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The Risk of Serious Bacterial Infection in Febrile Infants 0-90 Days of Life With a Respiratory Viral Infection.
Nicholson, Erin G; Avadhanula, Vasanthi; Ferlic-Stark, Laura; Patel, Kirtida; Gincoo, Karen E; Piedra, Pedro A.
Affiliation
  • Nicholson EG; From the Department of Pediatrics.
  • Avadhanula V; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX.
  • Ferlic-Stark L; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX.
  • Patel K; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX.
  • Gincoo KE; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX.
  • Piedra PA; Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX.
Pediatr Infect Dis J ; 38(4): 355-361, 2019 04.
Article in En | MEDLINE | ID: mdl-30882724
ABSTRACT

BACKGROUND:

Molecular diagnostic methods enhance the sensitivity and broaden the spectrum of detectable respiratory viruses in febrile infants ≤90 days of life. We describe the occurrence of respiratory viruses in this population, as well as the rates of serious bacterial infection (SBI) and respiratory viral coinfection with regard to viral characteristics.

METHODS:

This was a prospective observational cohort study performed in the emergency department that included previously healthy febrile infants ≤90 days of life. Clinical and historical characteristics were documented, and a respiratory nasal wash specimen was obtained from each patient. This sample was tested for 17 common respiratory pathogens, and a chart review was conducted to ascertain whether the infant was diagnosed with an SBI.

RESULTS:

In a 12-month period, 67% of the 104 recruited febrile infants were positive for a respiratory virus. The most commonly detected viruses were rhinovirus, respiratory syncytial virus, enterovirus and influenza. The rate of respiratory viral and SBI coinfection was 9% overall, and infants with either a systemic respiratory virus or negative viral testing were 3 times more likely to have an SBI than those with viruses typically restricted to the respiratory mucosa (95% confidence interval 1.1, 9.7).

CONCLUSIONS:

Respiratory viruses are readily detectable via nasopharyngeal wash in febrile infants ≤90 days of life. With the enhanced sensitivity of molecular respiratory diagnostics, rates of coinfection of respiratory viruses and SBI may be higher than previously thought. Further investigation utilizing molecular diagnostics is needed to guide usage in febrile infants ≤90 days.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Tract Infections / Bacterial Infections / Virus Diseases Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: Pediatr Infect Dis J Journal subject: DOENCAS TRANSMISSIVEIS / PEDIATRIA Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Tract Infections / Bacterial Infections / Virus Diseases Type of study: Etiology_studies / Observational_studies / Risk_factors_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: Pediatr Infect Dis J Journal subject: DOENCAS TRANSMISSIVEIS / PEDIATRIA Year: 2019 Document type: Article