Early antibiotic treatment for Pseudomonas aeruginosa eradication in patients with cystic fibrosis: a randomised multicentre study comparing two different protocols

被引:81
作者
Taccetti, Giovanni [1 ]
Bianchini, Elisa [2 ]
Cariani, Lisa [3 ]
Buzzetti, Roberto
Costantini, Diana [4 ]
Trevisan, Francesca [1 ]
Zavataro, Lucia [1 ]
Campana, Silvia [1 ]
机构
[1] Univ Florence, Anna Meyer Childrens Univ Hosp, Dept Sci Woman & Childs Hlth, Cyst Fibrosis Ctr, I-50139 Florence, Italy
[2] AOU Careggi Pad San Damiano, Ctr Coordinamento Sperimentaz Clin ITT, Florence, Italy
[3] Ca Granda Osped Maggiore Policlin, Fdn IRCCS, Lab Cyst Fibrosis Microbiol, Milan, Italy
[4] Ca Granda Osped Maggiore Policlin, Fdn IRCCS, Cyst Fibrosis Ctr, Milan, Italy
关键词
STENOTROPHOMONAS-MALTOPHILIA; INHALED TOBRAMYCIN; YOUNG-CHILDREN; LUNG-FUNCTION; COLONIZATION; INFECTION; THERAPY; COLISTIN; REGIMENS;
D O I
10.1136/thoraxjnl-2011-200832
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
100201 [内科学];
摘要
Background Pseudomonas aeruginosa chronic pulmonary infection is an unfavourable event in cystic fibrosis. Bacterial clearance is possible with an early antibiotic treatment upon pathogen isolation. Currently, no best practice exists for early treatment. The efficacy of two different regimens against initial P aeruginosa infection was assessed. Methods In a randomised, open-label, parallel-group study involving 13 centres, the superiority of inhaled tobramycin/oral ciprofloxacin compared with inhaled colistin/oral ciprofloxacin (reference treatment) over 28 days was evaluated. Patients were eligible if they were older than 1 year with first or new P aeruginosa isolation. Treatments were assigned equally by centralised balanced randomisation, stratified by age and forced expiratory volume in 1 s values. The participants and those giving the intervention were not masked to arm assignments. The primary endpoint was P aeruginosa eradication, defined as three successive negative cultures in 6 months. Analysis was by intention to treat. This trial was registered with EudraCT, number 2008-006502-42. Results 105 patients were assigned to inhaled colistin/oral ciprofloxacin (arm A) and 118 to inhaled tobramycin/oral ciprofloxacin (arm B). All patients were analysed. P aeruginosa was eradicated in 66 (62.8%) patients in arm A and in 77 (65.2%) in arm B (OR 0.90, 95% CI 0.52 to 1.55, p=0.81). Following treatment, an increase in Stenotrophomonas maltophilia was noted (OR 3.97, 95% CI 2.27 to 6.94, p=0.001) with no differences between the two arms (OR 0.89, 95% CI 0.44 to 1.78, p=0.88). Conclusions No superiority of treatment under study was demonstrated in comparison to the reference treatment. Early eradication treatment was associated with an increase in S maltophilia.
引用
收藏
页码:853 / 859
页数:7
相关论文
共 37 条
[1]
Open follow-up study of tobramycin nebuliser solution and colistin in patients with cystic fibrosis [J].
Adeboyeku, David ;
Scott, Sandra ;
Hodson, Margaret E. .
JOURNAL OF CYSTIC FIBROSIS, 2006, 5 (04) :261-263
[2]
[Anonymous], 2004, PSEUD AER INF PEOPL
[3]
Chronic pulmonary infection with Stenotrophomonas maltophilia and lung function in patients with cystic fibrosis [J].
Dalboge, C. S. ;
Hansen, C. R. ;
Pressler, T. ;
Hoiby, N. ;
Johansen, H. K. .
JOURNAL OF CYSTIC FIBROSIS, 2011, 10 (05) :318-325
[4]
Stenotrophomonas maltophilia contamination of nebulizers used to deliver aerosolized therapy to inpatients with cystic fibrosis [J].
Denton, M ;
Rajgopal, A ;
Mooney, L ;
Qureshi, A ;
Kerr, KG ;
Keer, V ;
Pollard, K ;
Peckham, DG ;
Conway, SP .
JOURNAL OF HOSPITAL INFECTION, 2003, 55 (03) :180-183
[5]
Doring Gerd, 2004, J Cyst Fibros, V3, P67, DOI 10.1016/j.jcf.2004.03.008
[6]
Acquisition and eradication of P. aeruginosa in young children with cystic fibrosis [J].
Douglas, T. A. ;
Brennan, S. ;
Gard, S. ;
Berry, L. ;
Gangell, C. ;
Stick, S. M. ;
Clements, B. S. ;
Sly, P. D. .
EUROPEAN RESPIRATORY JOURNAL, 2009, 33 (02) :305-311
[7]
Implementation of European standards of care for cystic fibrosis - Control and treatment of infection [J].
Elborn, J. S. ;
Hodson, M. ;
Bertram, C. .
JOURNAL OF CYSTIC FIBROSIS, 2009, 8 (03) :211-217
[8]
Frederiksen B, 1997, PEDIATR PULM, V23, P330, DOI 10.1002/(SICI)1099-0496(199705)23:5<330::AID-PPUL4>3.0.CO
[9]
2-O
[10]
Significant microbiological effect of inhaled tobramycin in young children with cystic fibrosis [J].
Gibson, RL ;
Emerson, J ;
McNamara, S ;
Burns, LL ;
Rosenfeld, M ;
Yunker, A ;
Hamblett, N ;
Accurso, F ;
Dovey, M ;
Hiatt, P ;
Konstan, MW ;
Moss, R ;
Retsch-Bogart, G ;
Wagener, J ;
Waltz, D ;
Wilmott, R ;
Zeitlin, PL ;
Ramsey, B .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 167 (06) :841-849