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用于骨软骨缺损修复的合成多相聚合物支架的计算机断层扫描评估。

A computed tomography scan assessment of synthetic multiphase polymer scaffolds used for osteochondral defect repair.

机构信息

Plano Orthopedic Sports Medicine and Spine Center, Plano, Texas, USA.

出版信息

Arthroscopy. 2011 Jan;27(1):60-4. doi: 10.1016/j.arthro.2010.06.023. Epub 2010 Oct 16.

DOI:10.1016/j.arthro.2010.06.023
PMID:20952149
Abstract

PURPOSE

To evaluate the radiographic response of a synthetic multiphase implant at various intervals after implantation and assess the nature of bone ingrowth into the implant location.

METHODS

Patients undergoing autologous osteochondral transplantation for full-thickness condylar defects with the donor sites filled by use of a synthetic implant were evaluated by computed tomography (CT) scan for the density at both donor and recipient sites. Hounsfield unit (HU) readings were obtained at the synthetic implant, transplanted autograft plug, soft-tissue, cancellous bone, and cortical bone sites. The implant site material was graded by an established ossification quality score (range, 1 to 4).

RESULTS

Nine patients underwent CT scans at intervals ranging from 2 to 63 months after surgery. This sequence of images tracked the potential development of bone ingrowth activity. Postoperative imaging confirmed complete autograft bone plug healing. The synthetic implant site CT scans showed a drop in density from 84 HU at 4 months to 19 HU by 13 months (fibrous scar density). The ossification quality score for all synthetic implants was 1 (tract filled with soft-tissue density) instead of 4 (cancellous bone). The transplanted autograft plug densities were consistent with and completely incorporated into the adjacent cancellous bone.

CONCLUSIONS

The synthetic multiphase implant showed no evidence of bone ingrowth, osteoconductivity, or ossification. The implant density declined over time to that of fibrous scar. This synthetic plug does not provide subchondral structural support for any tissue that grows over it. This study does not support the use of this implant for the primary repair of articular cartilage lesions.

LEVEL OF EVIDENCE

Level IV, therapeutic case series.

摘要

目的

评估一种合成多相植入物在植入后不同时间的放射学反应,并评估骨向内生长到植入部位的性质。

方法

对接受自体软骨移植治疗全层髁状突缺损的患者进行 CT 扫描,评估供体和受区的密度。在合成植入物、移植自体移植物塞、软组织、松质骨和皮质骨部位获得亨氏单位 (HU) 读数。使用既定的成骨质量评分(范围 1 至 4)对植入部位材料进行分级。

结果

9 例患者在手术后 2 至 63 个月的时间间隔内进行了 CT 扫描。这些图像序列跟踪了骨向内生长活动的潜在发展。术后影像学检查证实了完整的自体移植物骨塞愈合。合成植入物部位 CT 扫描显示,密度从术后 4 个月的 84 HU 下降到 13 个月的 19 HU(纤维瘢痕密度)。所有合成植入物的成骨质量评分均为 1(填充有软组织密度的通道),而非 4(松质骨)。移植的自体移植物塞密度与相邻的松质骨一致,并完全融合。

结论

合成多相植入物没有显示出骨向内生长、骨引导或成骨的证据。植入物的密度随时间下降到纤维瘢痕的密度。这种合成塞子不能为生长在其上方的任何组织提供软骨下结构支撑。本研究不支持将这种植入物用于关节软骨损伤的主要修复。

证据水平

IV 级,治疗性病例系列。

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