Cost-Utility Analysis of Glucagon-Like Peptide-1 Agonists Compared with Dipeptidyl Peptidase-4 Inhibitors or Neutral Protamine Hagedorn Basal Insulin as Add-On to Metformin in Type 2 Diabetes in Sweden

被引:24
作者
Kiadaliri, Aliasghar A. [1 ,2 ]
Gerdtham, Ulf G. [1 ,3 ]
Eliasson, Bjorn [4 ]
Carlsson, Katarina Steen [1 ,5 ]
机构
[1] Lund Univ, Dept Clin Sci Malmo, Hlth Econ, SE-22381 Lund, Sweden
[2] Univ Tehran Med Sci, Sch Publ Hlth, Dept Hlth Management & Econ, Tehran, Iran
[3] Lund Univ, Dept Econ, SE-22381 Lund, Sweden
[4] Univ Gothenburg, Sahlgrenska Univ Hosp, Dept Med, Gothenburg, Sweden
[5] Swedish Inst Hlth Econ, Lund, Sweden
基金
瑞典研究理事会;
关键词
Cost-utility analysis; DPP-4; inhibitors; GLP-1; agonists; Insulin; Sweden; Type; 2; diabetes; LIFETIME HEALTH OUTCOMES; NPH INSULIN; OPEN-LABEL; MELLITUS; MODEL; GLARGINE; COMPLICATIONS; EFFICACY; THERAPY; SAFETY;
D O I
10.1007/s13300-014-0080-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: This study aimed to assess the costs and benefits of three alternative second-line treatment strategies for Swedish patients with type 2 diabetes mellitus (T2DM) who fail to reach glycated hemoglobin (HbA1c) <= 7% with metformin treatment alone: glucagon-like peptide-1 (GLP-1) receptor agonists, dipeptidyl peptidase-4 (DPP-4) inhibitors, and neutral protamine Hagedorn (NPH) insulin. Methods: A previously developed cohort model for T2DM was applied over a 35-year time horizon. Data on T2DM patients on metformin monotherapy with HbA1c > 7% were collected from the Swedish National Diabetes Register. Treatment effects were taken from published studies. Costs and effects were discounted at 3% per annum, and the analysis was conducted from a societal perspective. The robustness of the results was evaluated using one-way and probabilistic sensitivity analyses. Results: Treatment with GLP-1 agonists was associated with a discounted incremental benefit of 0.10 and 0.25 quality-adjusted life years (QALYs) and higher discounted costs of Swedish Krona (SEK) 34,865 and SEK 40,802 compared with DPP-4 inhibitors and NPH insulin, respectively. Assuming willingness-to-pay (WTP) of SEK 500,000 per QALY, treatment strategy with GLP-1 agonists was a cost-effective option with incremental cost-effectiveness ratios of SEK 353,172 and SEK 160,618 per QALY gained versus DPP-4 inhibitors and NPH insulin, respectively. The results were most sensitive to incidence rate of moderate/major hypoglycemia and disutilities associated with insulin treatment, body mass index (BMI), and hypoglycemia. Conclusion: Assuming a WTP of SEK 500,000 per QALY, treatment strategy with GLP-1 agonists is a cost-effective strategy in comparison to DPP-4 inhibitors and NPH insulin among T2DM patients inadequately controlled with metformin alone in a Swedish setting.
引用
收藏
页码:591 / 607
页数:17
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