骨外动脉直径与距骨穹隆骨软骨损伤的关系

Foot & ankle international Pub Date : 2024-11-01 Epub Date: 2024-10-16 DOI:10.1177/10711007241278672
Lercan Aslan, Samir Ghandour, Soheil Ashkani-Esfahani, Cemil Cihad Gedik, Daniel Guss, Gregory Waryasz, Lorena Bejarano-Pineda, Christopher W DiGiovanni, John Y Kwon
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引用次数: 0

摘要

背景:距骨骨软骨损伤(OLT)的病因是多因素的,可能是由于创伤、遗传或血管功能低下引起的。距骨穹隆由胫后动脉(PTA)供应,其次是距骨窦动脉(STA)。关于距骨穹隆血管过少对 OLT 的影响,研究仍然很少。我们旨在确定 PTA(dPTA)和 STA(dSTA)直径与距骨 OLT 的发生率和特征之间的关系:这项回顾性研究包括 77 名 OLT 患者和 77 名作为匹配对照组的受试者(年龄范围:30-40 岁)。通过磁共振成像,在胫骨骺板上方 1 厘米、骺板处和内侧踝尖水平测量了 dPTA。同样,在距骨颈水平也测量了 dSTA。同时还记录了OLT的面积、体积、深度、定位和手术干预情况:与对照组(分别为 1.25 ± 0.23 mm、1.20 ± 0.22 mm、1.14 ± 0.18 mm)相比,研究组三个水平的 dPTA 均明显较小(近端至远端分别为 1.05 ± 0.22 mm、0.99 ± 0.18 mm、0.98 ± 0.31 mm)(P P = .001)。预测 OLT 发生的平均 dPTA(所有 3 个水平)临界值为 1.1 毫米,灵敏度为 74%,特异度为 75%。在 OLT 面积和动脉直径之间观察到了明显的反相关性(P 结论:OLT 面积越大,动脉直径越小:管腔较小的 dPTA 和 dSTA 似乎与较高的 OLT 发生率有关,缺损大小与动脉直径成反比。
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Association of Extraosseous Arterial Diameter With Talar Dome Osteochondral Lesions.

Background: Etiology of osteochondral lesions of the talus (OLT) is multifactorial and may develop from trauma, genetics, or hypovascularity. The talar dome is supplied by the posterior tibial artery (PTA) and, to a lesser degree, the sinus tarsi artery (STA). The role of talar dome hypovascularity on OLT remains poorly studied. We aimed to determine any relationship between the diameter of PTA (dPTA) and STA (dSTA) and the incidence and characteristics of talus OLT.

Methods: This retrospective study included 77 patients with OLT and 77 subjects as a matched control group (age range: 30-40 years). Using magnetic resonance imaging, the dPTA was measured 1 cm above the tibial plafond, at the plafond, and at the level of medial malleolar tip. Likewise, dSTA was measured at the level of the talar neck. The area, volume, depth, localization, and surgical intervention for OLT were recorded as well.

Results: The study group had significantly smaller dPTA at all 3 levels (1.05 ± 0.22 mm, 0.99 ± 0.18 mm, 0.98 ± 0.31 mm, proximal to distal, respectively) compared with controls (1.25 ± 0.23 mm, 1.20 ± 0.22 mm, 1.14 ± 0.18 mm, respectively) (P < .001). The dSTA was also significantly smaller in the study group compared with the control group (0.5 ± 0.11 mm vs 0.57 ± 0.08 mm, respectively; P = .001). The mean dPTA (of all 3 levels) cutoff value for predicting the occurrence of OLT was 1.1 mm with 74% sensitivity and 75% specificity. A significant inverse correlation was observed between OLT area and arterial diameters (P < .001).

Conclusion: Smaller luminal dPTA and dSTA appear to be associated with higher incidence of OLT, with defect size inversely correlated to arterial diameter.

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