Patient Satisfaction and Glycemic Control After 1 Year With Inhaled Insulin (Exubera) in Patients With Type 1 or Type 2 Diabetes
- Julio Rosenstock, MD1,
- Joseph C. Cappelleri, PHD, MPH2,
- Björn Bolinder3 and
- Robert A. Gerber, PHARMD, MA2
- 1Dallas Diabetes and Endocrine Center, Dallas, Texas
- 2Pfizer Global Research and Development, Groton, Connecticut
- 3Aventis Pharmaceuticals, Bridgewater, New Jersey
- Address correspondence and reprint requests to Robert A. Gerber, PharmD, MA, Pfizer, MS 8260-208, Global ResearchDevelopment, Eastern Point Road, Groton, CT 06340. E-mail: robert_a_gerber{at}groton.pfizer.com
Abstract
OBJECTIVE—The aim of this study was to determine patient satisfaction in patients with type 1 or type 2 diabetes receiving an inhaled insulin or subcutaneous insulin regimen, as assessed by pooled analysis of two 12-week parent studies and 1-year extension studies.
RESEARCH DESIGN AND METHODS—In the 12-week parent studies, patients with type 1 (n = 70) or type 2 (n = 51) diabetes were randomized to an inhaled insulin or subcutaneous insulin regimen. In the 1-year extension studies, patients were allowed to select either treatment regimen. Patient satisfaction was assessed at baseline, week 12, and 1 year using the Patient Satisfaction with Insulin Therapy questionnaire.
RESULTS—Of the 60 patients who received inhaled insulin during the parent studies, 85.0% (n = 51) chose to continue treatment, 13.3% (n = 8) switched to subcutaneous insulin, and 1.7% (n = 1) did not continue. Of the 61 patients who received subcutaneous insulin, 21.3% (n = 13) chose to continue treatment, 75.4% (n = 46) switched to inhaled insulin, and 3.3% (n = 2) did not continue. From baseline (parent studies) to 1 year (extension studies), HbA1c reductions of 0.8% were sustained, and greater improvements were observed in the inhaled insulin group compared with the subcutaneous insulin group in terms of overall satisfaction (37.9 vs. 3.1%; P < 0.01) and ease of use (43.2 vs. −0.9%; P < 0.01).
CONCLUSIONS—Inhaled insulin was preferred over subcutaneous insulin, which resulted in greater patient satisfaction up to 1 year in patients with type 1 or type 2 diabetes with durable effects on HbA1c levels.
Footnotes
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J.R. has received research grants from Bristol-Myers Squibb, GlaxoSmithKline, Eli Lilly, Novo Nordisk, Pfizer, Aventis, Novartis, Takeda, and Astra-Zeneca; has been a paid consultant for Aventis, Johnson and Johnson, GlaxoSmithKline, Takeda, and Novo Nordisk; and has been on speakers bureaus for Aventis, Bristol-Myers Squibb, Novo Nordisk, GlaxoSmithKline, and Takeda.
A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.
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- Accepted February 26, 2004.
- Received October 13, 2003.
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