The autologous chondrocyte implantation (ACI) technique described by Peterson, which we adopted in 1997, is not suitable for an arthroscopic application. Since November 2000 we have been moving towards a system based on a solid collagenic scaffold (MACI^®, Verigen) which allowed us to develop an entirely arthroscopic procedure applicable to all knee joint areas.

A total of 47 patients (mean age 31 years), accounting for a total of 52 focal, non-degenerative chondral defects with an average size of 4.7 cm² (range: 3.2 – 6.2 cm²), have been treated arthroscopically. All were mobilised on the first and discharged on the second day after surgery. Partial weight-bearing was introduced after 4 weeks and increased to the full extent after 8 weeks. They were clinically evaluated by Modified Cincinnati, IKDC and Visual Analogue Scale (VAS). In two cases, after specific informed consent, an arthroscopic second look was performed1 year after surgery. The regeneration was assessed macroscopically (ICRS Cartilage Repair Assessment score) and histologically (histomorphometry and immunochemistry).

We re-assessed the first 30 knee joints with a mean follow-up of 23 months (min 12, max 36). Cincinnati Scores improved from 2.8±1.14 (baseline Clinician) to 9.4±0.73, and from 2.5±0.90 (baseline Patient) to 9.7±0.50 at 3 years, respectively. IKDC and VAS results paralleled the Cincinnati scores. The two second- lookprocedures performed showed a regenerated tissue assessed as normal according to ICRS, a finding also supported by the histological evaluation.

The arthroscopic technique can be considered an established approach for second-generation ACI application, even in case of multiple lesions, and mainly for medial femoral condyle localisations. Our approach, based on traditional arthroscopic tools and procedures, can be easily performed by other adequately trained surgeons, thanks to the optimal mechanical properties of the membrane, characterised by a high resistance to tears, also after prolonged exposure to the intra-articular perfusion fluids. From the surgical perspective, the procedure is easy and fast, also when compared to the open-ceiling techniques, and in particular for non-condylar localisations (patella, trochlea and tibial plate), with clinical and histological outcomes that seem comparable to those obtained with liquid-suspension systems.

Proximal juxta-articular leg fractures are often high-energy injuries, involving the tibial articular surface as well as diaphyseal segments. Young, active people are frequently affected, and optimal reduction, effective stabilization, early function and a rapid return to daily-life are the goals of treatment.

These fractures are, as well known, difficult to treat, because of the frequent articular involvement, fragment comminution and extension of the fracture rim: if not adequately treated, they might result in mal-union, non-union, articular stiffness and late arthrosis.

Mal-union, both angular and rotational, are, in many cases, very difficult lesions to treat, almost always requiring osteotomies, osteointegration and stable fixation: we present our experience in the treatment of these lesions, with the results obtained in 31 cases treated with a minimum of 1 year of follow-up. The same protocol was used in all patients: direct surgical approach to the lesion, removal of any implanted device, careful débridement of the mal-union site (mainly directed to complete interposed fibrous tissue removal), deformity correction, stable internal fixation and osteointegration, whenever necessary, by autologous or homologous bone. We evaluated all cases in terms of patient satisfaction, deformity correction, bone healing and functional recovery: one major complication occurred (nail failure); delayed skin healing was seen in three patients (one requiring re-operation), and one patient there was rupture of a distal locking screw. In conclusion, this method is effective in the treatment of these lesions.

The identification of different substances able to promote a cellular response in terms of proliferation and differentiation the so-called “morphogenetic proteins”, has expanded research, aiming to identify the cellular elements that produce these proteins, in order to find a source for clinical application.

Platelets have been identified as the main source of morphogenetic protein production: they can be separated in human blood samples and thus it is possible to create a concentration of these elements that, used both in bone as well as in soft tissues, promote a cellular response useful for tissue repair in terms of bone formation and soft tissue regeneration.

Our experience takes into account different fields of application of this new technology: revision surgery, non-union treatment and repair of soft tissue in 18 patients.

The same manufacturing process was utilized for all cases: ”Haemonetics” MCS”+ technology for apheresis, concentration of platelets and plasma/cryoprecipitate obtained, then mixed with autologous thrombin and calcium gluconate to obtain a gel. Usually, for bone surgery, platelet gel is mixed with an autologous iliac crest bone graft or, in some instances, with a homologous bone bank graft, usually morcelized chips.

For soft tissue applications, after surgical débridement, the gel is directly applied over the site and covered by a soft bandage. No adverse effects have been observed: good results, in terms of bone healing and soft tissue repair, were obtained in all cases.