Arthroscopic debridement and lavage |
Arthroscopic or minimally invasive |
Progressive deterioration Recurring symptoms |
Cost-effective |
Short rehabilitation time |
|
Microfracture or marrow stimulation |
Cost-effective Surgically reproducible |
Fibrocartilage formation |
Partial defect filling |
|
Functional deterioration after 18–24 months4
|
Osteochondral autograft transplantation and mosaicplasty |
Restoration of hyaline cartilage articulating surface Good chondrocyte survival rateGood clinical results at medium long-term follow-up5
|
Lack of cartilage integration |
Poor matching of graft and host cartilage congruency |
|
Donor site morbidity |
Limited tissue availability |
|
Potential chondrocyte apoptosis during graft impaction6,7
|
Osteochondral allograft transplantation |
Restoration of hyaline cartilage articulating surface |
Potential immunological response and disease transmission |
Treatment of large defects |
Limited graft availability |
Good long-term clinical results and graft survival8
|
Potential chondrocyte apoptosis during graft impaction6,7
|
Autologous chondrocyte implantation (ACI) and matrix-assisted ACI (MACI) |
Arthroscopic or minimally invasivePotential for hyaline cartilage repair tissue Use of autologous cells |
Expensive |
Two-stage procedure |
|
Variable repair tissue type: hyaline like, fibrocartilage and mixed9
|
|
Limited defect filling and integration10
|