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用于治疗半月板部分缺损的聚氨酯半月板支架:5年随访结果:一项欧洲多中心研究

Polyurethane Meniscal Scaffold for the Treatment of Partial Meniscal Deficiency: 5-Year Follow-up Outcomes: A European Multicentric Study.

作者信息

Toanen Cecile, Dhollander Aad, Bulgheroni Paolo, Filardo Giuseppe, Zaffagnini Stefano, Spalding Tim, Monllau Joan Carles, Gelber Pablo, Verdonk Rene, Beaufils Philippe, Pujol Nicolas, Bulgheroni Erica, Asplin Laura, Verdonk Peter

机构信息

Investigation performed at the Orthopedic Department, Centre Hospitalier de Versailles, Le Chesnay, France.

出版信息

Am J Sports Med. 2020 May;48(6):1347-1355. doi: 10.1177/0363546520913528. Epub 2020 Apr 8.

Abstract

BACKGROUND

A biodegradable polyurethane scaffold was developed to treat patients with the challenging clinical condition of painful partial meniscal defects.

HYPOTHESIS

The use of an acellular polyurethane scaffold in patients with symptomatic partial meniscal defects would result in both midterm pain relief and improved function.

STUDY DESIGN

Case series; Level of evidence, 4.

METHODS

A total of 155 patients with symptomatic partial meniscal defects (101 medial and 54 lateral) were implanted with a polyurethane scaffold in a prospective, single-arm, multicentric study with a minimum 5-year follow-up. Clinical outcomes were measured with the visual analog scale for pain, International Knee Documentation Committee subjective knee evaluation form, Lysholm knee scale, and Knee injury and Osteoarthritis Outcome Score at baseline and at 2- and 5-year follow-ups. Magnetic resonance imaging (MRI) was used to evaluate the knee joint, meniscal implant, and meniscal extrusion. Kaplan-Meier survival analysis was also performed. Removal of the scaffold, conversion to a meniscal transplant, and unicompartmental/total knee arthroplasty were used as endpoints.

RESULTS

Eighteen patients were lost to follow-up (11.6%). The patients who were included in this study showed significant clinical improvement after surgery as indicated by the different outcome measures ( = .01). However, the clinical improvement tended to stabilize between 2 and 5 years of follow-up. MRI scans of the scaffolds in 56 patients showed a smaller-sized implant in the majority of the cases when compared with the native meniscus with an irregular surface at the 5-year follow-up. During the follow-up period, 87.6% of the implants survived in this study. At 5 years of follow-up, 87.9% of the medial scaffolds were still functioning versus 86.9% of the lateral scaffolds. In total, 23 treatments had failed: 10 removed scaffolds because of breakage, 7 conversions to meniscal allograft transplantation, 4 conversions to unicompartmental knee arthroplasty, and 2 conversions to total knee arthroplasty.

CONCLUSION

The polyurethane meniscal implant was able to improve knee joint function and reduce pain in patients with segmental meniscal deficiency over 5 years after implantation. The MRI appearance of this scaffold was different from the original meniscal tissue at the midterm follow-up. The treatment survival rates of 87.9% of the medial scaffolds and 86.9% of the lateral scaffolds in the present study compared favorably with those published concerning meniscal allograft transplantation after total meniscectomy.

摘要

背景

开发了一种可生物降解的聚氨酯支架,用于治疗具有挑战性的疼痛性部分半月板缺损临床病症的患者。

假设

对有症状的部分半月板缺损患者使用无细胞聚氨酯支架将导致中期疼痛缓解和功能改善。

研究设计

病例系列;证据等级,4级。

方法

在一项前瞻性、单臂、多中心研究中,对155例有症状的部分半月板缺损患者(101例内侧和54例外侧)植入聚氨酯支架,进行至少5年的随访。在基线以及2年和5年随访时,使用视觉模拟疼痛量表、国际膝关节文献委员会主观膝关节评估表、Lysholm膝关节评分量表以及膝关节损伤和骨关节炎结局评分来测量临床结果。使用磁共振成像(MRI)评估膝关节、半月板植入物和半月板挤出情况。还进行了Kaplan-Meier生存分析。将支架取出、转换为半月板移植以及单髁/全膝关节置换作为终点指标。

结果

18例患者失访(11.6%)。本研究纳入的患者术后在不同结局指标方面均显示出显著的临床改善(P = 0.01)。然而,临床改善在随访2至5年期间趋于稳定。56例患者的支架MRI扫描显示,与5年随访时表面不规则的天然半月板相比,大多数情况下植入物尺寸较小。在随访期间,本研究中87.6%的植入物存活。在5年随访时,87.9%的内侧支架仍在发挥作用,而外侧支架为86.9%。总共有23例治疗失败:10例因支架断裂而取出,7例转换为半月板同种异体移植,4例转换为单髁膝关节置换,2例转换为全膝关节置换。

结论

聚氨酯半月板植入物能够在植入后5年内改善节段性半月板缺损患者的膝关节功能并减轻疼痛。在中期随访时,该支架的MRI表现与原始半月板组织不同。本研究中内侧支架87.9%和外侧支架86.9%的治疗生存率与全半月板切除术后半月板同种异体移植的相关报道相比具有优势。

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