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Prospective comparison of the detection rates of human enterovirus and parechovirus RT-qPCR and viral culture in different pediatric specimens

  • S. C. M. de Crom*
  • , C. C. Obihara
  • , R. A. de Moor
  • , E. J. M. Veldkamp
  • , A. M. van Furth
  • , J. W. A. Rossen
  • *Corresponding author for this work
  • Department of Medical Oncology, Elisabeth-Tweesteden Hospital, Tilburg, The Netherlands
  • Maastricht UMC+
  • Amphia Hospital
  • Amsterdam UMC - Vrije Universiteit Amsterdam
  • University of Amsterdam
  • University of Groningen, University Medical Center Groningen

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background: Reverse-transcriptase quantitative real-time polymerase chain reaction (RT-qPCR) has become the gold standard for the diagnosis of human enterovirus (EV) and parechovirus (HPeV) infections. The detection rate of RT-qPCR in different pediatric body specimens has not been compared prospectively in a multicentre study. Objectives: This study compared the diagnostic detection rates of EV and HPeV RT-qPCR and viral culture in different specimens (feces, nasopharynx, blood, urine and cerebrospinal fluid (CSF)) of pediatric patients. Study design: This prospective, multicenter study performed an EV and HPeV RT-qPCR on nasopharynx, blood, urine, feces and CSF specimens and a viral culture on nasopharynx, feces and CSF specimens in symptomatic children. <. 16 years. Results: Of 285 included children EV was detected in 140 (49%) and HPeV in 44 (15%) children. Both EV and HPeV RT-qPCR had a higher sensitivity and negative predictive value than EV and HPeV viral culture, respectively. EV and HPeV RT-qPCR in feces specimen had the highest sensitivity (99.2% and 95.1%) of all specimens. Pooling results of specimens increased the detection rate for both viruses. Conclusion: Of all specimens, RT-qPCR in feces had the highest detection rate for both EV and HPeV in symptomatic pediatric patients. An EV was detected in all EV positive patients if a RT-qPCR was performed on both feces and CSF specimens or in both feces and urine specimens. HPeV was detected in all HPeV positive patients if a RT-qPCR was performed on both feces and CSF specimens, feces and nasopharynx specimens or CSF and nasopharynx specimens. © 2013 Elsevier B.V.
Original languageEnglish
Pages (from-to)449-454
JournalJournal of clinical virology
Volume58
Issue number2
DOIs
Publication statusPublished - Oct 2013

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