Suppr超能文献

孤立性非畸形终末期踝关节关节炎行全踝关节置换术、关节镜下踝关节融合术和开放式踝关节融合术的疗效比较。

Outcomes of Total Ankle Replacement, Arthroscopic Ankle Arthrodesis, and Open Ankle Arthrodesis for Isolated Non-Deformed End-Stage Ankle Arthritis.

机构信息

Division of Distal Extremities, Department of Orthopaedics, University of British Columbia, Vancouver, British Columbia, Canada.

Footbridge Centre for Integrated Orthopaedic Care, Vancouver, British Columbia, Canada.

出版信息

J Bone Joint Surg Am. 2019 Sep 4;101(17):1523-1529. doi: 10.2106/JBJS.18.01012.

Abstract

BACKGROUND

End-stage ankle arthritis is a disabling condition that has a similar effect on morbidity, pain, and loss of function to hip arthritis. We compared clinical outcomes of total ankle replacement (TAR) involving the HINTEGRA prosthesis (Integra LifeSciences), arthroscopic ankle arthrodesis (AAA), and open ankle arthrodesis (OAA) in patients with isolated, non-deformed end-stage ankle arthritis.

METHODS

Patients ≥18 years old who underwent TAR, AAA, or OAA from 2002 to 2012 with a minimum follow-up of 2 years were retrospectively identified from the Canadian Orthopaedic Foot and Ankle Society (COFAS) Prospective Ankle Reconstruction Database. All patients had symptomatic COFAS Type-1 end-stage ankle arthritis without intra-articular or extra-articular deformity or surrounding joint arthritis. Clinical outcomes included the Ankle Osteoarthritis Scale (AOS) and Short Form-36 (SF-36). Revision was defined as removal of 1 or both metal ankle prosthesis components for TAR and as reoperation for malposition, malunion, or nonunion for AAA and OAA.

RESULTS

Analysis included 238 ankles (88 TAR, 50 AAA, and 100 OAA) in 229 patients with a mean follow-up of 43.3 ± 18.5 months. The TAR group had more female patients (55%; p = 0.0318) and a higher mean age (p = 0.0005). Preoperative AOS pain, disability, and total scores were similar for all groups. SF-36 physical and mental component summary scores were similar across groups, both preoperatively and postoperatively. Improvement in AOS total score was significantly larger for TAR (34.4 ± 22.6) and AAA (38.3 ± 23.6) compared with OAA (25.8 ± 25.5; p = 0.005). Improvement in AOS disability score was also significantly larger for TAR (36.7 ± 24.3) and AAA (40.5 ± 26.4) compared with OAA (26.0 ± 26.2; p = 0.0013). However, the greater improvements did not meet the minimal clinically important difference. The TAR group underwent more reoperations than AAA and OAA groups (p < 0.0001). Revision rates were similar for all 3 groups (p = 0.262).

CONCLUSIONS

AAA and OAA resulted in comparable clinical outcomes to TAR in patients with non-deformed, COFAS Type-1 end-stage ankle arthritis. The rate of component revision in patients who underwent TAR was similar to the rate of revision for patients who underwent AAA or OAA; however, TAR patients underwent a greater number of additional procedures. Overall, AAA and TAR involving the HINTEGRA prosthesis were not significantly different surgical options in terms of short-term outcomes; patients should be counseled regarding higher reoperation rates for TAR.

LEVEL OF EVIDENCE

Therapeutic Level III. See Instructions for Authors for a complete description of levels of evidence.

摘要

背景

终末期踝关节关节炎是一种致残性疾病,其在发病率、疼痛和功能丧失方面与髋关节关节炎相似。我们比较了涉及 HINTEGRA 假体(英特格拉生命科学公司)的全踝关节置换术(TAR)、关节镜下踝关节融合术(AAA)和开放式踝关节融合术(OAA)在患有孤立性、非畸形终末期踝关节关节炎患者中的临床结果。

方法

从加拿大矫形足踝学会(COFAS)前瞻性踝关节重建数据库中回顾性确定了 2002 年至 2012 年间接受 TAR、AAA 或 OAA 治疗且随访时间至少 2 年的≥18 岁患者。所有患者均有症状性 COFAS 1 型终末期踝关节关节炎,无关节内或关节外畸形或周围关节关节炎。临床结果包括踝关节骨关节炎量表(AOS)和简短形式 36 项健康调查(SF-36)。翻修为 TAR 去除 1 个或 2 个金属踝关节假体组件,AAA 和 OAA 为位置不正、愈合不良或不愈合的再手术。

结果

分析纳入了 229 名患者的 238 个踝关节(88 个 TAR、50 个 AAA 和 100 个 OAA),平均随访 43.3±18.5 个月。TAR 组女性患者比例更高(55%;p=0.0318),平均年龄更高(p=0.0005)。所有组的术前 AOS 疼痛、残疾和总分相似。SF-36 生理和心理成分综合评分在各组中均相似,术前和术后均相似。TAR(34.4±22.6)和 AAA(38.3±23.6)的 AOS 总分改善明显大于 OAA(25.8±25.5;p=0.005)。TAR(36.7±24.3)和 AAA(40.5±26.4)的 AOS 残疾评分改善也明显大于 OAA(26.0±26.2;p=0.0013)。然而,更大的改善并没有达到最小临床重要差异。TAR 组的再手术率高于 AAA 和 OAA 组(p<0.0001)。三组的翻修率相似(p=0.262)。

结论

在非畸形 COFAS 1 型终末期踝关节关节炎患者中,AAA 和 OAA 与 TAR 相比具有相似的临床结果。接受 TAR 治疗的患者的假体翻修率与接受 AAA 或 OAA 治疗的患者相似;然而,TAR 患者接受了更多的附加手术。总体而言,在短期结果方面,TAR 涉及的 HINTEGRA 假体与 AAA 没有明显的差异;应告知患者 TAR 较高的再手术率。

证据水平

治疗性 III 级。有关证据水平的完整说明,请参见作者指南。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验