Treatment of AVN using the induction chamber technique and a biological-based approach: Indications and clinical results

被引:31
作者
Calori, G. M. [1 ]
Mazza, E. [1 ]
Colombo, M. [1 ]
Mazzola, S. [1 ]
Mineo, G. V. [2 ]
Giannoudis, P. V. [3 ]
机构
[1] Univ Milan, Orthopaed Inst Gaetano Pini, Orthopaed Reparat Surg Dept, I-20122 Milan, Italy
[2] Univ Milan, Orthopaed Inst Gaetano Pini, Univ Dept Orthopaed, I-20122 Milan, Italy
[3] Univ Leeds, Sch Med, Acad Dept Trauma & Orthopaed, Leeds LS2 9JT, W Yorkshire, England
来源
INJURY-INTERNATIONAL JOURNAL OF THE CARE OF THE INJURED | 2014年 / 45卷 / 02期
关键词
Avascular necrosis; AVN; Mesenchymal stem cells; Core decompression; rhBMP; Osteonecrosis; Femoral head; Early stage; Autologous implantation; Biological chamber; FEMORAL-HEAD; BONE-MARROW; NON-UNIONS; AVASCULAR NECROSIS; CORE DECOMPRESSION; PROXIMAL FEMUR; HIP-ARTHROPLASTY; STEM-CELL; OSTEONECROSIS; IMPLANTATION;
D O I
10.1016/j.injury.2013.09.014
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objective: To determine the efficacy of core decompression (CD) technique combined with recombinant morphogenetic proteins, autologous mesenchymal stem cells (MSCs) and xenograft bone substitute into the necrotic lesion of the femoral head on clinical symptoms and on the progression of osteonecrosis of the femoral head. Patients and methods: A total of 38 patients (40 hips) with early stage osteonecrosis of the femoral head were studied over a 4-year period. Results: CD technique combined with recombinant morphogenetic proteins, autologous MSCs and xenograft bone substitute was associated with a significant reduction in both pain and joint symptoms and reduced the incidence of fractural stages. At 36 months, 33 patients achieved clinical and radiographic healing. Conclusion: This long-term follow-up study confirmed that CD technique combined with recombinant morphogenetic proteins, autologous MSCs and xenograft bone substitute may be an effective treatment for patients with early stage osteonecrosis of the femoral head. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:369 / 373
页数:5
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