Literature DB >> 16547960

Are lower airway or throat cultures predictive of sinus bacteriology in cystic fibrosis?

Marianne S Muhlebach1, Melissa B Miller, Charity Moore, Joel P Wedd, Amelia F Drake, Margaret W Leigh.   

Abstract

The choice of antibiotics for sinusitis in children with cystic fibrosis (CF) is empirical or based on lower airway cultures, because sinus cultures are difficult to obtain. The aim of this study was to identify the main organisms cultured from CF children with chronic sinusitis, and to evaluate the concordance of concomitant sinus, oropharyngeal swab (OP), and bronchoalveolar lavage fluid (BALF) cultures. OP and BALF cultures were done preoperatively, and sinus cultures were obtained during clinically indicated sinus surgery. The genetic identity of the bacteria was compared if the same organisms were present in upper and lower airway cultures. In total, 45 paired sinus-BALF cultures from 31 patients were included. Twenty-four of these had matched OP cultures. The mean age of patients was 9.5 +/- 4.3 years, and 19 patients were DeltaF508 homozygous. Bacterial sinus infection was present in 96%, caused by S. aureus (49%), P. aeruginosa (42%), and H. influenzae (22%). The diagnostic accuracy of BALF or OP cultures was low in predicting sinus infection, particularly at younger ages. Positive and negative predictive values (PPV and NPV) of BALF for P. aeruginosa infection were 65% and 67%, and for S. aureus, 76% and 63%, respectively. Predictive values for OP cultures were similar. Bacterial species were the same in sinus and OP or BALF samples of 12 patients of these bacteria 83% showed genetic identity. We conclude that S. aureus is an important pathogen in pediatric CF sinusitis, and that BALF or oropharyngeal cultures are poor predictors for organisms present in the sinuses.

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Year:  2006        PMID: 16547960     DOI: 10.1002/ppul.20396

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  16 in total

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Authors:  Mohamad R Chaaban; Alexandra Kejner; Steven M Rowe; Bradford A Woodworth
Journal:  Am J Rhinol Allergy       Date:  2013 Sep-Oct       Impact factor: 2.467

2.  Pseudomonas aeruginosa and Periodontal Pathogens in the Oral Cavity and Lungs of Cystic Fibrosis Patients: a Case-Control Study.

Authors:  Rocio Rivas Caldas; Florence Le Gall; Krista Revert; Gilles Rault; Michèle Virmaux; Stephanie Gouriou; Geneviève Héry-Arnaud; Georges Barbier; Sylvie Boisramé
Journal:  J Clin Microbiol       Date:  2015-04-08       Impact factor: 5.948

3.  16S rRNA gene sequencing reveals site-specific signatures of the upper and lower airways of cystic fibrosis patients.

Authors:  Sarah K Lucas; Robert Yang; Jordan M Dunitz; Holly C Boyer; Ryan C Hunter
Journal:  J Cyst Fibros       Date:  2017-08-18       Impact factor: 5.482

4.  Clinical predictors of cystic fibrosis chronic rhinosinusitis severity.

Authors:  Anna C Zemke; Seyed Mehdi Nouraie; John Moore; Jordan R Gaston; Nicholas R Rowan; Joseph M Pilewski; Jennifer M Bomberger; Stella E Lee
Journal:  Int Forum Allergy Rhinol       Date:  2019-06-04       Impact factor: 3.858

5.  Evolution and diversification of Pseudomonas aeruginosa in the paranasal sinuses of cystic fibrosis children have implications for chronic lung infection.

Authors:  Susse Kirkelund Hansen; Martin Holm Rau; Helle Krogh Johansen; Oana Ciofu; Lars Jelsbak; Lei Yang; Anders Folkesson; Hanne Østergaard Jarmer; Kasper Aanæs; Christian von Buchwald; Niels Høiby; Søren Molin
Journal:  ISME J       Date:  2011-06-30       Impact factor: 10.302

6.  Plasma TGF-β₁ in pediatric cystic fibrosis: potential biomarker of lung disease and response to therapy.

Authors:  William T Harris; Marianne S Muhlebach; Robert A Oster; Michael R Knowles; J P Clancy; Terry L Noah
Journal:  Pediatr Pulmonol       Date:  2011-02-18

7.  Secretory IgA-mediated immune response in saliva and early detection of Pseudomonas aeruginosa in the lower airways of pediatric cystic fibrosis patients.

Authors:  Renan Marrichi Mauch; Claudio Lucio Rossi; Marcos Tadeu Nolasco da Silva; Talita Bianchi Aiello; José Dirceu Ribeiro; Antônio Fernando Ribeiro; Niels Høiby; Carlos Emilio Levy
Journal:  Med Microbiol Immunol       Date:  2019-01-31       Impact factor: 3.402

Review 8.  Sinus bacteriology in patients with cystic fibrosis or primary ciliary dyskinesia: A systematic review.

Authors:  Maria E Møller; Mikkel C Alanin; Christian Grønhøj; Kasper Aanæs; Niels Høiby; Christian von Buchwald
Journal:  Am J Rhinol Allergy       Date:  2017-09-01       Impact factor: 2.467

9.  Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.

Authors:  Eugene H Chang; Alejandro A Pezzulo; David K Meyerholz; Andrea E Potash; Tanner J Wallen; Leah R Reznikov; Jessica C Sieren; Philip H Karp; Sarah Ernst; Thomas O Moninger; Nicholas D Gansemer; Paul B McCray; David A Stoltz; Michael J Welsh; Joseph Zabner
Journal:  Laryngoscope       Date:  2012-06-18       Impact factor: 3.325

10.  Mucus clearance, MyD88-dependent and MyD88-independent immunity modulate lung susceptibility to spontaneous bacterial infection and inflammation.

Authors:  A Livraghi-Butrico; E J Kelly; E R Klem; H Dang; M C Wolfgang; R C Boucher; S H Randell; W K O'Neal
Journal:  Mucosal Immunol       Date:  2012-03-14       Impact factor: 7.313

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