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股骨远端内翻截骨术中内侧铰链骨折风险的实验研究。

Experimental study of risk of medial hinge fracture during distal femoral varus osteotomy.

机构信息

Service de Chirurgie Orthopédique et de Traumatologie, Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, 1, avenue Molière, 67098 Strasbourg cedex, France; Laboratoire ICube, CNRS UMR 7357, 2-4, rue Boussingault, 67000 Strasbourg, France.

Service de Chirurgie Orthopédique et de Traumatologie, Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, 1, avenue Molière, 67098 Strasbourg cedex, France.

出版信息

Orthop Traumatol Surg Res. 2023 Jun;109(4):103527. doi: 10.1016/j.otsr.2022.103527. Epub 2022 Dec 20.

Abstract

INTRODUCTION

Lateral opening wedge distal femoral osteotomy (LOWDFO) is indicated for isolated lateral osteoarthritis in the valgus morphotype. Medial hinge fracture is a factor for poor prognosis. The present study had two aims: (1) to assess the impact of a temporary K-wire on hinge fracture risk; and (2) to assess the impact of LOWDFO opening speed.

HYPOTHESIS

The main study hypothesis was that a temporary hinge K-wire reduces hinge fracture risk. The second hypothesis was that faster opening speed increases fracture risk.

MATERIAL AND METHOD

Twenty femurs were produced by 3D printing from a CT database, reproducing LOWDFO anatomy. The ABS® polymer showed the same breaking-point behavior as human bone. Ten specimens were included in the "K-wire" group (KW+) and 10 in the "No K-wire" group (KW-). To determine high and low speed, a motion-capture glove was used by 2 operators, providing 3D modeling of the surgeon's hand. High speed was defined as 152mm/min and low speed as 38mm/min. The KW+ and KW- groups were subdivided into high- and low-speed subgroups (HS, LS) of 5 each. Compression tests were conducted using an Instron® mechanical test machine up to hinge fracture. The main endpoint was maximum breaking-point force (N); the secondary endpoints were maximum displacement (mm) and maximum speed (min) at breaking point.

RESULTS

The K-wire significantly increased maximum breaking-point force (LS, 143.08N vs. 93.71N, p<0.01; and HS, 186.98N vs. 95.22N, p<0.01), but not maximum displacement (LS, 26.17mm vs. 24.11mm, p=0.31; and HS 26.18mm vs. 23.66mm, p=0.14) or maximum time (LS, 27.07s vs. 24.94s, p=0.31; and HS, 5.24s vs. 4.73s, p=0.14). Speed did not affect maximum force (KW+, 143.08N vs. 186.98N, p=0.06; and KW-, 93.71N vs. 95.22N, p=0.42) or maximum displacement (KW+, 26.17mm vs. 26.18mm, p=1; and KW-, 24.11mm vs. 23.66mm, p=0.69). Only maximum time was greater at low speed (KW+, 27.07s vs. 5.24s, p>0.01; and KW-, 24.94s vs. 4.73s, p<0.01), which is obvious for constant distance.

DISCUSSION

The first study hypothesis was confirmed, with significantly lower hinge fracture risk with the K-wire, independently of opening speed. The second hypothesis was not confirmed. The study was performed under strict experimental conditions, unprecedented to our knowledge in the literature. However, complementary clinical studies are needed to confirm the present findings.

LEVEL OF EVIDENCE

IV, experimental study.

摘要

简介

外侧开口楔形股骨远端截骨术(LOWDFO)适用于外侧关节炎伴内翻畸形的病例。内侧铰链骨折是预后不良的一个因素。本研究有两个目的:(1)评估临时 K 线对铰链骨折风险的影响;(2)评估 LOWDFO 开口速度的影响。

假说

主要研究假设是临时铰链 K 线可降低铰链骨折的风险。第二个假设是更快的开口速度会增加骨折的风险。

材料和方法

使用 CT 数据库通过 3D 打印制作了 20 个股骨标本,模拟了 LOWDFO 的解剖结构。ABS®聚合物的断裂特性与人体骨骼相同。10 个标本纳入“K 线”组(KW+),10 个标本纳入“无 K 线”组(KW-)。为了确定高、低速度,两名操作人员使用运动捕捉手套,提供了手术医生手部的 3D 建模。高速度定义为 152mm/min,低速度为 38mm/min。KW+和 KW-组分别分为高、低速度亚组(HS,LS),每组 5 个。使用 Instron®机械试验机进行压缩试验,直至铰链骨折。主要终点是最大断裂点力(N);次要终点是断裂点的最大位移(mm)和最大速度(min)。

结果

K 线显著增加了最大断裂点力(LS,143.08N 比 93.71N,p<0.01;HS,186.98N 比 95.22N,p<0.01),但不增加最大位移(LS,26.17mm 比 24.11mm,p=0.31;HS,26.18mm 比 23.66mm,p=0.14)或最大时间(LS,27.07s 比 24.94s,p=0.31;HS,5.24s 比 4.73s,p=0.14)。速度不影响最大力(KW+,143.08N 比 186.98N,p=0.06;KW-,93.71N 比 95.22N,p=0.42)或最大位移(KW+,26.17mm 比 26.18mm,p=1;KW-,24.11mm 比 23.66mm,p=0.69)。仅低速时最大时间更长(KW+,27.07s 比 5.24s,p>0.01;KW-,24.94s 比 4.73s,p<0.01),这在恒定距离下很明显。

讨论

第一个研究假设得到了证实,与不使用 K 线相比,使用 K 线显著降低了铰链骨折的风险,与开口速度无关。第二个假设未得到证实。本研究在严格的实验条件下进行,据我们所知,这在文献中是前所未有的。然而,需要进行补充的临床研究来证实目前的发现。

证据等级

IV,实验研究。

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