Polyurethane scaffold in lateral meniscus segmental defects: Clinical outcomes at 24 months follow-up

被引:50
作者
Bouyarmane, H. [1 ,2 ]
Beaufils, P. [1 ]
Pujol, N. [1 ]
Bellemans, J. [3 ]
Roberts, S. [4 ]
Spalding, T. [5 ]
Zaffagnini, S. [6 ]
Marcacci, M. [6 ]
Verdonk, P. [7 ]
Womack, M. [8 ]
Verdonk, R. [9 ]
机构
[1] Univ Versailles St Quentin, Ctr Hosp Versailles, Serv Orthopedie Traumatol, F-78150 Le Chesnay, France
[2] Orthopaed Surg Ctr, Casablanca 20060, Morocco
[3] Catholic Univ Hosp, Langdorp, Belgium
[4] Orthoped Hosp, Oswestry, Shrops, England
[5] Univ Hosp, Coventry, W Midlands, England
[6] Ist Ortoped Rizzoli, Bologna, Italy
[7] Antwerpen Orthopaed Ctr, Antwerp, Belgium
[8] Orteq Sports Med, London, England
[9] Univ Ghent, B-9000 Ghent, Belgium
关键词
Lateral meniscus; Meniscectomy; Scaffold; Arthroscopy; Knee; PARTIAL MENISCECTOMY; REPAIR; IMPLANT; ARROWS; FIX;
D O I
10.1016/j.otsr.2013.10.011
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: Segmental tissue loss in the lateral meniscus is associated with pain and increased risk of osteoarthritis even when indications have been carefully considered. Hypothesis: Repairing the defect using a novel biodegradable scaffold will reduce pain and restore the knee function. Methods: In this prospective multicenter study, a total of 54 patients (37 males/17 females; mean age: 28 years [16-50]) were enrolled. All patients presented with postmeniscectomy syndrome and segmental lateral meniscus loss, and were treated with a polyurethane biodegradable scaffold (Actifit (R), Orteq) implanted arthroscopically. Clinical outcomes were assessed at 6, 12 and 24 months using Visual Analogue Scale (VAS), International Knee Documentation Committee Score (IKDC) and Knee Injury and Osteoarthritis Outcome Score (KOOS). Results: VAS decreased from 5.5 at baseline to 3.6 at 6 months, 3.4 at 12 months and 2.9 at 24 months. IKDC improved from 47.0 at baseline to 60.2, 67.0 and 67.0 at 6, 12 and 24 months. All KOOS subscores improved between baseline and 24 months. Discussion: Clinical results of this study demonstrate clinically and statistically significant improvements of pain and function scores (VAS, IKDC, and all KOOS subscales except sport), at the 6 months follow-up and on all clinical outcomes at the 2-year follow-up. The Actifit (R) scaffold is safe and effective in treating lateral meniscus defects. (C) 2013 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:153 / 157
页数:5
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