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      BST-CarGel® Treatment Maintains Cartilage Repair Superiority over Microfracture at 5 Years in a Multicenter Randomized Controlled Trial

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          Abstract

          Objective

          The efficacy and safety of BST-CarGel®, a chitosan scaffold for cartilage repair was compared with microfracture alone at 1 year during a multicenter randomized controlled trial in the knee. This report was undertaken to investigate 5-year structural and clinical outcomes.

          Design

          The international randomized controlled trial enrolled 80 patients, aged 18 to 55 years, with grade III or IV focal lesions on the femoral condyles. Patients were randomized to receive BST-CarGel® treatment or microfracture alone, and followed standardized 12-week rehabilitation. Co-primary endpoints of repair tissue quantity and quality were evaluated by 3-dimensional MRI quantification of the degree of lesion filling (%) and T2 relaxation times. Secondary endpoints were clinical benefit measured with WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index) questionnaires and safety. General estimating equations were used for longitudinal statistical analysis of repeated measures.

          Results

          Blinded MRI analysis demonstrated that BST-CarGel®-treated patients showed a significantly greater treatment effect for lesion filling ( P = 0.017) over 5 years compared with microfracture alone. A significantly greater treatment effect for BST-CarGel® was also found for repair tissue T2 relaxation times ( P = 0.026), which were closer to native cartilage compared to the microfracture group. BST-CarGel® and microfracture groups showed highly significant improvement at 5 years from pretreatment baseline for each WOMAC subscale ( P < 0.0001), and there were no differences between the treatment groups. Safety was comparable for both groups.

          Conclusions

          BST-CarGel® was shown to be an effective mid-term cartilage repair treatment. At 5 years, BST-CarGel® treatment resulted in sustained and significantly superior repair tissue quantity and quality over microfracture alone. Clinical benefit following BST-CarGel® and microfracture treatment were highly significant over baseline levels.

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          Most cited references59

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          Chitosan chemistry and pharmaceutical perspectives.

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            SF-36 health survey update.

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              Novel injectable neutral solutions of chitosan form biodegradable gels in situ.

              A novel approach to provide, thermally sensitive neutral solutions based on chitosan/polyol salt combinations is described. These formulations possess a physiological pH and can be held liquid below room temperature for encapsulating living cells and therapeutic proteins; they form monolithic gels at body temperature. When injected in vivo the liquid formulations turn into gel implants in situ. This system was used successfully to deliver biologically active growth factors in vivo as well as an encapsulating matrix for living chondrocytes for tissue engineering applications. This study reports for the first time the use of polymer/polyol salt aqueous solutions as gelling systems, suggesting the discovery of a prototype for a new family of thermosetting gels highly compatible with biological compounds.
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                Author and article information

                Journal
                Cartilage
                Cartilage
                CAR
                spcar
                Cartilage
                SAGE Publications (Sage CA: Los Angeles, CA )
                1947-6035
                1947-6043
                April 2015
                April 2015
                : 6
                : 2
                : 62-72
                Affiliations
                [1 ]Piramal Healthcare (Canada) Ltd., Laval, Quebec, Canada
                [2 ]Department of Surgery, Dalhousie University, Halifax, Nova Scotia, Canada
                [3 ]Department of Orthopedic Surgery, University of British Columbia, Vancouver, British Columbia, Canada
                [4 ]School of Medicine, CEU San Pablo University, Madrid, Spain
                [5 ]University of Calgary Sports Medicine Centre, Calgary, Alberta, Canada
                [6 ]Department of Orthopedics, CHA-Pavillon Enfant-Jésus, Quebec, Quebec, Canada
                [7 ]Hôpital Charles LeMoyne, Greenfield Park, Quebec, Canada
                [8 ]Department of Epidemiology and Biostatistics, University of South Florida, Tampa, Florida, USA
                Author notes
                [*]Matthew S. Shive, 475 Armand-Frappier Blvd, Laval, Quebec, Canada H7V 4B3. Email: matthewshive1@ 123456gmail.com
                Article
                10.1177_1947603514562064
                10.1177/1947603514562064
                4462252
                26069709
                ea35d29f-bab8-4f2d-9d60-662e8276f3a6
                © The Author(s) 2014
                History
                Categories
                Article

                cartilage repair,chitosan,quantitative mri,microfracture,scaffold

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