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胫骨近端大假体植入治疗创伤后感染性骨缺损后髌腱的重建。

Reconstruction of patellar tendon following implantation of proximal tibia megaprosthesis for the treatment of post-traumatic septic bone defects.

作者信息

Calori Giorgio M, Mazza Emilio Luigi, Vaienti Luca, Mazzola Simone, Colombo Alessandra, Gala Luca, Colombo Massimiliano

机构信息

Reparative Orthopaedic Surgery Department - ASST Pini-CTO, University of Milan, Italy.

Department of Plastic and Reconstructive Surgery, I.R.C.C.S. Policlinico San Donato, University of Milan, Italy.

出版信息

Injury. 2016 Dec;47 Suppl 6:S77-S82. doi: 10.1016/S0020-1383(16)30843-9.

Abstract

INTRODUCTION

Latest advances made in joint replacement implants allows reconstruction of entire limbs. These special prostheses or megaprostheses were originally designed for the treatment of severe oncological bone loss. Nowadays, however, the indications and applications of these devices are expanding to other orthopaedic and trauma clinical conditions. Since 2008 we have implanted 152 megaprostheses in non-oncological conditions: 87 were implanted for post-traumatic failures aseptic/septic (represented by complex non-unions and critical size bone defects); 26 total femur, 52 distal femur and 9 proximal tibia. In this group of patients bone and soft tissues conditions are completely different compared to patients with oncological back ground. The presence of infection and previous surgeries can lead to adhesion, scar interference, muscular and tendon impairment and skin problems that lead to reduced function and severe joint stiffness. The purpose of this study is to evaluate the results of treatment of reconstruction of patellar tendon during implantation of proximal tibia megaprosthesis for the treatment of septic post traumatic critical bone defects.

PATIENTS AND METHODS

In this retrospective study, we evaluated 9 patients treated with proximal tibia megaprosthesis who underwent patellar tendon reconstruction. All patients presented a complete patellar tendon disruption at the time of prosthesis implantation. Procedures of reconstruction included a tendon-plasty of quadriceps and/or patellar tendons, a pie crusting of quadriceps fascia, a reinforcement of the apparatus with synthetic tendon graft substitutes (LARS) and a medial gastrocnemius muscular flap to reconstruct the extensor mechanism and obtain skin coverage when needed. The average follow up was 18 months (9-36). For each of the cases, we analysed the complications occurred regarding septic recurrence, patellar fracture, quadriceps and patellar tendon rupture and number of reinterventions. The clinical outcome was assessed by the WOMAC Score.

RESULTS

In all cases there was no infection recurrence or skin related problems. None of the patients require prosthesis revision due to loosening or device failure. No patellar fracture or quadriceps tendon failure was recorded. One patient presented a rupture of the reconstructed patellar tendon due to a trauma incident 18 months after the implantation and he required revision surgery. From a clinical point of view the average WOMAC score was 62.4 at 1 month rising to 72.6 at 3 months, 78.2 at 6 months, 76.4 at 1 year and 74.8 at 18 months.

CONCLUSION

When proximal tibia megaprosthesis is implanted and there are soft tissue and patellar tendon deficiency, soft tissue reconstruction can be achieved by appropriate lengthening of the tendon and a gastrocnemius flap reinforced by LARS. Such an approach allows restoration of the extensor mechanism and coverage of the prosthesis in an area where skin problems are frequently very common.

摘要

引言

关节置换植入物的最新进展使得全肢体重建成为可能。这些特殊的假体或大型假体最初是为治疗严重的肿瘤性骨缺损而设计的。然而如今,这些装置的适应证和应用正在扩展到其他骨科和创伤临床情况。自2008年以来,我们已在非肿瘤性情况下植入了152个大型假体:87个用于创伤后无菌/感染性失败(以复杂骨不连和临界尺寸骨缺损为代表);26个用于全股骨,52个用于股骨远端,9个用于胫骨近端。在这组患者中,其骨骼和软组织状况与有肿瘤背景的患者完全不同。感染的存在和既往手术可能导致粘连、瘢痕干扰、肌肉和肌腱损伤以及皮肤问题,进而导致功能减退和严重的关节僵硬。本研究的目的是评估在植入胫骨近端大型假体治疗创伤后感染性临界骨缺损时重建髌腱的治疗结果。

患者与方法

在这项回顾性研究中,我们评估了9例接受胫骨近端大型假体植入并进行髌腱重建的患者。所有患者在假体植入时均出现髌腱完全断裂。重建手术包括股四头肌和/或髌腱的腱成形术、股四头肌筋膜的“饼皮样”处理、用合成肌腱移植替代物(LARS)加强该装置以及采用内侧腓肠肌肌瓣来重建伸膝机制并在需要时获得皮肤覆盖。平均随访时间为18个月(9 - 36个月)。对于每例患者,我们分析了发生的关于感染复发、髌骨骨折、股四头肌和髌腱断裂以及再次干预次数的并发症。通过WOMAC评分评估临床结果。

结果

所有病例均未出现感染复发或与皮肤相关的问题。没有患者因假体松动或装置故障而需要翻修假体。未记录到髌骨骨折或股四头肌肌腱断裂。1例患者在植入后18个月因外伤导致重建的髌腱断裂,他需要进行翻修手术。从临床角度来看,平均WOMAC评分在1个月时为62.4,3个月时升至72.6,6个月时为78.2,1年时为76.4,18个月时为74.8。

结论

当植入胫骨近端大型假体且存在软组织和髌腱缺损时,可通过适当延长肌腱并用LARS加强的腓肠肌瓣来实现软组织重建。这种方法能够恢复伸膝机制并在皮肤问题通常非常常见的区域覆盖假体。

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