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Community-acquired pneumonia in children: cell-free plasma sequencing for diagnosis and management.
Farnaes, Lauge; Wilke, Julianne; Ryan Loker, Kathleen; Bradley, John S; Cannavino, Christopher R; Hong, David K; Pong, Alice; Foley, Jennifer; Coufal, Nicole G.
Afiliação
  • Farnaes L; University of California San Diego, Department of Pediatrics, Division of Infectious Disease; Rady Children's Institute of Genomic Medicine. Electronic address: lfarnaes@rchsd.org.
  • Wilke J; University of California San Diego, Department of Pediatrics, Division of Critical Care.
  • Ryan Loker K; University of California San Diego, Department of Pediatrics, Division of Infectious Disease.
  • Bradley JS; University of California San Diego, Department of Pediatrics, Division of Infectious Disease.
  • Cannavino CR; University of California San Diego, Department of Pediatrics, Division of Infectious Disease.
  • Hong DK; Karius Inc. Redwood City, CA.
  • Pong A; University of California San Diego, Department of Pediatrics, Division of Infectious Disease.
  • Foley J; University of California San Diego, Department of Pediatrics, Division of Critical Care.
  • Coufal NG; University of California San Diego, Department of Pediatrics, Division of Critical Care.
Diagn Microbiol Infect Dis ; 94(2): 188-191, 2019 Jun.
Article em En | MEDLINE | ID: mdl-30819624
Community-acquired pneumonia (CAP) is a common cause of pediatric hospital admission. Empiric antibiotic therapy for hospitalized children with serious CAP now targets the most likely pathogen(s), including those that may demonstrate significant antibiotic resistance. Cell-free plasma next-generation sequencing (CFPNGS) was first made available for Pediatric Infectious Diseases physicians in June 1, 2017, to supplement standard-of-care diagnostic techniques. A retrospective chart review was performed for children hospitalized with CAP between June 1, 2017, and January 22, 2018, to evaluate the impact of CFPNGS. We identified 15 hospitalized children with CAP without other underlying medical conditions for whom CFPNGS was performed. CFPNGS identified a pathogen in 13 of 15 (86%) children compared with 47% for those using standard culture and PCR-based methods alone. Changes in antibiotic management were made in 7 of 15 (47%) of children as a result of CFPNGS.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasma / Bactérias / DNA Bacteriano / Infecções Comunitárias Adquiridas / Pneumonia Bacteriana / Técnicas de Diagnóstico Molecular / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Plasma / Bactérias / DNA Bacteriano / Infecções Comunitárias Adquiridas / Pneumonia Bacteriana / Técnicas de Diagnóstico Molecular / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article