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Treating Type 1 Diabetes Mellitus with a Rapid-Acting Analog Insulin Regimen vs. Regular Human Insulin in Germany: A Long-Term Cost-Effectiveness Evaluation

机译:用快速作用的模拟胰岛素方案对德国常规人胰岛素治疗1型糖尿病:长期成本效益评估

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Objective The aim of the present study was to evaluate the cost effectiveness of rapid-acting analog insulin relative to regular human insulin in adults with type 1 diabetes mellitus in Germany. Methods The PRIME Diabetes Model, a patient-level, discrete event simulation model, was used to project long-term clinical and cost outcomes for patients with type 1 diabetes from the perspective of a German healthcare payer. Simulated patients had a mean age of 21.5 years, duration of diabetes of 8.6 years, and baseline glycosylated hemoglobin of 7.39%. Regular human insulin and rapid-acting analog insulin regimens reduced glycosylated hemoglobin by 0.312 and 0.402%, respectively. Compared with human insulin, hypoglycemia rate ratios with rapid-acting analog insulin were 0.51 (non-severe nocturnal) and 0.80 (severe). No differences in non-severe diurnal hypoglycemia were modeled. Discount rates of 3% were applied to future costs and clinical benefits accrued over the 50-year time horizon. Results In the base-case analysis, rapid-acting analog insulin was associated with an improvement in quality-adjusted life expectancy of 1.01 quality-adjusted life-years per patient (12.54 vs. 11.53 quality-adjusted life-years). Rapid-acting analog insulin was also associated with an increase in direct costs of €4490, resulting in an incremental cost-effectiveness ratio of €4427 per quality-adjusted life-year gained vs. human insulin. Sensitivity analyses showed that the base case was driven predominantly by differences in hypoglycemia; abolishing these differences reduced incremental quality-adjusted life expectancy to 0.07 quality-adjusted life-years, yielding an incremental cost-effectiveness ratio of €74,622 per quality-adjusted life-year gained. Conclusions Rapid-acting analog insulin is associated with beneficial outcomes in patients with type 1 diabetes and is likely to be considered cost effective in the German setting vs. regular human insulin.
机译:目的本研究的目的是评估德国1型糖尿病患者常规人胰岛素的快速作用模拟胰岛素的成本效力。方法方法,患者水平,离散事件仿真模型的主要糖尿病模型用于从德国医疗保健付款人的角度来看,为1型糖尿病患者的长期临床和成本结果。模拟患者的平均年龄为21.5岁,糖尿病持续时间为8.6岁,基线糖基化血红蛋白为7.39%。常规人胰岛素和快速作用的模拟胰岛素方案分别将糖基化血红蛋白减少0.312和0.402%。与人胰岛素相比,具有快速作用模拟胰岛素的低血糖率比为0.51(非严重夜间)和0.80(严重)。没有模拟非严重昼夜低血糖的差异。 3%的折扣率适用于50年来的未来成本和临床福利,而在50年的时间范围内累计。结果在基本情况下,快速作用模拟胰岛素与质量调整后寿命的提高有关1.01质量调整后的每位患者的寿命(12.54与11.53质量调整的寿命)。快速作用的模拟胰岛素也与直接成本的增加有关,导致每个质量调整的生命年龄与人类胰岛素的增量成本效益比为4427欧元。敏感性分析表明,基本情况主要受到低血糖症的差异的推动;废除这些差异将增量质量调整后的寿命降低至0.07质量调整的寿命,从而增加每个质量调整的救生年度的增量成本效益为74,622欧元。结论快速作用模拟胰岛素与1型糖尿病患者的有益结果有关,并且可能被认为是德国环境与常规人胰岛素的成本效益。

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