No Difference in Graft Signal Intensity on MRI or Clinical Outcome Between Anterior Cruciate Ligament Reconstruction With and Without Suture Augmentation.

Keiji Tensho, Tomoya Iwaasa, Suguru Koyama, Hiroki Shimodaira, Tsuneari Takahashi, Jun Takahashi
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Abstract

Purpose: To evaluate the safety of anterior cruciate ligament reconstruction (ACLR) with suture augmentation (SA) through clinical evaluations, monitoring of complications, and evaluation of early graft remodeling using magnetic resonance imaging (MRI).

Methods: Data of participants who underwent anatomic double-bundle ACLR using hamstring tendon autografts, with a minimum 2-year follow-up, were retrospectively reviewed. Participants undergoing ACLR with SA were propensity-matched with those without SA. Postoperative clinical evaluations, including Lysholm and Tegner activity scores, International Knee Documentation Committee (IKDC) evaluation scores, KT-1000 side-to-side difference for knee stability at a 2-year follow-up, and complications, were recorded. The minimal clinically important difference (MCID) was calculated for IKDC scores. The anteromedial bundle graft was categorized into distal, middle, and proximal regions on the 6-month and 1-year postoperative MRI. The signal-to-noise quotient (SNQ) of each region of interest was calculated to evaluate the graft signal intensity, which was compared between the two groups using Welch's t-test.

Results: Fifty-three participants were included in each group. No significant differences were observed between the non-SA and SA groups in the Lysholm scores (96.6 ± 6.2; 95.3 ± 5.8, P = 0.25), Tegner activity scores (4.8 ± 1.4; 5.0 ± 1.3, P = 0.49), IKDC scores (90.4 ± 10.8; 87.1 ± 12.9, P = 0.15), percentage of patients meeting the MCID (94.3%; 83.0%, P = 0.12), or postoperative KT-1000 side-to-side difference (0.9 ±1.2; 0.7 ± 1.8 mm, P = 0.56). One (1.8%) and two (3.7%) cases of re-tears occurred in the non-SA and SA groups, respectively; no other complications occurred. The postoperative SNQ measurements revealed no significant differences in signal changes in all regions of the grafts between the two groups.

Conclusions: This study confirmed no difference in graft signal intensity on MRI or clinical outcome between ACLR with and without SA at the 2-year follow-up.

Level of evidence: Level III, retrospective, comparative study.

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前十字韧带重建术中缝合增量与不缝合增量在核磁共振成像上的移植物信号强度和临床效果上无差异。
目的:通过临床评估、并发症监测以及使用磁共振成像(MRI)评估早期移植物重塑情况,评估使用缝合增强(SA)进行前交叉韧带重建(ACLR)的安全性:方法:对使用腘绳肌腱自体移植物进行解剖学双束前交叉韧带重建且随访至少 2 年的患者数据进行回顾性回顾。接受前交叉韧带置换术的患者与未接受前交叉韧带置换术的患者进行了倾向性匹配。记录了术后临床评估,包括 Lysholm 和 Tegner 活动评分、国际膝关节文献委员会(IKDC)评估评分、2 年随访时膝关节稳定性的 KT-1000 侧-侧差异以及并发症。计算了 IKDC 评分的最小临床重要性差异(MCID)。术后 6 个月和 1 年的磁共振成像将前内侧束移植分为远端、中间和近端区域。计算每个感兴趣区的信噪比商(SNQ)以评估移植物信号强度,并使用韦尔奇 t 检验比较两组之间的信号强度:两组各有 53 名参与者。非 SA 组和 SA 组在 Lysholm 评分(96.6 ± 6.2;95.3 ± 5.8,P = 0.25)、Tegner 活动评分(4.8 ± 1.4;5.0 ± 1.3,P = 0.49)、IKDC 评分(90.4 ± 10.8;87.1 ± 12.9,P = 0.15)、符合 MCID 的患者比例(94.3%;83.0%,P = 0.12)或术后 KT-1000 侧-侧差异(0.9 ± 1.2;0.7 ± 1.8 mm,P = 0.56)。非SA组和SA组分别有1例(1.8%)和2例(3.7%)再次撕裂,未出现其他并发症。术后 SNQ 测量显示,两组移植物所有区域的信号变化无显著差异:这项研究证实,在两年的随访中,使用和不使用SA的前交叉韧带置换术在磁共振成像上的移植物信号强度和临床结果上没有差异:证据等级:III级,回顾性比较研究。
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来源期刊
CiteScore
9.30
自引率
17.00%
发文量
555
审稿时长
58 days
期刊介绍: Nowhere is minimally invasive surgery explained better than in Arthroscopy, the leading peer-reviewed journal in the field. Every issue enables you to put into perspective the usefulness of the various emerging arthroscopic techniques. The advantages and disadvantages of these methods -- along with their applications in various situations -- are discussed in relation to their efficiency, efficacy and cost benefit. As a special incentive, paid subscribers also receive access to the journal expanded website.
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