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      Challenges and Opportunities for Lung Ultrasound in Novel Coronavirus Disease (COVID-19)

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          Abstract

          Novel coronavirus disease (COVID-19) is responsible for hundreds of thousands of hospitalizations worldwide, and this number is still increasing rapidly in many countries as of mid-April 2020. Diagnostic and clinical approaches differ between countries and even within countries because of inconsistent presence of testing materials and variable access to chest imaging. Severe acute respiratory syndrome-coronavirus-2 reverse transcriptase–polymerase chain reaction from nasopharyngeal or throat swabs has a high specificity but moderate sensitivity. Although patients with COVID-19 can present with a normal chest X-ray early in the disease, 1 abnormalities on chest images have a higher sensitivity to detect the disease than molecular testing, but lack specificity. 2 Typical findings on a chest X-ray include bilateral and multi-lobar infiltrates that can progress rapidly over the first days of illness. Chest X-ray is the most commonly used imaging technique in suspected COVID-19 in resource-limited settings. However, the image quality is often poor, and follow-up chest X-rays are difficult in settings with constraints on infrastructure, human resources, and personal protective equipment. Chest computed tomography (CT) scan is more sensitive that chest X-ray to detect early COVID-19. Typical findings on chest CT include bilateral and multi-lobar “ground-glass” or “crazy-paving” opacities, surrounded by spared lung tissue. 3,4 Ground-glass and crazy-paving opacities can, however, also be seen in many other pulmonary diseases. The COVID-19 working group of the Dutch Radiological Society recently coined the “CO-RADS classification” for diagnosing COVID-19, grading the level of suspicion for COVID-19 from very low (“CO-RADS 1”) to very high (“CO-RADS 5”). 5 Chest CT scan findings, however, are of limited value in resource-limited settings where access to CT scanners is in general very limited. Chest CT scan access may even be limited in resource-rich settings when hospital systems are overwhelmed with huge numbers of patients with suspected COVID-19. In addition, obtaining a chest CT scan is highly impractical once a patient is intubated and ventilated because transportation to the CT scanner is labor intensive and not without risk. Last, but not least, an additional burden is that the CT scanner needs to be thoroughly cleaned after each suspected case of COVID-19, to prevent the spread of the infection to other patients and healthcare personnel. Point-of-care lung ultrasound (LUS) could play an important role in COVID-19 management. Lung ultrasound is a noninvasive, rapid, repeatable, and sensitive bedside method to detect a range of pulmonary (and extrapulmonary) pathologies, including pneumothorax, pleural effusions, pulmonary infiltrates, and lung consolidations. In this issue of the American Journal of Tropical Medicine and Hygiene, Yasukawa and Taro 6 report their first experience with LUS in a case series of COVID-19 patients in the United States. All patients had “comet tails” (or “glass rockets”), with or without a “white lung” (“Birolleau variant”), and confluent B lines. Irregular pleural lines were also present in all patients, and half of the patients had small subpleural consolidations. In the one patient with a concomitant chest CT scan, peripheral opacification on the CT scan matched with a white lung area on the LUS images. The good sensitivity of bedside LUS to detect lung lesions in COVID-19 makes this an attractive additional diagnostic tool in patients suspected of COVID-19, often nursed in isolation rooms or on isolation wards. Lung ultrasound has been implemented for this purpose in several COVID-19–designated hospitals in Thailand. These centers are now also gaining experience in performing daily LUS for early detection of disease progression in COVID-19, with results important for decisions on escalation of care. 7 One challenge with LUS is defining consistent systems for reporting and interpretation of findings. One frequently used approach is semi-quantification of lung aeration across 12 lung regions into a numerical “global score,” in which the presence of A lines counts as “0,” less or more B lines count as “1” or “2,” and consolidation counts as “3.” 8 Scores are then summed to a global score that ranges from 0 (i.e., “no abnormalities at all”) to 36 (i.e., “consolidations in all regions”). Global LUS scores combined with SpO2/FiO2 in a resource-limited setting, 9 and with PaO2/FiO2 in a resource-rich setting, 10 showed good performance for diagnosing acute respiratory distress syndrome (ARDS) and for assessing ARDS severity. 11 Of note, current global LUS scores do not include pleural thickening and subpleural abnormalities, which seem often present in COVID-19. We should evaluate urgently whether a global LUS score has diagnostic and prognostic value in COVID-19, whether scores correlate with disease severity and CT findings, and how pleural thickening and subpleural abnormalities should be incorporated in the scoring system. Lung ultrasound could potentially also be an important tool for optimizing invasive ventilation in patients with severe COVID-19. 12 Although patients with COVID-19 receiving invasive ventilation will often have non-recruitable lung lesions early on, recruitable lesions may develop later in the disease course. In patients with lung lesions that can be opened up, recruitment maneuvers and higher positive end-expiratory pressure (PEEP) may be beneficial. 13 It is currently not well defined how these recruitable lung areas can be best identified. Comparing the same lung lesion on chest CT scan at different PEEP levels (10 and 20 cm H2O) can show whether a lesion becomes aerated (Schultz, personal experience in Amsterdam). However, this procedure is impractical, especially in resource-limited settings. In patients with ARDS, it has been shown that PEEP-induced lung recruitment can be adequately estimated with bedside LUS. 14 A study to assess LUS as a tool to detect recruitable lung lesions in patients with severe COVID-19 is currently underway in Amsterdam, the Netherlands, and Brussels, Belgium. In summary, the report from Yasukawa and Taro 6 shows that LUS is a promising additional lung imaging tool in COVID-19, in particular in settings with limited resources. This easy-to-perform bedside tool could prove to be important in diagnosis, prognostication, and follow-up of patients, and might also enable identification of recruitable lung lesions to guide invasive ventilation.

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          Coronavirus Disease 2019 (COVID-19): A Systematic Review of Imaging Findings in 919 Patients

          OBJECTIVE. Available information on CT features of the 2019 novel coronavirus disease (COVID-19) is scattered in different publications, and a cohesive literature review has yet to be compiled. MATERIALS AND METHODS. This article includes a systematic literature search of PubMed, Embase (Elsevier), Google Scholar, and the World Health Organization database. RESULTS. Known features of COVID-19 on initial CT include bilateral multilobar ground-glass opacification (GGO) with a peripheral or posterior distribution, mainly in the lower lobes and less frequently within the right middle lobe. Atypical initial imaging presentation of consolidative opacities superimposed on GGO may be found in a smaller number of cases, mainly in the elderly population. Septal thickening, bronchiectasis, pleural thickening, and subpleural involvement are some of the less common findings, mainly in the later stages of the disease. Pleural effusion, pericardial effusion, lymphadenopathy, cavitation, CT halo sign, and pneumothorax are uncommon but may be seen with disease progression. Follow-up CT in the intermediate stage of disease shows an increase in the number and size of GGOs and progressive transformation of GGO into multifocal consolidative opacities, septal thickening, and development of a crazy paving pattern, with the greatest severity of CT findings visible around day 10 after the symptom onset. Acute respiratory distress syndrome is the most common indication for transferring patients with COVID-19 to the ICU and the major cause of death in this patient population. Imaging patterns corresponding to clinical improvement usually occur after week 2 of the disease and include gradual resolution of consolidative opacities and decrease in the number of lesions and involved lobes. CONCLUSION. This systematic review of current literature on COVID-19 provides insight into the initial and follow-up CT characteristics of the disease.
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            Performance of radiologists in differentiating COVID-19 from viral pneumonia on chest CT

            Background Despite its high sensitivity in diagnosing COVID-19 in a screening population, chest CT appearances of COVID 19 pneumonia are thought to be non-specific. Purpose To assess the performance of United States (U.S.) and Chinese radiologists in differentiating COVID-19 from viral pneumonia on chest CT. Methods A total of 219 patients with both positive COVID-19 by RT-PCR and abnormal chest CT findings were retrospectively identified from 7 Chinese hospitals in Hunan Providence, China from January 6 to February 20, 2020. A total of 205 patients with positive Respiratory Pathogen Panel for viral pneumonia and CT findings consistent with or highly suspicious for pneumonia by original radiology interpretation within 7 days of each other were identified from Rhode Island Hospital in Providence, RI. Three Chinese radiologists blindly reviewed all chest CTs (n=424) to differentiate COVID-19 from viral pneumonia. A sample of 58 age-matched cases was randomly selected and evaluated by 4 U.S. radiologists in a similar fashion. Different CT features were recorded and compared between the two groups. Results For all chest CTs, three Chinese radiologists correctly differentiated COVID-19 from non-COVID-19 pneumonia 83% (350/424), 80% (338/424), and 60% (255/424) of the time, respectively. The seven radiologists had sensitivities of 80%, 67%, 97%, 93%, 83%, 73% and 70% and specificities of 100%, 93%, 7%, 100%, 93%, 93%, 100%. Compared to non-COVID-19 pneumonia, COVID-19 pneumonia was more likely to have a peripheral distribution (80% vs. 57%, p<0.001), ground-glass opacity (91% vs. 68%, p<0.001), fine reticular opacity (56% vs. 22%, p<0.001), and vascular thickening (59% vs. 22%, p<0.001), but less likely to have a central+peripheral distribution (14.% vs. 35%, p<0.001), pleural effusion (4.1 vs. 39%, p<0.001) and lymphadenopathy (2.7% vs. 10.2%, p<0.001). Conclusion Radiologists in China and the United States distinguished COVID-19 from viral pneumonia on chest CT with high specificity but moderate sensitivity. A translation of this abstract in Farsi is available in the supplement. - ترجمه چکیده این مقاله به فارسی، در ضمیمه موجود است.
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              Bedside ultrasound assessment of positive end-expiratory pressure-induced lung recruitment.

              In the critically ill patients, lung ultrasound (LUS) is increasingly being used at the bedside for assessing alveolar-interstitial syndrome, lung consolidation, pneumonia, pneumothorax, and pleural effusion. It could be an easily repeatable noninvasive tool for assessing lung recruitment. Our goal was to compare the pressure-volume (PV) curve method with LUS for assessing positive end-expiratory pressure (PEEP)-induced lung recruitment in patients with acute respiratory distress syndrome/acute lung injury (ARDS/ALI). Thirty patients with ARDS and 10 patients with ALI were prospectively studied. PV curves and LUS were performed in PEEP 0 and PEEP 15 cm H₂O₂. PEEP-induced lung recruitment was measured using the PV curve method. Four LUS entities were defined: consolidation; multiple, irregularly spaced B lines; multiple coalescent B lines; and normal aeration. For each of the 12 lung regions examined, PEEP-induced ultrasound changes were measured, and an ultrasound reaeration score was calculated. A highly significant correlation was found between PEEP-induced lung recruitment measured by PV curves and ultrasound reaeration score (Rho = 0.88; P < 0.0001). An ultrasound reaeration score of +8 or higher was associated with a PEEP-induced lung recruitment greater than 600 ml. An ultrasound lung reaeration score of +4 or less was associated with a PEEP-induced lung recruitment ranging from 75 to 450 ml. A statistically significant correlation was found between LUS reaeration score and PEEP-induced increase in Pa(O₂) (Rho = 0.63; P < 0.05). PEEP-induced lung recruitment can be adequately estimated with bedside LUS. Because LUS cannot assess PEEP-induced lung hyperinflation, it should not be the sole method for PEEP titration.
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                Author and article information

                Journal
                Am J Trop Med Hyg
                Am. J. Trop. Med. Hyg
                tpmd
                tropmed
                The American Journal of Tropical Medicine and Hygiene
                The American Society of Tropical Medicine and Hygiene
                0002-9637
                1476-1645
                June 2020
                24 April 2020
                24 April 2020
                : 102
                : 6
                : 1162-1163
                Affiliations
                [1 ]Mahidol–Oxford Tropical Medicine Research Unit (MORU), Mahidol University, Bangkok, Thailand;
                [2 ]Nuffield Department of Medicine, Mahidol University, Bangkok, Thailand;
                [3 ]Department of Intensive Care, Amsterdam University Medical Centers, Amsterdam, The Netherlands;
                [4 ]Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand
                Author notes
                [* ]Address correspondence to Marcus J. Schultz, Amsterdam University Medical Centers, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands. E-mail: marcus.j.schultz@ 123456gmail.com

                Authors’ addresses: Marcus J. Schultz and Arjen M. Dondorp, Mahidol–Oxford Tropical Medicine Research Unit (MORU), Mahidol University, Bangkok, Thailand, Nuffield Department of Medicine, Mahidol University, Bangkok, Thailand, and Department of Intensive Care, Amsterdam University Medical Centers, Amsterdam, The Netherlands, E-mails: marcus.j.schultz@ 123456gmail.com and arjen@ 123456tropmedres.ac . Chaisith Sivakorn, Department of Clinical Tropical Medicine, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand, E-mail: chaisith.siv@ 123456mahidol.edu .

                Article
                tpmd200323
                10.4269/ajtmh.20-0323
                7253115
                32333546
                f4c5d906-6d2f-4246-8614-87320cd2b665
                © The American Society of Tropical Medicine and Hygiene

                This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 19 April 2020
                : 20 April 2020
                Page count
                Pages: 2
                Categories
                Editorial

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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