Impact of pharmacy services on cystic fibrosis medication adherence
Jeffery T Zobell1,2, Elizabeth Schwab3, Dave S Collingridge4
1Pharmacy, Intermountain Primary Children's Hospital, Salt Lake City, Utah.
Insights
Pharmacy services significantly improved medication adherence for pediatric cystic fibrosis (CF) patients. Integrated pharmacy models increased adherence to dornase alfa, reducing hospitalizations.
Area of Science:
- Pediatric Pulmonology
- Clinical Pharmacy
- Health Outcomes Research
Background:
- Cystic Fibrosis (CF) requires consistent medication adherence for optimal management.
- Dornase alfa is a key therapy for CF, but adherence can be challenging.
- The role of integrated pharmacy services in improving pediatric CF care is not fully characterized.
Purpose of the Study:
- To evaluate the impact of pharmacy services on medication adherence in pediatric CF patients.
- To assess the effect of pharmacy services on hospitalization rates for CF-related pulmonary exacerbations.
- To compare adherence rates before and after the implementation of an integrated pharmacy team.
Main Methods:
- Retrospective analysis of health insurance claims and medical charts (2014-2016).
- Inclusion of patients from the Pediatric Intermountain CF Center.
- Measurement of dornase alfa adherence using Medication Possession Ratio (MPR) and review of hospital admissions.
Main Results:
- Mean yearly dornase alfa MPR increased from 0.75 in 2014 to 0.92 in 2016.
- Patients were 2.8 times more likely to be adherent with an integrated pharmacy team (P < 0.001).
- Patients were 2.4 times more likely to be adherent with a dedicated CF clinic pharmacist (P = 0.001).
Conclusions:
- Pharmacy services demonstrably improve dornase alfa adherence in pediatric CF patients.
- Integrated and dedicated CF clinic pharmacy models enhance medication adherence.
- These findings support the integration of pharmacy services in CF care to improve patient outcomes.
Objectives:
The purpose of this study is to characterize the impact of pharmacy services on medication adherence and hospitalizations for pediatric cystic fibrosis (CF) patients.
Methods:
A retrospective health insurance claims analysis and patient medical charts review from January 1, 2014 to December 31, 2016 of patients from the Pediatric Intermountain CF Center was performed. Adherence to dornase alfa and hospital admissions for pulmonary exacerbations pre and post the implementation of an integrated pharmacy team were reviewed. Dornase alfa adherence was measured by the medication possession ratio (MPR) both monthly and yearly.
Results:
Fifty-four patients met inclusion criteria. The mean dornase alfa yearly MPR improved from 0.75 (2014) to 0.92 (2016). Patients were 2.8 times more likely to be adherent to dornase alfa when followed by integrated pharmacy team model (P < 0.001), and 2.4 times more likely to be adherent when followed by a dedicated CF clinic pharmacist only (P = 0.001).
Conclusion:
The study demonstrated that pharmacy services improved adherence to dornase alfa.
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