Graichen H, Strauch M, Scior W, Morgan-Jones R
Endoprothetik - Zentrum, Asklepios Orthopädische Klinik Lindenlohe, Lindenlohe 18, 92421, Schwandorf, Deutschland,
Oper Orthop Traumatol. 2015 Feb;27(1):24-34. doi: 10.1007/s00064-014-0333-0. Epub 2015 Jan 28.
Primary and long-term fixation of cementless metaphyseal implants in knee revision arthroplasty cases with large bone defects.
All tibial and femoral bone defects AORI grade 2 and 3.
Cases where stable uncemented fixation of the metaphyseal implant is not possible.
Pre-operative evaluation of the failure mode and implant fixation planning. After opening the joint, a synovectomy and mobilisation of medial and lateral recesses routinely performed. Testing of ligamentous stability and implant fixation undertaken before explantation. Removal of the bearing, femoral and tibial components with osteotomes or oscillating saw. Tibial diaphysis prepared with reamers, and metaphyseal preparation with broaches and stem extension. Placement of the metaphyseal broach for height with respect to the tibial joint line and rotational stability assessed. Tibial tray size and position determined before implanting the sleeve, stem and tray trial. The tibial trial provides a stable platform for analysis of the extension and flexion gaps with spacer blocks. Diaphyseal reamers used to identify the anterior femoral bow. Metaphyseal broaches used to achieve stable fixation up to the resection line marked on the handle. Distal femoral freshening cut in 5° or 7° of valgus made to accommodate distal augments as needed. Positioning of the 4-in-1 block with reconstruction of the posterior off-set and cutting for posterior augmentation. Selection of a box cut corresponding to the amount of constraint needed. Trial insert with appropriate, stem, sleeve, condylar femur and augments introduced. Bearing size, joint stability and ROM assessed. Patella alignment and the need for patella replacement or revision determined. The definitive implants are cemented at the joint surface, with metaphyseal sleeves and diaphyseal stems are uncemented.
Full weight bearing as tolerated, physiotherapy, lymph drainage and pain therapy are routine with no specific post-operative management required.
Between 2007 and 2011, 193 sleeves (119 tibial/74 femoral) were implanted in 121 aspetic knee revision arthroplasties. After average of 3.6 years they were analysed clinically and radiographically. The AKSS (American Knee Society Score) increased from 88 ± 18 to 147 ± 23 points (p < 0.01). ROM (range of motion) increased from 89 ± 6° to 114 ± 4°. Overall revision rate was 11.6 %. Only 4 sleeves revised for aseptic loosening (2 % of total sleeves). An additional 10 revisions performed mainly for infection (3.3 %) or ligament instability (3.3 %).
在存在大骨缺损的膝关节翻修置换病例中对非骨水泥型干骺端植入物进行初次和长期固定。
所有AORI 2级和3级的胫骨和股骨骨缺损。
无法实现干骺端植入物稳定非骨水泥固定的病例。
术前评估失败模式并进行植入物固定规划。打开关节后,常规进行滑膜切除以及内外侧隐窝的松解。在取出植入物前测试韧带稳定性和植入物固定情况。用骨刀或摆动锯取出承重部件、股骨和胫骨部件。用扩孔钻准备胫骨干,用拉刀和柄部延长器准备干骺端。根据胫骨关节线放置干骺端拉刀以确定高度,并评估旋转稳定性。在植入套筒、柄部和托盘试模前确定胫骨托盘的尺寸和位置。胫骨试模为使用间隔块分析伸直和屈曲间隙提供稳定平台。用骨干扩孔钻确定股骨前弓。使用干骺端拉刀实现直至手柄上标记的切除线的稳定固定。根据需要进行5°或7°外翻的股骨远端修整切口,以容纳远端增强物。放置四合一块并重建后方偏移,进行后方增强物的切割。选择与所需约束量相对应的盒式切口。插入合适的试模、柄部、套筒、股骨髁和增强物。评估承重部件尺寸、关节稳定性和活动范围。确定髌骨对线情况以及是否需要进行髌骨置换或翻修。关节表面的最终植入物使用骨水泥固定,干骺端套筒和骨干柄部不使用骨水泥。
根据耐受情况完全负重,物理治疗、淋巴引流和疼痛治疗为常规操作,无需特殊的术后管理。
在2007年至2011年期间,121例无菌性膝关节翻修置换术中植入了193个套筒(119个胫骨/74个股骨)。平均3.6年后,对其进行临床和影像学分析。美国膝关节协会评分(AKSS)从88±18分提高到147±23分(p<0.01)。活动范围(ROM)从89±6°增加到114±4°。总体翻修率为11.6%。仅4个套筒因无菌性松动进行翻修(占套筒总数的2%)。另外10次翻修主要针对感染(3.3%)或韧带不稳定(3.3%)。