ECONCARE LP, Athens, Greece.
Diabetes Centre, Department of Internal Medicine, Konstantopouleio Hospital, Athens, Greece.
Clin Drug Investig. 2021 Apr;41(4):371-380. doi: 10.1007/s40261-021-01013-w. Epub 2021 Mar 9.
Type 2 diabetes mellitus (T2DM) accounts for approximately 95% of all diabetes cases and is associated with a substantially elevated risk for cardiovascular disease (CVD) that is 2- to 4-times higher in patients with T2DM compared to those without. The aim of present study was to evaluate the cost effectiveness of empagliflozin compared to dapagliflozin for the treatment of patients with T2DM and established CVD in Greece.
A published health economic model was used to project clinical and economic outcomes of T2DM patients receiving empagliflozin compared to those receiving dapagliflozin. Individual patient-level discrete-event simulation was conducted to predict time-to-event for CV, renal, and adverse events over patients' lifetimes. Hazard ratios for dapagliflozin versus empagliflozin on each clinical event was estimated from DECLARE-TIMI 58 and EMPA-REG OUTCOME trials' data using an indirect treatment comparison. Following a public payer perspective, only direct medical costs related to drug acquisition, fatal/non-fatal diabetes-related complications and adverse events were considered (€2020). Model extrapolated outcomes included life years (LY), quality-adjusted life years (QALYs), costs as well as incremental cost-effectiveness ratio (ICER). Sensitivity analyses explored the impact of changes in input data.
Over a patient's lifetime, empagliflozin was associated with longer mean survival (17.23 LY with empagliflozin vs 16.07 LY with dapagliflozin) and reduced rate of CV mortality resulting in 0.48 more QALYs (9.27 vs 8.79), at additional costs of €462. The generated ICER of empagliflozin was €965 per QALY gained. Deterministic sensitivity analysis confirmed empagliflozin's cost-effective profile. Probabilistic sensitivity analysis revealed that the probability of empagliflozin being cost effective over dapagliflozin was 100%, at the defined threshold of €36,000 per QALY gained.
Empagliflozin was estimated to be a highly cost-effective treatment option compared to dapagliflozin for the treatment of T2DM patients with established CVD in Greece.
2 型糖尿病(T2DM)约占所有糖尿病病例的 95%,与心血管疾病(CVD)风险显著升高相关,T2DM 患者的 CVD 风险比无 T2DM 患者高 2-4 倍。本研究旨在评估恩格列净相对于达格列净治疗希腊 T2DM 合并已确诊 CVD 患者的成本效果。
使用已发表的卫生经济学模型预测接受恩格列净治疗的 T2DM 患者与接受达格列净治疗的患者的临床和经济结局。通过个体患者水平的离散事件模拟,预测 CVD、肾脏和不良事件在患者一生中的发生时间。使用间接治疗比较,从 DECLARE-TIMI 58 和 EMPA-REG OUTCOME 试验的数据中估计达格列净与恩格列净在每个临床事件上的风险比。基于公共支付者的角度,仅考虑与药物获取、致命/非致命糖尿病相关并发症和不良事件相关的直接医疗成本(€2020)。模型外推结果包括寿命年(LY)、质量调整寿命年(QALY)、成本以及增量成本效益比(ICER)。敏感性分析探讨了输入数据变化的影响。
在患者的一生中,恩格列净与更长的平均生存期相关(恩格列净治疗组为 17.23 LY,达格列净治疗组为 16.07 LY),并降低了 CVD 死亡率,导致 QALY 增加 0.48(9.27 比 8.79),额外成本为€462。恩格列净的增量成本效益比为每获得 1 QALY 增加€965。确定性敏感性分析证实了恩格列净的成本效益状况。概率敏感性分析表明,恩格列净相对于达格列净的成本效益比在 100%的概率上超过了€36,000 每获得 1 QALY 的阈值。
与达格列净相比,恩格列净在希腊 T2DM 合并已确诊 CVD 患者的治疗中被估计为一种具有高度成本效益的治疗选择。