Cost-effectiveness of basal insulin from a US health system perspective: Comparative analyses of detemir, glargine, and NPH

被引:35
作者
Valentine, William J.
Palmer, Andrew J.
Erny-Albrecht, Katrina M.
Ray, Joshua A.
Cobden, David
Foos, Volker
Lurati, Francisco M.
Roze, Stephane
机构
[1] CORE Ctr Outcomes Res, CH-4102 Binningen, Switzerland
[2] Novo Nordisk Inc, Princeton, NJ USA
关键词
type; 1; diabetes; NPH; detemir; insulin glargine; modeling; costs; life expectancy; quality-adjusted life expectancy; cost-effectiveness;
D O I
10.1007/BF02850126
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The purpose of this study was to compare in clinical and economic terms the long-acting insulin analogue detemir with intermediate-acting Neutral Protamine Hagedorn (NPH) insulin and with long-acting insulin glargine. Investigators used the validated Center for Outcomes Research (CORE) Diabetes Model to project clinical and cost outcomes over a 35-year base case time horizon; outcome data were extracted directly from randomized, controlled trials designed to compare detemir with NPH and with insulin glargine. Modeled patient characteristics were derived from corresponding trials, and simulations incorporated published quality-of-life utilities with cost data obtained from a Medicare perspective. Detemir, when compared with NPH, increased quality-adjusted life expectancy by 0.698 quality-adjusted life-years (QALYs). Lifetime direct medical costs were increased by $10,451 per patient, although indirect costs were reduced by $4688. On the basis of direct costs, the cost per QALY gained with detemir was $14,974. In comparison with glargine, detemir increased quality-adjusted life expectancy by 0.063 QALYs, reduced direct medical costs by $2072 per patient, and decreased indirect costs by $3103 (dominant). Reductions in diabetes-related comorbidities were also associated with detemir in both instances, most notably in the complications of retinopathy and nephropathy. Relative reductions in rates of complications were greatest in the comparison of detemir with NPH. Results were most sensitive to variation in hemoglobin A(1c) (HbA(1c)) levels. However, variation among any of the key assumptions, including HbA(1c), did not alter the relative results. Detemir represents an attractive clinical and economic intervention in the US health care setting compared with both NPH insulin and insulin glargine.
引用
收藏
页码:191 / 207
页数:17
相关论文
共 32 条
[1]  
*AM ASS CLIN END, 2002, MED GUID MAN DIAB ME
[2]   INSULIN PHARMACOKINETICS [J].
BINDER, C ;
LAURITZEN, T ;
FABER, O ;
PRAMMING, S .
DIABETES CARE, 1984, 7 (02) :188-199
[3]  
Briggs AH, 1997, HEALTH ECON, V6, P327, DOI 10.1002/(SICI)1099-1050(199707)6:4<327::AID-HEC282>3.0.CO
[4]  
2-W
[5]   Differences in hypoglycemia event rates and associated cost-consequence in patients initiated on long-acting and intermediate-acting insulin products [J].
Bullano, MF ;
Al-Zakwani, IS ;
Fisher, MD ;
Menditto, L ;
Willey, VJ .
CURRENT MEDICAL RESEARCH AND OPINION, 2005, 21 (02) :291-298
[6]  
DAVIES R, 2005, IMPACT HLTH RELATED
[7]  
DCCT Res Grp, 1991, AM J MED, V90, P450, DOI 10.1016/0002-9343(91)80085-Z
[8]  
DCCT Res Grp, 1988, DIABETES CARE, V11, P567
[9]   Impact of overweight on chronic microvascular complications in type 1 diabetic patients [J].
De Block, CEM ;
De Leeuw, IH ;
Van Gaal, LF .
DIABETES CARE, 2005, 28 (07) :1649-1655
[10]   The impact of insulin glargine on clinical and humanistic outcomes in patients uncontrolled on other insulin and oral agents: an office-based naturalistic study [J].
Fischer, JS ;
McLaughlin, T ;
Loza, L ;
Beauchamp, R ;
Schwartz, S ;
Kipnes, M .
CURRENT MEDICAL RESEARCH AND OPINION, 2004, 20 (11) :1703-1710