Improving evidence-based care in cystic fibrosis through quality improvement
Gary L McPhail1, Jeanne Weiland, James D Acton
1Division of Pulmonary Medicine, University of Cincinnati, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio 45229-3039, USA. gary.mcphail@cchmc.org
Insights
Improving clinician adherence to cystic fibrosis (CF) medication guidelines is achievable. Educating providers and families, alongside monitoring, significantly boosts adherence to evidence-based recommendations for pediatric CF care.
Area of Science:
- Pediatric Pulmonology
- Clinical Quality Improvement
- Evidence-Based Medicine
Background:
- Cystic Fibrosis (CF) management requires adherence to specific pulmonary medication guidelines.
- Variability in clinician prescribing practices can impact patient outcomes in CF.
Purpose of the Study:
- To enhance clinician adherence to established prescribing guidelines for pulmonary medications in pediatric patients with CF.
- To implement and evaluate a quality improvement initiative targeting medication prescribing in CF.
Main Methods:
- A quality improvement project utilizing a multiple time series design was conducted at a US tertiary care pediatric hospital.
- Interventions included developing evidence-based guidelines, educating clinicians and families, and implementing a monitoring system with accountability measures.
- Adherence was tracked via a CF database and record reviews for children eligible for azithromycin, dornase alfa, or inhaled tobramycin.
Main Results:
- Initial clinician adherence to prescribing guidelines was 62% among 170 pediatric CF patients.
- After 3 months, adherence increased to 87% (OR=4.6, 95% CI: 3.0-7.0).
- This improvement in adherence was sustained over 21 months of follow-up.
Conclusions:
- Educating clinicians on prescribing guidelines is crucial for improving adherence.
- Engaging families by sharing guidelines enhances the effectiveness of adherence interventions.
- Continuous monitoring and accountability mechanisms are key to sustaining improved prescribing practices in CF care.
Objective:
To increase clinician adherence to prescribing guidelines for pulmonary medications in children with cystic fibrosis (CF).
Design:
Quality improvement project with multiple time series design.
Setting:
The CF center at a tertiary care pediatric hospital in the United States.
Patients:
Children with CF who were eligible to receive oral azithromycin, nebulized dornase alfa, or inhaled tobramycin sulfate based on prescribing guidelines for CF lung disease.
Intervention:
Evidence-based prescribing guidelines were designed by a local committee to reflect consensus recommendations from the CF Foundation. Clinicians and families were educated about guidelines. Adherence to prescribing guidelines was tracked using a local CF database and record reviews. Weekly meetings were used to highlight adherence failures and promote clinician accountability.
Main Outcome Measure:
The rate of clinician adherence to prescribing guidelines.
Results:
One hundred seventy patients with CF were included. At the start of the project, the rate of clinician adherence to prescribing guidelines was 62%. After 3 months of the project, the rate of clinician adherence to prescribing guidelines was 87% (odds ratio = 4.6; 95% confidence interval, 3.0-7.0). The improvements in adherence to prescribing guidelines were sustained for 21 months of follow-up.
Conclusions:
Educating clinicians about prescribing guidelines, sharing guidelines with families, and monitoring clinician adherence improve prescribing adherence to evidence-based recommendations.
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