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当前生产的肿瘤假体的存活率:并发症、功能结果和比较统计分析。

Survival of current production tumor endoprostheses: complications, functional results, and a comparative statistical analysis.

机构信息

Department of Orthopaedics, University of Bologna, Istituto Ortopedico Rizzoli, Bologna, Italy.

出版信息

J Surg Oncol. 2013 Nov;108(6):403-8. doi: 10.1002/jso.23414. Epub 2013 Sep 4.

Abstract

BACKGROUND AND OBJECTIVES

Retrospectively analyze outcomes of current-generation Global Modular Replacement System (GMRS) modular tumor endoprosthesis for the lower limb in primary and secondary implantation procedures.

METHODS

Two hundred ninety five prostheses were implanted, 197 were primary implants, 98 were for revision surgery; revision procedures included 84 failed tumor reconstructions and 14 failed non-tumor reconstructions. Anatomic sites included: distal femur 199; proximal tibia 60; proximal femur 32;total femur 4. Endoprosthesis failures were classified as soft-tissue failures (Type 1), aseptic loosening (Type 2), structural fracture (Type 3), infection (Type 4), and tumor recurrence (Type 5). MSTS functional scores were measured.

RESULTS

The overall failure rate was 28.8% and failure occurred at a median of 1.7 years (range, 1 month to 7 years). At a mean oncologic follow up of 4.2 years (range, 2-8 years), 195 patients are continuously NED, 43 NED after treatment of relapse, 10 AWD, 33 DWD. There was a significant difference in implant survival of all modes of failure between primary and revision implants (P = 0.03). No prosthetic fracture occurred. The average functional score was 81.6% (24.5).

CONCLUSIONS

Mid-term results with GMRS are promising, with good functional results and low incidence of complications for primary implants.

LEVEL OF EVIDENCE

Therapeutic study, level IV-1 (case series).

摘要

背景与目的

回顾分析当前一代全球模块化置换系统(GMRS)模块化肿瘤假体在原发性和继发性植入手术中的应用效果。

方法

共植入 295 例假体,197 例为原发性植入,98 例为翻修手术;翻修手术包括 84 例肿瘤重建失败和 14 例非肿瘤重建失败。解剖部位包括:股骨远端 199 例;胫骨近端 60 例;股骨近端 32 例;全股骨 4 例。假体失败分为软组织失败(1 型)、无菌性松动(2 型)、结构断裂(3 型)、感染(4 型)和肿瘤复发(5 型)。测量 MSTS 功能评分。

结果

总的失败率为 28.8%,中位失败时间为 1.7 年(范围 1 个月至 7 年)。平均肿瘤随访 4.2 年(范围 2-8 年),195 例患者持续无瘤生存(NED),43 例经治疗后复发的患者 NED,10 例疾病稳定(AWD),33 例疾病进展(DWD)。原发性和翻修假体在所有失败模式下的假体存活率有显著差异(P=0.03)。无假体骨折发生。平均功能评分为 81.6%(24.5)。

结论

GMRS 的中期结果令人鼓舞,原发性植入假体功能结果良好,并发症发生率低。

证据水平

治疗性研究,IV 级-1(病例系列)。

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