Clinical Outcomes After Initial Pseudomonas Acquisition in Cystic Fibrosis

被引:52
作者
Zemanick, Edith T. [1 ]
Emerson, Julia [2 ,3 ]
Thompson, Valeria [4 ]
McNamara, Sharon [2 ,3 ]
Morgan, Wayne [5 ]
Gibson, Ronald L. [2 ,3 ]
Rosenfeld, Margaret [2 ,3 ]
机构
[1] Univ Colorado, Sch Med, Dept Pediat, Aurora, CO USA
[2] Seattle Childrens Hosp, Dept Pediat, Seattle, WA USA
[3] Univ Washington, Sch Med, Seattle, WA USA
[4] Seattle Childrens Hosp, Cyst Fibrosis Fdn, Therapeut Dev Network, Coordinating Ctr, Seattle, WA USA
[5] Univ Arizona, Dept Pediat, Tucson, AZ 85721 USA
关键词
cystic fibrosis; P; aeruginosa; clinical outcomes; pulmonary exacerbations; microbiology; epidemiology; AERUGINOSA INFECTION; PULMONARY-FUNCTION; YOUNG-CHILDREN; LUNG-DISEASE; DIAGNOSIS; PATHOPHYSIOLOGY; EXACERBATIONS; DECLINE; ADULTS;
D O I
10.1002/ppul.23036
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
ObjectivesTo evaluate clinical outcomes associated with initial isolation of Pseudomonas aeruginosa (Pa) in a large U.S. cystic fibrosis (CF) cohort in the current era of widespread early Pa eradication therapy. MethodsParticipants were children with CF enrolled in the Early Pseudomonas Infection Control (EPIC) Observational Study who had no isolation of Pa from respiratory cultures prior to enrollment. Population-averaged regression models using generalized estimating equation methods were used to estimate the effect of Pa acquisition on endpoints including lung function, growth, pulmonary exacerbation rate, respiratory signs and symptoms, and respiratory cultures. ResultsEight hundred thirty-eight subjects were observed for a mean 4.6 (SD 1.2) years during which 431 (51%) acquired Pa. There was no statistically significant effect of Pa acquisition on the slopes of FEV1% predicted or growth parameters. Pulmonary exacerbation rate was statistically significantly greater after Pa acquisition (incident rate ratio 1.40, 95% CI 1.07, 1.84) as were odds of crackles or wheeze on physical exam (OR 1.23, 95% CI 1.00, 1.52). Odds of isolation of MRSA (OR 1.86, 95% CI 1.38, 2.49) and S. maltophilia (OR 2.11, 95% CI 1.49, 2.98) increased after Pa acquisition, while the odds of H. influenzae (OR 0.54, 95% CI 0.46, 0.64) decreased. ConclusionsIn this large U.S. cohort, we did not detect an association between acquisition of Pa and deterioration in lung function or nutrition. Pa acquisition was associated with significantly increased pulmonary exacerbation rate and odds of crackles or wheeze. Pa infection may be the cause of these outcomes or a marker of more severe disease. Pediatr Pulmonol. 2015; 50:42-48. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:42 / 48
页数:7
相关论文
共 25 条
[1]   The Effect of Early Pseudomonas aeruginosa Treatment on Lung Function in Pediatric Cystic Fibrosis [J].
Amin, Reshma ;
Lam, Michelle ;
Dupuis, Annie ;
Ratjen, Felix .
PEDIATRIC PULMONOLOGY, 2011, 46 (06) :554-558
[2]   Treatment of lung infection in patients with cystic fibrosis: Current and future strategies [J].
Doering, Gerd ;
Flume, Patrick ;
Heijerman, Harry ;
Elborn, J. Stuart ;
Angyalosi, G. ;
Assael, B. ;
Bell, S. ;
Bilton, D. ;
De Boeck, K. ;
Bush, A. ;
Campbell, P. W., III ;
Cattaneo, A. ;
Dembowsky, K. ;
Drevinek, P. ;
Dubois, C. ;
Eichler, I. ;
Elborn, J. S. ;
Flume, P. A. ;
Foweraker, J. E. ;
Gallagher, C. ;
Gartner, S. ;
Geller, D. E. ;
Goldman, M. ;
Goss, C. H. ;
Gupta, R. ;
Heijerman, H. G. ;
Henig, N. ;
Higgins, M. ;
Hjelte, L. ;
Hoiby, N. ;
Jongejan, R. ;
Knoch, M. ;
Konstan, M. W. ;
Muhlebach, M. S. ;
Nieuwenhuizen, P. W. ;
Parkins, M. D. ;
Pressler, T. ;
Quittner, A. L. ;
Ratjen, F. ;
Ramsey, B. W. ;
Smyth, A. ;
Thieroff-Ekerdt, R. ;
Tullis, E. ;
van der Ent, C. K. ;
Vazquez, C. ;
Wainwright, C. E. .
JOURNAL OF CYSTIC FIBROSIS, 2012, 11 (06) :461-479
[3]   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
[4]   Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis [J].
Emerson, J ;
Rosenfeld, M ;
McNamara, S ;
Ramsey, B ;
Gibson, RL .
PEDIATRIC PULMONOLOGY, 2002, 34 (02) :91-100
[5]   Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report [J].
Farrell, Philip M. ;
Rosenstein, Beryl J. ;
White, Terry B. ;
Accurso, Frank J. ;
Castellani, Carlo ;
Cutting, Garry R. ;
Durie, Peter R. ;
LeGrys, Vicky A. ;
Massie, John ;
Parad, Richard B. ;
Rock, Michael J. ;
Campbell, Preston W., III .
JOURNAL OF PEDIATRICS, 2008, 153 (02) :S4-S14
[6]   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
[7]   Spirometric reference values from a sample of the general US population [J].
Hankinson, JL ;
Odencrantz, JR ;
Fedan, KB .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (01) :179-187
[8]   MUCOID PSEUDOMONAS-AERUGINOSA IS A MARKER OF POOR SURVIVAL IN CYSTIC-FIBROSIS [J].
HENRY, RL ;
MELLIS, CM ;
PETROVIC, L .
PEDIATRIC PULMONOLOGY, 1992, 12 (03) :158-161
[9]   PROGNOSTIC IMPLICATIONS OF INITIAL OROPHARYNGEAL BACTERIAL-FLORA IN PATIENTS WITH CYSTIC-FIBROSIS DIAGNOSED BEFORE THE AGE OF 2 YEARS [J].
HUDSON, VL ;
WIELINSKI, CL ;
REGELMANN, WE .
JOURNAL OF PEDIATRICS, 1993, 122 (06) :854-860
[10]   Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis [J].
Konstan, Michael W. ;
Morgan, Wayne J. ;
Butler, Steven M. ;
Pasta, David J. ;
Craib, Marcia L. ;
Silva, Stefanie J. ;
Stokes, Dennis C. ;
Wohl, Mary Ellen B. ;
Wagener, Jeffrey S. ;
Regelmann, Warren E. ;
Johnson, Charles A. .
JOURNAL OF PEDIATRICS, 2007, 151 (02) :134-139