Real-world health care utilization in asthma patients using albuterol sulfate inhalation aerosol (ProAir^® HFA) with and without integrated dose counters

Abstract

Background

Accurate tracking of the administered dose of asthma rescue inhalers is critical for optimal disease management and is related to reductions in rates of unscheduled health care utilization in asthma patients. There are few published data on the real-world impact of rescue inhalers with integrated dose counters (IDCs) on health care resource utilization (HRU) for asthma patients. This study evaluates HRU among users of ProAir^® hydrofluoroalkane (HFA) (albuterol sulfate inhalation aerosol), with IDC versus without IDC, in asthma patients.

Methods

This was a retrospective administrative claims study of asthma patients receiving a new prescription for albuterol inhalation aerosol without IDC during 2 years (January 2011–December 2012) or with IDC during the first full year after IDC implementation in the USA (July 2013–July 2014). Six months of continuous enrollment with medical and prescription drug benefits were required before and after the first prescription during the study period. Data on respiratory-related hospitalizations and emergency department (ED) visits were collected during the follow-up period.

Results

A total of 135,305 (32%) patients used albuterol inhalation aerosol with IDC, and 287,243 (68%) patients received albuterol inhalation aerosol without IDC. After adjusting for baseline confounding factors, the odds ratio (OR) for experiencing a respiratory-related hospitalization (OR=0.92; 95% confidence interval [CI] 0.88–0.96) or ED visit (OR=0.92; 95% CI 0.90–0.94) was significantly lower among patients using albuterol inhalation aerosol with IDC versus without IDC.

Conclusion

In a real-world setting, asthma patients using ProAir HFA with IDC experienced significantly fewer hospitalizations and ED visits compared with patients using ProAir HFA without IDC. Dosage information provided by IDCs may allow providers to better understand patients’ disease severity and aid in titrating controller medications and also decrease the likelihood that the canister will be empty when needed, thereby enhancing disease management and reducing HRU.

Keywords:

• asthma
• ProAir
• integrated dose counters
• respiratory-related hospitalizations
• emergency department visits
• lower respiratory tract infections-related outpatient visits

Acknowledgments

This study was sponsored by Teva Pharmaceutical Industries Ltd and conducted by Truven Health Analytics. Medical writing assistance was provided by Truven Health Analytics. Editorial support for this manuscript was provided by Santosh Tiwari, an employee of Truven Health Analytics, and by Peloton Advantage, Parsippany, NJ, and was funded by Teva Pharmaceutical Industries Ltd. Teva provided a full review of the article.

Disclosure

Edward M Kerwin has served on advisory boards and speaker panels, or received travel reimbursement, from Amphastar, AstraZeneca, Forest, Ironwood, Merck, Mylan, Novartis, Pearl, Pfizer, Sanofi Aventis, Sunovion, Targacept, Teva, and Theravance, and has conducted multicenter clinical research trials for ~40 pharmaceutical companies including Teva. Thomas J Ferro, Rinat Ariely, and Ruchir Parikh are employees of Teva Pharmaceuticals. Debra E Irwin discloses that her institution receives funding from all major pharmaceutical companies to conduct research studies, but she does not personally receive any support. The authors report no other conflicts of interest in this work.