Sridharan Natalie Domenick, Liang Nathan, Robinson Darve, Avgerinos Efthymios, Tzeng Edith, Makaroun Michel S, Chaer Rabih A, Eslami Mohammad H
Division of Vascular Surgery, Department of Surgery, UPMC, Pittsburgh, Pa.
Division of Vascular Surgery, Department of Surgery, UPMC, Pittsburgh, Pa.
J Vasc Surg. 2018 Nov;68(5):1465-1472. doi: 10.1016/j.jvs.2018.02.040. Epub 2018 May 18.
Initial data on drug-eluting stents (DES) shows that they may increase the durability of endovascular treatment of superficial femoral artery disease compared with traditional bare-metal stents (BMS). Observed decreased target lesion revascularization (TLR) rates have potential for cost savings despite an increased initial cost. The purpose of this study was to run a simulation model of progressive transition from BMS to DES over 5 years evaluating the overall cost impact of that transition.
Florida State Ambulatory Databases were searched for all patients undergoing superficial femoral artery stenting in 2013 using Current Procedural Terminology codes 37226 and 37227. A simulation model was developed to estimate the impact of a progressive transition from BMS to DES over a 5-year horizon in this patient population. Cost estimates were determined from available cost charge ratio data. For the 5-year model, 2013 served as the initial year with each subsequent year based on the expected number of interventions per year. Up to one TLR per patient was assumed for the model. The 5-year TLR rates for DES and other parameter estimates were based on pooled data from the literature. Institutional data were used to estimate that up to 48% of superficial femoral artery lesions would fit the instructions for use for the Zilver PTX (Cook Medical, Bloomington, Ind), which is currently the only DES approved by the U.S. Food and Drug Administration for peripheral interventions. The net budget impact was expressed as the difference in total costs (primary stenting and reinterventions) for a scenario where BMS is progressively replaced by Zilver PTX compared with a scenario of BMS only. Multiple sensitivity analyses were performed on the base scenario.
We identified 4107 peripheral interventions in the first year that fit our study. The overall cost for these procedures in Florida database was $51,362,142.00. In the base case scenario, DES was introduced slowly into the population at a rate of 8% per year up to 48% at the end of the model. This strategy resulted in an overall cost savings of $1,688,953.72 compared with the model with BMS alone. Sensitivity analyses including slower adoption of DES up to only 24% at 5 years, a 20% increase in TLR rates per year for the DES, and a 10% reduction in TLR rates per year for BMS still resulted in a net savings. As long as the additional cost of a DES compared with BMS is less than $677, the DES model remains less expensive.
The adoption of DES in lieu of traditional BMS can lead to significant cost savings in a single state model over a short time horizon.
药物洗脱支架(DES)的初步数据表明,与传统裸金属支架(BMS)相比,它们可能会提高股浅动脉疾病血管内治疗的持久性。尽管初始成本增加,但观察到的靶病变血管重建(TLR)率降低有节省成本的潜力。本研究的目的是建立一个模拟模型,评估5年内从BMS逐步过渡到DES的总体成本影响。
使用当前程序术语代码37226和37227在佛罗里达州门诊数据库中搜索2013年所有接受股浅动脉支架置入术的患者。开发了一个模拟模型,以估计在该患者群体中5年内从BMS逐步过渡到DES的影响。成本估计是根据可用的成本收费比率数据确定的。对于5年模型,2013年作为初始年份,随后每年根据每年预期的干预次数确定。模型假设每位患者最多进行一次TLR。DES的5年TLR率和其他参数估计基于文献中的汇总数据。机构数据用于估计高达48%的股浅动脉病变符合Zilver PTX(库克医疗公司,印第安纳州布卢明顿)的使用说明,Zilver PTX是目前美国食品药品监督管理局批准用于外周干预的唯一DES。净预算影响表示为Zilver PTX逐步取代BMS的情况下与仅使用BMS的情况下总成本(初次支架置入和再次干预)的差异。对基础情景进行了多次敏感性分析。
我们在第一年确定了4107例符合我们研究的外周干预。佛罗里达数据库中这些手术的总成本为51362142.00美元。在基础情景中,DES以每年8%的速度缓慢引入人群,到模型结束时达到48%。与仅使用BMS的模型相比,该策略总体节省成本1688953.72美元。敏感性分析包括DES采用速度较慢,到5年时仅达到24%,DES每年的TLR率增加20%,BMS每年的TLR率降低10%,仍然导致净节省。只要DES与BMS相比的额外成本低于677美元,DES模型的成本仍然较低。
在一个单一州的模型中,在短时间内采用DES代替传统BMS可导致显著的成本节省。