Stenotrophomonas maltophilia: A marker of lung disease severity

被引:35
作者
Berdah, Laura [1 ]
Taytard, Jessica [1 ]
Leyronnas, Sophie [1 ]
Clement, Annick [1 ,2 ]
Boelle, Pierre-Yves [3 ,4 ]
Corvol, Harriet [1 ,5 ]
机构
[1] Hop Trousseau, APHP, Cyst Fibrosis Ctr, Paris, France
[2] UPMC Univ Paris 06, Sorbonne Univ, INSERM, Paris, France
[3] UPMC Univ Paris 06, Sorbonne Univ, IPLESP, INSERM,UMRS 1136, Paris, France
[4] Hop St Antoine, AP HP, Dept Publ Hlth, Paris, France
[5] UPMC Univ Paris 06, Sorbonne Univ, CRSA, INSERM, Paris, France
关键词
children; cystic fibrosis; lung function; pulmonary exacerbation Stenotrophomonas maltophilia; CYSTIC-FIBROSIS PATIENTS; RISK-FACTORS; ASSOCIATION; EMERGENCE;
D O I
10.1002/ppul.23943
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundWhile the prevalence of Stenotrophomonas maltophilia lung infection in cystic fibrosis (CF) patients has increased in the last decades, its pathogenicity remains controversial. The aim of this study was to investigate the effects of S. maltophilia initial infection on the progression of lung disease in CF children. MethodsThis case-control retrospective study took place in a pediatric CF center. A total of 23 cases defined by at least one sputum culture positive for S. maltophilia, were matched for age, sex, and CFTR mutations to 23 never infected CF controls. The clinical data were collected for 2 years before and after S. maltophilia initial infection and comprised lung function analyses, rates of exacerbations and of antibiotic courses. ResultsCompared with controls, cases had lower lung function (P=0.05), more frequent pulmonary exacerbations (P=0.01), hospitalizations (P=0.02), and intravenous antibiotic courses (P=0.04) before S. maltophilia acquisition. In the year following S. maltophilia initial infection, lung function decline was similar in cases and controls but cases remained more severe, with more frequent pulmonary exacerbations (P=0.01), hospitalizations (P=0.02) and intravenous antibiotic courses (P=0.02). ConclusionsS. maltophilia seems to be a marker of CF lung disease severity and international recommendations to reduce lung infection by this pathogen should rapidly emerge.
引用
收藏
页码:426 / 430
页数:5
相关论文
共 24 条
[1]  
Amin R, 2012, COCHRANE DB SYST REV, V5
[2]  
Amin R, 2016, COCHRANE DB SYST REV, V7, DOI [10.1002/14651858.CD009249, DOI 10.1002/14651858.CD009249]
[3]  
Amin R, 2014, COCHRANE DB SYST REV, V4
[4]  
[Anonymous], 2016, 2015 ANN DAT REP
[5]  
Bellis G, 2016, REGISTRE FRANCAIS MU
[6]   Microbiology of sputum from patients at cystic fibrosis centers in the United States [J].
Burns, JL ;
Emerson, J ;
Stapp, JR ;
Yim, DL ;
Krzewinski, J ;
Louden, L ;
Ramsey, BW ;
Clausen, CR .
CLINICAL INFECTIOUS DISEASES, 1998, 27 (01) :158-163
[7]   Risk factors for lung function decline in a large cohort of young cystic fibrosis patients [J].
Cogen, Jonathan ;
Emerson, Julia ;
Sanders, Don B. ;
Ren, Clement ;
Schechter, Michael S. ;
Gibson, Ronald L. ;
Morgan, Wayne ;
Rosenfeld, Margaret .
PEDIATRIC PULMONOLOGY, 2015, 50 (08) :763-770
[8]   Translating the genetics of cystic fibrosis to personalized medicine [J].
Corvol, Harriet ;
Thompson, Kristin E. ;
Tabary, Olivier ;
Le Rouzic, Philippe ;
Guillot, Loic .
TRANSLATIONAL RESEARCH, 2016, 168 :40-49
[9]   Role of anti-pseudomonal antibiotics in the emergence of Stenotrophomonas maltophilia in cystic fibrosis patients [J].
Denton, M ;
Todd, NJ ;
Littlewood, JM .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 1996, 15 (05) :402-405
[10]   Pathophysiology and management of pulmonary infections in cystic fibrosis [J].
Gibson, RL ;
Burns, JL ;
Ramsey, BW .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2003, 168 (08) :918-951