Related Experiment Video
Updated: Jan 12, 2026

Visualization of Pseudomonas aeruginosa within the Sputum of Cystic Fibrosis Patients
Published on: July 16, 2020
The Increased Risk for Postinfluenza Pneumonia Among Cystic Fibrosis Carriers-A Population-Based Study
Aaron C Miller1, D Erik Boonstra2, Joe E Cavanaugh2
1Department of Internal Medicine, Division of Infectious Diseases, University of Iowa, Iowa City, Iowa, USA.
Background:
Influenza is strongly associated with an increased risk for subsequent bacterial pneumonia. Moreover, cystic fibrosis (CF) carriers are at increased risk for some pulmonary infections. The purpose of this study was to determine whether CF carriers are at greater risk for postinfluenza pneumonia than noncarriers.
Methods:
Using MarketScan insurance claims data (2001-2023), we identified a study cohort of 38 047 CF carriers and a cohort of 380 470 matched controls. We conducted 2 analyses using these cohorts. First, we assessed individual-level risk for experiencing pneumonia following an influenza infection. Second, because many cases of influenza often do not result in medical visits, we conducted a cohort-level analysis comparing the weekly incidence of pneumonia between CF carriers and noncarriers while accounting for weekly Centers for Disease Control and Prevention-reported influenzalike illnesses across multiple influenza seasons.
Results:
At an individual level, we found that the odds of developing pneumonia following a diagnosis of influenza were approximately 34% greater among CF carriers compared with noncarriers. Second, we found that while the incidence of influenza is not elevated among CF carriers, the incidence rate of pneumonia was about 55% greater among CF carriers compared with our control population.
Conclusions:
Because 2%-11% of the population acquires influenza each year, and because there are >10-15 million CF carriers in the United States alone, a substantial number of cases of secondary pneumonia may be attributable to the CF carrier state.
Related Concept Videos
Cystic Fibrosis: Management
Sinus disease and chronic...
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Pneumonia I: Introduction
Risk Factors
Various factors influence the likelihood of developing pneumonia. Age plays a crucial role, with infants, children under two, and individuals over 65 at increased risk due to their...
Pneumonia V: Nursing management and Prevention
The nurse must practice strict medical asepsis and adhere to infection control guidelines to minimize healthcare-associated infections.
Enhance airway patency
Position the patient correctly to facilitate drainage of the affected lung segments. Manual or mechanical percussion and vibration can also be employed....
Pneumonia II: Pathophysiology
Transmission-based Precautions II: Airborne and Protective Environment
Airborne precautions:
Use airborne precautions when treating patients known or suspected to have diseases that spread through the air—for example, tuberculosis or measles. These organisms are present in smaller droplets expelled by an infected person and...

