The Royal Orthopaedic Hospital, Birmingham, UK.
The Robert Jones and Agnes Hunt, Oswestry, UK.
J Med Econ. 2023 Jan-Dec;26(1):537-546. doi: 10.1080/13696998.2023.2194805.
For patients with cartilage defects of the knee, a new biocompatible and cross-linkable albumin-hyaluronan-based hydrogel has been developed for matrix-associated autologous chondrocyte implantation (M-ACI) - NOVOCART Inject plus (Ninject; TETEC AG, Reutlingen, Germany). We aimed to estimate the potential cost-effectiveness of NInject, that is not available on the market, yet compared to spheroids of human autologous matrix-associated chondrocytes (Spherox; CO.DON GmbH, Leipzig, Germany) and microfracture.
An early Markov model was developed to estimate the cost-effectiveness in the United Kingdom (UK) from the payer perspective. Transition probabilities, response rates, utility values and costs were derived from literature. Since NInject has not yet been launched and no prices are available, its costs were assumed equal to those of Spherox. Cycle length was set at one year and the time horizon chosen was notional patients' remaining lifetime. Model robustness was evaluated with deterministic and probabilistic sensitivity analyses (DSA; PSA) and value of information analysis (VOIA). The Markov model was built using TreeAge Pro Healthcare.
NInject was cost-effective compared to microfracture (ICER: ₤5,147) while Spherox was extendedly dominated. In sensitivity analyses, the ICER exceeded conventional WTP threshold of ₤20,000 only when the utility value after successful first treatment with NInject was decreased by 20% (ICER: ₤69,620). PSA corroborated the cost-effectiveness findings of NInject, compared to both alternatives, with probabilities of 60% of NInject undercutting the aforementioned WTP threshold and being the most cost-effective alternative. The VOIA revealed that obtaining additional evidence on the new technology will likely not be cost-effective for the UK National Health Service.
This early Markov model showed that NInject is cost-effective for the treatment of articular cartilage defects in the knee, compared to Spherox and microfracture. However, as the final price of NInject has yet to be determined, the cost-effectiveness analysis performed in this study is provisional, assuming equal prices for NInject and Spherox.
对于膝关节软骨缺损的患者,我们开发了一种新型的生物相容性和可交联的白蛋白-透明质酸水凝胶,用于基质相关的自体软骨细胞植入(M-ACI)-NOVOCART Inject plus(Ninject;TETEC AG,德国雷廷根)。我们旨在评估尚未在市场上推出的 NOVOCART Inject plus(Ninject)的潜在成本效益,将其与同种异体基质相关软骨细胞的球体(Spherox;CO.DON GmbH,德国莱比锡)和微骨折进行比较。
从支付者的角度出发,我们开发了一种早期的 Markov 模型来估计英国(UK)的成本效益。转移概率、反应率、效用值和成本均来自文献。由于 NOVOCART Inject plus(Ninject)尚未推出,且尚无价格信息,因此假设其成本与 Spherox 相同。周期长度设定为一年,选择的时间范围为患者的剩余预期寿命。使用 TreeAge Pro Healthcare 构建 Markov 模型。
与微骨折相比,NOVOCART Inject plus(Ninject)具有成本效益(ICER:₤5,147),而 Spherox 则被广泛超越。在敏感性分析中,只有当成功进行首次 NOVOCART Inject plus(Ninject)治疗后的效用值降低 20%时(ICER:₤69,620),ICER 才超过传统的意愿支付阈值₤20,000。PSA 证实了与替代方案相比,NOVOCART Inject plus(Ninject)的成本效益,NOVOCART Inject plus(Ninject)的概率为 60%,低于上述意愿支付阈值,是最具成本效益的替代方案。VOIA 表明,对于英国国家医疗服务体系(NHS)来说,获得有关新技术的额外证据可能不会具有成本效益。
本早期 Markov 模型表明,与 Spherox 和微骨折相比,NOVOCART Inject plus(Ninject)治疗膝关节关节软骨缺损具有成本效益。然而,由于尚未确定 NOVOCART Inject plus(Ninject)的最终价格,因此本研究中的成本效益分析是暂定的,假设 NOVOCART Inject plus(Ninject)和 Spherox 的价格相同。