Physiologic Preoperative Knee Hyperextension Is Not Associated With Postoperative Laxity, Subjective Knee Function, or Revision Surgery After ACL Reconstruction With Hamstring Tendon Autografts.

Gunnar Edman,Kristian Samuelsson,Eric Hamrin Senorski,Romain Seil,Riccardo Cristiani
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Abstract

BACKGROUND There is concern that physiologic knee hyperextension may be associated with inferior outcomes after anterior cruciate ligament reconstruction (ACLR) using hamstring tendon (HT) autografts. PURPOSE To assess whether there is an association between contralateral passive preoperative knee hyperextension (≤-5°) and postoperative anterior knee laxity, subjective knee function, or revision surgery after ACLR using HT autografts. STUDY DESIGN Cohort study; Level of evidence, 3. METHODS Patients without concomitant ligament injuries who underwent primary ACLR using an HT autograft at Capio Artro Clinic, Stockholm, Sweden, between January 1, 2005, and December 31, 2018, were identified. The cohort was dichotomized into the hyperextension group (≤-5°) and the no hyperextension group (>-5°) depending on preoperative contralateral passive knee extension degree. Anterior knee laxity (KT-1000 arthrometer; 134 N) was assessed preoperatively and at 6 months postoperatively. The Knee injury and Osteoarthritis Outcome Score (KOOS) was collected preoperatively and at 1, 2, and 5 years postoperatively. Patients who underwent revision ACLR at any institution in Sweden within 5 years of the primary surgery were identified in the Swedish National Knee Ligament Registry. RESULTS A total of 6104 patients (53.5% male) for whom knee range of motion measurements were available were identified (hyperextension group [≤-5°]: 2350 [38.5%]; mean extension, -6.1°± 2.3° [range, -20° to -5°]; no hyperextension group [>-5°]: 3754 [61.5%]; mean extension, 0°± 1.4° [range, -4° to 15°]). There were no intergroup differences in anterior knee laxity preoperatively (hyperextension group, 3.6 ± 2.8 mm; no hyperextension group, 3.7 ± 2.7 mm; P = .24) or postoperatively (hyperextension group, 1.8 ± 2.3 mm; no hyperextension group, 1.8 ± 2.2 mm; P = .41). The only significant but nonclinically relevant intergroup differences were seen in the KOOS Symptoms subscale at the 1-year follow-up (hyperextension group, 81.4 ± 16.0; no hyperextension group, 80.3 ± 16.5; P = .03) and in the Sport and Recreation subscale at the 5-year follow-up (hyperextension group, 73.0 ± 25.6; no hyperextension group, 75.7 ± 24.3; P = .02). No other significant intergroup differences were noted preoperatively or at 1, 2, or 5 years postoperatively in any of the KOOS subscales. The overall revision ACLR rate at ≤5 years after the primary surgery was 4.9% (302 of 6104 patients). The hazard for revision ACLR in the no hyperextension group (4.5%; 170 of 3754 patients) was not significantly different from that in the hyperextension group (5.6%; 132 of 2350 patients) (hazard ratio, 0.89; 95% CI, 0.71 to -1.12; P = .34). A subsequent subanalysis showed that the hazard of revision ACLR in patients with no hyperextension was not significantly different from that of patients with ≤-10° of extension (5.8%; 27 of 467 patients) (hazard ratio, 0.91; 95% CI, 0.61 to 1.36; P = .65). CONCLUSION Preoperative passive contralateral knee hyperextension (≤-5°) was not associated with postoperative anterior knee laxity, subjective knee function, or revision surgery ≤5 years after ACLR using HT autografts. Therefore, the presence of knee hyperextension alone should not be considered a contraindication per se for the use of HT autografts in ACLR.
使用腘绳肌腱自体移植物进行前交叉韧带重建术后,术前膝关节生理过伸与术后松弛、主观膝关节功能或翻修手术无关。
目的评估使用腘绳肌腱(HT)自体移植物进行前交叉韧带重建(ACLR)后,对侧被动术前膝关节过伸(≤-5°)与术后膝关节前部松弛、主观膝关节功能或翻修手术之间是否存在关联。研究设计队列研究;证据级别,3.方法确定了2005年1月1日至2018年12月31日期间在瑞典斯德哥尔摩Capio Artro诊所使用HT自体移植物进行初次前交叉韧带置换术的无并发韧带损伤患者。根据术前对侧膝关节被动伸展程度,将患者分为膝关节过度伸展组(≤-5°)和无过度伸展组(>-5°)。对术前和术后 6 个月的膝关节前松弛度(KT-1000 关节测量计;134 N)进行评估。术前和术后 1 年、2 年和 5 年收集膝关节损伤和骨关节炎结果评分(KOOS)。瑞典国家膝关节韧带注册中心对初次手术后 5 年内在瑞典任何机构接受翻修性 ACLR 的患者进行了鉴定。结果共鉴定出 6104 例可进行膝关节活动范围测量的患者(男性占 53.5%)(过度伸展组 [≤-5°]:2350 [38.5%];平均伸展度为 -6.1°± 2.3°[范围为 -20° 至 -5°];无过度伸展组 [>-5°]:3754 [61.5%];平均伸展度为 -6.1°± 2.3°[范围为 -20°至 -5°]):3754例[61.5%];平均伸展度为0°± 1.4°[范围为-4°至15°])。术前(过度伸展组,3.6 ± 2.8 mm;无过度伸展组,3.7 ± 2.7 mm;P = .24)或术后(过度伸展组,1.8 ± 2.3 mm;无过度伸展组,1.8 ± 2.2 mm;P = .41)膝关节前松弛度没有组间差异。随访 1 年时,KOOS 症状分量表(过度伸展组,81.4 ± 16.0;无过度伸展组,80.3 ± 16.5;P = .03)和随访 5 年时,运动和娱乐分量表(过度伸展组,73.0 ± 25.6;无过度伸展组,75.7 ± 24.3;P = .02)出现了唯一显著但与临床无关的组间差异。在术前、术后 1 年、2 年或 5 年的任何 KOOS 分量表中,均未发现其他明显的组间差异。初次手术后≤5年的前交叉韧带翻修率为4.9%(6104例患者中有302例)。无过度伸展组(4.5%;3754 例患者中的 170 例)与过度伸展组(5.6%;2350 例患者中的 132 例)的前交叉韧带复发风险无显著差异(风险比,0.89;95% CI,0.71 至-1.12;P = .34)。随后的一项子分析表明,无过度伸展的患者与伸展≤-10°的患者(5.8%;467 例患者中的 27 例)的前交叉韧带翻修危险性无显著差异(危险比,0.91;95% CI,0.结论术前被动对侧膝关节过伸(≤-5°)与术后膝关节前部松弛、主观膝关节功能或使用 HT 自体移植物进行 ACLR 后 5 年内的翻修手术无关。因此,膝关节过伸本身不应被视为在前交叉韧带置换术中使用 HT 自体移植物的禁忌症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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