Use of a cell-free collagen type-I matrix for the - Arthro
Transcription
Use of a cell-free collagen type-I matrix for the - Arthro
Klinik für Orthopädie und Rheumatologie Direktorin: Univ.-Prof. Dr. Susanne Fuchs-Winkelmann Universitätsklinikum Gießen und Marburg, Standort Marburg 62nd Annual Meeting of the Association of South German orthopedic surgeons e.V. Use of a cell-free collagen type-I matrix for the therapy of larger cartilage defects of knee joints Schüttler KF, Pfister B, Struewer J, Roessler PP, FuchsWinkelmann S, Efe T Cartilage Lesions Cartilage lesions of the knee joint are are often • 43% of all arthroskopies (Figueroa D, 2007 Arthroscopy) • 61% of all arthroskopies (Hjelle K, 2002 Arthroscopy) • 66% of all arthroskopies (Aaron A, 2004 Am J Sport Med) Surgical Options Stimulation Repair 1. Generation Regeneration 2..Generation Stimulation 2.and. 3..Generation Regeneration Mikrofrakture, Pridie-Drilling, Abrasion OsteochondralImplantation (OATS) Autologeous Chondrocyte Implantation (ACI) Autologeous Matrix-Induced Chondrogenesis (AMIC) Collagen-covered ACI (C-ACI), 2nd Generation fibrocartilage donor defect Next Generation?: Cell-free implants CaReS-1S®; GelrinC® Matrix-Induced ACI (MACI) 3rd Generation two-stage, periosteal hypertrophy fibrocartilage, Osseous hypertrophy Two-stage Decision on the defect size MACI AMIC Method Cell-free Implants OATS Microfracture 0cm2 1cm2 2cm2 3cm2 4cm2 5cm2 6cm2 7cm2 8cm2 Defect Size Matrix • • • • Cell-free collagen type-I matrix 4,8mg/ml collagen type-I, in PBS stired at 2-25°C CaReS-1S®, ArthroKinetics, Austria Previously been used successfully as a matrix within the MACT (CaReS) (Andereya S, 2006 Z Orthop Ihre Grenzgeb.) Cell-free – which defect size is possible? ? ? Cartilage Cartilage Cell-free matrix ? ? Bone ? ? Morales TI, 2007 Osteoarthritis Cartilage Prospective case series – Implantation of the matrix after previous ASK using a mini-arthrotomy – 22 patients treated with a collagen type-I matrix (6 female; 16 male; average age: 32 years) Clinical examination after 3, 6, 12 months – Clinical evaluation by SF-36 and IKDC score (SF-36: Tarlov AR, 1989 JAMA; IKDC: Irrgang JJ, 2001 Am J Sports Med) Radiological examination after 6, 12 months – Evaluation of the regenerated tissue by MRI (MOCART score; Marlovits S, 2006 Eur J Radiol) Inclusion criteria • Inclusion criteria: – preserved cartilage shoulder – corresponding intact articular surface (no „kissing-lesions“) – intact menisci and ligaments – physiological leg axis – free ROM – Defects acc. to ICRS: grade III and IV Patients • Mean defect size: 4,33cm2 (2cm2 - 6,25cm2) • Defect localization: – 19x femoral condyle; 3x patellofemoral • solitary defects • 15x caused by trauma, 5x OD, 2x idiopathic • all patients were followed up • no perioperative complications Results I • subjective satisfaction: – 80% (18/22 patients) „good“ und „excellent“ SF-‐‑36 mentally 70 * 60 * SF-‐‑36 physically * 50 * 50 * * 40 40 30 30 20 20 10 10 0 60 präoperativ 3 Monate 6 Monate 12 Monate 0 * p < 0,05 präoperativ 3 Monate 6 Monate 12 Monate Results II IKDC 70 * 60 * 50 40 30 20 10 0 präoperativ 3 Monate 6 Monate 12 Monate Results III • MOCART score: – 6 months postoperative 52 / 100 – 12 months postoperative 59 / 100 • Complete filling of the defects in 20 of 22 patients • 1 patient with incomplete integration to border zone • 1 patient with incomplete filling of the defect (hypothroph) • No evidence of infection, synovitis Limitations of the study • no control group • current follow-up until 1 year • small collective • Where are the cells derived from? Summary • The implantation of a cell-free collagen type I matrix results in good to very good results 12 months postoperatively • Also defects of a size up to 6.25 cm2 can be successfully treated with cell-free implants