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, Jahrgang 133, Nr. 11, 01.11.2013, S. 1575-8.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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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 -