Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where J.C. Reichert is active.

Publication


Featured researches published by J.C. Reichert.


American Journal of Sports Medicine | 2011

A Prospective Multicenter Study on the Outcome of Type I Collagen Hydrogel–Based Autologous Chondrocyte Implantation (CaReS) for the Repair of Articular Cartilage Defects in the Knee

U. Schneider; Lars Rackwitz; Stefan Andereya; Sebastian Siebenlist; Florian Fensky; J.C. Reichert; Ingo Löer; Thomas Barthel; Maximilian Rudert; Ulrich Nöth

Background: The Cartilage Regeneration System (CaReS) is a novel matrix-associated autologous chondrocyte implantation (ACI) technique for the treatment of chondral and osteochondral lesions (Outerbridge grades III and IV). For this technology, no expansion of the chondrocytes in a monolayer culture is needed, and a homogeneous cell distribution within the gel is guaranteed. Purpose: To report a prospective multicenter study of matrix-associated ACI of the knee using a new type I collagen hydrogel (CaReS). Study Design: Case series; Level of evidence, 4. Methods: From 2003 to 2008, 116 patients (49 women and 67 men; mean age, 32.5 ± 8.9 years) had CaReS implantation of the knee in 9 different centers. On the basis of the International Cartilage Repair Society (ICRS) Cartilage Injury Evaluation Package 2000, the International Knee Documentation Committee (IKDC) score, pain score (visual analog scale [VAS]), SF-36 score, overall treatment satisfaction and the IKDC functional status were evaluated. Patient follow-up was performed at 3, 6, and 12 months after surgery and annually thereafter. Mean follow-up was 30.2 ± 17.4 months (range, 12-60 months). There were 67 defects of the medial condyle, 14 of the lateral, 22 of the patella/trochlea, and 3 of the tibial plateau, and 10 patients had 2 lesions. The mean defect size was 5.4 ± 2.4 cm2. Thirty percent of the defects were <4 cm2 and 70% were >4 cm2. Results: The IKDC score improved significantly from 42.4 ± 13.8 preoperatively to 70.5 ± 18.7 (P < .001) at latest follow-up. Global pain level significantly decreased (P < .001) from 6.7 ± 2.2 preoperatively to 3.2 ± 3.1 at latest follow-up. There also was a significant increase of both components of the SF-36 score. The overall treatment satisfaction was judged as very good or good in 88% by the surgeon and 80% by the patient. The IKDC functional knee status was grade I in 23.4%, II in 56.3%, III in 17.2%, and IV in 3.1% of the patients. Conclusion: Matrix-associated ACI employing the CaReS technology for the treatment of chondral or osteochondral defects of the knee is a safe and clinically effective treatment that yields significant functional improvement and improvement in pain level. However, further investigation is necessary to determine the long-term viability and clinical outcome of this procedure.


Orthopade | 2012

Bone tissue engineering. Reconstruction of critical sized segmental bone defects in the ovine tibia

J.C. Reichert; Devakara R. Epari; Martin E. Wullschleger; Arne Berner; Siamak Saifzadeh; Ulrich Nöth; Ian C. Dickinson; Michael Schuetz; Dietmar W. Hutmacher

Well-established therapies for bone defects are restricted to bone grafts which face significant disadvantages (limited availability, donor site morbidity, insufficient integration). Therefore, the objective was to develop an alternative approach investigating the regenerative potential of medical grade polycaprolactone-tricalcium phosphate (mPCL-TCP) and silk-hydroxyapatite (silk-HA) scaffolds.Critical sized ovine tibial defects were created and stabilized. Defects were left untreated, reconstructed with autologous bone grafts (ABG) and mPCL-TCP or silk-HA scaffolds. Animals were observed for 12 weeks. X-ray analysis, torsion testing and quantitative computed tomography (CT) analyses were performed. Radiological analysis confirmed the critical nature of the defects. Full defect bridging occurred in the autograft and partial bridging in the mPCL-TCP group. Only little bone formation was observed with silk-HA scaffolds. Biomechanical testing revealed a higher torsional moment/stiffness (p < 0.05) and CT analysis a significantly higher amount of bone formation for the ABG group when compared to the silk-HA group. No significant difference was determined between the ABG and mPCL-TCP groups. The results of this study suggest that mPCL-TCP scaffolds combined can serve as an alternative to autologous bone grafting in long bone defect regeneration. The combination of mPCL-TCP with osteogenic cells or growth factors represents an attractive means to further enhance bone formation.


Orthopade | 2012

Knochen-Tissue-Engineering@@@Bone tissue engineering: Rekonstruktion segmentaler Knochendefekte kritischer Größe in der Schafstibia@@@Reconstruction of critical sized segmental bone defects in the ovine tibia

J.C. Reichert; Devakar Epari; Martin E. Wullschleger; Arne Berner; Siamak Saifzadeh; Ulrich Nöth; Ian C. Dickinson; Michael Schuetz; Dietmar W. Hutmacher

Well-established therapies for bone defects are restricted to bone grafts which face significant disadvantages (limited availability, donor site morbidity, insufficient integration). Therefore, the objective was to develop an alternative approach investigating the regenerative potential of medical grade polycaprolactone-tricalcium phosphate (mPCL-TCP) and silk-hydroxyapatite (silk-HA) scaffolds.Critical sized ovine tibial defects were created and stabilized. Defects were left untreated, reconstructed with autologous bone grafts (ABG) and mPCL-TCP or silk-HA scaffolds. Animals were observed for 12 weeks. X-ray analysis, torsion testing and quantitative computed tomography (CT) analyses were performed. Radiological analysis confirmed the critical nature of the defects. Full defect bridging occurred in the autograft and partial bridging in the mPCL-TCP group. Only little bone formation was observed with silk-HA scaffolds. Biomechanical testing revealed a higher torsional moment/stiffness (p < 0.05) and CT analysis a significantly higher amount of bone formation for the ABG group when compared to the silk-HA group. No significant difference was determined between the ABG and mPCL-TCP groups. The results of this study suggest that mPCL-TCP scaffolds combined can serve as an alternative to autologous bone grafting in long bone defect regeneration. The combination of mPCL-TCP with osteogenic cells or growth factors represents an attractive means to further enhance bone formation.


Advanced Drug Delivery Reviews | 2013

How smart do biomaterials need to be? A translational science and clinical point of view

Boris Michael Holzapfel; J.C. Reichert; Jan-Thorsten Schantz; Uwe Gbureck; Lars Rackwitz; Ulrich Nöth; Franz Jakob; Maximilian Rudert; Jürgen Groll; Dietmar W. Hutmacher


Institute of Health and Biomedical Innovation; Science & Engineering Faculty | 2013

Autologous vs. allogenic mesenchymal progenitor cells for the reconstruction of critical-sized segmental tibial bone defects in aged sheep

Arne Berner; J.C. Reichert; Maria A. Woodruff; Siamak Saifzadeh; Anthony Morris; Devakar Epari; Michael Nerlich; Michael Schuetz; Dietmar W. Hutmacher


Orthopade | 2012

Reconstruction of osteochondral defects with a collagen I hydrogel. Results of a prospective multicenter study

L. Rackwitz; U. Schneider; S. Andereya; S. Siebenlist; J.C. Reichert; F. Fensky; J. Arnholdt; I. Löer; Grossstück R; W. Zinser; T. Barthel; Maximilian Rudert; Ulrich Nöth


Orthopade | 2012

Rekonstruktion von Gelenkknorpeldefekten mit einem Kollagen-I-Hydrogel

L. Rackwitz; U. Schneider; S. Andereya; S. Siebenlist; J.C. Reichert; F. Fensky; J. Arnhold; I. Löer; R. Großstück; W. Zinser; T. Barthel; Maximilian Rudert; Ulrich Nöth


Archive | 2012

Implants Containing BMP-7

J.C. Reichert; Dietmar W. Hutmacher


Orthopade | 2018

Zellbasierte und zukünftige Therapieansätze der Femurkopfnekrose

L. Rackwitz; J.C. Reichert; M. Haversath; Ulrich Nöth; Marcus Jäger


School of Biomedical Sciences; Faculty of Health; Institute of Health and Biomedical Innovation | 2017

A humanised tissue-engineered bone model allows species-specific breast cancer-related bone metastasis in vivo

Vmc Quent; Anna Taubenberger; J.C. Reichert; Laure Martine; Judith A. Clements; Dietmar W. Hutmacher; Daniela Loessner

Collaboration


Dive into the J.C. Reichert's collaboration.

Top Co-Authors

Avatar

Ulrich Nöth

University of Würzburg

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Dietmar W. Hutmacher

Queensland University of Technology

View shared research outputs
Top Co-Authors

Avatar

Arne Berner

Queensland University of Technology

View shared research outputs
Top Co-Authors

Avatar

Siamak Saifzadeh

Queensland University of Technology

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Ian C. Dickinson

Princess Alexandra Hospital

View shared research outputs
Top Co-Authors

Avatar

Martin E. Wullschleger

Queensland University of Technology

View shared research outputs
Top Co-Authors

Avatar

Michael Schuetz

Queensland University of Technology

View shared research outputs
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge