Aims: Surgical joint stabilisation can be achieved by capsular plication or thermal shrinkage. We hypothesised that there was no difference in mechanical and morphological properties after reduction of laxity in ligaments treated by either technique.

Methods: 30 skeletally mature female rabbits underwent either ‘thermal’ treatment, or ‘plication’ of their left medial collateral ligament (MCL). After 12 weeks convalescence, MCL complexes were procured from left and contralateral knees to undergo viscoelastic (creep) testing, quantitative transmission electron microscopy (TEM) and immunohistochemistry.

Results: Mean creep strain in both thermal (1.85 +/− 0.32%) and plicated ligaments (1.92 +/− 0.36%) was almost twice that of the control group (1.04 +/− 0.15%), although there was no difference between treatment modalities. However, collagen morphological parameters of all three groups were significantly different (p< 0.001). The thermal ligaments demonstrated predominantly small fibrils, whilst the plicated group displayed an intermediate distribution of heterogeneous fibrils (Fig. I). Immunohistochemistry followed by TEM revealed a random distribution of alpha-smooth muscle actin staining fibroblasts in both thermal and plicated groups.

Conclusion: Susceptibility to creep, and residual deformation after recovery, is similar after thermal shrinkage or plication, although inferior to intact ligaments. However, a different pattern of remodelling was revealed in the treatment groups. The plicated results suggest remodelling on a pre-existing fibrillar scaffold, yet the thermal group demonstrated histomorphometry similar to scar tissue, suggesting de novo synthesis. The absence of contractile myofibroblasts suggests that these cells may play an insignificant role in regulation of matrix tension during healing.

Surgical joint stabilisation can be achieved by ligamentous plication or thermal shrinkage, and as such, we hypothesized that there is no difference in mechanical and morphological properties after reduction of laxity in ligaments treated by either technique.

Methods: 30 mature female rabbits underwent either ‘thermal’ treatment of their left medial collateral ligament (MCL) using a bipolar radiofrequency probe, or plication with two 4/O non-absorbable sutures following division along its midsubstance and loaded positioning of the free ends. After 12 weeks convalescence, the animals were euthanised and MCL complexes were procured from left and contralateral knees to undergo viscoelastic (creep) testing, quantitative Transmission Electron Microscopy (TEM) and immunohistochemistry. The TEM data was quantified by two data procurement protocols; computational analysis and manual graticule.

Mean creep strain in both thermal (1.85 +/− 0.32%) and plicated ligaments (1.92+/−0.36%) was almost twice that of the control (1.04+/−0.15%), although there was no difference between treatment modalities. Similar findings were seen in the thermal (1.77+/−0.45%), plication (1.85+/−0.40%) and control groups (0.92+/−0.20%) for viscoplastic deformation. However, collagen morphological parameters of all three groups were significantly different (p< 0.001). The thermal ligaments demonstrated predominantly small fibrils, whilst the plicated group displayed an intermediate distribution of heterogenous fibrils. Immunohistochemistry followed by TEM revealed a sparse random distribution of alpha-smooth muscle actin staining fibroblasyts in both thermal and plicated groups. There was an insignificant difference in computational and manual procurement methods (p=0.84).

Susceptibility to creep, and residual deformation after recovery, is similar after thermal shrinkage or plication, although inferior to intact ligaments. However, the plicated results suggest remodeling on a pre-existing fibrillar scaffold, yet the thermal group demonstrated histomorphometry similar to scar tissue, suggesting de novo synthesis. The absence of contractile myofibroblasts suggests that these cells may have an insignificant role in regulation of matrix tension during healing.