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在前交叉韧带重建中,自体腘绳肌腱小于 8mm 与混合移植物 8mm 或更大的移植物在翻修风险方面没有差异。

No difference in revision risk between autologous hamstring graft less than 8 mm versus hybrid graft 8 mm or larger in anterior cruciate ligament reconstruction.

机构信息

Department of Orthopedic Surgery, Southern California Permanente Medical Group, 1011 Baldwin Park Blvd, Baldwin Park, CA, 91706, USA.

Medical Device Surveillance and Assessment, Kaiser Permanente, San Diego, CA, USA.

出版信息

Knee Surg Sports Traumatol Arthrosc. 2023 Aug;31(8):3465-3473. doi: 10.1007/s00167-023-07437-5. Epub 2023 May 4.

Abstract

PURPOSE

Hamstring autograft (HA) is commonly used for primary anterior cruciate ligament reconstruction (ACLR). However, if the harvested HA is inadequate in diameter, it is often augmented with an allograft tendon, forming a hybrid graft (HY). This study sought to evaluate aseptic revision risk following HA versus HY ACLR.

METHODS

A retrospective cohort study was performed using data obtained from our healthcare system's ACLR registry. Patients ≤ 25 years of age who underwent primary isolated ACLR were identified (2005-2020). Graft type and diameter size was the primary exposure of interest: < 8 mm HA and ≥ 8 mm HY. A secondary analysis was performed to examine 7 mm HA and 7.5 mm HA vs ≥ 8 mm HY. Propensity score-weighted Cox proportional hazard regression was used to evaluate the risk of aseptic revision.

RESULTS

The study sample included 1,945 ACLR: 548 ≥ 8 mm HY, 651 7 mm HA, and 672 7.5 mm HA. The crude cumulative aseptic revision probability at 8-years for ≥ 8 mm HY was 9.1%, 11.1% for 7 mm HA, and 11.2% for 7.5 mm HA. In adjusted analysis, no difference in revision risk was observed for < 8 mm HA (hazard ratio [HR] 1.15, 95% confidence interval [CI] 0.72-1.82), 7 mm HA (HR 1.23, 95% CI 0.71-2.11), or 7.5 mm HA (HR 1.16, 95% CI 0.74-1.82) compared to ≥ 8 mm HY.

CONCLUSION

In a US-based cohort of ACLR patients aged ≤ 25 years, we failed to observe any differences in aseptic revision risk for HA < 8 mm compared to HY ≥ 8 mm. Augmentation of a HA as small as 7 mm is not necessary to prevent a revision surgery.

LEVEL OF EVIDENCE

Level III.

摘要

目的

腘绳肌腱自体移植物(HA)常用于初次前交叉韧带重建(ACLR)。然而,如果所采集的 HA 直径不足,通常会使用同种异体肌腱进行增强,形成混合移植物(HY)。本研究旨在评估 HA 与 HY ACLR 后无菌性翻修的风险。

方法

本研究使用我们医疗保健系统的 ACLR 注册中心获取的数据进行回顾性队列研究。确定了年龄≤25 岁的初次孤立 ACLR 患者(2005-2020 年)。感兴趣的主要暴露因素是移植物类型和直径大小:<8mm 的 HA 和≥8mm 的 HY。进行了二次分析,以检查 7mm HA 和 7.5mm HA 与≥8mm HY。采用倾向评分加权 Cox 比例风险回归评估无菌性翻修的风险。

结果

研究样本包括 1945 例 ACLR:548 例≥8mm HY、651 例 7mm HA 和 672 例 7.5mm HA。8 年时,≥8mm HY 的未感染性翻修概率的粗累积率为 9.1%,7mm HA 为 11.1%,7.5mm HA 为 11.2%。在调整分析中,<8mm HA(风险比[HR]1.15,95%置信区间[CI]0.72-1.82)、7mm HA(HR 1.23,95%CI 0.71-2.11)或 7.5mm HA(HR 1.16,95%CI 0.74-1.82)与≥8mm HY 相比,翻修风险无差异。

结论

在一项基于美国的 ACLR 患者队列中,年龄≤25 岁,我们未观察到 HA<8mm 与 HY≥8mm 相比,无菌性翻修风险有任何差异。增强直径小至 7mm 的 HA 并非预防翻修手术所必需。

证据水平

III 级。

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