Setting
Four hospitals in Lombardy region participated to the study: three located in Milan area (ASST Fatebenefratelli Ospedale Luigi Sacco, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico, ASST Rhodense—Presidio Ospedaliero di Garbagnate Milanese), and one in Lodi (ASST Lodi—Ospedale Maggiore di Lodi).
This retrospective cross-sectional study, with a longitudinal component, was conducted in accordance with the principles of the Declaration of Helsinki. Each institutional review board approved the study according to General Data Protection Regulation (GDPR).
Patients
All consecutive adult (> 18 years) patients referred to the Emergency Department (ED), with laboratory-identified SARS-CoV-2 infection by real time Reverse Transcription-Polymerase Chain Reaction (RT-PCR), were enrolled between February 22nd, 2020, and March 18th, 2020. All patients had at least one CXR at presentation.
The following clinical variables were extracted from patient’s charts: age, sex, exposure history, comorbid conditions, symptoms.
A repeat CXR was performed in the admission ward, when clinically indicated by the attending physician.
RT-PCR test
Nasopharyngeal and oropharyngeal specimens collected with synthetic fiber swabs (manufactured by Copan) were laboratory tested with real time RT-PCR to detect SARS-CoV-2 nucleotides.
The real time RT-PCR Tests were performed using GeneFinder™ COVID-19 Plus RealAmp Kit manufactured by OSANG Healtcare (CE-IVD marked, fulfilling European Directive 98/79/EC) and Allplex™ 2019-nCoV Assay manufactured by Seegene (approved by Korean Food and Drug Administration).
Imaging acquisition and interpretation
The majority of CXR were performed bedside with portable digital radiographic equipment, owing to the impossibility to move the patient and/or to avoid his transportation from isolation areas. In the other cases CXR were acquired with patient standing with standard two projections.
Different digital radiographic equipment has been used: Ysio Max system and MOBILETT Elara Max mobile system (Siemens Healthcare) [Hospital A], Adora System (NRT X-RAY A/S) and MAC mobile X-ray unit (General Medical Merate) [Hospital B], AXIOM Luminos dRF system (Siemens Healthcare) and FCR Go 2 portable system (Fujifilm) [Hospital C], FDR AcSelerate system and FDR Go PLUS portable system (Fujifilm) [Hospital D].
In each Hospital, two radiologists (with more than 10 years of experience in interpreting CXR imaging), reviewed all images, and classified CXR as suggestive or not suggestive for COVID-19 pneumonia. In case of disagreement, the same radiologists reviewed together the images to reach a consensus on the basis of the available radiological literature data.
The epidemiological history and clinical symptoms (cough, fever, weakness, etc.) were available for both readers.
The presence of lung parenchymal abnormalities on each CXR was recorded in accordance with the Glossary of Terms for Thoracic Imaging of the Fleischner Society and defined as: (a) ground glass opacity (GGO); (b) lung consolidation; (c) reticular pattern [8].
GGO is defined as an area of hazy increased lung opacity, less opaque than consolidation, within which margins of pulmonary vessels may be indistinct (Fig. 1a, b). Consolidation is defined as a homogeneous increase in pulmonary parenchymal attenuation that obscures the margins of vessels and airway walls (Fig. 2a). Reticular pattern is defined as a collection of innumerable small linear opacities that, by summation, produce an appearance resembling a net (Fig. 1c, d, Fig. 2b).
Patients were considered to have findings suggestive for COVID-19 pneumonia if they had at least one of the above-mentioned features.
The distribution of the abnormal findings was recorded considering three criteria: (a) laterality (unilateral or bilateral); (b) axial distribution (central and/or peripheral); (c) longitudinal distribution (superior and/or middle and/or inferior).
Associated findings such as pleural effusion, pneumothorax and pneumomediastinum, were also recorded.
In addition, on follow-up CXR radiologists evaluated the evolution of the radiographic findings describing if any improvement, a worsening or no significant changes occurred.
Statistical analysis
The study sample size was targeted at least 1000 patients, to be able to estimate proportions with precision at least 3.2%. Descriptive statistics were produced for demographic, clinical and laboratory characteristics of cases. Mean and standard deviation (SD) are presented for normally distributed variables, and median and interquartile range (IQR) for non-normally distributed variables, number and percentages for categorical variables. Groups were compared with parametric or nonparametric tests, according to data distribution, for continuous variables, and with Pearson’s χ2 test (Fisher exact test where appropriate) for categorical variables. Differences between first and second CXR were tested by means of the McNemar test (χ2 for paired data). In all cases, 2-tailed tests were used. P value significance cut-off was 0.05. Stata computer software version 16.0 (Stata Corporation, 4905 Lakeway Drive, College Station, Texas 77845, USA) was used for statistical analysis.