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Volume 87, Issue 1, Pages 108-116 (January 2010)


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Direct costs associated with initiating NPH insulin versus glargine in patients with type 2 diabetes: A retrospective database analysis

Lauren J. Leea, Andrew P. Yub, Scott J. JohnsonbCorresponding Author Informationemail address, Howard G. Birnbaumb, Pavel Atanasovb, Don P. Bueschinga, Jeffrey A. Jacksonc, Jaime A. Davidsond

Received 12 November 2008; received in revised form 27 August 2009; accepted 28 September 2009. published online 06 November 2009.

Abstract 

Aims

To compare total costs and risk of hypoglycemia in patients with type 2 diabetes (T2D) initiated on NPH insulin versus glargine in a real-world setting.

Methods

This study used claims data (10/2001 to 06/2005) from a privately insured U.S. population of adult T2D patients who were initiated on NPH or glargine following a 6-month insulin-free period. A sample of 1698 glargine-treated and 400 NPH-treated patients met the inclusion criteria. Total and diabetes-related costs (inflation-adjusted to 2006) were calculated for 6-month pre- and post-index periods and compared between 400 patient pairs matched by a propensity score method.

Results

In the post-index 6-month period, glargine patients incurred higher diabetes-related drug costs than NPH patients ($785 versus $632, p<0.0001) but there were no significant differences in diabetes-related medical or total costs, or all other total cost categories. Compared to the pre-index period, glargine patient costs declined by $2420 (p=0.058) whereas NPH patient costs declined by $4200 (p=0.046), with no statistically significant group differences (p=0.469). Among patients with hypoglycemia-related claims (0.75% in both groups), mean hypoglycemia-related costs were $85 and $202 for NPH and glargine patients, respectively (p=0.564).

Conclusion

Initiation of either NPH or glargine was associated with major cost reductions and infrequent hypoglycemia-related claims.

a Eli Lilly and Company, Global Health Outcomes, Indianapolis, IN, United States

b Analysis Group, Inc., Boston, MA, United States

c Lilly USA, LLC, US Medical Division, Indianapolis, IN, United States

d Department of Medicine, University of Texas, Southwestern Medical School, Dallas, TX, United States

Corresponding Author InformationCorresponding author at: Analysis Group, Inc., New York, NY 10020, United States. Tel.: +1 212 492 8130; fax: +1 212 492 8188.

PII: S0168-8227(09)00415-X

doi:10.1016/j.diabres.2009.09.023


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