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用于治疗拇僵硬的聚乙烯醇水凝胶植入物在短期随访中并发症发生率高,失败率中等:系统评价。

Polyvinyl alcohol hydrogel implant for the treatment of hallux rigidus is associated with a high complication rate and moderate failure rate at short-term follow-up: a systematic review.

机构信息

Foot and Ankle Division, Department of Orthopaedic Surgery, NYU Langone Health, 171 Delancey Street, 2nd Floor, New York, NY, 10002, USA.

Royal College of Surgeons in Ireland, Dublin, Ireland.

出版信息

Eur J Orthop Surg Traumatol. 2024 May;34(4):1765-1778. doi: 10.1007/s00590-024-03895-w. Epub 2024 Mar 30.

Abstract

PURPOSE

Moderate-to-severe hallux rigidus is a debilitating pathology that is optimally treated with surgical intervention. Arthrodesis produces reliable clinical outcomes but is limited by restriction in 1st metatarsophalangeal joint range of motion. The advent of polyvinyl alcohol hydrogel (PVA) implants have produced early promise based on initial trials, but more recent studies have called into question the efficacy of this procedure. The purpose of this systematic review was to evaluate the clinical and radiological outcomes following the use of PVA for hallux rigidus.

METHODS

The MEDLINE, EMBASE and Cochrane library databases were systematically reviewed using the preferred reporting items for systematic reviews and meta-analyses guidelines. 18 studies were included.

RESULTS

In total, 1349 patients (1367 feet) underwent PVA at a weighted mean follow-up of 24.1 ± 11.1 months. There were 168 patients (169 feet) included in the cheilectomy cohort and 322 patients (322 feet) included in the arthrodesis cohort. All 3 cohorts produced comparable improvements in subjective clinical outcomes. Postoperative imaging findings in the PVA cohort included joint space narrowing, peri-implant fluid, peri-implant edema and erosion of the proximal phalanx. The complication rate in the PVA cohort, cheilectomy cohort and arthrodesis cohort was 27.9%, 11.8% and 24.1%, respectively. The failure rates in the PVA cohort, cheilectomy cohort and arthrodesis cohort was 14.8%, 0.3% and 9.0%, respectively.

CONCLUSION

This systematic review demonstrated that PVA produced a high complication rate (27.9%) together with concerning postoperative imaging findings at short-term follow-up. In addition, a moderate failure rate (14.8%) and secondary surgical procedure rate (9.5%) was noted for the PVA cohort. The findings of this review calls into question the efficacy and safety of PVA for the treatment of hallux rigidus.

LEVEL OF EVIDENCE

IV.

摘要

目的

中度至重度拇僵硬是一种使人虚弱的病症,通过手术干预是最佳治疗方法。关节融合术可产生可靠的临床效果,但受到第一跖趾关节活动范围受限的限制。聚维酮醇水凝胶(PVA)植入物的出现基于最初的试验有了早期的希望,但最近的研究对该手术的疗效提出了质疑。本系统评价的目的是评估使用 PVA 治疗拇僵硬的临床和影像学结果。

方法

使用系统评价和荟萃分析首选报告项目,对 MEDLINE、EMBASE 和 Cochrane 图书馆数据库进行系统检索。共纳入 18 项研究。

结果

总共 1349 例患者(1367 足)接受了 PVA 治疗,加权平均随访时间为 24.1±11.1 个月。其中,趾切除术组 168 例(169 足),关节融合术组 322 例(322 足)。所有 3 个队列在主观临床结果方面均有相似的改善。PVA 队列的术后影像学发现包括关节间隙变窄、植入物周围积液、植入物周围水肿和近节趾骨侵蚀。PVA 队列、趾切除术组和关节融合术组的并发症发生率分别为 27.9%、11.8%和 24.1%。PVA 队列、趾切除术组和关节融合术组的失败率分别为 14.8%、0.3%和 9.0%。

结论

本系统评价表明,PVA 治疗拇僵硬的并发症发生率高(27.9%),且在短期随访时影像学发现令人担忧。此外,PVA 队列还存在中度失败率(14.8%)和二次手术率(9.5%)。本综述结果对 PVA 治疗拇僵硬的疗效和安全性提出了质疑。

证据水平

IV 级。

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