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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="para0001" class="elsevierStylePara elsevierViewall">After the declaration of the pandemic in March 2020&#44; we are still facing a persistent COVID 19 crisis worldwide&#46;<a class="elsevierStyleCrossRef" href="#bib0001"><span class="elsevierStyleSup">1</span></a> As the virus continues to spread globally and common symptoms overlap with those of other acute respiratory infections&#44; the need for adequate actions based on robust diagnostic tests that support active surveillance systems seems yet to be key&#46;<a class="elsevierStyleCrossRef" href="#bib0002"><span class="elsevierStyleSup">2</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0003"><span class="elsevierStyleSup">3</span></a> Huge scientific advances have been made in COVID-19 diagnosis&#44; and several high-performance technologies have been developed in recent years&#46;<a class="elsevierStyleCrossRefs" href="#bib0002"><span class="elsevierStyleSup">2&#8211;4</span></a> Consequently&#44; it is essential to select cost-effective diagnostic methods for monitoring in a different type of action settings&#44; especially in ambulatory care backgrounds&#44; where case management&#44; isolation&#44; contact tracing and quarantine are relevant to prevent viral transmission in the community&#46;<a class="elsevierStyleCrossRef" href="#bib0003"><span class="elsevierStyleSup">3</span></a></p><p id="para0002" class="elsevierStylePara elsevierViewall">Originally developed for being used in a pregnancy test&#44; lateral flow immunoassay &#40;LFI&#41;&#44; or &#34;point of care testing&#34; has been essential for in vitro diagnostics for a long time now&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">5</span></a> Typically&#44; they involved antibodies coupled to a nitrocellulose membrane as a line on an immuno-chromatographic strip&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">5</span></a> Lateral flow devices for COVID 19 asymptomatic mass testing are proving controversial&#44; and in a similar way&#44; its uses seem to be questionable too in symptomatic patients&#46;<a class="elsevierStyleCrossRef" href="#bib0006"><span class="elsevierStyleSup">6</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> In the study accomplished by Scotta et&#160;al&#46;&#44; the authors investigated the accuracy of a SARS-CoV-2 antibody LFI test in symptomatic children and adolescents compared to a real-time polymerase chain reaction &#40;RT-PCR&#41;&#44; as a reference test&#44; in acute care settings&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> To achieve this goal&#44; the authors designed a prospective multicenter observational study&#44; from May to November 2020&#44; where enrolled pediatric patients &#40;&#62;&#160;2 months and &#60;&#160;18 years&#41; that were admitted at emergency rooms &#40;ERs&#41; or visited outpatient clinics with a suspected diagnosis of COVID 19 within 14 days of onset of symptoms&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> The authors analyzed data from 175 enrolled patients&#44; of whom 51 &#40;29&#46;14&#37;&#41; were positive for SARS CoV-2 by RT-PCR and 36 &#40;20&#46;57&#37;&#41; by LFI&#46; <a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> To evaluate the antibody LFI test performance&#44; authors assessed the sensitivity&#44; specificity&#44; positive predictive value&#44; and negative predictive value&#46; They found that the LFI had a sensitivity of 70&#46;6&#37; and a specificity of 96&#46;8&#37; measured after 7 days of the onset of symptoms compared with RT-PCR&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> The performance of LFI did not improve statistically between 7 and 13 and after 14 days of symptoms onset and did not present significant differences between ages &#40;&#60;&#160;2 or &#62;&#160;2 years old&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> Furthermore&#44; the authors found even a lower performance of the LFI in comparison with the commercial description&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a></p><p id="para0003" class="elsevierStylePara elsevierViewall">Several explanations can be postulated on the low precision of LFI in acute SARS-CoV-2 infection in children&#46; First&#44; not all infected patients with SARS CoV-2 elicited IgG antibodies against the virus&#46;<a class="elsevierStyleCrossRef" href="#bib0008"><span class="elsevierStyleSup">8</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0009"><span class="elsevierStyleSup">9</span></a> In fact&#44; more than half of the children infected with SARS CoV-2 cannot elicit detectable antibodies in the acute phase of infection&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">10</span></a> Second&#44; the antibodies response seems to be higher in a convalescent period in comparison with the acute phase of infection in both children and adults&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">10</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0011"><span class="elsevierStyleSup">11</span></a> Sera kinetics from infected subjects showed that antibodies response is associated with time after symptoms onset&#46;<a class="elsevierStyleCrossRef" href="#bib0011"><span class="elsevierStyleSup">11</span></a> Third&#44; children have lower levels of Spike and Nucleocapsid antibodies than adults&#46;<a class="elsevierStyleCrossRef" href="#bib0012"><span class="elsevierStyleSup">12</span></a> This could explain why Scotta et&#160;al&#46; showed less performance than attributed by the manufacturer&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> The antibody lateral flow test explored in the study &#40;Wondfo Biotech Co&#46;&#44; Guangzhou&#44; China&#41; evaluates the presence of antibodies against the Spike protein of SARS CoV 2&#44; which may be lower in children and adolescents enrolled in the study&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0012"><span class="elsevierStyleSup">12</span></a> Lastly&#44; severe COVID-19 correlates with higher antibody levels in infected patients&#46;<a class="elsevierStyleCrossRef" href="#bib0011"><span class="elsevierStyleSup">11</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0013"><span class="elsevierStyleSup">13</span></a></p><p id="para0004" class="elsevierStylePara elsevierViewall">Scotta et&#160;al&#46; showed in this journal and others authors explored elsewhere that lateral flow tests based on antibodies measurement may not be the best approach for early diagnose of SARS CoV-2 acute infection in children&#46;<a class="elsevierStyleCrossRef" href="#bib0006"><span class="elsevierStyleSup">6</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> From this perspective&#44; the Centers for Disease Control and Prevention &#40;CDC&#41; and the European Centre for Disease Prevention and Control recommend that these methods should not be used to establish acute SARS-CoV-2 infection&#46;<a class="elsevierStyleCrossRef" href="#bib0014"><span class="elsevierStyleSup">14</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">15</span></a> Diagnostic methods based on virologic testing should be done to detect viral infection&#46;<a class="elsevierStyleCrossRef" href="#bib0016"><span class="elsevierStyleSup">16</span></a> However&#44; we understand that early&#44; quick&#44; and affordable acute COVID 19 detection is key for the management of triage&#44; isolation&#44; quarantine&#44; and follow-up of patients and their contacts&#44; mainly in health facilities of low-settings countries&#46; In this way&#44; antigen test represents an alternative to antibody tests&#44; RT-PCR&#44; or other nucleic acid amplification tests &#40;NAATs&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0017"><span class="elsevierStyleSup">17</span></a> However&#44; a correct interpretation of each test result is essential for case management&#46; Finally&#44; the &#8220;gold standard&#8221; for acute SARS-CoV-2 infection remains laboratory-based RT-PCR and NAATs&#46;<a class="elsevierStyleCrossRef" href="#bib0018"><span class="elsevierStyleSup">18</span></a> Thus&#44; LFI for antibody detection test or antigen-based test results should be confirmed with a laboratory-based NAAT&#44; especially if the result of the antigen test is inconsistent with the clinical context&#46;<a class="elsevierStyleCrossRef" href="#bib0017"><span class="elsevierStyleSup">17</span></a></p><p id="para0005" class="elsevierStylePara elsevierViewall">Facing the persistence of viral circulation in a context of low vaccine coverage in the developing world and in the emergence of new viral variants&#44; it is essential to clearly establish the correct use of diagnostic tests for acute SARS CoV2 infection&#46; Each diagnostic test should be applied for the correct purpose&#44; and its indication must be weighed against well-designed cost-effectiveness studies&#46; Then&#44; each country will have to decide which are the best affordable and possible strategies that can be applied for diagnosis and then design clear and consistent decision algorithms&#46;</p></span>"
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Editorial
Behind the curtain of a weak diagnosis of acute SARS-CoV-2 infection in children
Mauricio T. Caballero
Fundación INFANT, Consejo Nacional de Investigaciones Científicas y Técnicas (CONCIET), Buenos Aires, Argentina
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    "titulo" => "Behind the curtain of a weak diagnosis of acute SARS-CoV-2 infection in children<a class="elsevierStyleCrossRef" href="#fn1"><span class="elsevierStyleSup">&#8270;</span></a>"
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        "autoresLista" => "Mauricio T&#46; Caballero"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="para0001" class="elsevierStylePara elsevierViewall">After the declaration of the pandemic in March 2020&#44; we are still facing a persistent COVID 19 crisis worldwide&#46;<a class="elsevierStyleCrossRef" href="#bib0001"><span class="elsevierStyleSup">1</span></a> As the virus continues to spread globally and common symptoms overlap with those of other acute respiratory infections&#44; the need for adequate actions based on robust diagnostic tests that support active surveillance systems seems yet to be key&#46;<a class="elsevierStyleCrossRef" href="#bib0002"><span class="elsevierStyleSup">2</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0003"><span class="elsevierStyleSup">3</span></a> Huge scientific advances have been made in COVID-19 diagnosis&#44; and several high-performance technologies have been developed in recent years&#46;<a class="elsevierStyleCrossRefs" href="#bib0002"><span class="elsevierStyleSup">2&#8211;4</span></a> Consequently&#44; it is essential to select cost-effective diagnostic methods for monitoring in a different type of action settings&#44; especially in ambulatory care backgrounds&#44; where case management&#44; isolation&#44; contact tracing and quarantine are relevant to prevent viral transmission in the community&#46;<a class="elsevierStyleCrossRef" href="#bib0003"><span class="elsevierStyleSup">3</span></a></p><p id="para0002" class="elsevierStylePara elsevierViewall">Originally developed for being used in a pregnancy test&#44; lateral flow immunoassay &#40;LFI&#41;&#44; or &#34;point of care testing&#34; has been essential for in vitro diagnostics for a long time now&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">5</span></a> Typically&#44; they involved antibodies coupled to a nitrocellulose membrane as a line on an immuno-chromatographic strip&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">5</span></a> Lateral flow devices for COVID 19 asymptomatic mass testing are proving controversial&#44; and in a similar way&#44; its uses seem to be questionable too in symptomatic patients&#46;<a class="elsevierStyleCrossRef" href="#bib0006"><span class="elsevierStyleSup">6</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> In the study accomplished by Scotta et&#160;al&#46;&#44; the authors investigated the accuracy of a SARS-CoV-2 antibody LFI test in symptomatic children and adolescents compared to a real-time polymerase chain reaction &#40;RT-PCR&#41;&#44; as a reference test&#44; in acute care settings&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> To achieve this goal&#44; the authors designed a prospective multicenter observational study&#44; from May to November 2020&#44; where enrolled pediatric patients &#40;&#62;&#160;2 months and &#60;&#160;18 years&#41; that were admitted at emergency rooms &#40;ERs&#41; or visited outpatient clinics with a suspected diagnosis of COVID 19 within 14 days of onset of symptoms&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> The authors analyzed data from 175 enrolled patients&#44; of whom 51 &#40;29&#46;14&#37;&#41; were positive for SARS CoV-2 by RT-PCR and 36 &#40;20&#46;57&#37;&#41; by LFI&#46; <a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> To evaluate the antibody LFI test performance&#44; authors assessed the sensitivity&#44; specificity&#44; positive predictive value&#44; and negative predictive value&#46; They found that the LFI had a sensitivity of 70&#46;6&#37; and a specificity of 96&#46;8&#37; measured after 7 days of the onset of symptoms compared with RT-PCR&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> The performance of LFI did not improve statistically between 7 and 13 and after 14 days of symptoms onset and did not present significant differences between ages &#40;&#60;&#160;2 or &#62;&#160;2 years old&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> Furthermore&#44; the authors found even a lower performance of the LFI in comparison with the commercial description&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a></p><p id="para0003" class="elsevierStylePara elsevierViewall">Several explanations can be postulated on the low precision of LFI in acute SARS-CoV-2 infection in children&#46; First&#44; not all infected patients with SARS CoV-2 elicited IgG antibodies against the virus&#46;<a class="elsevierStyleCrossRef" href="#bib0008"><span class="elsevierStyleSup">8</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0009"><span class="elsevierStyleSup">9</span></a> In fact&#44; more than half of the children infected with SARS CoV-2 cannot elicit detectable antibodies in the acute phase of infection&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">10</span></a> Second&#44; the antibodies response seems to be higher in a convalescent period in comparison with the acute phase of infection in both children and adults&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">10</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0011"><span class="elsevierStyleSup">11</span></a> Sera kinetics from infected subjects showed that antibodies response is associated with time after symptoms onset&#46;<a class="elsevierStyleCrossRef" href="#bib0011"><span class="elsevierStyleSup">11</span></a> Third&#44; children have lower levels of Spike and Nucleocapsid antibodies than adults&#46;<a class="elsevierStyleCrossRef" href="#bib0012"><span class="elsevierStyleSup">12</span></a> This could explain why Scotta et&#160;al&#46; showed less performance than attributed by the manufacturer&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> The antibody lateral flow test explored in the study &#40;Wondfo Biotech Co&#46;&#44; Guangzhou&#44; China&#41; evaluates the presence of antibodies against the Spike protein of SARS CoV 2&#44; which may be lower in children and adolescents enrolled in the study&#46;<a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0012"><span class="elsevierStyleSup">12</span></a> Lastly&#44; severe COVID-19 correlates with higher antibody levels in infected patients&#46;<a class="elsevierStyleCrossRef" href="#bib0011"><span class="elsevierStyleSup">11</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0013"><span class="elsevierStyleSup">13</span></a></p><p id="para0004" class="elsevierStylePara elsevierViewall">Scotta et&#160;al&#46; showed in this journal and others authors explored elsewhere that lateral flow tests based on antibodies measurement may not be the best approach for early diagnose of SARS CoV-2 acute infection in children&#46;<a class="elsevierStyleCrossRef" href="#bib0006"><span class="elsevierStyleSup">6</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0007"><span class="elsevierStyleSup">7</span></a> From this perspective&#44; the Centers for Disease Control and Prevention &#40;CDC&#41; and the European Centre for Disease Prevention and Control recommend that these methods should not be used to establish acute SARS-CoV-2 infection&#46;<a class="elsevierStyleCrossRef" href="#bib0014"><span class="elsevierStyleSup">14</span></a><span class="elsevierStyleSup">&#44;</span><a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">15</span></a> Diagnostic methods based on virologic testing should be done to detect viral infection&#46;<a class="elsevierStyleCrossRef" href="#bib0016"><span class="elsevierStyleSup">16</span></a> However&#44; we understand that early&#44; quick&#44; and affordable acute COVID 19 detection is key for the management of triage&#44; isolation&#44; quarantine&#44; and follow-up of patients and their contacts&#44; mainly in health facilities of low-settings countries&#46; In this way&#44; antigen test represents an alternative to antibody tests&#44; RT-PCR&#44; or other nucleic acid amplification tests &#40;NAATs&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0017"><span class="elsevierStyleSup">17</span></a> However&#44; a correct interpretation of each test result is essential for case management&#46; Finally&#44; the &#8220;gold standard&#8221; for acute SARS-CoV-2 infection remains laboratory-based RT-PCR and NAATs&#46;<a class="elsevierStyleCrossRef" href="#bib0018"><span class="elsevierStyleSup">18</span></a> Thus&#44; LFI for antibody detection test or antigen-based test results should be confirmed with a laboratory-based NAAT&#44; especially if the result of the antigen test is inconsistent with the clinical context&#46;<a class="elsevierStyleCrossRef" href="#bib0017"><span class="elsevierStyleSup">17</span></a></p><p id="para0005" class="elsevierStylePara elsevierViewall">Facing the persistence of viral circulation in a context of low vaccine coverage in the developing world and in the emergence of new viral variants&#44; it is essential to clearly establish the correct use of diagnostic tests for acute SARS CoV2 infection&#46; Each diagnostic test should be applied for the correct purpose&#44; and its indication must be weighed against well-designed cost-effectiveness studies&#46; Then&#44; each country will have to decide which are the best affordable and possible strategies that can be applied for diagnosis and then design clear and consistent decision algorithms&#46;</p></span>"
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Article information
ISSN: 00217557
Original language: English
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