viral pneumonia 17 . In our study, compared with discharged patients with severe COVID-19, the deceased group has significantly higher incidence of ARDS. ARDS was an independent predictor of mortality risk in severe COVID-19 patients, which is similar to critically ill patients with SARS 18 . The incidence of ARDS in the present study is consistent with previous critically ill patients with www.nature.com/scientificreports/ COVID-19 10 , but which is slightly higher than that previously seen in patients with SARS 18, 19 and MERS 20 . Such a discrepancy may be due to failure to timely diagnosis and treatment in the situation of sudden increase in infected patients. Of note, the incidence of ARDS of survivors in the present study is significantly higher than that recently reported in Zhou's study 12 . The different inclusion criteria, our discharged group were all severe patients, may result in the problem. In future, the earlier recognition of ARDS and ongoing efforts to study potential mechanisms of pulmonary damage in severe COVID-19 are the keys to reduce mortality rate. In addition, hypertension, cardiovascular disease and diabetes are the most common comorbidities in severe patients, which is in keep with previous studies 9, 10 . Similarly, deceased patients had more comorbidities, such as hypertension, diabetes, and chronic pulmonary disease, than those discharged. Although comorbidities were not risk factors for death event in multivariable regression analysis, clinicians still require to focus on the clinical progression in severe patients. In terms of laboratory indexes, more than 80% of severe patients in the present study have lymphocytopenia on admission, and the lymphocyte count was significantly lower in deceased patients than discharged patients. This finding is similar to previous COVID-19, SARS and MERS patients 10, 21, 22 . Unlike Chen's study showed less than 40% of non-severe patients had only mild lymphocytopenia, the present study indicated the extent of lymphocytopenia may reflect the severity of SARS-CoV-2 infection. Furthermore, our study first demonstrated lymphocytopenia is an independent predictor of mortality risk in severe patients with COVID-19. Prior studies reported that severe SARS or MERS patients were prone to have lymphocytopenia. It may due to virus particle directly invading and damaging the lymphocyte cytoplasmic component or lymphocytes apoptosis 16, 22 . Unfortunately, the pathogenesis of lymphocytopenia in severe COVID-19 is still unclear by now, later basic immunology may be the key to solve the problem. Additionally, compared with discharged patients, deceased patients had lower hemoglobin and albumin level, higher LDH, Creatinine, D-dimer and hypersensitive troponin I level.

These abnormal results suggest that the severity of SARS-CoV-2 infection may be related to coagulation activation, myocardial damage and kidney damage. Unlike a previous study 9 , although more than 50% severe patients have elevated ALT and AST, no significant differences of ALT and AST level were found between deceased and discharged patients with severe COVID-19. Liver damage in patients with COVID-19 is common, especially in critically ill patients. The possible reasons are as follows: (1) liver cells are possibly directly infected with virus, (2) drug hepatotoxicity in the treatment, (3) immune-mediated inflammation, such as cytokine storm 23 . Although, liver damage is not a prognostic factor in the present study, further research still should pay close attention to the causes and evolution of liver injury in COVID-19. www.nature.com/scientificreports/ Of note, the present study showed that elevated baseline HRCT score is an independent prognostic factor of mortality risk in severe COVID-19 patients. CT score 24 was a semi quantitative parameter, which could quantify the severity of pulmonary abnormalities (GGO and consolidation dominated in COVID- 19) . Previous studies 22, 25 have demonstrated that the score was correlated with the degree of pulmonary lesions in pathologic specimens. CT score has been applied in the quantitative assessment of the evolution of pulmonary lesions in previous SARS 26 and COVID-19 patients 27 . To the best of our knowledge, this is the first study to assess the prognostic www.nature.com/scientificreports/ value of baseline CT score, which has a significant value for clinical decisions based on radiological risk stratification in severe COVID-19 patients. We have reasons to believe that CT scan after hospital admission may be an important imaging modality in assisting the diagnosis and assessment of outcome in patients with severe COVID-19. However, given the infectious risk of transporting patients with COVID-19 for other hospitalized patients and health care workers, it's necessary to select the appropriate timing for immediate CT imaging. First, in the outbreak stage of COVID-19, RT-PCR for SARS-CoV-2 viral nucleic acid was reported to have a sensitivity of less than 60% 15, 28 . Based on a higher sensitivity (80-90%) for COVID-19 15, 29 , HRCT can be considered as a primary tool for the current COVID-19 detection in epidemic areas. Second, With the improvement of (a,b) . The mediastinal window (c) shows a small pleural effusion at the right (arrow) and a small pericardial effusion (arrow). The patient died 4 days after this scan due to respiratory failure.

Transverse CT scans in a woman infected with SARS-CoV-2 and suffering type 2 diabetes for 10 years. Scan obtained on 16th day from onset of symptoms shows bilateral, diffuse consolidation, which predominantly involved the lower lobes. There was pneumomediastinum were also seen (a,b arrows). The patient died 7 days after this scan because of both circulatory and respiratory failure. www.nature.com/scientificreports/ the accuracy and rapidity of the RT-PCR testing, immediate CT imaging is mainly used for suspected positive patients 30, 31 . In addition, there were no pregnant women among the study, however, according to previous studies, HRCT examination for pregnant patients may be performed in the appropriate clinical settings 32 . Given the concern of radiation exposure to the fetus, for asymptomatic pregnant patients, self-quarantine until the results of RT-PCR (not CT) are available may be considered. For pregnant patients who are prone to severe COVID-19, CT scan after hospital admission may be an important tool in assisting reasonable risk stratification and timely clinical management. Like SARS and MERS, the CT findings of severe COVID-19 patients were nonspecific, which included diffusely bilateral GGO and consolidation of subsegmental areas. However, the extent of consolidation in severe COVID-19 patients was less severe than SARS patients 33 . Interestingly, although GGO was mainly diffuse in all patients, the consolidation proportion was comparatively higher in died patients than discharged patients. In a recent autopsy report of a deceased COVID-19 patient, Liu et al. 34 demonstrated that edema, inflammatory infiltrate, and exudation were common in affected lung areas. Those may explain the predominant pattern of GGO on CT images 35 . At present, the relation between the extent of consolidation and outcome is unclear, which needs further large sample autopsy and HRCT studies. In this study, 28% patients with severe COVID-19 had pleural effusion, and which was significantly more common in deceased patients than discharged patients. Due to the present study mainly included severe patients, the incidence of pleural effusion may be higher than previous studies [36] [37] [38] . Das et al. study 39 showed that the presence of pleural effusion was a poor prognostic factor in patients with MERS. Consequently, severe patients having abnormal pleural effusion deserve the attention of clinicians. All in all, baseline CT may be an important imaging modality in assisting the diagnosis and assessment of outcome in patients with severe COVID-19.

This study has several limitations. First, the sample size was small. Second, this is a retrospective study design, a few of clinical and laboratory results were missing in some patients, which may lead to unavoidable biases in analysis. Third, some survivors still hospitalized were not included the present study, the mortality rate of severe patients was overestimated in this study.

In conclusion, older age, ARDS, lymphocytopenia and elevated CT score were strong predictors of mortality risk in severe COVID-19 patients. Patients who are prone to severe COVID-19, CT scan after hospital admission may be an important imaging modality for assisting assessment of outcome in patients with severe COVID-19. Our findings may have important implications for clinical decisions based on risk stratification in severe pneumonia patients. As our study was retrospectively designed with possible selection bias, further prospective studies are needed to confirm our findings.

Study design and participants. A retrospective two-center study was performed in Wuhan Jin Yin-tan hospital and Wuhan Union hospital (Wuhan, Hubei province, China). From January 5, 2020, to Feb 22, 2020, we enrolled two groups of patients (deceased and discharged patients) with severe COVID-19, who underwent HRCT scan at admission. All patients of confirmed infection with SARS-CoV-2 are in accordance with World Figure 6 . Transverse CT scans in a man infected with SARS-CoV-2. Scan obtained on 10th day from onset of symptoms shows diffuse, heterogeneous consolidation that affected bilateral, subpleural lung parenchyma. The patient was discharged from hospital 7 days the scan. www.nature.com/scientificreports/ www.nature.com/scientificreports/ Health Organization (WHO) interim guidance 40 . Throat swab samples were collected for confirmation of SARS-CoV-2 by the real-time polymerase chain reaction assay as previously described 2,3 . The diagnostic criteria for adult severe pneumonia was according to WHO interim guidance 41 , which includes fever or suspected respiratory tract infection, plus one of followings: respiratory rate > 30 breaths/min, SpO2 < 90% on room air or severe respiratory distress. The discharge criteria for patients was according to the sixth edition of "pneumonia diagnosis and treatment plan for new coronavirus infection" in China 42 , which includes normal temperature for more than 3 days, both the respiratory symptoms and chest imaging showing significant improvement, and negative two consecutive respiratory pathogen nucleic acid tests with the interval at least 1 day. This study had ethics approval of the Ethics Commission of Wuhan Jin Yin-tan hospital and Wuhan Union hospital. All participants remained anonymous, and written informed consent was waived by ethics commission for rapid emerging infectious diseases. This study was conducted in compliance with the Declaration of Helsinki.

Clinical data collection. We reviewed the electronic medical records, nursing records, laboratory findings, and radiology findings in all patients. All data were independently reviewed and checked by four physicians (J.L., Y.L., X.H., Y.C.). We collected age, sex, exposure history, underlying disease, maximum body temperature, vital signs, onset of symptoms, and the laboratory finding at admission (complete blood count, liver and kidney function, coagulation profile, C-reactive protein, erythrocyte sedimentation rate, blood gas analysis etc.) and treatment measures [oxygen therapy, antiviral agents, antibacterial agents, corticosteroids, immunoglobulin, tracheal intubation and extracorporeal membrane oxygenation (ECMO)]. In addition, the durations from onset of disease to hospital admission, chest HRCT scan, ARDS and ICU admission were recorded. ARDS was diagnosed according to the Berlin definition 43 .

HRCT image acquisition. All patients underwent HRCT examination in the supine position on one of the three CT scanners: SOMATOM Definition AS+, SOMATOM Perspective, or SOMATOM Spirit (Siemens Healthineers, Germany). Scans were done from the thoracic inlet to the diaphragm, and no contrast medium was used. CT scan parameters were as described in our previous study 38 . All images were reconstructed using standard reconstruction algorithms with a slice thickness of 2 mm or 5 mm. The multiplanar reconstruction postprocessing was implemented on workstation and picture archiving and communication systems. www.nature.com/scientificreports/ HRCT image interpretation. All HRCT images were reviewed in random order by three radiologists (H.S., J.G., Y.F.) who were senior cardiothoracic radiologists. The readers independently assessed the CT features using both axial and MPR images, who were unaware of any other clinical and laboratory findings or outcome of the patients. After independent evaluation, discussion and consensus resolved the disagreements. For each severe pneumonia patients, the predominant HRCT patterns defined by the Fleischner Society glossary 44 were as following: ground-glass opacities (GGO), consolidation, interlobular septal thickening, crazypaving pattern, air bronchogram, pneumonectasis, pleural effusion and pneumomediastinum. The distribution of lesion was categorized as diffuse central area and peripheral area.

To quantify the extent of pulmonary abnormalities, a HRCT score system 24 was assigned on the basis of the area involved. And a previous study 22 has demonstrated that this system was correlated well with the degree of pulmonary lesions in pathologic specimens. Specifically, each of the five lung lobes was visually scored from 0 to 5 as: 0, no involvement; (1) < 5% of lobe (minimal but not normal), (2) 5-25% of lobe, (3) 26-49% of lobe; (4) 50-75% of lobe; (5) > 75% of lobe. Finally, the total CT severity score was calculated by summing the individual lobar scores (range of possible scores from 0 to 25).

The Kolmogorov-Smirnov test was used to checked the normality of all continuous data. Normally and non-normally distributed data and categorical variables are expressed as the mean (SD) and the medians (IQR) and number (%), respectively. We assessed differences between two groups of normally distributed variables using two-sample t test or Mann-Whitney U test depending on normally and non-normally distributed data for continuous variables and Fisher's exact test for categorical variables. The association between baseline clinical or HRCT Findings and incidence of death events was assessed with univariate logistic regression model (P < 0.1 in Tables 1, 2, 3) . From a clinical point of view, to ensure proper independent variable number and avoid variable overfitting of the final multivariable model, we implemented the following step: (1) first, a multivariable model (Model 1: baseline characteristics) was tested, including those baseline variables that showed an association (p < 0.1 in Table 4 ) with incidence of death events. (2) A second multivariable model (Model 2: laboratory findings) was tested, including those baseline laboratory findings that showed an association (p < 0.1 in Table 4 ) with incidence of death events. (3) A third multivariable model (Model 3: HRCT findings) was tested, including those baseline HRCT findings that showed an association (p < 0.1 in Table 4 ) with incidence of death events. (4) A final multivariable model (Model 4: baseline characteristics plus laboratory findings plus HRCT findings) included variables from Model 1-3 that were independently related to the incidence of death events. The minimum sample size of the study should be 10 times greater than the included independent variable number. Co-linearity of variables tested in multivariate regression model (Table 4 ) was evaluated using the tolerance statistic and the variance inflation factor (excessive if < 0.1 and if > 10, respectively). Statistical significance was considered a p value < 0.05 (2-tailed). Analyses were conducted using SPSS software (SPSS 21.0 for Windows, IBM, Chicago, IL, USA).

Ethics declarations. This study was approved by both ethics committees of Union hospital of Tongji Medical College of Huazhong University of Science and Technology and Wuhan Jin-yintan hospital. The written informed consent was waived by ethics commission for rapid emerging infectious diseases.

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

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We would like to thank all colleagues for helping us during the current study. This study was supported by Nation Science Foundation of China (82071921), Zhejiang University special scientific research fund for COVID-19 prevention and control and the Fundamental Research Funds for the Central Universities (2020kfyXGYJ019). 

The authors declare no competing interests.

Correspondence and requests for materials should be addressed to Y.F., H.W. or H.S.

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