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review.
COVID-19 outbreak in Italy: Experimental chest x-
ray scoring system for quantifying and
monitoring disease progression
CURRENT STATUS: POSTED
Andrea Borghesi
Department of Medical and Surgical Specialties, Radiological Sciences and Public Health,
University of Brescia, ASST Spedali Civili of Brescia, Piazzale Spedali Civili, 1, I - 25123
Brescia, Italy
andrea.borghesi@unibs.itCorresponding
Author ORCiD: https://orcid.org/0000-0002-4761-
2923
Roberto Maroldi
Department of Medical and Surgical Specialties, Radiological Sciences and Public Health,
University of Brescia, ASST Spedali Civili of Brescia, Piazzale Spedali Civili, 1, I - 25123
Brescia, Italy
1
DOI:
10.21203/rs.3.rs-19842/v1
Infectious Diseases
SUBJECT AREAS
Nuclear Medicine & Medical Imaging
KEYWORDS
SARS-CoV-2, COVID-19, Chest X-ray, Computed Tomography, Scoring System
2
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a new virus recently isolated
from
hum ans . SARS-CoV-2 was discovered to be the pathogen responsible for a cluster of
pneumonia associated with severe respiratory disease occurred in December 2019 in
China. This novel
pulmonary infection, formally called coronavirus disease 2019 (COVID-19), h as spread rapidly in
China and beyond. On 8 March 2020, the number of Italians with SARS-CoV-2 infection was 7375
with a 4 8 % hospitalization rate.
At present, chest computed tomography im aging is considered the most effective method for
detection of lung abnormalities in early-stage disease and for quantitative assessm ent of
severity and progression of COVID-19 infection. Although chest x-ray (CXR) is considered not
sensitive for the detection of pulmonary involvement in the early stage of disease, we believe
that, in the current em ergency setting, CXR can be a useful diagnostic tool for monitoring the
rapid progression of lung abnormalities in infected patients, particularly in intensive care units.
In this article we present our experimental CXR scoring system that we are applying in
hospitalized patients with COVID-19 pneum onia to quantify and monitor the severity and
progression of this new infectious disease. We also present the results of our preliminary
validation study on a sam ple of 100 hospitalized patients with SARS-CoV-2 infection for whom
the final outcome (recovery or death) was available.
Introduction
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV–2) is a new virus recently isolated
from
hum ans. This new virus is a betacoronavirus that belongs to the Orthocoronavirinae subfamily
of the Coronaviridae family [1, 2]. SARS-CoV–2 was discovered to be the pathogen responsible
for a cluster of pneum onia associated with severe respiratory disease occurred in December
2019 in China, in W uhan (the capital of the province of Hubei) [1]. This novel pulmonary
infection, formally called Coronavirus Disease 2019 (COVID–19) [3], has spread rapidly in m a n y
other Chinese provinces and beyond [2, 4].
On 21 February 2020, SARS-CoV–2 infection was also detected in Northern Italy. Since then, the
3
number of SARS-CoV–2 infection cases has grown exponentially. On 8 March 2020, the number
of
Italians with SARS-CoV–2 infection was 7375 with a 4 8 % hospitalization rate ( 1 8 % in
intensive care unit) and a 5 % mortality rate.
At present, the reference standard to m a k e a definitive diagnosis of SARS-CoV–2 infection
is the reverse-transcription-polymerase-chain-reaction a s s a y [5].
Radiological im aging plays a crucial role in the detection and m a n a g e m e n t of COVID–19
patients. Computed tomography (CT) im aging is considered the most effective method for
detection of lung abnormalities, particularly in the early stage of disease [4, 6–12]. Moreover,
serial chest CT im aging with different time intervals (from three to seven days) is also
effective to assess the disease evolution (from initial diagnosis of COVID–19 to patient
discharge) [6, 7, 13].
However, the increasing number of hospitalized patients and the consequent increase of
radiological examinations m a k e the constant use of chest CT scan (from diagnosis to discharge)
difficult to sustain over time. Therefore, in our Radiology Department we are trying to limit the use
of CT im aging for monitoring patients with confirmed infection.
Although chest x-ray (CXR) is considered not sensitive for the detection of pulmonary
involvement in early-stage disease [4, 14], we believe that, in the current em ergency setting,
CXR (standard or beside) can be a useful diagnostic tool for monitoring (“day after day”) the
rapid progression of lung abnormalities in COVID–19, particularly in critical patients admitted to
intensive care units.
The radiological quantification of severity and progression of lung abnormalities is of great
importance to define the appropriate clinical m a n a g e m e n t and respiratory support for infected
patients. At the present time, two different CT scoring system s and one CXR scoring system were
used to quantify the pulmonary involvement in COVID–19 infection [6, 7,11]. This CXR scoring
system is a simple five-point grading tool that was proposed in 2015, and it was designed for
non-radiologist clinicians [15]. The goal of this scoring system was to facilitate the clinical
grading of CXR reports into five different severity categories in hospitalized patients with acute
respiratory infection.
Therefore, to the best of our knowledge, there are no published papers in which a dedicated
4
The aim of this short communication is to present our experimental CXR scoring system that we
are
applying in hospitalized patients with COVID–19 pneumonia. We also assessed the validity of
this CXR scoring s ystem on a sam ple of 100 hospitalized patients with SARS-CoV–2 infection for
whom the final outcome (recovery or death) was available
Materials And
Methods CXR Scoring
S ys t e m
Based on current knowledge about the common chest CT finding in COVID-19 pneum onia
(ground-
glass opacity with or without patchy consolidation) [4, 6-8, 10-12] we ha ve designed a
dedicated CXR scoring system for hospitalized patients with SARS-CoV-2 infection (confirmed b y
RT-PCR).
Our CXR scoring system for COVID-19 pneum onia includes two steps of im aging analysis.
The first step is to divide the lungs into six zones on frontal chest projection
(posteroanterior or anteroposterior projection according to the patient position) (Fig. 1):
Upper zones (A and D): above the inferior wall of the aortic arch
Middle zones (B and E): below the inferior wall of the aortic arch and above the inferior wall of the
right inferior pulmonary vein (i.e. the hilar structures)
Lower zones (C and F): below the inferior wall of the right inferior pulmonary vein (i.e. the lung
bases)
For technical reasons (for exam ple bedside CXR in critical patients), it m a y be difficult to identify
som e anatomical landmarks. In these cases, we recommend dividing each lung into three
equal zones.
The second step is to assign a score (from 0 to 3) to each zone based on the lung
abnormalities detected on frontal chest projection a s follows (Fig 2):
Score 0: no lung
abnormalities Score 1:
interstitial infiltrates
Score 2: interstitial and alveolar infiltrates (interstitial
predominance) Score 3: interstitial and alveolar infiltrates
(alveolar predominance)
The scores of the six lung zones are then added to obtain a n overall “CXR SCORE” ranging from 0
to
18.
The “CXR SCORE” is entered at the end of the descriptive report. Near to the overall score, the
partial score of each zone (from A to F) is also entered between square brackets.
5
An exam ple of our CXR report is shown below:
CHEST X-RAY
Symmetrical lung expansion
Interstitial and alveolar infiltrates in the middle and lower zones of both lungs, greater to
the left side. No pleural effusion.
Mediastinum and heart size within normal limits.
CXR SCORE: 10 [022033]
Validation st u d y s a m p l e a n d statistical a n a lysis
To assess the validity of our CXR scoring system , we selected 100 hospitalized patients with
SARS-
CoV-2 infection for whom the final outcome (recovery or death) was available. The selected
sam ple was obtained from a search in our departmental digital archive between March 4, 2020
and March 16, 2020. All CXR reports containing the new scoring system were retrieved. For each
patient, only the CXR report containing the highest score was considered for the validation study.
The frontal chest projection linked to these 100 CXR reports were independently read by a n
experienced thoracic radiologist who reassigned the score for each CXR exam.
To determine the agreem ent between radiologists in applying the new CXR scoring system , the
first score of each CXR examination was compared with the second score reassigned by the
experienced thoracic radiologist. To assess this agreem ent, the weighted k appa and 9 5 %
confidence interval (CI) were calculated. We use the weighted k appa (specifically the linear
weighted kappa) because the CXR score system was designed on a n 18-point continuous-ordinal
scale and the degree of disagreement between the scores had a different weight. The Mann-
Whitney U-test was also used to compare the CXR scores with the final outcome (recovery or
death) of the selected patients. We used this non- parametric test because the CXR score was not
normally distributed. The statistical analyses were performed using commercial software
(MedCalc Statistical Software version 19, Ostend, Belgium). P- values of <0.05 were considered
statistically significant.
Results
The score entered in the 100 CXR reports ranged from 0 to 16 (median, 6.5; interquartile range,
2–
6
11). The CXR score reassigned by the thoracic radiologist ranged from 0 to 15 (median, 7;
interquartile range, 3–10). The CXR scoring agreem ent was very good (kw, 0.82; 9 5 % CI, 0.79–
0.86).
For both semi-quantitative analyses (retrieved from report, and performed by the thoracic
radiologist), the CXR score was significantly higher in patients who died than those discharged
from the hospital (p ≤ 0.002).
Discussion
In this article we presented our original CXR scoring system for COVID–19 pneumonia. This severity
scoring system is designed exclusively for semi-quantitative assessm ent of severity and
progression of pulmonary involvement in hospitalized patients with COVID–19 infection (Fig. 3).
It is quite simple and can be easily replicated in other clinical realities.
We obviously realize that this method required further studies to confirm its validity because its
score depends m ainly on the quality of the CXR im a g e s and the experience of the observers.
However, in our preliminary validation study we found that the inter-rater agreem ent was very
good and the CXR score is a useful parameter for predicting mortality in hospitalized patients with
SARS-CoV–2 infection. In conclusion, we consider this scoring tool to be very promising due to its
ability to provide, in a very clear and straightforward way, relevant information for clinicians
enhancing the role of radiologists in this long and tiring battle against this new viral pneumonia.
Declarations
Funding
The author states that this work has not received a n y funding
Compliance with ethical standards
Conflict of interest/Competing interests
The authors declare that they have no conflict of interest
Ethical standards
All procedures followed were in accordance with the ethical standards of the responsible
committee on h um a n experimentation and with the Helsinki Declaration of 1975, a s revised in
2008. This study was submitted to our local ethics committee a s a retrospective analysis.
Given the retrospective
7
nature of this study and in accordance with current legislation, the need for informed consent for
informed consent was waived.
References
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P n e u m o n i a : S e r ia l C o m p u t e d T o m o g r a p h y F i n d i n g s . Korean J Radiol.
h t t p s : / / d o i. o r g / 1 0 . 3 3 4 8 / k j r . 2 0 2 0 . 0 1 1 2
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R a d io lo g ic F i n d i n g s a n d Literature R e v i e w . Radiol Cardiothorac I m a g i n g
2 : e 2 0 0 0 3 4 . h t t p s : / / d o i. o r g / 1 0 . 1 1 4 8 / r yc t . 2 0 2 0 2 0 0 0 3 4
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Figures
Figure 1
Division of lungs into six zones on frontal chest radiograph. The Line A is drawn at the
level of the inferior wall of the aortic arch. The Line B is drawn at the level of the inferior
wall of the right inferior pulmonary vein. A and D upper zones; B and E middle zones; C
and F lower zones
9
10
Figure 2
Exam ples of CXR scoring system in two different patients with COVID-19
pneumonia
11
Figure 3
Serial chest x-ray findings in a 72-year-old m ale patient with COVID-19 pneumonia. a
Baseline frontal chest radiograph performed on the d a y of admission (one d a y after
onset of fever). b, c The radiographic follow-up performed four and five days after
hospitalization shows rapid progression of the lung disease.
12
13

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2020 COVID-19 outbreak in Italy Experimental chest x-ray scoring system for quantifying and monitoring.pptx

  • 1. Preprint: Please note that this article has not completed peer review. COVID-19 outbreak in Italy: Experimental chest x- ray scoring system for quantifying and monitoring disease progression CURRENT STATUS: POSTED Andrea Borghesi Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, ASST Spedali Civili of Brescia, Piazzale Spedali Civili, 1, I - 25123 Brescia, Italy andrea.borghesi@unibs.itCorresponding Author ORCiD: https://orcid.org/0000-0002-4761- 2923 Roberto Maroldi Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, ASST Spedali Civili of Brescia, Piazzale Spedali Civili, 1, I - 25123 Brescia, Italy 1 DOI: 10.21203/rs.3.rs-19842/v1 Infectious Diseases SUBJECT AREAS Nuclear Medicine & Medical Imaging KEYWORDS SARS-CoV-2, COVID-19, Chest X-ray, Computed Tomography, Scoring System
  • 2. 2 Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a new virus recently isolated from hum ans . SARS-CoV-2 was discovered to be the pathogen responsible for a cluster of pneumonia associated with severe respiratory disease occurred in December 2019 in China. This novel pulmonary infection, formally called coronavirus disease 2019 (COVID-19), h as spread rapidly in China and beyond. On 8 March 2020, the number of Italians with SARS-CoV-2 infection was 7375 with a 4 8 % hospitalization rate. At present, chest computed tomography im aging is considered the most effective method for detection of lung abnormalities in early-stage disease and for quantitative assessm ent of severity and progression of COVID-19 infection. Although chest x-ray (CXR) is considered not sensitive for the detection of pulmonary involvement in the early stage of disease, we believe that, in the current em ergency setting, CXR can be a useful diagnostic tool for monitoring the rapid progression of lung abnormalities in infected patients, particularly in intensive care units. In this article we present our experimental CXR scoring system that we are applying in hospitalized patients with COVID-19 pneum onia to quantify and monitor the severity and progression of this new infectious disease. We also present the results of our preliminary validation study on a sam ple of 100 hospitalized patients with SARS-CoV-2 infection for whom the final outcome (recovery or death) was available. Introduction Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV–2) is a new virus recently isolated from hum ans. This new virus is a betacoronavirus that belongs to the Orthocoronavirinae subfamily of the Coronaviridae family [1, 2]. SARS-CoV–2 was discovered to be the pathogen responsible for a cluster of pneum onia associated with severe respiratory disease occurred in December 2019 in China, in W uhan (the capital of the province of Hubei) [1]. This novel pulmonary infection, formally called Coronavirus Disease 2019 (COVID–19) [3], has spread rapidly in m a n y other Chinese provinces and beyond [2, 4]. On 21 February 2020, SARS-CoV–2 infection was also detected in Northern Italy. Since then, the
  • 3. 3 number of SARS-CoV–2 infection cases has grown exponentially. On 8 March 2020, the number of Italians with SARS-CoV–2 infection was 7375 with a 4 8 % hospitalization rate ( 1 8 % in intensive care unit) and a 5 % mortality rate. At present, the reference standard to m a k e a definitive diagnosis of SARS-CoV–2 infection is the reverse-transcription-polymerase-chain-reaction a s s a y [5]. Radiological im aging plays a crucial role in the detection and m a n a g e m e n t of COVID–19 patients. Computed tomography (CT) im aging is considered the most effective method for detection of lung abnormalities, particularly in the early stage of disease [4, 6–12]. Moreover, serial chest CT im aging with different time intervals (from three to seven days) is also effective to assess the disease evolution (from initial diagnosis of COVID–19 to patient discharge) [6, 7, 13]. However, the increasing number of hospitalized patients and the consequent increase of radiological examinations m a k e the constant use of chest CT scan (from diagnosis to discharge) difficult to sustain over time. Therefore, in our Radiology Department we are trying to limit the use of CT im aging for monitoring patients with confirmed infection. Although chest x-ray (CXR) is considered not sensitive for the detection of pulmonary involvement in early-stage disease [4, 14], we believe that, in the current em ergency setting, CXR (standard or beside) can be a useful diagnostic tool for monitoring (“day after day”) the rapid progression of lung abnormalities in COVID–19, particularly in critical patients admitted to intensive care units. The radiological quantification of severity and progression of lung abnormalities is of great importance to define the appropriate clinical m a n a g e m e n t and respiratory support for infected patients. At the present time, two different CT scoring system s and one CXR scoring system were used to quantify the pulmonary involvement in COVID–19 infection [6, 7,11]. This CXR scoring system is a simple five-point grading tool that was proposed in 2015, and it was designed for non-radiologist clinicians [15]. The goal of this scoring system was to facilitate the clinical grading of CXR reports into five different severity categories in hospitalized patients with acute respiratory infection. Therefore, to the best of our knowledge, there are no published papers in which a dedicated
  • 4. 4 The aim of this short communication is to present our experimental CXR scoring system that we are applying in hospitalized patients with COVID–19 pneumonia. We also assessed the validity of this CXR scoring s ystem on a sam ple of 100 hospitalized patients with SARS-CoV–2 infection for whom the final outcome (recovery or death) was available Materials And Methods CXR Scoring S ys t e m Based on current knowledge about the common chest CT finding in COVID-19 pneum onia (ground- glass opacity with or without patchy consolidation) [4, 6-8, 10-12] we ha ve designed a dedicated CXR scoring system for hospitalized patients with SARS-CoV-2 infection (confirmed b y RT-PCR). Our CXR scoring system for COVID-19 pneum onia includes two steps of im aging analysis. The first step is to divide the lungs into six zones on frontal chest projection (posteroanterior or anteroposterior projection according to the patient position) (Fig. 1): Upper zones (A and D): above the inferior wall of the aortic arch Middle zones (B and E): below the inferior wall of the aortic arch and above the inferior wall of the right inferior pulmonary vein (i.e. the hilar structures) Lower zones (C and F): below the inferior wall of the right inferior pulmonary vein (i.e. the lung bases) For technical reasons (for exam ple bedside CXR in critical patients), it m a y be difficult to identify som e anatomical landmarks. In these cases, we recommend dividing each lung into three equal zones. The second step is to assign a score (from 0 to 3) to each zone based on the lung abnormalities detected on frontal chest projection a s follows (Fig 2): Score 0: no lung abnormalities Score 1: interstitial infiltrates Score 2: interstitial and alveolar infiltrates (interstitial predominance) Score 3: interstitial and alveolar infiltrates (alveolar predominance) The scores of the six lung zones are then added to obtain a n overall “CXR SCORE” ranging from 0 to 18. The “CXR SCORE” is entered at the end of the descriptive report. Near to the overall score, the partial score of each zone (from A to F) is also entered between square brackets.
  • 5. 5 An exam ple of our CXR report is shown below: CHEST X-RAY Symmetrical lung expansion Interstitial and alveolar infiltrates in the middle and lower zones of both lungs, greater to the left side. No pleural effusion. Mediastinum and heart size within normal limits. CXR SCORE: 10 [022033] Validation st u d y s a m p l e a n d statistical a n a lysis To assess the validity of our CXR scoring system , we selected 100 hospitalized patients with SARS- CoV-2 infection for whom the final outcome (recovery or death) was available. The selected sam ple was obtained from a search in our departmental digital archive between March 4, 2020 and March 16, 2020. All CXR reports containing the new scoring system were retrieved. For each patient, only the CXR report containing the highest score was considered for the validation study. The frontal chest projection linked to these 100 CXR reports were independently read by a n experienced thoracic radiologist who reassigned the score for each CXR exam. To determine the agreem ent between radiologists in applying the new CXR scoring system , the first score of each CXR examination was compared with the second score reassigned by the experienced thoracic radiologist. To assess this agreem ent, the weighted k appa and 9 5 % confidence interval (CI) were calculated. We use the weighted k appa (specifically the linear weighted kappa) because the CXR score system was designed on a n 18-point continuous-ordinal scale and the degree of disagreement between the scores had a different weight. The Mann- Whitney U-test was also used to compare the CXR scores with the final outcome (recovery or death) of the selected patients. We used this non- parametric test because the CXR score was not normally distributed. The statistical analyses were performed using commercial software (MedCalc Statistical Software version 19, Ostend, Belgium). P- values of <0.05 were considered statistically significant. Results The score entered in the 100 CXR reports ranged from 0 to 16 (median, 6.5; interquartile range, 2–
  • 6. 6 11). The CXR score reassigned by the thoracic radiologist ranged from 0 to 15 (median, 7; interquartile range, 3–10). The CXR scoring agreem ent was very good (kw, 0.82; 9 5 % CI, 0.79– 0.86). For both semi-quantitative analyses (retrieved from report, and performed by the thoracic radiologist), the CXR score was significantly higher in patients who died than those discharged from the hospital (p ≤ 0.002). Discussion In this article we presented our original CXR scoring system for COVID–19 pneumonia. This severity scoring system is designed exclusively for semi-quantitative assessm ent of severity and progression of pulmonary involvement in hospitalized patients with COVID–19 infection (Fig. 3). It is quite simple and can be easily replicated in other clinical realities. We obviously realize that this method required further studies to confirm its validity because its score depends m ainly on the quality of the CXR im a g e s and the experience of the observers. However, in our preliminary validation study we found that the inter-rater agreem ent was very good and the CXR score is a useful parameter for predicting mortality in hospitalized patients with SARS-CoV–2 infection. In conclusion, we consider this scoring tool to be very promising due to its ability to provide, in a very clear and straightforward way, relevant information for clinicians enhancing the role of radiologists in this long and tiring battle against this new viral pneumonia. Declarations Funding The author states that this work has not received a n y funding Compliance with ethical standards Conflict of interest/Competing interests The authors declare that they have no conflict of interest Ethical standards All procedures followed were in accordance with the ethical standards of the responsible committee on h um a n experimentation and with the Helsinki Declaration of 1975, a s revised in 2008. This study was submitted to our local ethics committee a s a retrospective analysis. Given the retrospective
  • 7. 7 nature of this study and in accordance with current legislation, the need for informed consent for informed consent was waived. References 1. Zhu N, Z h a n g D, W a n g W, et a l ( 2 0 2 0 ) A Novel Coronavirus f rom P a t i e n t s with P n e u m o n i a in C h in a , 2 0 1 9 . N E n g l J M e d 7 2 7 – 7 3 3 . h t t p s : / / d o i . o r g / 1 0 . 1 0 5 6 / n e j m o a 2 0 0 1 0 1 7 2 . S u n P, Lu X, Xu C, S u n W, P a n B ( 2 0 2 0 ) U n d e r s t a n d i n g of COVID-1 9 b a s e d on current e v i d e n c e . J M e d Virol 1–4. h t t p s : / / d o i . o r g / 1 0 . 1 0 0 2 / j m v . 2 5 7 2 2 3. World H e a lt h O r g a n iza t io n ( 2 0 2 0 ) WHO Director-G e n e r a l' s r e m a r k s a t the m e d i a b r ie f in g on 2 0 1 9 - n C o V . h t t p s : / / w w w . w h o . i n t / d g / s p e e c h e s / d e t a i l / w h o - director- g e n e r a l - s - r e m a r k s - a t - t h e - m e d i a - b r i e f i n g - on-2 0 1 9 - n c o v - on-1 1 - f e b r u a r y- 2 0 2 0 . 4. Zu ZY, J i a n g MD, Xu PP, Chen W, Ni QQ, Lu GM, Z h a n g LJ ( 2 0 2 0 ) Coronavirus D is e a s e 2 0 1 9 (COVID-1 9 ) : A P e r s p e c t i v e f rom C h in a . R a d i o l o g y 2 0 0 4 9 0 . h t t p s : / / d o i. o r g / 1 0 . 1 1 4 8 / r a d io l. 2 0 2 0 2 0 0 4 9 0 5 . C h in e s e S o c i e t y of R a d i o l o g y ( 2 0 2 0 ) R a d i o l o g i c a l d i a g n o s i s of n e w coronavirus i n f e c t e d p n e u m o n i t i s : Expert r e c o m m e n d a t i o n f rom the C h in e s e S o c i e t y of R a d io lo g y (First edition). Chin J Radiol 5 4 : E 0 0 1 - E 0 0 1 . 6 . B e r n h e i m A, Mei X, H u a n g M, et a l ( 2 0 2 0 ) Chest CT F i n d i n g s in Coronavirus Disease - 1 9 (COVID-1 9 ) : R e l a t i o n s h i p to Duration of Inf ection. R a d i o l o g y 2 0 0 4 6 3 . h t t p s : / / d o i. o r g / 1 0 . 1 1 4 8 / r a d io l. 2 0 2 0 2 0 0 4 6 3 7 . P a n F, Ye T, S u n P, et a l ( 2 0 2 0 ) T im e Course of L u n g C h a n g e s On Chest CT During R e c o v e r y From 2 0 1 9 Novel Coronavirus (COVID-1 9 ) P n e u m o n i a . R a d i o l o g y 2 0 0 3 7 0 . h t t p s : / / d o i. o r g / 1 0 . 1 1 4 8 / r a d io l. 2 0 2 0 2 0 0 3 7 0 8 . S h i H, H a n X, J i a n g N, et a l ( 2 0 2 0 ) R a d i o l o g i c a l f i n d i n g s f rom 8 1 p a t i e n t s with COVID- 1 9 p n e u m o n i a in W u h an , C h in a : a d e s c r ip t ive s t u d y. L a n c e t Inf ect Dis 3 0 9 9 : 1 – 1 0 .
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  • 9. Figure 1 Division of lungs into six zones on frontal chest radiograph. The Line A is drawn at the level of the inferior wall of the aortic arch. The Line B is drawn at the level of the inferior wall of the right inferior pulmonary vein. A and D upper zones; B and E middle zones; C and F lower zones 9
  • 10. 10
  • 11. Figure 2 Exam ples of CXR scoring system in two different patients with COVID-19 pneumonia 11
  • 12. Figure 3 Serial chest x-ray findings in a 72-year-old m ale patient with COVID-19 pneumonia. a Baseline frontal chest radiograph performed on the d a y of admission (one d a y after onset of fever). b, c The radiographic follow-up performed four and five days after hospitalization shows rapid progression of the lung disease. 12
  • 13. 13