Healthcare expenditure of intravitreal anti-vascular endothelial growth factor inhibitors compared with dexamethasone implant for diabetic macular oedema

被引:2
作者
Hertzberg, Silvia N. W. [1 ,2 ]
Moe, Morten Carstens [1 ,2 ]
Jorstad, Oystein Kalsnes [1 ,2 ]
Petrovski, Beata Eva [1 ,2 ]
Burger, Emily [3 ,4 ]
Petrovski, Goran [1 ,2 ]
机构
[1] Oslo Univ Hosp, Fac Med, Ctr Eye Res, Dept Ophthalmol, Kirkeveien 166, N-0450 Oslo, Norway
[2] Univ Oslo, Inst Clin Med, Kirkeveien 166, N-0450 Oslo, Norway
[3] Univ Oslo, Dept Hlth Management & Hlth Econ, Oslo, Norway
[4] Harvard TH Chan Sch Publ Hlth, Ctr Hlth Decis Sci, Boston, MA USA
关键词
Avastin; diabetic macular edema; Eylea; healthcare expenditure; intravitreal injections; Ozurdex; COST-EFFECTIVENESS; RANIBIZUMAB TREATMENT; BEVACIZUMAB; AFLIBERCEPT; OUTCOMES; INJECTIONS; EFFICACY; SAFETY; TRIAL;
D O I
10.1111/aos.15151
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose The aim of this study was to estimate the 1-year costs associated with treating diabetic macular oedema (DME) patients using current intravitreal anti-vascular endothelial growth factor (anti-VEGF) biologics compared with the dexamethasone implant. Methods We conducted a descriptive cost-evaluation analysis using data from Oslo University Hospital and literature to compare three different intravitreal drugs for DME: bevacizumab, aflibercept and dexamethasone. Stratification of patients into 'Naive' or 'Switch' group was based on treatment history. We estimated the costs from healthcare and 'extended' healthcare perspectives. Sensitivity analysis evaluated the impact of various parameters. Results The average injections per patient per year for the Naive group (bevacizumab), Switch group (aflibercept) and dexamethasone were 9.5, 9.1 and 3.0 respectively. From a healthcare perspective, the 1-year costs for the Naive group were 15% lower (bevacizumab, euro3619), and for the Switch group, 23% higher (aflibercept, euro5226) compared with dexamethasone (euro4252). The 'extended' healthcare perspective showed the cost per patient per year for bevacizumab remained nominally lower in the Naive group, while dexamethasone remained lower for the Switch group (euro5116 for dexamethasone, compared to euro4987 for bevacizumab and euro6537 for aflibercept). Conclusions From a primary healthcare perspective, the dexamethasone as a first-line DME treatment may increase economic costs in settings where bevacizumab is used off-label. Treating resistant DMEwith dexamethasone may reduce the costs and treatment burden compared with switching to aflibercept.
引用
收藏
页码:E1630 / E1640
页数:11
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