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自体骨软骨移植与异体骨软骨移植治疗复发性或大型距骨骨软骨损伤的比较

Comparison of Osteochondral Autografts and Allografts for Treatment of Recurrent or Large Talar Osteochondral Lesions.

作者信息

Ahmad Jamal, Jones Kennis

机构信息

Orthopaedic Surgery, Rothman Institute Orthopaedics at Thomas Jefferson University Hospital, Philadelphia, PA, USA

Rothman Institute Orthopaedics at Thomas Jefferson University Hospital, Philadelphia, PA, USA.

出版信息

Foot Ankle Int. 2016 Jan;37(1):40-50. doi: 10.1177/1071100715603191. Epub 2015 Sep 2.

Abstract

BACKGROUND

The purpose of this study was to prospectively evaluate and compare the long-term clinical and radiographic outcomes of using osteochondral autograft and allograft to manage either recurrent or large osteochondral lesions of the talar dome (OLT) in a single surgeon's practice.

METHODS

Between January 2008 and January 2014, a total of 40 patients presented with either a recurrent OLT that failed initial arthroscopic treatment (ie, excision, curettage, debridement, and micro-fracture) or a primary OLT greater than 1.5 cm2 that had undergone no prior surgery. Before surgery, 20 patients were randomized to receive osteochondral autograft plugs (Arthrex, Naples, FL) from the ipsilateral superolateral distal femoral condyle whereas the remaining 20 were randomized to receive osteochondral allograft plugs from a fresh size-matched donor talus (Joint Restoration Foundation, Centennial, CO, and Arthrex, Naples, FL), but 4 of these were excluded that received a hemi-talus allograft with internal fixation. Preoperative and postoperative function and pain was graded using the Foot and Ankle Ability Measures (FAAM) scoring system and a Visual Analog Scale (VAS) of pain, respectively. Radiographs were assessed for osteochondral graft healing, joint congruency, and degenerative changes. Data regarding postoperative complications and revision surgeries were also recorded.

RESULTS

Of the 20 patients who received osteochondral autograft, the mean FAAM score increased from 54.4 preoperatively to 85.5 at the time of final follow-up. The mean VAS pain score decreased from 7.9 of 10 preoperatively to 2.2 of 10 at final follow-up. Two patients (10%) that received osteochondral autograft, 1 for a recurrent OLT of 1.3 cm2 and 1 for a primary OLT of 2.0 cm2, developed a symptomatic nonunion at the entire graft site. Both of these patients had their autograft converted to talar allograft plugs and achieved full osteochondral healing. At the time of final follow-up, no patients who received osteochondral autograft developed ankle degenerative changes or knee complications. The mean FAAM score of the 16 patients who received osteochondral allograft plugs increased from 55.2 preoperatively to 80.7 at the time of final follow-up. This postoperative score was lower than that of the osteochondral autograft group, but not to a statistically significant degree (P = .25). The mean VAS pain score decreased from 7.8 of 10 preoperatively to 2.7 of 10 at final follow-up. This postoperative score was higher than that of the osteochondral autograft group but not to a statistically significant degree (P = .15). Three patients (18.8%) that received osteochondral talar allograft, 2 for recurrent OLTs less than 1.5 cm2 and 1 for a primary OLT of 2.2 cm2, developed a symptomatic nonunion at the entire graft site. Two of these 3 patients had their allograft converted to osteochondral autograft plugs harvested from the ipsilateral superolateral distal femoral condyle and achieved full osteochondral healing. At the time of final follow-up, 1 of these 16 (6.3%) patients who received talar allograft as OLT treatment had developed asymptomatic anterior ankle arthritis upon radiographs.

CONCLUSION

Using fresh talar osteochondral allograft provided results that were comparable to the use of distal femoral osteochondral autograft for treating recurrent or large OLTs. Although the use of allograft avoided the risk of knee complications when harvesting autograft from the distal femur, fresh talar allograft may have lower healing rates than osteochondral autograft.

LEVEL OF EVIDENCE

Level II, comparative case series.

摘要

背景

本研究的目的是前瞻性评估并比较在单一外科医生的实践中,使用自体骨软骨移植和异体骨软骨移植治疗距骨穹窿部复发性或大型骨软骨损伤(OLT)的长期临床和影像学结果。

方法

在2008年1月至2014年1月期间,共有40例患者,其中一些患者患有复发性OLT,初始关节镜治疗(即切除、刮除、清创和微骨折)失败,另一些患者患有面积大于1.5 cm²的原发性OLT且此前未接受过手术。手术前,20例患者被随机分配接受来自同侧股骨外侧髁远端的自体骨软骨移植栓(Arthrex,那不勒斯,佛罗里达州),而其余20例被随机分配接受来自新鲜大小匹配的供体距骨的异体骨软骨移植栓(关节修复基金会,百年纪念,科罗拉多州,以及Arthrex,那不勒斯,佛罗里达州),但其中4例接受半距骨异体移植并内固定的患者被排除。术前和术后功能及疼痛分别使用足踝能力测量(FAAM)评分系统和视觉模拟疼痛量表(VAS)进行分级。对X线片进行评估,以观察骨软骨移植愈合情况、关节一致性和退变改变。还记录了术后并发症和翻修手术的数据。

结果

在接受自体骨软骨移植的20例患者中,FAAM平均评分从术前的54.4分增加到最后随访时的85.5分。VAS疼痛平均评分从术前的10分中的7.9分降至最后随访时的10分中的2.2分。2例(10%)接受自体骨软骨移植的患者,1例为1.3 cm²的复发性OLT,1例为2.0 cm²的原发性OLT,在整个移植部位出现了有症状的骨不连。这2例患者均将其自体移植转换为距骨异体移植栓,并实现了完全的骨软骨愈合。在最后随访时,接受自体骨软骨移植的患者中没有出现踝关节退变改变或膝关节并发症。接受异体骨软骨移植栓的16例患者的FAAM平均评分从术前的55.2分增加到最后随访时的80.7分。这个术后评分低于自体骨软骨移植组,但差异无统计学意义(P = 0.25)。VAS疼痛平均评分从术前的10分中的7.8分降至最后随访时的10分中的2.7分。这个术后评分高于自体骨软骨移植组,但差异无统计学意义(P = 0.15)。3例(18.8%)接受距骨异体骨软骨移植的患者,2例为面积小于1.5 cm²的复发性OLT,1例为2.2 cm²的原发性OLT,在整个移植部位出现了有症状的骨不连。这3例患者中的2例将其异体移植转换为从同侧股骨外侧髁远端采集的自体骨软骨移植栓,并实现了完全的骨软骨愈合。在最后随访时,这16例接受距骨异体移植作为OLT治疗的患者中有1例(6.3%)在X线片上出现了无症状的前踝关节关节炎。

结论

使用新鲜距骨骨软骨异体移植的结果与使用股骨远端骨软骨自体移植治疗复发性或大型OLT的结果相当。虽然使用异体移植避免了从股骨远端采集自体移植时出现膝关节并发症的风险,但新鲜距骨异体移植的愈合率可能低于骨软骨自体移植。

证据水平

II级,比较病例系列。

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