Literature DB >> 29534149

Changing Rates of Chronic Pseudomonas aeruginosa Infections in Cystic Fibrosis: A Population-Based Cohort Study.

Matthew R Crull1, Ranjani Somayaji1,2, Kathleen J Ramos1, Ellen Caldwell1, Nicole Mayer-Hamblett3, Moira L Aitken1, David P Nichols3, Ali Rowhani-Rahbar4, Christopher H Goss1.   

Abstract

Background: Chronic Pseudomonas aeruginosa lung infection is associated with significant morbidity and mortality in cystic fibrosis (CF). It is not known whether recent advances in care have affected the rates of chronic infection. We aimed to determine if the rates of developing new chronic P. aeruginosa infection among adolescents and adults with CF significantly changed over time.
Methods: The cohort consisted of individuals with CF followed in the Cystic Fibrosis Foundation Patient Registry aged ≥13 years without chronic P. aeruginosa at baseline. Multivariable regression models accounting for within-patient correlation were used to assess the change in rate of developing chronic P. aeruginosa infection between 2003 and 2012.
Results: A total of 15504 individuals were followed for a median of 5 (interquartile range, 2-9) years. The annual rates of developing new chronic P. aeruginosa decreased from 14.3% in 2003 to 6.4% in 2012. After adjusting for potential confounders, relative risk (RR) of developing chronic P. aeruginosa infection decreased significantly over time compared to 2003 (P value test of trend < .001). Compared with 2003, the RR of developing chronic P. aeruginosa infection in 2012 was 0.33 (95% confidence interval, 0.30-0.37). No significant increases in risk of chronic infections with other major CF bacterial pathogens relative to 2003 were identified. Conclusions: Among individuals with CF, a significant decrease in the risk and rates of developing chronic P. aeruginosa infection between 2003 and 2012 was observed. Whether this decline results in changes in clinical outcomes warrants further exploration.

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Year:  2018        PMID: 29534149      PMCID: PMC6137120          DOI: 10.1093/cid/ciy215

Source DB:  PubMed          Journal:  Clin Infect Dis        ISSN: 1058-4838            Impact factor:   9.079


  37 in total

1.  Mucoid Pseudomonas aeruginosa is a marker of poor survival in cystic fibrosis.

Authors:  R L Henry; C M Mellis; L Petrovic
Journal:  Pediatr Pulmonol       Date:  1992-03

2.  Duration of treatment effect after tobramycin solution for inhalation in young children with cystic fibrosis.

Authors:  Ronald L Gibson; Julia Emerson; Nicole Mayer-Hamblett; Jane L Burns; Sharon McNamara; Frank J Accurso; Michael W Konstan; Barbara A Chatfield; George Retsch-Bogart; David A Waltz; James Acton; Pamela Zeitlin; Peter Hiatt; Richard Moss; Judy Williams; Bonnie W Ramsey
Journal:  Pediatr Pulmonol       Date:  2007-07

3.  Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis.

Authors:  Michael W Konstan; Wayne J Morgan; Steven M Butler; David J Pasta; Marcia L Craib; Stefanie J Silva; Dennis C Stokes; Mary Ellen B Wohl; Jeffrey S Wagener; Warren E Regelmann; Charles A Johnson
Journal:  J Pediatr       Date:  2007-06-22       Impact factor: 4.406

4.  Impact of Sustained Eradication of New Pseudomonas aeruginosa Infection on Long-term Outcomes in Cystic Fibrosis.

Authors:  Nicole Mayer-Hamblett; Margaret Kloster; Margaret Rosenfeld; Ronald L Gibson; George Z Retsch-Bogart; Julia Emerson; Valeria Thompson; Bonnie W Ramsey
Journal:  Clin Infect Dis       Date:  2015-05-13       Impact factor: 9.079

5.  Changes in cystic fibrosis sputum microbiology in the United States between 1995 and 2008.

Authors:  Julia Emerson; Sharon McNamara; Anne Marie Buccat; Kelly Worrell; Jane L Burns
Journal:  Pediatr Pulmonol       Date:  2010-04

6.  Longevity of patients with cystic fibrosis in 2000 to 2010 and beyond: survival analysis of the Cystic Fibrosis Foundation patient registry.

Authors:  Todd MacKenzie; Alex H Gifford; Kathryn A Sabadosa; Hebe B Quinton; Emily A Knapp; Christopher H Goss; Bruce C Marshall
Journal:  Ann Intern Med       Date:  2014-08-19       Impact factor: 25.391

7.  Clinical outcome after early Pseudomonas aeruginosa infection in cystic fibrosis.

Authors:  G M Nixon; D S Armstrong; R Carzino; J B Carlin; A Olinsky; C F Robertson; K Grimwood
Journal:  J Pediatr       Date:  2001-05       Impact factor: 4.406

8.  Comparative efficacy and safety of 4 randomized regimens to treat early Pseudomonas aeruginosa infection in children with cystic fibrosis.

Authors:  Miriam M Treggiari; George Retsch-Bogart; Nicole Mayer-Hamblett; Umer Khan; Michal Kulich; Richard Kronmal; Judy Williams; Peter Hiatt; Ronald L Gibson; Terry Spencer; David Orenstein; Barbara A Chatfield; Deborah K Froh; Jane L Burns; Margaret Rosenfeld; Bonnie W Ramsey
Journal:  Arch Pediatr Adolesc Med       Date:  2011-09

9.  The changing prevalence of pulmonary infection in adults with cystic fibrosis: A longitudinal analysis.

Authors:  Kay A Ramsay; Harpreet Sandhu; James B Geake; Emma Ballard; Peter O'Rourke; Claire E Wainwright; David W Reid; Timothy J Kidd; Scott C Bell
Journal:  J Cyst Fibros       Date:  2016-08-08       Impact factor: 5.482

10.  Eradication of Pseudomonas aeruginosa in adults with cystic fibrosis.

Authors:  S L Kenny; T D Shaw; D G Downey; J E Moore; J C Rendall; J S Elborn
Journal:  BMJ Open Respir Res       Date:  2014-04-23
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  15 in total

1.  The O2-independent pathway of ubiquinone biosynthesis is essential for denitrification in Pseudomonas aeruginosa.

Authors:  Chau-Duy-Tam Vo; Julie Michaud; Sylvie Elsen; Bruno Faivre; Emmanuelle Bouveret; Frédéric Barras; Marc Fontecave; Fabien Pierrel; Murielle Lombard; Ludovic Pelosi
Journal:  J Biol Chem       Date:  2020-05-14       Impact factor: 5.157

2.  Systemic levels of anti-PAD4 autoantibodies correlate with airway obstruction in cystic fibrosis.

Authors:  Ruchi Yadav; Dae-Goon Yoo; J Michelle Kahlenberg; S Louis Bridges; Oluwadamilola Oni; Hanwen Huang; Arlene Stecenko; Balázs Rada
Journal:  J Cyst Fibros       Date:  2019-01-10       Impact factor: 5.482

3.  Increased Innate Immune Susceptibility in Hyperpigmented Bacteriophage-Resistant Mutants of Pseudomonas aeruginosa.

Authors:  Nitasha D Menon; Samuel Penziner; Elizabeth T Montaño; Raymond Zurich; David T Pride; Bipin G Nair; Geetha B Kumar; Victor Nizet
Journal:  Antimicrob Agents Chemother       Date:  2022-07-06       Impact factor: 5.938

4.  Pseudomonas aeruginosa Detection Using Conventional PCR and Quantitative Real-Time PCR Based on Species-Specific Novel Gene Targets Identified by Pangenome Analysis.

Authors:  Chufang Wang; Qinghua Ye; Aiming Jiang; Jumei Zhang; Yuting Shang; Fan Li; Baoqing Zhou; Xinran Xiang; Qihui Gu; Rui Pang; Yu Ding; Shi Wu; Moutong Chen; Qingping Wu; Juan Wang
Journal:  Front Microbiol       Date:  2022-05-04       Impact factor: 6.064

5.  Early acquisition and conversion of Pseudomonas aeruginosa in Hispanic youth with cystic fibrosis in the United States.

Authors:  Meghan E McGarry; Chiung-Yu Huang; Dennis W Nielson; Ngoc P Ly
Journal:  J Cyst Fibros       Date:  2020-11-05       Impact factor: 5.482

6.  Cystic Fibrosis Patients Infected With Epidemic Pseudomonas aeruginosa Strains Have Unique Microbial Communities.

Authors:  Nicole Acosta; Barbara Waddell; Alya Heirali; Ranjani Somayaji; Michael G Surette; Matthew L Workentine; Harvey R Rabin; Michael D Parkins
Journal:  Front Cell Infect Microbiol       Date:  2020-04-24       Impact factor: 5.293

7.  Characterization and Genomic Analyses of Pseudomonas aeruginosa Podovirus TC6: Establishment of Genus Pa11virus.

Authors:  Chaofei Tang; Chuanjiang Deng; Yi Zhang; Cong Xiao; Jing Wang; Xiancai Rao; Fuquan Hu; Shuguang Lu
Journal:  Front Microbiol       Date:  2018-10-25       Impact factor: 5.640

8.  Developing Inhaled Antibiotics in Cystic Fibrosis: Current Challenges and Opportunities.

Authors:  Dave P Nichols; Anthony G Durmowicz; Ann Field; Patrick A Flume; Donald R VanDevanter; Nicole Mayer-Hamblett
Journal:  Ann Am Thorac Soc       Date:  2019-05

9.  Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis.

Authors:  Diana Bilton; Tacjana Pressler; Isabelle Fajac; John Paul Clancy; Dorota Sands; Predrag Minic; Marco Cipolli; Ivanka Galeva; Amparo Solé; Alexandra L Quittner; Keith Liu; John P McGinnis; Gina Eagle; Renu Gupta; Michael W Konstan
Journal:  J Cyst Fibros       Date:  2019-08-23       Impact factor: 5.527

10.  Pulmonary Outcomes Associated with Long-Term Azithromycin Therapy in Cystic Fibrosis.

Authors:  Dave P Nichols; Katherine Odem-Davis; Jonathan D Cogen; Christopher H Goss; Clement L Ren; Michelle Skalland; Ranjani Somayaji; Sonya L Heltshe
Journal:  Am J Respir Crit Care Med       Date:  2020-02-15       Impact factor: 21.405

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