聚氨酯半月板支架植入治疗部分半月板缺陷的长期临床和MRI结果:至少10年的随访研究。

Vasileios S Akrivos, George A Komnos, Bela Ujvari, Artemis Hante, Eleftheria Adaktylidou, Theofilos Karachalios, Michael Hantes
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引用次数: 0

摘要

目的:对半月板部分切除术后慢性节段性半月板缺损植入聚氨酯支架进行长期随访,评估其临床和磁共振成像(MRI)结果。研究设计:IV级,回顾性病例系列。方法:32例膝关节因半月板缺陷接受关节镜植入Actifit®聚氨酯半月板植入物。临床结果采用患者报告的结果评分进行评估,包括膝关节损伤和骨关节炎结果评分(oos)、Lysholm、Tegner活动量表和疼痛和满意度视觉模拟量表(VAS)。术前MRI扫描、最后随访x线片和MRI评估评估支架形态、组织整合和关节软骨状态。结果:平均随访11.4年。临床结果有显著改善,kos从术前平均47.75(标准差[SD]: 16.88)改善到78.62 (SD: 15.45), Lysholm评分从46.62 (SD: 16.96)改善到84.62 (SD: 13.03), Tegner活动量表从1.8改善到4.1。疼痛VAS评分从术前平均5.62 (SD: 2.54)降至2.12 (SD: 2.02)。使用Genovese分类的MRI评估显示,23个膝关节为II型支架,0个膝关节为III型支架,9个膝关节为I型支架。27个膝关节未出现骨水肿,5个膝关节表现为I型骨水肿。24例膝关节部分挤压,8例膝关节完全挤压。对侧半月板28例正常,2例为Reicher 1级。kelgren - lawrence分类显示15个膝关节有I型骨关节炎改变,10个有II型骨关节炎改变,7个有III型骨关节炎改变。结论:关节镜下使用聚氨酯半月板植入物治疗慢性节段性半月板缺失患者在减轻疼痛和膝关节功能方面可以获得可持续的长期效果。然而,MRI并未显示所有病例的半月板正常。证据等级:四级。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term clinical and MRI outcomes of a polyurethane meniscal scaffold implantation for the treatment of partial meniscal deficiency: A minimum 10-year follow-up study.

Purpose: To assess the clinical and magnetic resonance imaging (MRI) results after implantation of a polyurethane scaffold for chronic segmental meniscus deficiency following partial meniscectomy in a long-term follow-up.

Study design: Level IV, retrospective case series.

Methods: Thirty-two knees received arthroscopic implantation of an Actifit® polyurethane meniscal implant for deficiency of the meniscus. Clinical outcomes were assessed using patient-reported outcome scores, including Knee injury and Osteoarthritis Outcome Score (KOOS), Lysholm, Tegner Activity Scale and visual analogue scale (VAS) for pain and satisfaction. Preoperative MRI scans and final follow-up radiographs and MRI evaluations were performed to assess scaffold morphology, tissue integration and the status of the articular cartilage.

Results: The mean follow-up was 11.4 years. Significant improvements were observed in clinical outcomes, with KOOS improving from a preoperative mean of 47.75 (standard deviation [SD]: 16.88) to a 78.62 (SD: 15.45), Lysholm scores from 46.62 (SD: 16.96) to 84.62 (SD: 13.03), Tegner Activity Scale improving from 1.8 to 4.1 at the final follow-up. The VAS for pain decreased from a preoperative mean of 5.62 (SD: 2.54) to 2.12 (SD: 2.02). MRI evaluations using the Genovese classification showed 23 knees with Type II scaffolds, 0 with Type III and 9 with Type I. Bone oedema was not present in 27 knees, with 5 knees showing Type I bone oedema. Meniscal extrusion was observed in 24 knees with partial extrusion and 8 knees with complete extrusion. The contralateral meniscus was normal in 28 knees and graded as Reicher Grade 1 in 2 knees. The Kellgren-Lawrence classification revealed 15 knees with Type I osteoarthritic changes, 10 with Type II changes and 7 with Type III changes.

Conclusion: Arthroscopic treatment for patients with chronic segmental meniscal loss using a polyurethane meniscal implant can achieve sustainable long-term results regarding pain reduction and knee function. However, the MRI did not reveal normal menisci in all cases.

Level of evidence: Level IV.

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