Get Arthroplasty of the Spine PDF

By Robert Gunzburg, H. Michael Mayer, Marek Szpalski, Max Aebi

ISBN-10: 3540202951

ISBN-13: 9783540202950

ISBN-10: 3642185088

ISBN-13: 9783642185083

Joint alternative is a logical step within the therapy of serious joint pathologies with irreversible lesions resisting conservative treatment. on the spinal point, arthrodesis turned, very early, the ultimate of therapy for serious intervertebral disc pathologies. the following logical step used to be to examine sensible substitute, and this step used to be taken as early as 1956, whilst the 1st intervertebral implant was once defined. despite the fact that, it took many extra years and a superb number of proposed implant designs earlier than medical purposes should be attempted.

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As of late January 2002, 49 of the patients have been followed for I year and 10 patients have been followed for 2 years. Table 2 details the demographic variables of the patients. The duration of preoperative symptoms ranged from 3 weeks to more than 2 years. Reflexes on a four-point scale (right and left sides) Biceps Triceps Brachioradialis Knees Ankles Sensory function on a four-point scale (right and left sides) C4 dermatome C5 dermatome C6 dermatome C7 dermatome Operative technique Neck pain severity on a six-point scale Arm pain severity on a six-point scale Ability to function with respect to activities of daily living on a four-point scale (n=97) Several patients presented with multiple diagnoses and/or etiology a Age range Gender Clinical diagnosis a Primary etiologya Duration of symptoms Levels implanted Size implanted • Excellent: improvement in most (at least 80%) of the preoperative signs and symptoms, with little deterioration (not more than 10%) • Good: improvement in some (at least 70%) of the preoperative signs and symptoms, with some deterioration (not more than 15%) • Fair: improvement in half (at least 50%) of the preoperative signs and symptoms, with some deterioration (not more than 20%) • Poor: improvement in few (less than 50%) of the preoperative signs and symptoms, or significant deterioration (more than 20%) Radiographs were analyzed independently to determine ROM and assess device migration and/or subsidence.

LLC, New York Vincent E. Bryan Jr The clinical investigators involved in this study were: I Goffin, MD, PhD; A Casey, MD; P Kehr, MD; K Liebig, MD, PhD; B Lind, MD, PhD; C Logroscino; V Pointillart, MD, PhD; F Van Calenbergh, MD; and I van Loon, MD. The clinical data were gathered from the following sites: Universitaire Ziekenhuizen, Leuven, Belgium; the National Hospital for Neurology and Neurosurgery, London, UK; Centre de Traumatologie et d'Orthopedie, Illkirch, France; Orthopadische Abteilung des Waldkrankenhauses St.

When combined with extensive in vitro testing, the robust chimpanzee and goat study results collectively demonstrated device safety and supported the initiation of clinical trials during the first week of January 2000. The operative procedures represent the combined work of nine neuro- and orthopedic surgeons at seven centers in Europe. Study design Patients were concurrently enrolled in a multi-center evaluation of the prosthesis for the treatment of single-level DDD of the cervical spine. The prospective study was approved by the ethics committee and, as required, the regulatory agencies for each center.

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Arthroplasty of the Spine by Robert Gunzburg, H. Michael Mayer, Marek Szpalski, Max Aebi

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