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Published on: April 19, 2024
Incidence and prevalence of common respiratory pathogens before and after implementation of the Cystic Fibrosis
Christy Kim1, Elizabeth delaRiva-Velasco1, Arvind Budhram1
1New York Medical College and Maria Fareri Children's Hospital at Westchester Medical Center Division of Pediatric Pulmonology, Allergy and Sleep Medicine and the Armond V. Mascia Cystic Fibrosis Center, Valhalla, NY, USA.
Insights
The 2013 Cystic Fibrosis Foundation
Area of Science:
- Medical Research
- Infectious Disease Epidemiology
- Pulmonology
Background:
- The Cystic Fibrosis Foundation's Infection Prevention and Control Guideline (CFF IP&C) was established in 2013.
- The guideline aimed to minimize the risk of respiratory pathogen acquisition and transmission in cystic fibrosis (CF) patients.
Purpose of the Study:
- To evaluate the impact of the CFF IP&C guideline on the incidence of common respiratory pathogens in CF patients.
- To test the hypothesis that guideline implementation would decrease pathogen incidence.
Main Methods:
- A retrospective analysis of respiratory cultures from CF patients between August 2012 and August 2017.
- Inclusion criteria required at least one culture per year for incidence analysis.
- Quarterly data were collected for one year pre-guideline and three years post-guideline implementation.
Main Results:
- No significant changes were observed in the quarterly or annual incidence rates of common respiratory organisms.
- The prevalence rates of these organisms also remained unchanged during the study period.
Conclusions:
- The initial three years following CFF IP&C guideline implementation showed no significant effect on the incidence or prevalence of common respiratory pathogens.
- Further long-term follow-up is necessary to ascertain any delayed effects of the guideline.
Background:
The 2013 Cystic Fibrosis Foundation's Infection Prevention and Control Guideline (CFF IP&C) was developed to reduce the risk of acquisition and transmission of respiratory pathogens in patients with cystic fibrosis (CF).
Objective:
We hypothesised that the incidence of common CF respiratory pathogens would decrease at our centre after implementation of the guideline.
Methods:
All patients with CF seen at our centre from August 2012 through August 2017 who had respiratory cultures were included. Patients were excluded from incidence analysis if they did not have at least one culture per year. Quarterly data were collected for one year before and three years after implementation of the guidelines to determine the incidence and prevalence of seven organisms commonly found in respiratory cultures of patients with CF.
Results:
Quarterly and annual incidence and prevalence rates of common organisms did not change during the study period.
Discussion:
There were no significant differences in the incidence or prevalence of common respiratory organisms in the first three years after implementation of the CF IP&C guideline. Long-term follow-up is needed to determine if changes occur over time.
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