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Pseudomonas aeruginosa serology and risk for re-isolation in the EPIC trial

  • Michael Anstead
  • , Sonya L. Heltshe
  • , Umer Khan
  • , Joseph T. Barbieri
  • , Markus Langkamp
  • , Gerd Döring
  • , Shimoni Dharia
  • , Ronald L. Gibson
  • , Miriam M. Treggiari
  • , James Lymp
  • , Margaret Rosenfeld
  • , Bonnie Ramsey

Producción científica: Articlerevisión exhaustiva

33 Citas (Scopus)

Resumen

Background: The prognostic value of Pseudomonas aeruginosa serology for antibiotic therapy in cystic fibrosis patients is not well understood. Methods: Using five antigens from two ELISAs, we assessed whether positive serology in CF patients participating in the multi-center Early Pseudomonas Infection in Children (EPIC) trial would predict treatment failure, time to pulmonary exacerbation and risk for recurrent P. aeruginosa isolation post eradication. Results: Baseline positive P. aeruginosa serology was not significantly associated with failure of initial P. aeruginosa eradication measured at week 10 (adjusted for baseline culture) but seropositivity to the antigens alkaline protease and exotoxin A was significantly associated with increased risk for recurrent P. aeruginosa isolation during the 60. week post eradication follow-up period (p=0.003 and p=0.001 respectively). There was no association between baseline seropositivity and time to pulmonary exacerbation. Conclusion: P. aeruginosa serology may complement culture results in clinicians' efforts to successfully monitor recurrence of early P. aeruginosa in CF patients.

Idioma originalEnglish
Páginas (desde-hasta)147-153
Número de páginas7
PublicaciónJournal of Cystic Fibrosis
Volumen12
N.º2
DOI
EstadoPublished - mar 2013

Nota bibliográfica

Funding Information:
This study was supported by CFFT RAMSEY10A0 and CFFT EPIC04K0 from the US Cystic Fibrosis Foundation and NIH P30 DK089507 , NIH U01 HL80310 , and NIH-R01 AI30162 from The National Institutes of Health .

Financiación

This study was supported by CFFT RAMSEY10A0 and CFFT EPIC04K0 from the US Cystic Fibrosis Foundation and NIH P30 DK089507 , NIH U01 HL80310 , and NIH-R01 AI30162 from The National Institutes of Health .

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)U01HL080310, P30DK089507
National Institutes of Health (NIH)
National Institute of Allergy and Infectious DiseasesR01AI030162
National Institute of Allergy and Infectious Diseases
Cystic Fibrosis Foundation HeadquartersNIH-R01 AI30162, P30 DK089507, U01 HL80310
Cystic Fibrosis Foundation Headquarters
Cystic Fibrosis Foundation Therapeutics IncorporatedEPIC04K0, RAMSEY10A0
Cystic Fibrosis Foundation Therapeutics Incorporated

    ASJC Scopus subject areas

    • Pediatrics, Perinatology, and Child Health
    • Pulmonary and Respiratory Medicine

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