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Failed joint unloading implant system in the treatment of medial knee osteoarthritis

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Failed joint unloading implant system in the treatment of medial knee osteoarthritis. / Citak, Mustafa; Kendoff, Daniel; O Loughlin, Padhraig F; Klatte, Till O; Gebauer, Matthias; Gehrke, Thorsten; Haasper, Carl.

In: ARCH ORTHOP TRAUM SU, Vol. 133, No. 11, 01.11.2013, p. 1575-8.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Citak, M, Kendoff, D, O Loughlin, PF, Klatte, TO, Gebauer, M, Gehrke, T & Haasper, C 2013, 'Failed joint unloading implant system in the treatment of medial knee osteoarthritis', ARCH ORTHOP TRAUM SU, vol. 133, no. 11, pp. 1575-8. https://doi.org/10.1007/s00402-013-1830-6

APA

Citak, M., Kendoff, D., O Loughlin, P. F., Klatte, T. O., Gebauer, M., Gehrke, T., & Haasper, C. (2013). Failed joint unloading implant system in the treatment of medial knee osteoarthritis. ARCH ORTHOP TRAUM SU, 133(11), 1575-8. https://doi.org/10.1007/s00402-013-1830-6

Vancouver

Citak M, Kendoff D, O Loughlin PF, Klatte TO, Gebauer M, Gehrke T et al. Failed joint unloading implant system in the treatment of medial knee osteoarthritis. ARCH ORTHOP TRAUM SU. 2013 Nov 1;133(11):1575-8. https://doi.org/10.1007/s00402-013-1830-6

Bibtex

@article{c0038f90ec5048f8982b649bc7f81590,
title = "Failed joint unloading implant system in the treatment of medial knee osteoarthritis",
abstract = "In the setting of end-stage osteoarthritis of the knee, total knee arthroplasty is the gold-standard treatment. Recently, a minimally invasive, joint preserving treatment option in the treatment of medial osteoarthritis of the knee has been developed. It is called the KineSpring({\textregistered}) (Moximed({\textregistered}) International GmbH, Zurich, Switzerland). The goal of this novel device is to reduce medial compartment loading without significantly affecting the loading of the lateral compartment. In this context, the current authors present a case of device failure using these new implants, which at 7 months post-op necessitated revision surgery with complete removal of the device.",
keywords = "Aged, Female, Humans, Orthopedic Procedures, Osteoarthritis, Knee, Prostheses and Implants, Prosthesis Design, Prosthesis Failure",
author = "Mustafa Citak and Daniel Kendoff and {O Loughlin}, {Padhraig F} and Klatte, {Till O} and Matthias Gebauer and Thorsten Gehrke and Carl Haasper",
year = "2013",
month = nov,
day = "1",
doi = "10.1007/s00402-013-1830-6",
language = "English",
volume = "133",
pages = "1575--8",
journal = "ARCH ORTHOP TRAUM SU",
issn = "0936-8051",
publisher = "Springer",
number = "11",

}

RIS

TY - JOUR

T1 - Failed joint unloading implant system in the treatment of medial knee osteoarthritis

AU - Citak, Mustafa

AU - Kendoff, Daniel

AU - O Loughlin, Padhraig F

AU - Klatte, Till O

AU - Gebauer, Matthias

AU - Gehrke, Thorsten

AU - Haasper, Carl

PY - 2013/11/1

Y1 - 2013/11/1

N2 - In the setting of end-stage osteoarthritis of the knee, total knee arthroplasty is the gold-standard treatment. Recently, a minimally invasive, joint preserving treatment option in the treatment of medial osteoarthritis of the knee has been developed. It is called the KineSpring(®) (Moximed(®) International GmbH, Zurich, Switzerland). The goal of this novel device is to reduce medial compartment loading without significantly affecting the loading of the lateral compartment. In this context, the current authors present a case of device failure using these new implants, which at 7 months post-op necessitated revision surgery with complete removal of the device.

AB - In the setting of end-stage osteoarthritis of the knee, total knee arthroplasty is the gold-standard treatment. Recently, a minimally invasive, joint preserving treatment option in the treatment of medial osteoarthritis of the knee has been developed. It is called the KineSpring(®) (Moximed(®) International GmbH, Zurich, Switzerland). The goal of this novel device is to reduce medial compartment loading without significantly affecting the loading of the lateral compartment. In this context, the current authors present a case of device failure using these new implants, which at 7 months post-op necessitated revision surgery with complete removal of the device.

KW - Aged

KW - Female

KW - Humans

KW - Orthopedic Procedures

KW - Osteoarthritis, Knee

KW - Prostheses and Implants

KW - Prosthesis Design

KW - Prosthesis Failure

U2 - 10.1007/s00402-013-1830-6

DO - 10.1007/s00402-013-1830-6

M3 - SCORING: Journal article

C2 - 23912420

VL - 133

SP - 1575

EP - 1578

JO - ARCH ORTHOP TRAUM SU

JF - ARCH ORTHOP TRAUM SU

SN - 0936-8051

IS - 11

ER -