Impact of Oral Antihyperglycemic Therapy on All-Cause Mortality Among Patients With Diabetes in the Veterans Health Administration
- Kristijan H. Kahler, PHD, RPH1,
- Mangala Rajan, MBA1,
- George G. Rhoads, MPH2,
- Monika M. Safford, MD3,
- Kitaw Demissie, PHD, MD2,
- Shou-En Lu, PHD2 and
- Leonard M. Pogach, MD1
- 1Center for Health Care Knowledge and Management, VA New Jersey Health Care System, East Orange, New Jersey
- 2School of Public Health, University of Medicine and Dentistry of New Jersey, Piscataway, New Jersey
- 3Deep South Center on Effectiveness, Birmingham VA Medical Center, Birmingham, Alabama
- Address correspondence and reprint requests to Kristijan H. Kahler, PhD, RPh, Novartis Pharmaceuticals, One Health Plaza, Room 405/3117, East Hanover, NJ 07936. E-mail: kristijan.kahler{at}novartis.com
Abstract
OBJECTIVE— The objective of this analysis was to evaluate the impact of several classes of oral antihyperglycemic therapy relative to sulfonylurea monotherapy on all-cause mortality among a cohort of patients with diabetes from the Veterans Health Administration (VHA).
RESEARCH DESIGN AND METHODS— A retrospective cohort study using data obtained from the VHA Diabetes Epidemiology Cohort was used. Users of oral antihyperglycemic therapy were classified into the following cohorts: sulfonylurea monotherapy, metformin monotherapy, metformin plus sulfonylurea, thiazolidinedione (TZD) use alone or in combination with other oral agents (TZD users), and no drug therapy. All-cause mortality was the outcome of interest. Multivariate mixed models incorporating a propensity score to account for imbalance among cohorts were used to estimate drug effects on mortality with associated 95% CIs.
RESULTS— A total of 39,721 patients with diabetes were included in the study. Adjusted odds ratios and 95% CIs for all-cause mortality were 0.87 (0.68–1.10) for metformin monotherapy users, 0.92 (0.82–1.05) for metformin plus sulfonylurea users, and 1.04 (0.75–1.46) for TZD users, relative to sulfonylurea monotherapy users.
CONCLUSIONS— We did not find any significant drug effect on all-cause mortality for any oral treatment cohorts relative to sulfonylurea oral monotherapy.
- DEpiC, Diabetes Epidemiology Cohort
- LHSVE, Large Health Survey of Veteran Enrollees
- TZD, thiazolidinedione
- UKPDS, U.K. Prospective Diabetes Study
- VHA, Veterans Health Administration
Footnotes
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Published ahead of print at http://care.diabetesjournals.org on 17 April 2007. DOI: 10.2337/dc06-2272.
K.H.K. is currently affiliated with Novartis Pharmaceuticals, East Hanover, New Jersey.
Additional information for this article can be found in an online appendix at http://dx.doi.org/10.2337/dc06-2272.
A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C Section 1734 solely to indicate this fact.
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- Accepted April 11, 2007.
- Received November 5, 2006.
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