Effectiveness of inhaled tobramycin in eradicating Pseudomonas aeruginosa in children with cystic fibrosis

作者: Sanja Stanojevic , Valerie Waters , Joseph L. Mathew , Louise Taylor , Felix Ratjen

DOI: 10.1016/J.JCF.2013.09.002

关键词:

摘要: Abstract Background Inhaled tobramycin therapy has been shown to be efficacious in clinical trials for the eradication of initial Pseudomonas aeruginosa infection children with cystic fibrosis (CF). However, effectiveness different regimens eradicating P. and preventing development chronic actual settings yet determined. Methods This was an observational study ( from 2005–2012 based on data collected Toronto CF Database medical charts. Patients who received inhaled (80mg/2ml twice daily 365days) were compared those inhalation solution (TIS) (300mg/5ml 28days) respect infection. We also examined risk factors recurrence Results During period, 65 patients identified incident , which 7 (11%) failed therapy. Eradication failure similar between two treatment groups. A total 4 (6%) developed 12months following end no differences Female gender, older age, pancreatic insufficiency, lower lung function worse nutritional status as Conclusions Both have practice. Further work is needed, however, identify patient characteristics bacterial that play a role failure, order develop more effective antimicrobial rescue strategies.

参考文章(33)
Katherine M Flegal, Lester R Curtin, Clifford L Johnson, Zuguo Mei, Rong Wei, Cynthia L Ogden, Laurence M Grummer-Strawn, Robert J Kuczmarski, Shumei S Guo, Alex F Roche, 2000 CDC Growth Charts for the United States: methods and development. Vital and health statistics. Series 11, Data from the National Health Survey. pp. 1- 190 ,(2002)
Nicole Mayer-Hamblett, Margaret Rosenfeld, Miriam M. Treggiari, Michael W. Konstan, George Retsch-Bogart, Wayne Morgan, Jeff Wagener, Ronald L. Gibson, Umer Khan, Julia Emerson, Valeria Thompson, Eric P. Elkin, Bonnie W. Ramsey, , Standard care versus protocol based therapy for new onset Pseudomonas aeruginosa in cystic fibrosis Pediatric Pulmonology. ,vol. 48, pp. 943- 953 ,(2013) , 10.1002/PPUL.22693
Petra Schelstraete, Filomeen Haerynck, Sabine Van daele, Sarah Deseyne, Frans De Baets, Eradication therapy for Pseudomonas aeruginosa colonization episodes in cystic fibrosis patients not chronically colonized by P. aeruginosa Journal of Cystic Fibrosis. ,vol. 12, pp. 1- 8 ,(2013) , 10.1016/J.JCF.2012.07.008
Margaret Rosenfeld, Julia Emerson, Sharon McNamara, Valeria Thompson, Bonnie W Ramsey, Wayne Morgan, Ronald L Gibson, EPIC Study Group, None, Risk factors for age at initial Pseudomonas acquisition in the cystic fibrosis epic observational cohort Journal of Cystic Fibrosis. ,vol. 11, pp. 446- 453 ,(2012) , 10.1016/J.JCF.2012.04.003
Heinz Georg Wiesemann, Gratiana Steinkamp, Felix Ratjen, Adolf Bauernfeind, Barbara Przyklenk, Gerd Döring, Horst von der Hardt, Placebo-controlled, double-blind, randomized study of aerosolized tobramycin for early treatment ofPseudomonas aeruginosa colonization in cystic fibrosis Pediatric Pulmonology. ,vol. 25, pp. 88- 92 ,(1998) , 10.1002/(SICI)1099-0496(199802)25:2<88::AID-PPUL3>3.0.CO;2-J
M. Proesmans, F. Vermeulen, L. Boulanger, J. Verhaegen, K. De Boeck, Comparison of two treatment regimens for eradication of Pseudomonas aeruginosa infection in children with cystic fibrosis Journal of Cystic Fibrosis. ,vol. 12, pp. 29- 34 ,(2013) , 10.1016/J.JCF.2012.06.001
Deanna M Green, Kathryn E McDougal, Scott M Blackman, Patrick R Sosnay, Lindsay B Henderson, Kathleen M Naughton, J Michael Collaco, Garry R Cutting, Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients Respiratory Research. ,vol. 11, pp. 140- 140 ,(2010) , 10.1186/1465-9921-11-140
Judith H. Maselli, Marci K. Sontag, Jill M. Norris, Todd MacKenzie, Jeff S. Wagener, Frank J. Accurso, Risk factors for initial acquisition of Pseudomonas aeruginosa in children with cystic fibrosis identified by newborn screening. Pediatric Pulmonology. ,vol. 35, pp. 257- 262 ,(2003) , 10.1002/PPUL.10230
Richard L. Henry, Craig M. Mellis, Lea Petrovic, Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis. Pediatric Pulmonology. ,vol. 12, pp. 158- 161 ,(1992) , 10.1002/PPUL.1950120306