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1.
Rofo ; 177(12): 1670-6, 2005 Dec.
Article in German | MEDLINE | ID: mdl-16333790

ABSTRACT

PURPOSE: Kyphoplasty and vertebroplasty offer two minimally invasive operative stabilization procedures for vertebral compression fractures. The purpose of this prospective study was to investigate whether both procedures are able to reduce pain and to preserve postoperative vertebral height during a 1-year follow up. MATERIALS AND METHODS: Osteoporotic vertebral fractures were treated in 42 cases, 20 patients (15 female, 5 male) underwent vertebroplasty, 22 patients (14 female, 8 male) underwent kyphoplasty. 32 vertebral fractures were treated with vertebroplasty and 35 vertebral fractures were treated with kyphoplasty. Symptomatic levels were identified by correlating the clinical presentation with conventional radiographs, CT or/and MRI. During the follow up reduction of pain was determined. Radiographic scans were performed pre- and postoperatively and after 3, 6 and 12 months. The vertebral height and endplate angles were measured to assess the restoration of the sagittal alignment. The effects on pain symptoms were measured on a self-reported Visual Analog Scale (VAS) and the Oswestry score was documented. RESULTS: The median pain scores (VAS) decreased significantly for kyphoplasty and vertebroplasty from pre- to post-treatment, as did the Oswestry score (p < 0.05). No significant differences could be found between both groups for the median pain score (VAS) and the Oswestry score. Kyphoplsty led to a significant restoration of the vertebral height and reduction of kyphosis (p < 0.05). During the 1-year follow up both operation techniques were able to stabilize the height of the vertebral body. CONCLUSION: Kyphoplasty and vertebroplasty are effective minimally invasive procedures for the stabilization of osteoporotic vertebral fractures leading to a statistically significant reduction in pain. Kyphoplasty restores significantly vertebral body height in fresh fractures. The restoration of vertebral height and reduction of kyphosis may have an influence on the long term clinical outcome. This has to be evaluated in a long term prospective study.


Subject(s)
Orthopedic Procedures , Osteoporosis/complications , Spinal Fractures/etiology , Spinal Fractures/therapy , Aged , Aged, 80 and over , Female , Follow-Up Studies , Fractures, Spontaneous , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Pain Measurement , Prospective Studies , Spinal Fractures/diagnostic imaging , Time Factors , Tomography, X-Ray Computed
2.
Chirurg ; 75(7): 694-701, 2004 Jul.
Article in German | MEDLINE | ID: mdl-15258751

ABSTRACT

INTRODUCTION: Due to a recent increase in the commercial availability of expandable cages for vertebral body replacement, this study was designed to gain more information about their biomechanical properties. All three expandable cages evaluated in this study are approved for clinical use, but little knowledge about their biomechanical properties exists. MATERIAL AND METHODS: Human thoracolumbar spines (T11 to L3) ( n=32) were tested in flexion, extension, axial rotation, and lateral bending with a nondestructive stiffness method. Three-dimensional displacement was measured using an optical measurement system. All motion segments were tested intact. After L1 corporectomy, cages were implanted and the following groups ( n=8 each) were tested: (1) meshed titanium cage (nonexpandable cage, DePuy Acromed), (2) X-tenz (expandable cage, DePuy Acromed), (3) Synex (expandable Cage, Synthes), and (4) VBR (expandable cage, Ulrich). Finally, posterior stabilization and posterior-anterior stabilization, both using USS (Synthes), and anterior plating (LCDCP, Synthes) was applied. The mean apparent stiffness values, ranges of motion, and neutral and elastic zones were calculated from the corresponding load/displacement curves. RESULTS: No significant differences were found between the in vitro biomechanical properties of expandable and nonexpandable cages. Compared to the intact motion segment, isolated anterior stabilization using cages and anterior plating significantly decreased stiffness and increased range of motion in all directions. Additional posterior stabilization significantly increased stiffness and decreased range of motion in all directions compared to the intact motion segment. Combined anterior-posterior stabilization demonstrated the greatest stiffness results. CONCLUSION: Design variations of expandable cages for vertebral body replacement do not show any significant effect on the biomechanical results. There was no significant difference found, between the biomechanical properties of expandable and non-expandable cages. After corporectomy, isolated implantation of expandable cages plus anterior plating was not able to restore normal stability of the motion segment. As a consequence, isolated anterior stabilization using cages plus LCDCP should not be used for vertebral body replacement in the thoraco-lumbar spine.


Subject(s)
Equipment Failure Analysis , Lumbar Vertebrae/surgery , Prosthesis Implantation , Spinal Fusion/instrumentation , Thoracic Vertebrae/surgery , Biomechanical Phenomena , Equipment Design , Humans , Prosthesis Design
3.
Acta Chir Orthop Traumatol Cech ; 69(1): 16-21, 2002.
Article in English | MEDLINE | ID: mdl-11951564

ABSTRACT

PURPOSE OF THE STUDY: The purpose of the study was the examination of the osseous integration of hydroxyapatite grafts used for the filling of metaphyseal bone defects in tibia head fractures. MATERIAL: Four patients with lateral tibia plateau fractures AO-type B3 (12) were included in the study. Patients were treated by arthroscopically assisted reduction and percutaneous screw fixation. The metaphyseal bone defects were filled with prepared solid hydroxyapatite graft blocks (Endobon Fa. Merk Darmstadt, Germany). In all of the patients a CT study for the osseous integration of hydroxyapatite grafts used for the filling of metaphyseal bone defects in tibial head fractures was performed. Measurements of density were performed of the implant region, the periimplant region, the distant periimplant region and the fibula bone. Follow-up CT examinations of these specific regions were performed 6 and 12 months postoperative. RESULTS: In all cases an increase of density of the hydroxyapatite graft after 6 months and 12 months follow-up was detected. The periimplant region showed in all cases a decrease of density. A progressive decrease of the periimplant and the distant cancellous tibial bone region was also detectable after 6 and 12 months post-op. A similar decrease of density was visible in the region of the cancellous bone of the fibula. In the interface region a direct bone formation between the hydroxyapatite graft and the adjected cancellous bone was visible in all cases during follow-up. CONCLUSION: The increase of density of the hydroxyapatite grafts and the direct bone formation in the interface region between the hydroxyapatite graft and the adjacent cancellous bone are clear radiomorphological signs for an osteointegration of hydroxyapatite grafts in the metaphyseal region.


Subject(s)
Bone Substitutes , Durapatite , Osseointegration , Tibial Fractures/surgery , Tomography, X-Ray Computed , Adult , Arthroscopy , Female , Fracture Fixation, Internal , Humans , Male , Middle Aged , Tibial Fractures/diagnostic imaging
4.
J Neurosurg ; 95(1 Suppl): 80-7, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11453436

ABSTRACT

OBJECT: The placement of an anterior atlantoaxial plate after transoral odontoid resection has been described by Harms. Recently, the authors of biomechanical and clinical studies have shown that this procedure, especially in combination with posterior wiring, is a good alternative to established, isolated posterior atlantoaxial fixation techniques. Reports on the anatomy of the atlas and axis primarily focus on the posterior surgical approach. Scarce research regarding the quantitative anatomy of the anterior aspect of C-1 and C-2 has been reported. This study was undertaken to measure relevant dimensions of C-1 and C-2 and their relation to the anterior transoral approach. The aim of the study was to determine "safe zones" for screw placement in anterior atlantoaxial plate fixation. METHOD: Fifty human dry C-1 and C-2 vertebrae were obtained for direct anatomical, radiographic, and computerized tomography (CT) measurements. Thirty-two linear and four angular parameters were evaluated. All measurements were made using a digital caliper, ruler, or goniometer. Anatomical measurements were correlated with radiographic (anteroposterior, lateral, and craniocaudal) and CT (0.5-mm-slice thickness) measurements of the corresponding vertebrae. Additionally, bone mineral density (BMD) measurements of C-1 and C-2 were obtained in 20 patients. A safe zone for anterior screw placement in an atlas of bilateral trapezoid shape could be characterized. The average medial and lateral height of the trapezoid was 4.1 +/- 1.01 mm (range 1.4-6.7 mm) and 12.9 +/- 1.73 mm (range 8.7-17.4 mm), respectively. The distance between the sagittal plane and the medial and lateral walls of the trapezoid was 10.2 +/- 1.42 mm (range 8.9-12.8 mm) and 23.5 +/- 2.98 mm (range 21.7-30.7 mm), respectively. The average depth of the lateral masses was 22.3 +/- 2.04 mm (range 17.0-26.7 mm) in the sagittal plane. The average BMD in the safe zone of C-1 was 0.89 +/- 0.11 g/cm3 (range 0.75-1.01 g/cm3). Bone mineral density measurements at C-2 revealed a spheroid zone of low density at the basis of the dens (0.68 +/- 0.09 g/cm3). In contrast, high zones of BMD were found near the articular surfaces (C1-2: 0.97 +/- 0.11 g/cm3; C2-3: 0.94 +/- 0.12 g/cm3). The safe zone for anterior axis screw placement was V-shaped, limited cranially by a zone of low bone density and laterally by the vertebral artery groove. Correlations between radiographic and anatomical measurements were generally good (r2 = 0.78-0.95), but they were higher between CT and anatomical measurements (r2 = 0.86-0.99). CONCLUSIONS: A quantitative understanding of the anterior anatomy of C-1 and C-2 is necessary when considering anterior atlantoaxial plate fixation after transoral odontoid resection. In this study the authors defined safe zones for anterior atlas and axis screw placement. The anterior atlantoaxial plate, as originally described by Harms, only partially respects these safe zones.


Subject(s)
Atlanto-Axial Joint/surgery , Spinal Fusion/instrumentation , Adult , Aged , Atlanto-Axial Joint/pathology , Bone Density/physiology , Female , Humans , Image Processing, Computer-Assisted , Male , Mathematical Computing , Middle Aged , Mouth/surgery , Odontoid Process/surgery , Tomography, X-Ray Computed
6.
Chirurg ; 72(11): 1298-302, 2001 Nov.
Article in German | MEDLINE | ID: mdl-11766654

ABSTRACT

INTRODUCTION: A case of a 22-year-old patient with a malunited dens fracture and secondary atlanto-axial instability is presented. The significant narrowing of the spinal canal due to the atlanto-axial instability was associated with anterior myelon compression and neurological deficit. METHODS: A transoral approach with odontoid resection and anterior atlanto-axial plate fixation was performed. With this technique the atlanto-axial subluxation was reduced and the myelon was decompressed. RESULTS: The postoperative course was uneventful. The follow-up showed a complete remission of the neurological deficit and a bony fusion of the atlanto-axial joints. CONCLUSIONS: The presented case illustrates the importance of an accurate initial diagnosis of the degree of instability and the need for short-term follow-up examinations. If atlanto-axial pseudarthrosis or malunion with anterior spinal cord compression occurs, a transoral procedure with odontoid resection and atlanto-axial plate fixation seems to be an excellent salvage procedure.


Subject(s)
Atlanto-Axial Joint/injuries , Bone Plates , Fracture Fixation, Internal , Fractures, Malunited/surgery , Joint Instability/surgery , Odontoid Process/injuries , Adult , Atlanto-Axial Joint/diagnostic imaging , Atlanto-Axial Joint/surgery , Female , Fractures, Malunited/diagnostic imaging , Humans , Imaging, Three-Dimensional , Joint Instability/diagnostic imaging , Odontoid Process/diagnostic imaging , Odontoid Process/surgery , Reoperation , Spinal Stenosis/diagnostic imaging , Spinal Stenosis/surgery , Tomography, X-Ray Computed
7.
Chirurg ; 72(12): 1431-8, 2001 Dec.
Article in German | MEDLINE | ID: mdl-11824028

ABSTRACT

INTRODUCTION: A biodegradable interbody cage for lumbar spine fusion would be able to solve several problems associated with the use of metallic cages. In a biomechanical in vitro study using human lumbar spines three different biodegradable poly(L-lactide-co-D,L-lacitide)(PLDLLA) cages were compared to metallic cages of the same design. MATERIAL AND METHOD: 40 human cadaver lumbar specimens (L3-S1) were tested in flexion, extension, rotation, and bending with a non-destructive flexibility method using a nonconstrained testing apparatus. Seven different groups were examined: (1) control group (intact) (n = 40); (2) unstable group (after discectomy L4/5) (n = 40), (3) autologous iliac crest bone graft (n = 8), (4) BAK-Cage (n = 8), (5) BIO-Cage 1 (PLDLLA) (n = 8), (6) BIO-Cage 2 (PLD-LLA/hydroxylapatite-buffer) (n = 8) and (7) BIO-Cage 3 (PLDLLA/hydroxylapatite particles of different size) (n = 8). Additionally, destructive compression tests of all implants were performed. RESULTS: In comparison to the intact motion segment all cages showed significantly lower range of motion (ROM) in all test modes (P < 0.01). There was no significant difference in stiffness values and ROM between BIO-Cages and metallic cages. Axial compression stiffness and failure load were significantly highest for metallic BAK-cages (P < 0.05). No significant difference for failure load was observed between BIO-cage 1 and the intact motion segment. However, in comparison to the intact motion segment failure load was significantly lower for BIO-cage 2 and 3 (P < 0.05). CONCLUSION: The results of this study are encouraging, because the biodegradable cages were able to limit lumbar spine motion similar to the metallic cages. Especially, the biodegradable PLDLLA cage consisting of pure polymer (BIO-Cage 1) showed adequate initial compression strength. However, further in vivo animal experiments are essential prior to the clinical application of biodegradable lumbar interbody fusion cages.


Subject(s)
Absorbable Implants , Lumbar Vertebrae/surgery , Polyesters , Spinal Fusion/instrumentation , Adult , Aged , Diskectomy , Equipment Design , Equipment Failure Analysis , Female , Humans , Male , Middle Aged
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