Treatment satisfaction in cystic fibrosis: early patient experience with tobramycin inhalation powder
- PMID: 27822017
- PMCID: PMC5087789
- DOI: 10.2147/PPA.S102234
Treatment satisfaction in cystic fibrosis: early patient experience with tobramycin inhalation powder
Abstract
Background: This study assessed treatment satisfaction of cystic fibrosis (CF) patients in a routine clinical setting for tobramycin inhalation powder (TIP), the first dry powder-inhaled antibiotic for Pseudomonas aeruginosa infection.
Methods: CF patients aged 6 years or older treated with at least one cycle of TIP completed a web survey on experience with TIP, including the Treatment Satisfaction Questionnaire for Medication (TSQM). Regression analysis determined the factors associated with TSQM global satisfaction.
Results: Eighty patients (mean age ± standard deviation: 24.4±9.4 years; 57.5% female; mean forced expiratory volume in 1 second ± standard deviation: 67.1%±27.3% predicted) completed the survey. The majority expressed satisfaction with TIP's administration time (100%), time to clean (97.1%), portability (97.1%), and ease of use (94.3%). Effectiveness was significantly associated with TSQM global satisfaction (regression R-squared: 0.54).
Conclusion: Patient preferences for TIP were based on administration time and ease of use. Global satisfaction was related to greater patient-perceived effectiveness.
Keywords: cystic fibrosis; dry powder inhalers; patient satisfaction; tobramycin.
Conflict of interest statement
JBP and WWC are employees of Novartis Pharmaceuticals. DW and PS are employees of RTI Health Solutions. RTI Health Solutions and Boston Children’s Hospital each received funding from Novartis Pharmaceuticals for this study. The authors report no other conflicts of interest in this work.
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