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50-85 岁终末期踝关节炎患者行全踝关节置换术与踝关节融合术的疗效比较:TARVA RCT 研究

Total ankle replacement versus ankle arthrodesis for patients aged 50-85 years with end-stage ankle osteoarthritis: the TARVA RCT.

机构信息

Institute of Orthopaedics & Musculoskeletal Science, Division of Surgery, University College London, London, UK.

Comprehensive Clinical Trials Unit, Institute of Clinical Trials and Methodology, University College London, London, UK.

出版信息

Health Technol Assess. 2023 Mar;27(5):1-80. doi: 10.3310/PTYJ1146.

Abstract

BACKGROUND

We aimed to compare the clinical effectiveness, cost-effectiveness and complication rates of total ankle replacement with those of arthrodesis (i.e. ankle fusion) in the treatment of end-stage ankle osteoarthritis.

METHODS

This was a pragmatic, multicentre, parallel-group, non-blinded randomised controlled trial. Patients with end-stage ankle osteoarthritis who were aged 50-85 years and were suitable for both procedures were recruited from 17 UK hospitals and randomised using minimisation. The primary outcome was the change in the Manchester-Oxford Foot Questionnaire walking/standing domain scores between the preoperative baseline and 52 weeks post surgery.

RESULTS

Between March 2015 and January 2019, 303 participants were randomised using a minimisation algorithm: 152 to total ankle replacement and 151 to ankle fusion. At 52 weeks, the mean (standard deviation) Manchester-Oxford Foot Questionnaire walking/standing domain score was 31.4 (30.4) in the total ankle replacement arm ( = 136) and 36.8 (30.6) in the ankle fusion arm ( = 140); the adjusted difference in the change was -5.6 (95% confidence interval -12.5 to 1.4;  = 0.12) in the intention-to-treat analysis. By week 52, one patient in the total ankle replacement arm required revision. Rates of wound-healing issues (13.4% vs. 5.7%) and nerve injuries (4.2% vs. < 1%) were higher and the rate of thromboembolic events was lower (2.9% vs. 4.9%) in the total ankle replacement arm than in the ankle fusion arm. The bone non-union rate (based on plain radiographs) in the ankle fusion arm was 12.1%, but only 7.1% of patients had symptoms. A post hoc analysis of fixed-bearing total ankle replacement showed a statistically significant improvement over ankle fusion in Manchester-Oxford Foot Questionnaire walking/standing domain score (-11.1, 95% confidence interval -19.3 to -2.9;  = 0.008). We estimate a 69% likelihood that total ankle replacement is cost-effective compared with ankle fusion at the National Institute for Health and Care Excellence's cost-effectiveness threshold of £20,000 per quality-adjusted life-year gained over the patient's lifetime.

LIMITATIONS

This initial report contains only 52-week data, which must therefore be interpreted with caution. In addition, the pragmatic nature of the study means that there was heterogeneity between surgical implants and techniques. The trial was run across 17 NHS centres to ensure that decision-making streams reflected the standard of care in the NHS as closely as possible.

CONCLUSIONS

Both total ankle replacement and ankle fusion improved patients' quality of life at 1 year, and both appear to be safe. When total ankle replacement was compared with ankle fusion overall, we were unable to show a statistically significant difference between the two arms in terms of our primary outcome measure. The total ankle replacement versus ankle arthrodesis (TARVA) trial is inconclusive in terms of superiority of total ankle replacement, as the 95% confidence interval for the adjusted treatment effect includes both a difference of zero and the minimal important difference of 12, but it can rule out the superiority of ankle fusion. A post hoc analysis comparing fixed-bearing total ankle replacement with ankle fusion showed a statistically significant improvement of total ankle replacement over ankle fusion in Manchester-Oxford Foot Questionnaire walking/standing domain score. Total ankle replacement appears to be cost-effective compared with ankle fusion at the National Institute for Health and Care Excellence's cost-effectiveness threshold of £20,000 per quality-adjusted life-year gained over a patient's lifetime based on long-term economic modelling.

FUTURE WORK

We recommend long-term follow-up of this important cohort, in particular radiological and clinical progress. We also recommend studies to explore the sensitivity of clinical scores to detect clinically important differences between arms when both have already achieved a significant improvement from baseline.

TRIAL REGISTRATION

This trial is registered as ISRCTN60672307 and ClinicalTrials.gov NCT02128555.

FUNDING

This project was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme and will be published in full in ; Vol. 27, No. 5. See the NIHR Journals Library website for further project information.

摘要

背景

我们旨在比较全踝关节置换术与关节融合术(即踝关节融合)治疗终末期踝关节骨关节炎的临床疗效、成本效益和并发症发生率。

方法

这是一项实用的、多中心、平行组、非盲随机对照试验。从英国 17 家医院招募了年龄在 50-85 岁之间且适合两种手术的终末期踝关节骨关节炎患者,并使用最小化算法进行随机分组。主要结局是术前基线至术后 52 周时曼彻斯特-牛津足部问卷(Manchester-Oxford Foot Questionnaire)行走/站立域评分的变化。

结果

2015 年 3 月至 2019 年 1 月期间,303 名患者使用最小化算法进行随机分组:152 名患者接受全踝关节置换术,151 名患者接受踝关节融合术。在 52 周时,全踝关节置换组的曼彻斯特-牛津足部问卷行走/站立域评分的平均值(标准差)为 31.4(30.4)(n=136),踝关节融合组为 36.8(30.6)(n=140);意向治疗分析中的调整差异为-5.6(95%置信区间-12.5 至 1.4;=0.12)。到第 52 周时,全踝关节置换组中有 1 名患者需要翻修。全踝关节置换组的伤口愈合问题(13.4%比 5.7%)和神经损伤(4.2%比<1%)发生率较高,血栓栓塞事件发生率较低(2.9%比 4.9%)。踝关节融合组的骨不连率(基于平片)为 12.1%,但只有 7.1%的患者有症状。对固定轴承全踝关节置换的事后分析显示,在曼彻斯特-牛津足部问卷行走/站立域评分方面,全踝关节置换术显著优于踝关节融合术(-11.1,95%置信区间-19.3 至-2.9;=0.008)。我们估计,在国家卫生与保健卓越研究所(National Institute for Health and Care Excellence)的成本效益阈值为每获得 1 个质量调整生命年(quality-adjusted life-year)花费 2 万英镑的情况下,全踝关节置换术比踝关节融合术具有 69%的可能性更具成本效益。

局限性

本初始报告仅包含 52 周的数据,因此必须谨慎解释。此外,该实用研究的性质意味着手术植入物和技术之间存在异质性。该试验在 17 家 NHS 中心进行,以确保决策过程尽可能接近 NHS 的标准护理。

结论

全踝关节置换术和踝关节融合术均能在 1 年内改善患者的生活质量,且两种手术似乎均安全。当全踝关节置换术与踝关节融合术整体比较时,我们无法显示主要观察指标的两组之间存在统计学显著差异。TARVA 试验在全踝关节置换术的优越性方面没有定论,因为调整治疗效果的 95%置信区间既包含零差异,也包含 12 的最小重要差异,但可以排除踝关节融合术的优越性。固定轴承全踝关节置换术与踝关节融合术的事后分析显示,在曼彻斯特-牛津足部问卷行走/站立域评分方面,全踝关节置换术显著优于踝关节融合术。基于长期经济建模,全踝关节置换术与踝关节融合术相比,在国家卫生与保健卓越研究所的成本效益阈值(每获得 1 个质量调整生命年花费 2 万英镑)下具有成本效益。

未来工作

我们建议对这一重要队列进行长期随访,特别是影像学和临床进展。我们还建议开展研究,以探索当两支手臂都已从基线显著改善时,临床评分对检测手臂间临床重要差异的敏感性。

试验注册

本试验已在 ISRCTN60672307 和 ClinicalTrials.gov NCT02128555 上注册。

资金

本项目由英国国家卫生与保健研究院(NIHR)卫生技术评估计划资助,将在《Health Technology Assessment》杂志上全文发表;第 27 卷,第 5 期。有关该项目的更多信息,请访问 NIHR 期刊库网站。

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