Long-Term clinical outcomes of â € Prairie Epidemic Strain' Pseudomonas aeruginosa infection in adults with cystic fibrosis

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Abstract

Rationale Epidemic Pseudomonas aeruginosa (PA) plays an important role in cystic fibrosis (CF) lung disease. A novel strain, the â € Prairie Epidemic Strain' (PES), has been identified in up to 30% of patients in Prairie-based Canadian CF centres. Objective To determine the incidence, prevalence and long-Term clinical impact of PES infection. Methods A cohort of adults with CF was followed from 1980 to 2014 where bacteria isolated from clinical encounters were prospectively collected. Strain typing was performed using pulse-field gel electrophoresis and multilocus sequence typing. Patients were divided into one of four cohorts: no PA, transient PA, chronic PA with unique strains and chronic PES. Proportional Cox hazard and linear mixed models were used to assess for CF-Associated respiratory death or transplantation, and rates of %FEV 1 and body mass index (BMI) decline. Results 274 patients (51.7% male) were analysed: 44-no PA, 29-Transient PA, 137-unique PA, 64-PES. A total of 92 patients (33.6%) died or underwent lung transplantation (2423.0 patient-years). PES infection was associated with greater risk of respiratory death or lung transplant compared with the no PA group (aHR, 3.94 (95% CI 1.18 to 13.1); p=0.03) and unique PA group (aHR, 1.75 (95% CI 1.05 to 2.92) p=0.03). Rate of lung function decline (%FEV 1 predicted) was greatest in the PES group (1.73%/year (95% CI 1.63% to 1.82%); p<0.001). BMI improved over time but at an attenuated rate in the PES group (p=0.001). Conclusions Infection with PES was associated with increased patient morbidity through three decades and manifested in an increased risk of respiratory death and/or lung transplantation.

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Somayaji, R., Lam, J. C., Surette, M. G., Waddell, B., Rabin, H. R., Sibley, C. D., … Parkins, M. D. (2017). Long-Term clinical outcomes of â € Prairie Epidemic Strain’ Pseudomonas aeruginosa infection in adults with cystic fibrosis. Thorax, 72(4), 333–339. https://doi.org/10.1136/thoraxjnl-2015-208083

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