Skip to main content
Log in

Multiresistant non-fermentative Gram-negative bacteria in cystic fibrosis patients: the results of an Italian multicenter study

  • Published:
European Journal of Epidemiology Aims and scope Submit manuscript

Abstract

We carried out an epidemiological study on 2717 patients seen on a regular basis at Italian Cystic Fibrosis Centers with the aim of defining the prevalence of multiresistant Gram-negative strains in Italy. We found 272 multiresistant strains out of 1560 Gram-negative strains isolated in 1012 Italian cystic fibrosis patients. From our results in Italian cystic fibrosis patients we may conclude: (1)the beta-lactam antibiotics are moderately active; ceftazidime is the most efficacious even if 59.9% of multiresistant strains are not sensitive to this drug; (2)the aminoglycosides are poorly efficacious; 93% of multiresistant strains are resistant in vitro to tobramycin; and (3)the quinolones, notwithstanding their relatively recent introduction into clinical practice, have very poor activity against multiresistant strains, 89.7% of which are not sensitive.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Davis PB, Drumm M, Konstan MW. Cystic fibrosis. Am J Respir Crit Care Med 1996; 154: 1229–1256.

    Google Scholar 

  2. Hilman BC, Lewiston NJ. Clinical manifestations of cystic fibrosis. In: Hilman BC (ed), Pediatric respiratory disease: Diagnosis and treatment. Philadelphia: Saunders, 1993: 661–673.

    Google Scholar 

  3. Hoiby N. Microbiology of cystic fibrosis. In: Hodson ME, Geddes DM (eds), Cystic fibrosis. London: Chapman & Hall, 1995: 75–98.

    Google Scholar 

  4. Gilligan PH. Microbiology of airway disease in patients with cystic fibrosis. Clin Microbiol Rev 1991; 4: 35–51.

    Google Scholar 

  5. Govan JRW, Nelson JW. Microbiology of lung infection in cystic fibrosis. Br Med Bull 1992; 48: 919–930.

    Google Scholar 

  6. Govan JRW, Deretic V. Microbial pathogenesis in cystic fibrosis: Mucoid Pseudomonas aeruginosa and Burkholderia cepacia. Microbiol Rev 1996; 60: 539–574.

    Google Scholar 

  7. Vandamme P, Holmes B, Vancanneyt M, Coenye T, Hoste B, Coopman R, Revets H, Lauwers S, Gillis M, Kerster K, Govan JRW. Occurrence of multiple genomovars of Burkholderia cepacia in cystic fibrosis patients and proposal of Burkholderia multivorans sp.nov. Int J Syst Bacteriol 1997; 47: 1188–1200.

    Google Scholar 

  8. Cazzola G, Amalfitano G, Tonolli E, Perazzoli E, Piacentini I, Mastella G. Burkholderia (Pseudomonas) cepacia epidemiology in a cystic fibrosis population: A genome finger-printing study. Acta Paediatr 1996; 85: 554–557.

    Google Scholar 

  9. Cheng K, Smyth RL, Govan JRW, Doherty C, Winstanley C, Denning N, Heaf DP, van Saenen H, Hart CA. Spread of β-lactam-resistant Pseudomonas aeruginosa in a cystic fibrosis clinic. Lancet 1996; 348: 639–642.

    Google Scholar 

  10. Isles A, Macluskey I, Corey M, Gold R, Prober C, Fleming P, Levison H. Pseudomonas cepacia infection in cystic fibrosis: An emerging problem. J Pediatr 1984; 104: 206–210.

    Google Scholar 

  11. Saiman L, MacDonald NE, Whittier S. The microbiological basis for antimicrobial therapy. Tenth Annual North American Cystic Fibrosis Conference. Cystic Fibrosis Foundation, Orlando, October 24 1996.

  12. Bossi A, Padoan R, Gagliardini R, Manca A, Zanda M, Miano A, Marianelli L, Romano L, Magazzù G, Raia V, Pardo F, Grzincich G, Salvatore D, Quattrucci S, de Candussio G, Lucidi V, Faraguna D, Mastella G, Giunta A. The Italian Cystic Fibrosis patients registry. 20th European Cystic Fibrosis Conference. Brussels, 18–21 June 1995. P39.

  13. Taccetti G, Campana S. Microbiologic data overview of Italian cystic fibrosis patients. Eur J Epidemiol 1997; 13: 323–327.

    Google Scholar 

  14. Cystic Fibrosis Foundation. Microbiology and infectious disease in cystic fibrosis. Bethesda, Maryland, August 1996.

  15. Cystic Fibrosis Foundation, Consensus Conference — Microbiology and infectious disease in Cystic Fibrosis, Bethesda, Maryland, 17–18 May 1994 (Vol V; Section I: 19).

    Google Scholar 

  16. Cystic Fibrosis Foundation. Patient Registry 1993 Annual Data Report. Bethesda, Maryland, September 1994.

  17. FitzSimmons SC. The changing epidemiology of cystic fibrosis. J Pediatr 1993; 122: 1–9.

    Google Scholar 

  18. Observatoire National de la Mucoviscidose. Epidemiology of cystic fibrosis in France. Pediatr Pulmonol 1995; 19(suppl 12); A380.

    Google Scholar 

  19. Bingen E, Botzenhart K, Chabanon G, Doring G, Govan J, Hoiby N, LiPuma JJ, Michel-Briand Y, Ogle J, Romling U, Smith A, Speert D, Stern R, Tablan O, Wolz C. Epidemiology of pulmonary infections by Pseudomonas in patients with cystic fibrosis: A consensus report. In: Doing G, Schaffar L (eds), Paris: French Cystic Fibrosis Association, 1993: 9–11.

    Google Scholar 

  20. Winnie G, Hartigan E, Holt L. Chronic Alcaligenes xylosoxidans respiratory tract infection in patients with cystic fibrosis. Pediatr Pulmonol 1996; 20(suppl 13) A321.

    Google Scholar 

  21. Goldfarb J. New antimicrobial agents. Pediatr Clin North Am 1995; 42: 717–735.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Taccetti, G., Campana, S. & Marianelli, L. Multiresistant non-fermentative Gram-negative bacteria in cystic fibrosis patients: the results of an Italian multicenter study. Eur J Epidemiol 15, 85–88 (1999). https://doi.org/10.1023/A:1007504524034

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1007504524034

Navigation