4.4 Article

Randomized Trial of Biofilm Testing to Select Antibiotics for Cystic Fibrosis Airway Infection

Journal

PEDIATRIC PULMONOLOGY
Volume 46, Issue 2, Pages 184-192

Publisher

WILEY
DOI: 10.1002/ppul.21350

Keywords

Pseudomonas aeruginosa; intravenous antibiotics; antibiotic resistance; antibiotic susceptibility testing; broth microdilution testing; inhibitory quotient; sputum bacterial density; lung function

Funding

  1. Cystic Fibrosis Foundation [BURNS03A0]
  2. Clinical and Translational Science Center
  3. National Center for Research Resources [UL1 RR025014]
  4. University of Washington, Seattle [M01 RR000037]
  5. Ohio State University, Columbus [UL1 RR025755, M01 RR000034]
  6. University of Pittsburgh [UL1 RR024153, M01 RR000084]
  7. Washington University, St. Louis [UL1 RR024992, M01 RR000036]
  8. Baylor College of Medicine, Houston [M01 RR000188]
  9. University of Iowa [UL1 RR024979, M01 RR000059]
  10. University of Cincinnati [UL1 RR026314]
  11. Children's Hospital Medical Center, Cincinnati [M01 RR008084]
  12. National Heart Lung and Blood Institute [K08HL067903]
  13. Gilead Sciences for clinical research
  14. Boehringer-Ingelheim Pharmaceuticals
  15. Transave
  16. Vertex for clinical research
  17. PTC Pharmaceuticals
  18. Vertex
  19. Pharmaxis for clinical research
  20. KaloBios
  21. Chiesi for clinical research
  22. Cystic Fibrosis Foundation
  23. National Institutes of Health

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Rationale: In cystic fibrosis (CF), conventional antibiotic susceptibility results correlate poorly with clinical outcomes. We hypothesized that biofilm testing would more accurately reflect the susceptibilities of bacteria infecting CF airways. Methods: A multicenter randomized pilot trial was conducted to assess the efficacy and safety of using biofilm susceptibility testing of Pseudomonas aeruginosa sputum isolates to guide antibiotic regimens for chronic airway infections in clinically stable adolescent and adult CF patients. Thirty-nine participants were randomized to biofilm or conventional treatment groups; 14-day courses of two antibiotics were selected according to an activity-based algorithm using the corresponding susceptibility results. Results: Of the agents tested, meropenem was most active against biofilm-grown bacteria, and was included in regimens for about half of each study group. For 19 of 39 randomized participants, randomization to the other study group would not have changed the antibiotic classes of the assigned regimen. Study groups were comparable at baseline, and had similar mean decreases in bacterial density, measured in log, 0 colony forming units per gram of sputum (biofilm, -2.94 [SD 2.83] vs. conventional, -3.27 [SD 3.09]), and mean increases in forced expiratory volume in 1 sec, measured in liters (0.18 [SD 0.20] vs. 0.12 [SD 0.22]). Conclusions: In this pilot study, antibiotic regimens based on biofilm testing did not differ significantly from regimens based on conventional testing in terms of microbiological and clinical responses. The predictive value of biofilm testing may nonetheless warrant evaluation in an adequately powered clinical trial in younger CF patients or those experiencing acute pulmonary exacerbation. Pediatr Pulmonol. 2011; 46:184-192. (C) 2011 Wiley-Liss, Inc.

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