Arthroscopy: The Journal of Arthroscopic & Related Surgery
Original ArticleA Computed Tomography Scan Assessment of Synthetic Multiphase Polymer Scaffolds Used for Osteochondral Defect Repair
Section snippets
Methods
A consecutive series of 20 patients who had undergone autologous osteochondral transplantation for isolated full-thickness defects on either the medial or lateral femoral condyle since 2004 were identified. Those in whom a synthetic multiphase implant (TruFit) was used to backfill the donor sites were contacted and invited to be part of this institutional review board–approved study.
Inclusion criteria were patients aged 18 to 60 years (mean, 40 years; range, 26 to 58 years) who had a prior
Results
In this study 9 patients (8 men and 1 woman) who had undergone osteochondral autograft transplantation with the donor sites filled by use of the TruFit device agreed to return for physical, radiographic, and CT scan evaluation at intervals ranging from 2 to 63 months after surgery. This sequence of studies documented the synthetic implant degradation over time (first endpoint) (Figs 1 and 2) and the potential development of bone ingrowth activity (second endpoint). The HU density scores for the
Discussion
The purpose of this study was to evaluate the radiographic and CT scan responses of the TruFit synthetic implant over time and to look for the presence of bone ingrowth. No bone ingrowth was found. This sequential CT scan evaluation showed a significant change in the multiphase synthetic implant site density from 79 to 84 HU at 2 to 4 months, dropping to 19 HU by 13 months. This density (19 HU) is consistent with fibrous scar (Table 1). The synthetic implant site density remained at the fibrous
Conclusions
The synthetic multiphase implant showed no evidence of bone ingrowth, osteoconductivity, or ossification. The synthetic 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 synthetic implant for the primary repair of articular cartilage lesions.
Acknowledgment
The authors thank Jennifer Heldreth for her assistance with this project.
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Supported by the F. Alan Barber, MD, FACS Research Fund. The authors report no conflict of interest.