首页> 外文期刊>Clinical Orthopaedics and Related Research >Cemented distal femoral endoprostheses for musculoskeletal tumor: improved survival of modular versus custom implants.
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Cemented distal femoral endoprostheses for musculoskeletal tumor: improved survival of modular versus custom implants.

机译:骨水泥远端股骨假体用于肌肉骨骼肿瘤:模块化和定制植入物的存活率提高。

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BACKGROUND: Advocates of newer implant designs cite high rates of aseptic loosening and failure as reasons to abandon traditional cemented endoprosthetic reconstruction of the distal femur. QUESTIONS/PURPOSES: We asked whether newer, modular distal femoral components had improved survivorship compared with older, custom-casted designs. PATIENTS AND METHODS: We retrospectively reviewed 254 patients who underwent distal femoral endoprosthetic reconstruction. We excluded two patients with cementless implants, 27 with expandable prostheses, and 39 who had a nontumor diagnosis. This left 186 patients: 101 with older custom implants and 85 with contemporary modular implants. The minimum followup was 1 month (mean, 96.0 months; range, 1-336 months). The tumor was classified as Stage IIA/IIB in 122 patients, Stage IA/IB or benign in 43, and Stage III or metastatic in 21. RESULTS: Kaplan-Meier analysis revealed overall 10-, 20-, and 25-year implant survival rates of 77%, 58%, and 50%, respectively, using revision of the stemmed components as an end point. The 85 modular components had a greater 15-year survivorship than the 101 custom-designed implants: 93.7% versus 51.7%, respectively. Thirty-five stemmed components (18.8%) were revised for aseptic loosening in 22 patients, implant fatigue fracture in 10, infection in two, and local recurrence in one. CONCLUSIONS: Cemented modular rotating-hinge distal femoral endoprostheses demonstrated improved survivorship compared with custom-casted implants during this three-decade experience. Patients with low-grade disease and long-term survivors of high-grade localized disease should expect at least one or more revision procedures in their lifetime. LEVEL OF EVIDENCE: Level IV, therapeutic study. See the Guidelines for Authors for a complete description of levels of evidence.
机译:背景:较新的植入物设计的拥护者认为,无菌性松动和失败的发生率很高,这是放弃股骨远端传统的骨水泥内假体重建的原因。问题/目的:我们询问与较旧的定制铸造设计相比,较新的模块化股骨远端组件能否改善生存率。病人和方法:我们回顾性分析了254例接受股骨远端假体重建的患者。我们排除了两名无骨水泥植入物的患者,27名具有可扩张假体的患者和39名无肿瘤诊断的患者。剩下的186例患者:101例使用较旧的定制植入物,85例使用当代的模块化植入物。最小随访时间为1个月(平均96.0个月;范围1-336个月)。该肿瘤被分类为122例患者的IIA / IIB期,43例为IA / IB或良性,21例为III期或转移。结果:Kaplan-Meier分析显示植入物的总生存期为10、20和25年。以修改后的词干成分为终点,分别为77%,58%和50%。与101个定制设计的植入物相比,85个模块化组件的生存期更长:分别为93.7%和51.7%。修订了35根茎成分(18.8%),其中22例无菌松动,10例植入物疲劳性骨折,2例感染,1例局部复发。结论:在这三个十年的经验中,与定制铸造的植入物相比,骨水泥模块化的旋转铰接式股骨远端假体具有更好的生存率。患有低度疾病和长期局部高危幸存者的患者应在其一生中至少接受一种或多种修正程序。证据级别:IV级,治疗研究。有关证据水平的完整说明,请参见《作者指南》。

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