Real-World Cost-Effectiveness: Lower Cost of Treating Patients to Glycemic Goal with Liraglutide versus Exenatide

被引:20
作者
DeKoven, Mitch [1 ]
Lee, Won Chan [1 ]
Bouchard, Jonathan [2 ]
Massoudi, Marjan [2 ]
Langer, Jakob [2 ]
机构
[1] IMS Hlth, Hlth Econ & Outcomes Res, Alexandria, VA 22314 USA
[2] Novo Nordisk Inc, Plainsboro, NJ USA
关键词
Cost-effectiveness; Endocrinology; Exenatide; Glycated hemoglobin A1C goal attainment; Glycemic control; Liraglutide; Type; 2; diabetes; TYPE-2 DIABETES PATIENTS; INCRETIN-BASED THERAPIES; PARALLEL-GROUP; METFORMIN; EFFICACY; SITAGLIPTIN; GLIMEPIRIDE; 26-WEEK; PLACEBO; SAFETY;
D O I
10.1007/s12325-014-0098-8
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
While the liraglutide effect and action in diabetes (LEAD-6) clinical trial compared the efficacy and safety of liraglutide once daily (LIRA) to exenatide twice daily (EXEN) in adult patients with type 2 diabetes, few studies have explored the associated per-patient costs of glycemic goal achievement of their use in a real-world clinical setting. This retrospective cohort study used integrated medical and pharmacy claims linked with glycated hemoglobin A1C (A1C) results from the IMS Patient-Centric Integrated Data Warehouse. Patients' a parts per thousand yen18 years and na < ve to incretin therapies during a 6-month pre-index period, with a parts per thousand yen1 prescription for LIRA or EXEN between January 2010 and December 2010, were included. Patients with evidence of insulin use (pre- or post-index) were excluded. Only patients who were persistent on their index treatment during a 180-day post-index period were included. Follow-up A1C assessments were based on available laboratory data within 45 days before or after the 6-month post-index point in time. Diabetes-related pharmacy costs over the 6-month post-index period were captured and included costs for both the index drugs and concomitant diabetes medications. 234 LIRA and 182 EXEN patients were identified for the analysis. The adjusted predicted diabetes-related pharmacy costs per patient over the 6-month post-index period were higher for LIRA compared to EXEN ($2,002 [95% confidence interval (CI): $1,981, $2,023] vs. $1,799 [95% CI: $1,778, $1,820]; P < 0.001). However, a higher adjusted predicted percentage of patients on LIRA reached A1C < 7% goal (64.4% [95% CI: 63.5, 65.3] vs. 53.6% [95% CI: 52.6, 54.6]; P < 0.05), translating into lower average diabetes-related pharmacy costs per successfully treated patient for LIRA as compared to EXEN ($3,108 vs. $3,354; P < 0.0001). Although predicted diabetes-related pharmacy costs were greater with LIRA vs. EXEN, a higher proportion of patients on LIRA achieved A1C < 7%, resulting in a lower per-patient cost of A1C goal achievement with LIRA compared to EXEN.
引用
收藏
页码:202 / 216
页数:15
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