Understanding of the underlying pathogenesis and clinical findings of coronavirus disease 2019 (COVID‐19) is rapidly evolving since its initial presentation as an outbreak of severe respiratory illness in Wuhan, Hubei province, China in December 2019.
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Simultaneously, recognition of the characteristic imaging findings of acute COVID‐19 infection in pediatric patients has been advancing substantially with various imaging modalities. To date, the majority of published investigations of the imaging findings of pediatric COVID‐19 infection have focused on chest radiography (CXR) or computed tomography (CT) findings, because these are the most widely used and proven imaging modalities for evaluating lung disorders.
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Thinking outside of the box, Musolino and colleagues
have explored the feasibility, safety, and utility of lung ultrasound for the evaluation of pediatric COVID‐19 infection and reported their findings in this issue of the Journal.Despite inherent limitations (mainly stemming from small patient population, substantial number of excluded patients, and lack of gold standard for confirming ultrasound findings in all included cases), the authors’ study provides a step toward better understanding the role of ultrasound in diagnosing and monitoring pediatric COVID‐19 infection. Although the results are somewhat expected and in keeping with already known findings described with other imaging modalities, the most important aspect of the authors’ findings is the confirmation that ultrasound is technically feasible for detecting pleuropulmonary abnormalities associated with pediatric COVID‐19 infection, such as peripherally located consolidations and pleural effusions, specifically by recognizing the ultrasound findings of B lines, consolidations, and effusions.
As the authors concluded, it is plausible that perhaps ultrasound can be used to monitor these “sonographically visible” pleuropulmonary abnormalities in children with COVID‐19 infection instead of CXR or CT, which are associated with potentially harmful ionizing radiation exposure in the vulnerable pediatric population. In addition, it is reassuring to know that none of pediatricians who performed the ultrasounds in this study contracted COVID‐19 infection, confirming the safety of performing ultrasound for the operator in this clinical setting.At the present time, perhaps the next logical step is to focus on what we need to investigate now. The authors’ study provides much food for thought for future research. First, it would be important to investigate the utility and diagnostic accuracy of ultrasound: that is, whether ultrasound can actually provide a complete assessment of lung abnormalities associated with COVID‐19 infection in children by direct correlation with the current gold standard, such as CT. For example, the two most frequently observed lung abnormalities in pediatric COVID‐19 infection are ground‐glass opacity and consolidation. Although consolidation can be detected with ultrasound, often it is only visible if the consolidation is located in the peripheral portion of the lungs. Furthermore, ground‐glass opacity would be challenging to visualize with ultrasound. Second, the authors reported that pleural irregularities and simple pleural effusions were the two most commonly found abnormalities in their study population. However, these two pleural abnormalities have not been frequently detected on previously published studies of pediatric COVID‐19 infection focusing on CXR and CT findings.
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Interestingly, although the “pleural irregularity” that the authors described in their study is not well‐visualized on the provided figure, perhaps, this finding may be better detected with real‐time ultrasound; future studies, with less patient selection bias and larger patient population, confirming this finding will be important. Finally, direct correlation between the clinical status of affected pediatric patient and changes in ultrasound findings in different disease severity and various time points of infection (acute phase, subacute phase, resolution, and long‐term follow‐up period) will be beneficial to demonstrate the clinical utility of ultrasound as a monitoring tool in pediatric patients with COVID‐19 infection.Now that Musolino et al. have opened Pandora's box for investigating pleuropulmonary abnormalities associated with pediatric COVID‐19 infection with ultrasound, what can we expect in the future? Although the future is unknown, it is difficult to imagine that ultrasound will be used as an initial imaging modality for evaluating pediatric patients with COVID‐19 infection, particularly patients with mild or no symptoms. It may be more realistic to predict that ultrasound, as a noninvasive and radiation‐free imaging modality, may play a potentially useful role in monitoring and detecting complications of peripherally located consolidation from COVID‐19 infection that have been previously identified on CXR or CT. With the recent advent of contrast‐enhanced ultrasound, a promising new ultrasound technique, perhaps the lung and the sonographic findings of pediatric COVID‐19 infection can be better visualized; this may be an exciting area for future investigation. Finally, with the increasing recognition of pediatric patients with multisystem inflammatory syndrome in children (MIS‐C), a presumed postinfectious sequela of pediatric COVID‐19 infection, ultrasound (echocardiogram) may be crucial for diagnosis and follow‐up imaging assessment of children with MIS‐C who often present with heart failure (left ventricular systolic dysfunction), coronary artery dilatation, pulmonary edema, and pleural effusion.
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,Stepping outside the box of conventional approach to imaging, diagnosis, and management brings both challenges and opportunities. Despite some challenges and limitations in their study, the authors have provided us with an important stepping stone of information that may yield new opportunities to improve our understanding, diagnosis, and management of COVID‐19 infection in pediatric patients in the future.
AUTHOR CONTRIBUTIONS
Edward Y. Lee: Conceptualization (equal); project administration (equal); writing original draft (equal); writing review and editing (equal). Abbey J. Winant: Conceptualization (equal); project administration (equal); writing original draft (equal); writing review and editing (equal).
Authors: Alexandra M Foust; Abbey J Winant; Winnie C Chu; Karuna M Das; Grace S Phillips; Edward Y Lee Journal: AJR Am J Roentgenol Date: 2020-04-30 Impact factor: 3.959
Authors: Anna Maria Musolino; Maria Chiara Supino; Danilo Buonsenso; Raffaele Edo Papa; Sara Chiurchiù; Andrea Magistrelli; Maria Antonietta Barbieri; Massimiliano Raponi; Patrizia D'Argenio; Alberto Villani; Paolo Tomà Journal: Pediatr Pulmonol Date: 2021-01-12
Authors: Alexandra M Foust; Abbey J Winant; Ricardo Restrepo; Mark C Liszewski; Domen Plut; Edward Y Lee Journal: J Thorac Imaging Date: 2021-01 Impact factor: 3.000
Authors: Einat Blumfield; Terry L Levin; Jessica Kurian; Edward Y Lee; Mark C Liszewski Journal: AJR Am J Roentgenol Date: 2020-07-29 Impact factor: 3.959
Authors: Alexandra M Foust; Grace S Phillips; Winnie C Chu; Pedro Daltro; Karuna M Das; Pilar Garcia-Peña; Tracy Kilborn; Abbey J Winant; Edward Y Lee Journal: Radiol Cardiothorac Imaging Date: 2020-04-23
Authors: Abbey J Winant; Einat Blumfield; Mark C Liszewski; Jessica Kurian; Alexandra M Foust; Edward Y Lee Journal: Radiol Cardiothorac Imaging Date: 2020-07-30
Authors: Amir Pakray; David Walker; Alexander Figacz; Stephen Kilanowski; Casey Rhodes; Shashin Doshi; Mary Coffey Journal: Emerg Radiol Date: 2020-05-25
Authors: Alexandra Foust; Patrick R Johnston; Joanna Kasznia-Brown; Winnie C Chu; Pilar Garcia-Pena; Pedro Daltro; Karuna M Das; Domen Plut; Tracy Kilborn; Abbey J Winant; Edward Y Lee Journal: Radiol Cardiothorac Imaging Date: 2020-09-17
Authors: Alexandra M Foust; Alexander J McAdam; Winnie C Chu; Pilar Garcia-Peña; Grace S Phillips; Domen Plut; Edward Y Lee Journal: Pediatr Pulmonol Date: 2020-07-01