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个体化假体和工具的定制化保留后交叉韧带型全膝关节置换(iTotal™ CR G2)。

Patient-specific cruciate-retaining total knee replacement with individualized implants and instruments (iTotal™ CR G2).

机构信息

Department of Orthopedic Surgery, König-Ludwig-Haus, Julius-Maximilians-University Würzburg, Brettreichstraße 11, Würzburg, Germany.

Campus Bad Neustadt, Klinik für Orthopädie, Unfallchirurgie, Schulterchirurgie und Endoprothetik, Rhön Klinikum, Von-Guttenberg-Straße 11, 97616, Bad Neustadt a.d. Saale, Germany.

出版信息

Oper Orthop Traumatol. 2021 Apr;33(2):170-180. doi: 10.1007/s00064-020-00690-8. Epub 2020 Dec 8.

DOI:10.1007/s00064-020-00690-8
PMID:33289871
Abstract

OBJECTIVE

Treatment of tricompartimental osteoarthritis (OA) using customized instruments and implants for cruciate-retaining total knee arthroplasty. Use of patient-specific instruments and implants (ConforMIS iTotal CR G2) together with a 3D-planning protocol (iView®). Retropatellar resurfacing is optional.

INDICATIONS

Symptomatic tricompartmental OA of the knee (Kellgren-Lawrence stage IV) with preserved posterior cruciate ligament (PCL) after unsuccessful conservative or joint-preserving surgical treatment.

CONTRAINDICATIONS

Knee ligament instabilities of the posterior cruciate or collateral ligaments. Infection. Relative contraindication: knee deformities >15° (varus, valgus, flexion); prior partial knee replacement.

SURGICAL TECHNIQUE

Midline or parapatellar medial skin incision, medial arthrotomy; distal femoral resection with patient-specific cutting block; tibial resection using either a cutting jig for the anatomic slope or a fixed 5° slope. Balancing the knee in extension and flexion gap using patient-specific spacer. The final tibial preparation achieved with gap-balanced placement of the femoral cutting jigs. Kinematic testing using anatomic trial components. Final implant components are cemented in extension. Wound layers are sutured. Drainage is optional.

POSTOPERATIVE MANAGEMENT

Sterile wound dressing; compressive bandage. No limitation of the active and passive range of motion. Optional partial weight bearing during the first 2 weeks, then transition to full weight bearing. Follow-up directly after surgery, at 12 and 52 weeks, then every 1-2 years.

RESULTS

Overall 60 patients with tricompartmental knee OA and preserved PCL were treated. Mean age was 66 (range 45-76) years. Minimum follow-up was 12 months. There was 1 septic revision after a low-grade infection, 1 reoperation to replace the patellar due to patellar osteoarthritis and 3 manipulations under anesthesia (MUAs) to increase range of motion. Radiographic analyses demonstrated an ideal implant fit with less than 2 mm subsidence or overhang. The WOMAC score improved from 154.8 points preoperatively to 83.5 points at 1 year and 59.3 points at 2 years postoperatively. The EuroQol-5D Score also improved from 11.1 points preoperatively to 7.7 points at 1 year postoperatively.

摘要

目的

使用定制的器械和植入物治疗三分区骨关节炎(OA),用于保留十字韧带的全膝关节置换。使用患者特异性器械和植入物(ConforMIS iTotal CR G2)以及 3D 规划方案(iView®)。髌骨关节可选择再处理。

适应证

膝关节三分区 OA 伴未成功的保守或保膝手术治疗后保留的后十字韧带(PCL)(Kellgren-Lawrence 分期 IV 级)。

禁忌证

PCL 或侧副韧带不稳定的膝关节。感染。相对禁忌证:膝关节畸形>15°(内翻、外翻、屈曲);既往部分膝关节置换。

手术技术

正中或髌旁内侧皮肤切口,内侧入路;使用患者特异性截骨块进行股骨远端切除;胫骨截骨术使用解剖斜率截骨导向器或固定 5°斜率截骨导向器。使用患者特异性间隔物在膝关节伸展和屈曲间隙平衡。通过股骨截骨导向器的间隙平衡放置实现最终胫骨准备。使用解剖试模组件进行运动学测试。最终植入物组件在伸展位进行骨水泥固定。缝合各层切口。可选择引流。

术后处理

无菌伤口包扎;加压包扎。无主动和被动活动范围限制。术后 2 周内可部分负重,然后过渡到完全负重。术后即刻、术后 12 周和 52 周、之后每 1-2 年进行随访。

结果

共治疗 60 例三分区膝关节 OA 伴保留 PCL 的患者,平均年龄 66(45-76)岁。最小随访时间为 12 个月。1 例因低度感染发生感染性翻修,1 例因髌股关节炎更换髌骨,3 例因关节活动度增加行麻醉下手法复位(MUA)。影像学分析显示,假体适配理想,下沉或突出<2mm。WOMAC 评分从术前的 154.8 分改善至术后 1 年的 83.5 分和术后 2 年的 59.3 分。EuroQol-5D 评分从术前的 11.1 分改善至术后 1 年的 7.7 分。

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