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Orthopaedic Proceedings
Vol. 94-B, Issue SUPP_XXXVII | Pages 123 - 123
1 Sep 2012
Dhollander A Verdonk P Verdonk R Verbruggen G Almqvist K
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Aim

The present study was designed to evaluate the implantation of alginate beads containing human mature allogenic chondrocytes for the treatment of symptomatic cartilage defects in the knee.

Methods

A biodegradable, alginate-based biocompatible scaffold containing human mature allogenic chondrocytes was used for the treatment of chondral and osteochondral lesions in the knee. Twenty-one patients were clinically prospectively evaluated with use of the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and a Visual Analogue Scale (VAS) for pain preoperatively and at 3, 6, 9, 12, 24 and 36 months of follow-up.


Orthopaedic Proceedings
Vol. 94-B, Issue SUPP_IX | Pages 47 - 47
1 Mar 2012
Almqvist K Vanlauwe J Saris D Victor J Verdonk P Bellemans J Verdonk R
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Introduction

Autologous chondrocyte implantation presents a viable alternative to microfracture in the repair of damaged articular cartilage of the knee; however, outcomes for patellar lesions have been less encouraging. ChondroCelect (CC) is an innovative, advanced cell therapy product consisting of autologous cartilage cells expanded ex vivo through a highly controlled and consistent manufacturing process.

Purpose

To assess the effect of CC in the treatment of patellofemoral lesions, for which standard treatment options had failed and/or no other treatment options were considered feasible.


Orthopaedic Proceedings
Vol. 93-B, Issue SUPP_III | Pages 292 - 292
1 Jul 2011
Almqvist K Saris D Vanlauwe J Victor J Luyten F
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Purpose: Long-term follow-up was to determine clinical benefit of ChondroCelect (CC) in the repair of full-thickness femoral cartilage lesions as compared to microfracture (MF).

Methods: In a randomized controlled clinical trial CC (n=57) was compared to MF (n=61) in patients aged 18 to 50 years with single ICRS grade III/IV symptomatic cartilage defects of the femoral condyles. Clinical improvement was measured up to 36 months using the KOOS (Knee injury and Osteoarthritis Outcome Score). Safety was monitored throughout the study.

Results: At baseline, KOOS was comparable between treatment groups (Mean ± SD: CC, 56.30 ± 13.61 and MF, 59.53 ± 14.95). Improvement from baseline in adjusted mean ± SE for the Overall KOOS was 21.25 ± 3.60 for the CC group vs. 15.83 ± 3.48 for the MF group at 36 months. When using the mixed linear model analysis at 36 months, statistically significantly greater improvements were demonstrated in the CC group vs. the MF group in change from baseline for the overall KOOS (D 7.60%, P = 0.018), as well as in 4 of 5 KOOS domains (activities of daily living, pain, symptoms/stiffness, and quality of life). Percentages of treatment responders were 83% (n = 34/41) vs. 62% (n = 31/50) based on the KOOS for CC and MF groups, respectively. Two (3.9%) patients in the CC group and 7 (11.5%) patients in the MF group underwent a re-intervention and were therefore considered treatment failures. Both treatments were well tolerated and the proportion of patients reporting AEs diminished over time, indicating stabilization of the patients’ condition.

Conclusions: Implantation of ChondroCelect in the treatment of articular cartilage defects of the femoral condyles shows superior clinical benefit at 36 months vs. microfracture. Structural superiority in favour of the ChondroCelect group was previously demonstrated at 1 year follow up.


Orthopaedic Proceedings
Vol. 86-B, Issue SUPP_III | Pages 308 - 308
1 Mar 2004
Dominique C Vorlat P Byn P Almqvist K Verdonk R
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Aims: To assess the results of the Oxford unicompartmental knee prosthesis, and compare these with other prostheses. Methods: Ninety-seven prostheses (87 medial; 10 lateral) in 86 patients were evaluated with the HSS (Hospital for Special Surgery) score after 2–14 years (mean follow-up: 6 yrs-9 mos). Results: Five prostheses were lost to follow-up. Eight patients died after a mean of 7 years, none of them had undergone a revision. Fourteen revisions (of which 1 bilateral unicompartmental knee prosthesis), 11 medial and 3 lateral, were performed. The mean HSS-score of the 69 UKPñs is 178.8 (80% excellent, 10% good, 4% fair, 6% poor). Conclusions: With proper patient selection (i.e. degenerative medial unicompartmental arthritis, good range of motion, sedentary occupation and with a light body weight) and a consistent operating technique, the results are good. It is the þrst-choice prosthesis for the relatively young patient (with regard to later revisions). Since we also obtain good results in the elderly, it seems a good choice of treatment in this group.