Bone Joint J. 2024 Jun 1;106-B(6):589-595. doi: 10.1302/0301-620X.106B6.BJJ-2023-0783.R2.
The aim of this study was to evaluate the healthcare costs and benefits of enoxaparin compared to aspirin in the prevention of symptomatic venous thromboembolism (VTE) after total hip arthroplasty (THA) or total knee arthroplasty (TKA) using data from the CRISTAL trial.
This trial-based economic analysis reports value for money as incremental cost per quality-adjusted life-year (QALY) gained in 2022 Australian dollars, compared to a single threshold value of AUD$70,000 per QALY. Event costs were estimated based on occurrence of VTEs and bleeds, and on published guidelines for treatment. Unit costs were taken from Australian sources. QALYs were estimated using CRISTAL six-month follow-up data. Sensitivity analyses are presented that vary the cost of VTE treatment, and extend the analyses to two years.
The CRISTAL trial found that enoxaparin was more effective than aspirin in preventing symptomatic VTE within 90 days of THA or TKA (risk difference 1.97% (95% confidence interval (CI) 0.54% to 3.41%; p = 0.007)). The additional cost after a THA or TKA was AUD$83 (95% CI 68 to 97) for enoxaparin, and enoxaparin resulted in an additional 0.002 QALYs (95% CI -0.002 to 0.005). Incremental cost per QALY gained was AUD$50,567 (95% CI 15,513, dominated) for enoxaparin. We can be 60% confident that the incremental cost per QALY does not exceed the willingness-to-pay threshold of AUD$70,000. Increasing the cost of VTE treatment and extension of costs and consequences to two years suggested greater confidence that enoxaparin is good value for money (70% and 63% confidence, respectively).
This analysis provides strong evidence that enoxaparin thromboprophylaxis following THA or TKA reduced VTEs, but weak evidence of net economic benefits over aspirin. If the value of avoiding VTEs is high, and there is a strong likelihood of VTE-related health impairments, we can be more confident that enoxaparin is cost-effective compared to aspirin.
本研究旨在利用 CRISTAL 试验的数据,评估依诺肝素相对于阿司匹林在预防全髋关节置换术(THA)或全膝关节置换术(TKA)后症状性静脉血栓栓塞症(VTE)方面的医疗成本和效益。
本基于试验的经济学分析报告了 2022 年以澳元计的每增加一个质量调整生命年(QALY)的增量成本,与每 QALY 70000 澳元的单一阈值进行了比较。根据 VTE 和出血的发生情况以及治疗的已发表指南,估算了事件成本。单位成本取自澳大利亚的资料。使用 CRISTAL 六个月随访数据估算 QALYs。还进行了敏感性分析,改变了 VTE 治疗的成本,并将分析扩展到两年。
CRISTAL 试验发现,与阿司匹林相比,依诺肝素在 THA 或 TKA 后 90 天内预防症状性 VTE 更为有效(风险差异 1.97%(95%置信区间(CI)0.54%至 3.41%;p=0.007))。THA 或 TKA 后使用依诺肝素的额外成本为 83 澳元(95%CI 68 至 97),依诺肝素可增加 0.002 QALY(95%CI-0.002 至 0.005)。依诺肝素每增加一个 QALY 的增量成本为 50567 澳元(95%CI 15513,占主导地位)。我们有 60%的信心认为,依诺肝素每增加一个 QALY 的增量成本不超过 70000 澳元的支付意愿阈值。增加 VTE 治疗的成本,并将成本和后果延长至两年,表明依诺肝素更具性价比的可能性更大(分别为 70%和 63%的置信区间)。
本分析提供了强有力的证据表明,THA 或 TKA 后依诺肝素预防性抗血栓治疗可降低 VTE,但阿司匹林在经济上的净效益证据较弱。如果避免 VTE 的价值较高,且 VTE 相关健康损害的可能性较大,我们可以更有信心认为依诺肝素相对于阿司匹林更具成本效益。