Saint Luke's Mid America Heart Institute, University of Missouri-Kansas City (S.J.B., K.W., E.A.M., D.J.C.).
Premier Research Services Inc, Charlotte, NC (J.A.H.).
Circulation. 2019 Feb 12;139(7):877-888. doi: 10.1161/CIRCULATIONAHA.118.035236.
BACKGROUND: In patients with severe aortic stenosis (AS) at intermediate surgical risk, treatment with transcatheter aortic valve replacement (TAVR) or surgical aortic valve replacement (SAVR) results in similar rates of death or stroke at 2 years. Whether TAVR is cost-effective compared with SAVR for intermediate-risk patients remains uncertain. METHODS: Between 2011 and 2014, 3110 intermediate-risk AS patients were treated with TAVR or SAVR in the PARTNER 2 trial (Placement of Aortic Transcatheter Valves 2). A total of 2032 patients were randomized to receive TAVR using the SAPIEN XT valve (XT-TAVR) or SAVR in the PARTNER 2A trial, whereas the PARTNER S3i registry included an additional 1078 patients treated with TAVR using the SAPIEN 3 valve (S3-TAVR), which offers a lower delivery profile and sealing skirt designed to reduce paravalvular regurgitation compared with XT-TAVR. Procedural costs were estimated using measured resource utilization. Other in-trial costs were assessed by linkage of trial data with Medicare claims (n=2333) or by linear regression models for unlinked patients (n=682). Health utilities were estimated using the EQ-5D at baseline and 1, 12, and 24 months. Using a Markov model informed by in-trial costs, utilities, and survival data, lifetime cost-effectiveness from the perspective of the US healthcare system was estimated in terms of cost per quality-adjusted life-year gained. RESULTS: Although procedural costs were ≈$20 000 higher with TAVR than SAVR, total cost differences for the index hospitalization were only $2888 higher with XT-TAVR ( P=0.014) and were $4155 lower with S3-TAVR ( P<0.001) owing to reductions in length of stay with TAVR. Follow-up costs were significantly lower with XT-TAVR (Δ=-$9304; P<0.001) and S3-TAVR (Δ=-$11 377; P<0.001) than with SAVR. Over a lifetime horizon, TAVR was projected to lower total costs by $8000 to $10 000 and to increase quality-adjusted survival by 0.15 to 0.27 years. XT-TAVR and S3-TAVR were found to be economically dominant compared with SAVR in 84% and 97% of bootstrap replicates, respectively. CONCLUSIONS: Among intermediate-risk AS patients, TAVR is projected to be economically dominant from the perspective of the US healthcare system by providing both greater quality-adjusted life expectancy and lower long-term costs than SAVR. If long-term data demonstrate comparable late mortality with TAVR and SAVR, these findings suggest that TAVR might be the preferred treatment strategy for intermediate-risk AS patients based on both clinical and economic considerations. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov . Unique identifier: NCT01314313.
背景:在中危外科手术风险的严重主动脉瓣狭窄(AS)患者中,经导管主动脉瓣置换术(TAVR)或外科主动脉瓣置换术(SAVR)的治疗在 2 年内导致死亡或中风的发生率相似。对于中危患者,TAVR 是否比 SAVR 更具成本效益仍不确定。
方法:在 2011 年至 2014 年期间,PARTNER 2 试验(主动脉瓣经导管置换 2 期)中共有 3110 名中危 AS 患者接受了 TAVR 或 SAVR 治疗。共有 2032 名患者被随机分配接受 SAPIEN XT 瓣膜(XT-TAVR)的 TAVR 或 PARTNER 2A 试验中的 SAVR,而 PARTNER S3i 注册研究则包括另外 1078 名接受 SAPIEN 3 瓣膜(S3-TAVR)治疗的患者,该瓣膜提供了较低的输送轮廓和密封裙,旨在减少与 XT-TAVR 相比瓣周漏。使用测量的资源利用来估计程序成本。通过将试验数据与医疗保险索赔(n=2333)相关联,或通过未相关患者的线性回归模型(n=682)评估其他试验内成本。使用 EQ-5D 在基线、1、12 和 24 个月时估计健康效用。使用基于试验内成本、效用和生存数据的马尔可夫模型,从美国医疗保健系统的角度估计了 TAVR 在获得质量调整生命年方面的终生成本效益。
结果:尽管 TAVR 的程序成本比 SAVR 高约 20000 美元,但 XT-TAVR 的指数住院费用仅高出 2888 美元(P=0.014),S3-TAVR 的指数住院费用则低 4155 美元(P<0.001),这是由于 TAVR 的住院时间缩短所致。XT-TAVR(Δ=-9304 美元;P<0.001)和 S3-TAVR(Δ=-11377 美元;P<0.001)的随访成本明显低于 SAVR。在终生范围内,TAVR 预计将降低总成本 8000 至 10000 美元,并增加 0.15 至 0.27 年的质量调整生存。XT-TAVR 和 S3-TAVR 在 84%和 97%的 bootstrap 重复中分别被发现比 SAVR 更具经济性优势。
结论:在中危 AS 患者中,TAVR 预计将从美国医疗保健系统的角度具有经济性优势,因为它提供了更长的质量调整预期寿命和更低的长期成本,优于 SAVR。如果长期数据显示 TAVR 和 SAVR 的晚期死亡率相当,那么这些发现表明,基于临床和经济考虑,TAVR 可能是中危 AS 患者的首选治疗策略。
临床试验注册:网址:https://www.clinicaltrials.gov 。独特标识符:NCT01314313。
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