Bargar W L
University of California, Davis, School of Medicine, Sacramento.
Clin Orthop Relat Res. 1989 Dec(249):73-8.
Most authors agree that "fit" and "fill" of the endosteal canal is critical to the success of cementless femoral components. Yet, there exists a wide variation to the anatomic size and shape of this canal in the normal population. This paper reviews the rationale and the efficacy of using a computed tomography-generated CAD/CAM custom femoral component in cementless total hip arthroplasty. One hundred fifty-six cases (81 primary and 75 revisions) were reviewed with follow-up time of six weeks to three years (mean, 22 months). A subset of 48 hips (25 primary and 23 revisions) has been followed a minimum of two years. For the primary hips, the custom group was found to have statistically higher Harris pain scores (less pain) at all follow-up intervals as compared to a prior series by the same surgeon using an off-the-shelf (OTS) prosthesis. Revision customized hip implants had lower Harris pain and total scores than primary custom hips, but 80% were in the none or slight pain category. In revision cases, the use of custom components decreased the need for structural bone grafting and achieved stability on host bone in situations in which it was not possible using OTS components. Complications included failure by aseptic loosening of one primary and one revision case. Initial subsidence of more than 3 mm of the collarless custom design occurred in 8%, the majority being in revision cases. All cases but one appear to have stabilized. Subsidence occurred mainly in cases done early in the series.(ABSTRACT TRUNCATED AT 250 WORDS)
大多数作者都认为,髓腔的“适配”和“填充”对于非骨水泥型股骨假体的成功至关重要。然而,正常人群中该髓腔的解剖大小和形状存在很大差异。本文回顾了在非骨水泥型全髋关节置换术中使用计算机断层扫描生成的CAD/CAM定制股骨假体的理论依据和疗效。对156例病例(81例初次置换和75例翻修)进行了回顾,随访时间为6周至3年(平均22个月)。其中48例髋关节(25例初次置换和23例翻修)的随访时间至少为两年。对于初次置换的髋关节,与同一位外科医生之前使用现成(OTS)假体的系列研究相比,定制组在所有随访间隔的Harris疼痛评分在统计学上更高(疼痛较轻)。翻修定制髋关节假体的Harris疼痛和总分低于初次定制髋关节,但80%属于无疼痛或轻度疼痛类别。在翻修病例中,使用定制假体减少了结构性骨移植的需求,并在使用OTS假体无法实现的情况下在宿主骨上实现了稳定。并发症包括1例初次置换和1例翻修病例因无菌性松动而失败。无领定制设计的初始下沉超过3 mm的情况发生在8%的病例中,大多数为翻修病例。除1例病例外,所有病例似乎都已稳定。下沉主要发生在该系列早期进行的病例中。(摘要截短于250字)