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后稳定型全膝关节置换术中使用高度交联聚乙烯是否有益?一项随机试验。

Is There a Benefit to Highly Crosslinked Polyethylene in Posterior-stabilized Total Knee Arthroplasty? A Randomized Trial.

作者信息

Lachiewicz Paul F, Soileau Elizabeth S

机构信息

Chapel Hill Orthopedics Surgery & Sports Medicine, 101 Conner Drive, Suite 200, Chapel Hill, NC, 27514, USA.

出版信息

Clin Orthop Relat Res. 2016 Jan;474(1):88-95. doi: 10.1007/s11999-015-4241-x.

DOI:10.1007/s11999-015-4241-x
PMID:25762016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4686511/
Abstract

BACKGROUND

Polyethylene wear and osteolysis remain a concern with the use of modular, fixed-bearing total knee arthroplasty (TKA). A variety of highly crosslinked polyethylenes (XLPs) have been introduced to address this problem, but there are few data on the results and complications of this polyethylene in posterior-stabilized knee prostheses.

QUESTIONS/PURPOSES: In a randomized prospective study design comparing standard polyethylene (SP) tibial inserts with XLP inserts, we asked the following questions: (1) Are there any differences in the clinical results (as measured by the classic Knee Society scoring system) and radiographic results (as measured by an evaluation for radiolucencies and osteolysis) between these groups? (2) What is the frequency of reoperation in these two groups? (3) Are there any specific complications related to XLP liners?

METHODS

These are preliminary data from a single surgeon of a planned interim analysis of a prospective randomized study of one modular posterior-stabilized TKA. One hundred ninety-two patients (236 knees) were randomized to receive a SP compression-molded liner or a XLP (6.5 CGy electron beam-irradiated and remelted) polyethylene liner. There was no difference in the number of knees who were lost or refused followup (14 knees [13%] with XLP and 21 knees [17%] with SP). Patients were evaluated clinically using the original Knee Society scores, Lower Extremity Activity Score (LEAS), presence of knee effusion, and by standard radiographs for radiolucent lines and osteolytic lesions. This analysis was performed at a mean followup of 4.5 years (range, 2-8 years).

RESULTS

There were no clinical differences between 99 knees with SP and 94 knees with XLP in original Knee Society total score (SP mean 95, SD 5; XLP mean 94, SD 7 [p = 0.16]); change in total score (SP mean 41, 95% confidence interval [CI], 39-41; XLP mean 43, 95% CI, 39-48 [p = 0.56]); knee function score (SP mean 64 [SD 25]; XLP mean 64 [SD 24] p = 0.98; change in function score (SP mean 22, 95% CI, 17-27; XLP mean 21, 95% CI, 17-27 [p = 0.79]); LEAS score (both SP and XLP 9 [SD 2]; p = 0.88); and change in LEAS (both SP and XLP mean 1, 95% CI, 1-2 [p = 0.0.38]). There were no differences, with the numbers available, in the presence of effusion (two of 94 XLP and five of 99 SP) with 2 years minimum followup. There were no differences in the frequency of radiolucent lines (13 knees with SP and 15 with XLP) or of osteolysis (two knees with SP and none with XLP). There was no difference in frequency of reoperation between the two groups (three infections in 110 knees allocated to the XLP group and five (two infections, one femoral loosening, one instability, one fracture plating) in 122 knees allocated to the standard group. There were no complications related to the XLP liner.

CONCLUSIONS

In this interim analysis, with the numbers available, there were no complications, but no advantages, related to the use of this XLP tibial liner. Additional enrollment has continued, and longer followup of these patients will be necessary to determine whether long-term wear characteristics differ between the groups.

LEVEL OF EVIDENCE

Level I, therapeutic study.

摘要

背景

使用模块化、固定平台全膝关节置换术(TKA)时,聚乙烯磨损和骨溶解仍是令人担忧的问题。已引入多种高度交联聚乙烯(XLP)来解决这一问题,但关于这种聚乙烯在后方稳定型膝关节假体中的结果和并发症的数据较少。

问题/目的:在一项将标准聚乙烯(SP)胫骨衬垫与XLP衬垫进行比较的随机前瞻性研究设计中,我们提出了以下问题:(1)这些组之间的临床结果(通过经典膝关节协会评分系统测量)和影像学结果(通过评估透光线和骨溶解测量)是否存在差异?(2)这两组的再次手术频率是多少?(3)与XLP衬垫相关的特定并发症有哪些?

方法

这些是来自一位外科医生对一项前瞻性随机研究的计划中期分析的初步数据,该研究针对一种模块化后方稳定型TKA。192例患者(236个膝关节)被随机分配接受SP模压成型衬垫或XLP(6.5 cGy电子束辐照并重新熔融)聚乙烯衬垫。失访或拒绝随访的膝关节数量无差异(XLP组14个膝关节[13%],SP组21个膝关节[17%])。使用原始膝关节协会评分、下肢活动评分(LEAS)、膝关节积液情况对患者进行临床评估,并通过标准X线片评估透光线和溶骨性病变。该分析在平均随访4.5年(范围2 - 8年)时进行。

结果

99个使用SP的膝关节和94个使用XLP的膝关节在原始膝关节协会总分(SP平均95,标准差5;XLP平均94,标准差7 [p = 0.16])、总分变化(SP平均41,95%置信区间[CI],39 - 41;XLP平均43,95% CI,39 - 48 [p = 0.56])、膝关节功能评分(SP平均64 [标准差25];XLP平均64 [标准差24] p = 0.98;功能评分变化(SP平均22,95% CI,17 - 27;XLP平均21,95% CI,17 - 27 [p = 0.79])、LEAS评分(SP和XLP均为9 [标准差2];p = 0.88)以及LEAS变化(SP和XLP平均均为1,95% CI,1 - 2 [p = 0.38])方面无临床差异。在至少随访2年的情况下,积液情况(94个XLP中有2个,99个SP中有5个)在可用数据方面无差异。透光线频率(SP组13个膝关节,XLP组15个膝关节)或骨溶解频率(SP组2个膝关节,XLP组无)无差异。两组之间的再次手术频率无差异(分配到XLP组的110个膝关节中有3例感染,分配到标准组的122个膝关节中有5例(2例感染、1例股骨松动、1例不稳定、1例骨折内固定))。与XLP衬垫相关无并发症。

结论

在本次中期分析中,就现有数据而言,使用这种XLP胫骨衬垫无并发症,但也无优势。已继续进行额外入组,有必要对这些患者进行更长时间的随访,以确定两组之间的长期磨损特征是否不同。

证据水平

I级,治疗性研究。

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