Combs Joshua C, Dougherty Maura, Yamasaki Meghan U, DeCherney Alan H, Devine Kate M, Hill Micah J, Rothwell Erin, O'Brien Jeanne E, Nelson Richard E
Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland.
Walter Reed National Military Medical Center, Bethesda, Maryland.
F S Rep. 2023 Jun 13;4(3):300-307. doi: 10.1016/j.xfre.2023.06.001. eCollection 2023 Sep.
To evaluate the cost-effectiveness of in vitro fertilization with preimplantation genetic testing for monogenic disease (IVF + PGT-M) in the conception of a nonsickle cell disease (non-SCD) individual compared with standard of care treatment for a naturally conceived, sickle cell disease (SCD)-affected individual.
A Markov simulation model was constructed to evaluate a one-time IVF + PGT-M treatment compared with the lifetime standard of care costs of treatment for an individual potentially born with SCD. Using an annual discount rate of 3% for cost and outcome measures, quality-adjusted life years were constructed from utility weights and life expectancy values and then used as the effectiveness measurement. An incremental cost-effectiveness ratio was calculated for both treatment arms, and a willingness-to-pay threshold of $50,000 per quality-adjusted life year was assumed.
Tertiary care or university medical center.
A hypothetical cohort of 10,000 patients was analzyed over a lifetime horizon using yearly cycles.
In vitro fertilization with preimplantation genetic testing for monogenic disease use in conception of a non-SCD individual.
The primary outcomes of interest were the incremental cost and effectiveness of an IVF+PGT-M conception compared with the SOC treatment of an SCD-affected individual.
In vitro fertilization with preimplantation genetic testing for monogenic disease was the optimal strategy in 93.17% of the iterations. An incremental savings of $137,594 was demonstrated with a gain of 1.96 QALYs and 3.69 life years over a lifetime. Sensitivity analysis demonstrated that SOC treatment never met equivalent cost-effectiveness.
Our model demonstrates that IVF + PGT-M for selection against SCD, compared with lifetime SOC treatment for those affected, is the most cost-effective strategy within the United States healthcare sector.
评估单基因疾病植入前基因检测体外受精(IVF+PGT-M)用于非镰状细胞病(非SCD)个体受孕的成本效益,与自然受孕的镰状细胞病(SCD)患者的标准治疗相比。
构建马尔可夫模拟模型,评估一次性IVF+PGT-M治疗与潜在患SCD个体的终生标准治疗成本。成本和结果测量采用3%的年贴现率,根据效用权重和预期寿命值构建质量调整生命年,然后用作有效性测量。计算两个治疗组的增量成本效益比,并假设每质量调整生命年的支付意愿阈值为50,000美元。
三级医疗或大学医学中心。
使用年度周期对10,000名假设队列患者进行终生分析。
单基因疾病植入前基因检测体外受精用于非SCD个体受孕。
感兴趣的主要结局是IVF+PGT-M受孕与SCD患者标准治疗相比的增量成本和有效性。
单基因疾病植入前基因检测体外受精在93.17%的迭代中是最优策略。在一生中,显示出节省137,594美元,获得1.96个质量调整生命年和3.69个生命年。敏感性分析表明,标准治疗从未达到同等的成本效益。
我们的模型表明,与对SCD患者的终生标准治疗相比,IVF+PGT-M用于筛选SCD是美国医疗保健部门最具成本效益的策略。