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Single- and multiple viral respiratory infections in children: disease and management cannot be related to a specific pathogen.

Identifieur interne : 000044 ( Main/Exploration ); précédent : 000043; suivant : 000045

Single- and multiple viral respiratory infections in children: disease and management cannot be related to a specific pathogen.

Auteurs : Jérôme O. Wishaupt [Pays-Bas] ; Tjeerd Van Der Ploeg [Pays-Bas] ; Ronald De Groot [Pays-Bas] ; Florens G A. Versteegh [Pays-Bas, Belgique] ; Nico G. Hartwig [Pays-Bas]

Source :

RBID : pubmed:28077074

Descripteurs français

English descriptors

Abstract

BACKGROUND

The number of viral pathogens associated with pediatric acute respiratory tract infection (ARI) has grown since the introduction of reverse transcription real-time polymerase chain reaction (RT-PCR) assays. Multiple viruses are detected during a single ARI episode in approximately a quarter of all cases. The clinical relevance of these multiple detections is unclear, as is the role of the individual virus. We therefore investigated the correlation between clinical data and RT-PCR results in children with single- and multiple viral ARI.

METHODS

Data from children with ARI were prospectively collected during two winter seasons. RT-PCR testing for 15 viruses was performed in 560 ARI episodes. In the patients with a single-viral etiology, clinical data, laboratory findings, patient management- and outcome data were compared between the different viruses. With this information, we compared data from children of whom RT-PCR data were negative, with children with single- and multiple viral positive results.

RESULTS

The viral detection rate was 457/560 (81.6%) of which 331/560 (59.1%) were single infections and 126/560 (22.5%) were multiple infections. In single viral infections, some statistically significant differences in demographics, clinical findings, disease severity and outcome were found between children with different viral etiologies. However, no clinically recognizable pattern was established to be virus-specific. In a multivariate analysis, the only variables that were correlated with longer hospital stay were the use of oxygen and nebulizer therapy, irrespective of the viral pathogen. Children with RT-PCR positive test results had a significant higher disease severity, fever, length of hospital stay, days of extra oxygen supply, and days of antibiotic treatment than children with a negative RT-PCR test result. For children with single- versus children with multiple positive RT-PCR test results, these differences were not significant.

CONCLUSIONS

Disease (severity), management and outcome in pediatric ARI are not associated with a specific virus. Single- and multiple viral ARI do not significantly differ with regard to clinical outcome and patient management. For general pediatrics, RT-PCR assays should be restricted to pathogens for which therapy is available or otherwise may have clinical consequences. Further research with an extended panel of RT-PCR assays and a larger number of inclusions is necessary to further validate our findings.


DOI: 10.1186/s12879-016-2118-6
PubMed: 28077074
PubMed Central: PMC5225597


Affiliations:


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<term>Adenovirus Infections, Human (epidemiology)</term>
<term>Adenovirus Infections, Human (therapy)</term>
<term>Adenovirus Infections, Human (virology)</term>
<term>Anti-Bacterial Agents (therapeutic use)</term>
<term>Coinfection (epidemiology)</term>
<term>Coinfection (virology)</term>
<term>Coronavirus Infections (epidemiology)</term>
<term>Coronavirus Infections (therapy)</term>
<term>Coronavirus Infections (virology)</term>
<term>Female (MeSH)</term>
<term>Fever (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Infant (MeSH)</term>
<term>Influenza, Human (epidemiology)</term>
<term>Influenza, Human (therapy)</term>
<term>Influenza, Human (virology)</term>
<term>Length of Stay (MeSH)</term>
<term>Male (MeSH)</term>
<term>Multivariate Analysis (MeSH)</term>
<term>Nebulizers and Vaporizers (MeSH)</term>
<term>Netherlands (epidemiology)</term>
<term>Oxygen Inhalation Therapy (MeSH)</term>
<term>Picornaviridae Infections (epidemiology)</term>
<term>Picornaviridae Infections (therapy)</term>
<term>Picornaviridae Infections (virology)</term>
<term>Pneumonia (epidemiology)</term>
<term>Pneumonia (therapy)</term>
<term>Pneumonia (virology)</term>
<term>Prospective Studies (MeSH)</term>
<term>Real-Time Polymerase Chain Reaction (MeSH)</term>
<term>Respiratory Syncytial Virus Infections (epidemiology)</term>
<term>Respiratory Syncytial Virus Infections (therapy)</term>
<term>Respiratory Syncytial Virus Infections (virology)</term>
<term>Respiratory Tract Infections (epidemiology)</term>
<term>Respiratory Tract Infections (therapy)</term>
<term>Respiratory Tract Infections (virology)</term>
<term>Reverse Transcriptase Polymerase Chain Reaction (MeSH)</term>
<term>Seasons (MeSH)</term>
<term>Severity of Illness Index (MeSH)</term>
<term>Virus Diseases (epidemiology)</term>
<term>Virus Diseases (therapy)</term>
<term>Virus Diseases (virology)</term>
<term>Viruses (genetics)</term>
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<term>Antibactériens (usage thérapeutique)</term>
<term>Co-infection (virologie)</term>
<term>Co-infection (épidémiologie)</term>
<term>Durée du séjour (MeSH)</term>
<term>Femelle (MeSH)</term>
<term>Fièvre (MeSH)</term>
<term>Grippe humaine (thérapie)</term>
<term>Grippe humaine (virologie)</term>
<term>Grippe humaine (épidémiologie)</term>
<term>Humains (MeSH)</term>
<term>Indice de gravité de la maladie (MeSH)</term>
<term>Infections de l'appareil respiratoire (thérapie)</term>
<term>Infections de l'appareil respiratoire (virologie)</term>
<term>Infections de l'appareil respiratoire (épidémiologie)</term>
<term>Infections humaines à adénovirus (thérapie)</term>
<term>Infections humaines à adénovirus (virologie)</term>
<term>Infections humaines à adénovirus (épidémiologie)</term>
<term>Infections à Picornaviridae (thérapie)</term>
<term>Infections à Picornaviridae (virologie)</term>
<term>Infections à Picornaviridae (épidémiologie)</term>
<term>Infections à coronavirus (thérapie)</term>
<term>Infections à coronavirus (virologie)</term>
<term>Infections à coronavirus (épidémiologie)</term>
<term>Infections à virus respiratoire syncytial (thérapie)</term>
<term>Infections à virus respiratoire syncytial (virologie)</term>
<term>Infections à virus respiratoire syncytial (épidémiologie)</term>
<term>Maladies virales (thérapie)</term>
<term>Maladies virales (virologie)</term>
<term>Maladies virales (épidémiologie)</term>
<term>Mâle (MeSH)</term>
<term>Nourrisson (MeSH)</term>
<term>Nébuliseurs et vaporisateurs (MeSH)</term>
<term>Oxygénothérapie (MeSH)</term>
<term>Pays-Bas (épidémiologie)</term>
<term>Pneumopathie infectieuse (thérapie)</term>
<term>Pneumopathie infectieuse (virologie)</term>
<term>Pneumopathie infectieuse (épidémiologie)</term>
<term>RT-PCR (MeSH)</term>
<term>Réaction de polymérisation en chaine en temps réel (MeSH)</term>
<term>Saisons (MeSH)</term>
<term>Virus (génétique)</term>
<term>Études prospectives (MeSH)</term>
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<term>Anti-Bacterial Agents</term>
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<term>Adenovirus Infections, Human</term>
<term>Coinfection</term>
<term>Coronavirus Infections</term>
<term>Influenza, Human</term>
<term>Netherlands</term>
<term>Picornaviridae Infections</term>
<term>Pneumonia</term>
<term>Respiratory Syncytial Virus Infections</term>
<term>Respiratory Tract Infections</term>
<term>Virus Diseases</term>
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<term>Viruses</term>
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<term>Virus</term>
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<term>Adenovirus Infections, Human</term>
<term>Coronavirus Infections</term>
<term>Influenza, Human</term>
<term>Picornaviridae Infections</term>
<term>Pneumonia</term>
<term>Respiratory Syncytial Virus Infections</term>
<term>Respiratory Tract Infections</term>
<term>Virus Diseases</term>
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<term>Grippe humaine</term>
<term>Infections de l'appareil respiratoire</term>
<term>Infections humaines à adénovirus</term>
<term>Infections à Picornaviridae</term>
<term>Infections à coronavirus</term>
<term>Infections à virus respiratoire syncytial</term>
<term>Maladies virales</term>
<term>Pneumopathie infectieuse</term>
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<term>Antibactériens</term>
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<term>Co-infection</term>
<term>Grippe humaine</term>
<term>Infections de l'appareil respiratoire</term>
<term>Infections humaines à adénovirus</term>
<term>Infections à Picornaviridae</term>
<term>Infections à coronavirus</term>
<term>Infections à virus respiratoire syncytial</term>
<term>Maladies virales</term>
<term>Pneumopathie infectieuse</term>
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<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Adenovirus Infections, Human</term>
<term>Coinfection</term>
<term>Coronavirus Infections</term>
<term>Influenza, Human</term>
<term>Picornaviridae Infections</term>
<term>Pneumonia</term>
<term>Respiratory Syncytial Virus Infections</term>
<term>Respiratory Tract Infections</term>
<term>Virus Diseases</term>
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<term>Co-infection</term>
<term>Grippe humaine</term>
<term>Infections de l'appareil respiratoire</term>
<term>Infections humaines à adénovirus</term>
<term>Infections à Picornaviridae</term>
<term>Infections à coronavirus</term>
<term>Infections à virus respiratoire syncytial</term>
<term>Maladies virales</term>
<term>Pays-Bas</term>
<term>Pneumopathie infectieuse</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Female</term>
<term>Fever</term>
<term>Humans</term>
<term>Infant</term>
<term>Length of Stay</term>
<term>Male</term>
<term>Multivariate Analysis</term>
<term>Nebulizers and Vaporizers</term>
<term>Oxygen Inhalation Therapy</term>
<term>Prospective Studies</term>
<term>Real-Time Polymerase Chain Reaction</term>
<term>Reverse Transcriptase Polymerase Chain Reaction</term>
<term>Seasons</term>
<term>Severity of Illness Index</term>
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<keywords scheme="MESH" xml:lang="fr">
<term>Analyse multifactorielle</term>
<term>Durée du séjour</term>
<term>Femelle</term>
<term>Fièvre</term>
<term>Humains</term>
<term>Indice de gravité de la maladie</term>
<term>Mâle</term>
<term>Nourrisson</term>
<term>Nébuliseurs et vaporisateurs</term>
<term>Oxygénothérapie</term>
<term>RT-PCR</term>
<term>Réaction de polymérisation en chaine en temps réel</term>
<term>Saisons</term>
<term>Études prospectives</term>
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<p>
<b>BACKGROUND</b>
</p>
<p>The number of viral pathogens associated with pediatric acute respiratory tract infection (ARI) has grown since the introduction of reverse transcription real-time polymerase chain reaction (RT-PCR) assays. Multiple viruses are detected during a single ARI episode in approximately a quarter of all cases. The clinical relevance of these multiple detections is unclear, as is the role of the individual virus. We therefore investigated the correlation between clinical data and RT-PCR results in children with single- and multiple viral ARI.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>Data from children with ARI were prospectively collected during two winter seasons. RT-PCR testing for 15 viruses was performed in 560 ARI episodes. In the patients with a single-viral etiology, clinical data, laboratory findings, patient management- and outcome data were compared between the different viruses. With this information, we compared data from children of whom RT-PCR data were negative, with children with single- and multiple viral positive results.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>The viral detection rate was 457/560 (81.6%) of which 331/560 (59.1%) were single infections and 126/560 (22.5%) were multiple infections. In single viral infections, some statistically significant differences in demographics, clinical findings, disease severity and outcome were found between children with different viral etiologies. However, no clinically recognizable pattern was established to be virus-specific. In a multivariate analysis, the only variables that were correlated with longer hospital stay were the use of oxygen and nebulizer therapy, irrespective of the viral pathogen. Children with RT-PCR positive test results had a significant higher disease severity, fever, length of hospital stay, days of extra oxygen supply, and days of antibiotic treatment than children with a negative RT-PCR test result. For children with single- versus children with multiple positive RT-PCR test results, these differences were not significant.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>Disease (severity), management and outcome in pediatric ARI are not associated with a specific virus. Single- and multiple viral ARI do not significantly differ with regard to clinical outcome and patient management. For general pediatrics, RT-PCR assays should be restricted to pathogens for which therapy is available or otherwise may have clinical consequences. Further research with an extended panel of RT-PCR assays and a larger number of inclusions is necessary to further validate our findings.</p>
</div>
</front>
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<Abstract>
<AbstractText Label="BACKGROUND">The number of viral pathogens associated with pediatric acute respiratory tract infection (ARI) has grown since the introduction of reverse transcription real-time polymerase chain reaction (RT-PCR) assays. Multiple viruses are detected during a single ARI episode in approximately a quarter of all cases. The clinical relevance of these multiple detections is unclear, as is the role of the individual virus. We therefore investigated the correlation between clinical data and RT-PCR results in children with single- and multiple viral ARI.</AbstractText>
<AbstractText Label="METHODS">Data from children with ARI were prospectively collected during two winter seasons. RT-PCR testing for 15 viruses was performed in 560 ARI episodes. In the patients with a single-viral etiology, clinical data, laboratory findings, patient management- and outcome data were compared between the different viruses. With this information, we compared data from children of whom RT-PCR data were negative, with children with single- and multiple viral positive results.</AbstractText>
<AbstractText Label="RESULTS">The viral detection rate was 457/560 (81.6%) of which 331/560 (59.1%) were single infections and 126/560 (22.5%) were multiple infections. In single viral infections, some statistically significant differences in demographics, clinical findings, disease severity and outcome were found between children with different viral etiologies. However, no clinically recognizable pattern was established to be virus-specific. In a multivariate analysis, the only variables that were correlated with longer hospital stay were the use of oxygen and nebulizer therapy, irrespective of the viral pathogen. Children with RT-PCR positive test results had a significant higher disease severity, fever, length of hospital stay, days of extra oxygen supply, and days of antibiotic treatment than children with a negative RT-PCR test result. For children with single- versus children with multiple positive RT-PCR test results, these differences were not significant.</AbstractText>
<AbstractText Label="CONCLUSIONS">Disease (severity), management and outcome in pediatric ARI are not associated with a specific virus. Single- and multiple viral ARI do not significantly differ with regard to clinical outcome and patient management. For general pediatrics, RT-PCR assays should be restricted to pathogens for which therapy is available or otherwise may have clinical consequences. Further research with an extended panel of RT-PCR assays and a larger number of inclusions is necessary to further validate our findings.</AbstractText>
</Abstract>
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<LastName>Wishaupt</LastName>
<ForeName>Jérôme O</ForeName>
<Initials>JO</Initials>
<AffiliationInfo>
<Affiliation>Department of Pediatrics, Reinier de Graaf Hospital, P.O. Box 5011, 2600, GA, Delft, The Netherlands. wishaupt@rdgg.nl.</Affiliation>
</AffiliationInfo>
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<LastName>van der Ploeg</LastName>
<ForeName>Tjeerd</ForeName>
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<Affiliation>Pieter van Foreest Institute for Education and Research, Medical Centre Alkmaar, Alkmaar, The Netherlands.</Affiliation>
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<ForeName>Ronald</ForeName>
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<Affiliation>Laboratory of Pediatric Infectious Diseases, Department of Pediatrics, Radboud University Medical Centre, Nijmegen, The Netherlands.</Affiliation>
</AffiliationInfo>
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<LastName>Versteegh</LastName>
<ForeName>Florens G A</ForeName>
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<Affiliation>Department of Pediatrics, Groene Hart Ziekenhuis, Gouda, The Netherlands.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Pediatrics, Ghent University Hospital, Ghent, Belgium.</Affiliation>
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<LastName>Hartwig</LastName>
<ForeName>Nico G</ForeName>
<Initials>NG</Initials>
<AffiliationInfo>
<Affiliation>Department of Pediatrics, Franciscus Gasthuis en Vlietland, Rotterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Department of Pediatric Infectious Diseases and Immunology, ErasmusMC-Sophia, Rotterdam, The Netherlands.</Affiliation>
</AffiliationInfo>
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<Year>2017</Year>
<Month>01</Month>
<Day>11</Day>
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<Country>England</Country>
<MedlineTA>BMC Infect Dis</MedlineTA>
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<DescriptorName UI="D000258" MajorTopicYN="N">Adenovirus Infections, Human</DescriptorName>
<QualifierName UI="Q000453" MajorTopicYN="N">epidemiology</QualifierName>
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<QualifierName UI="Q000821" MajorTopicYN="N">virology</QualifierName>
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<Keyword MajorTopicYN="Y">Co-infection</Keyword>
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<Keyword MajorTopicYN="Y">Respiratory viruses</Keyword>
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