Arthroscopic matrix-associated, injectable autologous chondrocyte transplantation of the hip: significant improvement in patient-related outcome and good transplant quality in MRI assessment

被引:15
|
作者
Bretschneider, Henriette [1 ]
Trattnig, Siegfried [2 ,3 ]
Landgraeber, Stefan [4 ]
Hartmann, Albrecht [1 ]
Guenther, Klaus-Peter [1 ]
Dienst, Michael [5 ]
Schroeder, Joerg [6 ]
Fickert, Stefan [7 ,8 ]
机构
[1] Tech Univ Dresden, Univ Ctr Orthopaed & Trauma Surg, Univ Hosp Carl Gustav Carus, Fetscherstr 74,Bldg 29, D-01307 Dresden, Germany
[2] Med Univ Vienna, High Field MR Ctr, Dept Biomed Imaging & Image Guided Therapy, Vienna, Austria
[3] Christian Doppler Lab Clin Mol MR Imaging, Vienna, Austria
[4] Univ Duisburg Essen, Dept Orthopaed & Trauma Surg, Essen, Germany
[5] OCM Clin GmbH, Orthoped Surg Munchen, Munich, Germany
[6] Charite Univ Med Berlin, Ctr Musculoskeletal Surg, Campus Virchow Klinikum, Berlin, Germany
[7] Heidelberg Univ, Univ Med Ctr Mannheim, Med Fac Mannheim, Mannheim, Germany
[8] Sporthopaedicum Straubing Berlin Regensburg, Straubing, Germany
关键词
Hip arthroscopy; Matrix-associated autologous chondrocyte transplantation; MACT; Cartilage defect; CARTILAGE DEFECTS; CHONDRAL DEFECTS; FEMOROACETABULAR IMPINGEMENT; HIGH-RESOLUTION; OSTEOARTHRITIS; COMPLICATIONS; HYDROGEL; REPAIR; RISK;
D O I
10.1007/s00167-019-05466-7
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
Purpose Acetabular chondral lesions are common in patients with FAI. For large full-thickness cartilage defects, arthroscopic matrix-associated autologous chondrocyte transplantation (MACT) using an injectable in situ crosslinking product is an option. Aim of the study was to evaluate clinical and MRI results 12 months after MACT of acetabular cartilage defects in FAI patients. Methods We report data on 21 patients with a focal cartilage defect of the hip [2.97 +/- 1.44 cm(2) (mean +/- SD)] caused by FAI treated with an arthroscopically conducted MACT combined with FAI surgery. The results were assessed with patient-reported outcome measures (iHOT33, EQ-5D) pre- as well as post-operatively and by MRI using MOCART scoring system 6 and 12 months post-operatively. Results The iHOT33 score improved from 52.9 +/- 21.14 (mean +/- SD) pre-operative to 81.08 +/- 22.04 (mean +/- SD; p = 0.0012) 12 months post-operatively. The lower the pre-operative iHOT33 score and the larger the defect size, the greater the observed improvement compared to pre-operative scores at 12 months. Patients showed a significant improvement in EQ-5D-5L index value (p = 0.0015) and EQ-5D VAS (p = 0.0006). MRI analysis after 12 months revealed a complete integration of the transplant in 16 of 20 patients. Conclusions Injectable MACT is a promising minimally invasive treatment option for full-thickness cartilage defects of the hip caused by FAI. A significant improvement in symptoms and function associated with an increase in quality of life was detected in patients treated with injectable MACT combined with FAI surgery. This is of considerable clinical relevance, since, in addition to the elimination of the mechanical cause, MACT allows the successful therapy of consequential cartilage damage.
引用
收藏
页码:1317 / 1324
页数:8
相关论文
共 2 条
  • [1] Arthroscopic matrix-associated, injectable autologous chondrocyte transplantation of the hip: significant improvement in patient-related outcome and good transplant quality in MRI assessment
    Henriette Bretschneider
    Siegfried Trattnig
    Stefan Landgraeber
    Albrecht Hartmann
    Klaus-Peter Günther
    Michael Dienst
    Jörg Schröder
    Stefan Fickert
    Knee Surgery, Sports Traumatology, Arthroscopy, 2020, 28 : 1317 - 1324
  • [2] Two-Year Results of Injectable Matrix-Associated Autologous Chondrocyte Transplantation in the Hip Joint: Significant Improvement in Clinical and Radiological Assessment
    Riedl, Moritz
    Bretschneider, Henriette
    Dienst, Michael
    Guenther, Klaus-Peter
    Landgraeber, Stefan
    Schroeder, Jorg
    Trattnig, Siegfried
    Fickert, Stefan
    JOURNAL OF CLINICAL MEDICINE, 2023, 12 (17)