In vitro biomechanical analysis of three anterior thoracolumbar implants

2000 ◽  
Vol 93 (2) ◽  
pp. 252-258 ◽  
Author(s):  
Patrick W. Hitchon ◽  
Vijay K. Goel ◽  
Thomas N. Rogge ◽  
James C. Torner ◽  
Andrew P. Dooris ◽  
...  
Keyword(s):  
Axial Rotation ◽  
Biomechanical Analysis ◽  
Rigid Fixation ◽  
Angular Rotation ◽  
Content Type ◽  
Light Emitting ◽  
Vertebral Bodies ◽  
The Stability ◽  
Fine Print

Object. The goal of this study was to evaluate the comparative efficacy of three commonly used anterior thoracolumbar implants: the anterior thoracolumbar locking plate (ATLP), the smooth-rod Kaneda (SRK), and the Z-plate. Methods. In vitro testing was performed using the T9—L3 segments of human cadaver spines. An L-1 corpectomy was performed, and stabilization was achieved using one of three anterior devices: the ATLP in nine spines, the SRK in 10, and the Z-plate in 10. Specimens were load tested with 1.5-, 3-, 4.5-, and 6-Nm in flexion and extension, right and left lateral bending, and right and left axial rotation. Angular motion was monitored using two video cameras that tracked light-emitting diodes attached to the vertebral bodies. Testing was performed in the intact state in spines stabilized with one of the three aforementioned devices after the devices had been fatigued to 5000 cycles at ± 3 Nm and after bilateral facetectomy. There was no difference in the stability of the intact spines with use of the three devices. There were no differences between the SRK- and Z-plate—instrumented spines in any state. In extension testing, the mean angular rotation (± standard deviation) of spines instrumented with the SRK (4.7 ± 3.2°) and Z-plate devices (3.3 ± 2.3°) was more rigid than that observed in the ATLP-stabilized spines (9 ± 4.8°). In flexion testing after induction of fatigue, however, only the SRK (4.2 ± 3.2°) was stiffer than the ATLP (8.9 ± 4.9°). Also, in extension postfatigue, only the SRK (2.4 ± 3.4°) provided more rigid fixation than the ATLP (6.4 ± 2.9°). All three devices were equally unstable after bilateral facetectomy. The SRK and Z-plate anterior thoracolumbar implants were both more rigid than the ATLP, and of the former two the SRK was stiffer. Conclusions. The authors' results suggest that in cases in which profile and ease of application are not of paramount importance, the SRK has an advantage over the other two tested implants in achieving rigid fixation immediately postoperatively.

Biomechanical Assessment of Anchored Cervical Interbody Cages: Comparison of 2-Screw and 4-Screw Designs

2014 ◽  
Vol 10 (3) ◽  
pp. 412-417 ◽  
Author(s):  
Marco T. Reis ◽  
Phillip M. Reyes ◽  
Neil R. Crawford
Keyword(s):  
Axial Rotation ◽  
Anterior Plate ◽  
Biomechanical Assessment ◽  
Loading Mode ◽  
Variable Angle ◽  
Flexion Extension ◽  
Standard Plate ◽  
Vertebral Bodies ◽  
The Stability

Abstract BACKGROUND: A new anchored cervical interbody polyetheretherketone spacer was devised that uses only 2 integrated variable-angle screws diagonally into the adjacent vertebral bodies instead of the established device that uses 4 diagonal fixed-angle screws. OBJECTIVE: To compare in vitro the stability provided by the new 2-screw interbody spacer with that of the 4-screw spacer and a 4-screw anterior plate plus independent polyetheretherketone spacer. METHODS: Three groups of cadaveric specimens were tested with 2-screw anchored cage (n = 8), 4-screw anchored cage (n = 8), and standard plate/cage (n = 16). Pure moments (1.5 Nm) were applied to induce flexion, extension, lateral bending, and axial rotation while measuring 3-D motion optoelectronically. RESULTS: In all 3 groups, the mean range of motion (ROM) and lax zone were significantly reduced relative to the intact spine after discectomy and fixation. The 2-screw anchored cage allowed significantly greater ROM (P < .05) than the standard plate during flexion, extension, and axial rotation and allowed significantly greater ROM than the 4-screw cage during extension and axial rotation. The 4-screw anchored cage did not allow significantly different ROM or lax zone than the standard plate during any loading mode. CONCLUSION: The 2-screw variable-angle anchored cage significantly reduces ROM relative to the intact spine. Greater stability can be achieved, especially during extension and axial rotation, by using the 4-screw cage or standard plate plus cage.

Craniovertebral junction fixation with transarticular screws: biomechanical analysis of a novel technique

2003 ◽  
Vol 98 (2) ◽  
pp. 202-209 ◽  
Author(s):  
L. Fernando Gonzalez ◽  
Neil R. Crawford ◽  
Robert H. Chamberlain ◽  
Luis E. Perez Garza ◽  
Mark C. Preul ◽  
...  
Keyword(s):  
Three Dimensional ◽  
Axial Rotation ◽  
Craniovertebral Junction ◽  
Biomechanical Analysis ◽  
Lateral Bending ◽  
Content Type ◽  
Additional Stability ◽  
A New Technique ◽  
Flexion And Extension ◽  
Fine Print

Object. The authors compared the biomechanical stability resulting from the use of a new technique for occipitoatlantal motion segment fixation with an established method and assessed the additional stability provided by combining the two techniques. Methods. Specimens were loaded using nonconstraining pure moments while recording the three-dimensional angular movement at occiput (Oc)—C1 and C1–2. Specimens were tested intact and after destabilization and fixation as follows: 1) Oc—C1 transarticular screws plus C1–2 transarticular screws; 2) occipitocervical transarticular (OCTA) plate in which C1–2 transarticular screws attach to a loop from Oc to C-2; and (3) OCTA plate plus Oc—C1 transarticular screws. Occipitoatlantal transarticular screws reduced motion to well within the normal range. The OCTA loop and transarticular screws allowed a very small neutral zone, elastic zone, and range of motion during lateral bending and axial rotation. The transarticular screws, however, were less effective than the OCTA loop in resisting flexion and extension. Conclusions. Biomechanically, Oc—C1 transarticular screws performed well enough to be considered as an alternative for Oc—C1 fixation, especially when instability at C1–2 is minimal. Techniques for augmenting these screws posteriorly by using a wired bone graft buttress, as is currently undertaken with C1–2 transarticular screws, may be needed for optimal performance.

Biomechanical analysis of a newly designed bioabsorbable anterior cervical plate

2005 ◽  
Vol 3 (6) ◽  
pp. 465-470 ◽  
Author(s):  
Christopher P. Ames ◽  
Frank L. Acosta ◽  
Robert H. Chamberlain ◽  
Adolfo Espinoza Larios ◽  
Neil R. Crawford
Keyword(s):  
Axial Rotation ◽  
Metal Plate ◽  
Biomechanical Analysis ◽  
Fibular Graft ◽  
Disc Disease ◽  
Content Type ◽  
Flexion Extension ◽  
Cervical Plate ◽  
Anterior Cervical Plate ◽  
Fine Print

Object. The authors present a biomechanical analysis of a newly designed bioabsorbable anterior cervical plate (ACP) for the treatment of one-level cervical degenerative disc disease. They studied anterior cervical discectomy and fusion (ACDF) in a human cadaveric model, comparing the stability of the cervical spine after placement of the bioabsorbable fusion plate, a bioabsorbable mesh, and a more traditional metallic ACP. Methods. Seven human cadaveric specimens underwent a C6–7 fibular graft—assisted ACDF placement. A one-level resorbable ACP was then placed and secured with bioabsorbable screws. Flexibility testing was performed on both intact and instrumented specimens using a servohydraulic system to create flexion—extension, lateral bending, and axial rotation motions. After data analysis, three parameters were calculated: angular range of motion, lax zone, and stiff zone. The results were compared with those obtained in a previous study of a resorbable fusion mesh and with those acquired using metallic fusion ACPs. For all parameters studied, the resorbable plate consistently conferred greater stability than the resorbable mesh. Moreover, it offered comparable stability with that of metallic fusion ACPs. Conclusions. Bioabsorbable plates provide better stability than resorbable mesh. Although the results of this study do not necessarily indicate that a resorbable plate confers equivalent stability to a metal plate, the resorbable ACP certainly yielded better results than the resorbable mesh. Bioabsorbable fusion ACPs should therefore be considered as alternatives to metal plates when a graft containment device is required.

Biomechanical studies of an artificial disc implant in the human cadaveric spine

2005 ◽  
Vol 2 (3) ◽  
pp. 339-343 ◽  
Author(s):  
Patrick W. Hitchon ◽  
Kurt Eichholz ◽  
Christopher Barry ◽  
Paige Rubenbauer ◽  
Aditya Ingalhalikar ◽  
...  
Keyword(s):  
Biomechanical Testing ◽  
Axial Rotation ◽  
Load Testing ◽  
Artificial Disc ◽  
Lateral Bending ◽  
Content Type ◽  
Intact State ◽  
Flexion Extension ◽  
Fine Print

Object. The authors compared the biomechanical performance of the human cadaveric spine implanted with a metallic ball-and-cup artificial disc at L4–5 with the spine's intact state and after anterior discectomy. Methods. Seven human L2—S1 cadaveric spines were mounted on a biomechanical testing frame. Pure moments of 0, 1.5, 3.0, 4.5, and 6.0 Nm were applied to the spine at L-2 in six degrees of motion (flexion, extension, right and left lateral bending, and right and left axial rotation). The spines were tested in the intact state as well as after anterior L4–5 discectomy. The Maverick disc was implanted in the discectomy defect, and load testing was repeated. The artificial disc created greater rigidity for the spine than was present after discectomy, and the spine performed biomechanically in a manner comparable with the intact state. Conclusions. The results indicate that in an in vitro setting, this model of artificial disc stabilizes the spine after discectomy, restoring motion comparable with that of the intact state.

Effects of neck movements on stability and subsidence in cervical interbody fusion: an in vitro study

2001 ◽  
Vol 94 (1) ◽  
pp. 97-107 ◽  
Author(s):  
Annette Kettler ◽  
Hans-Joachim Wilke ◽  
Lutz Claes
Keyword(s):  
Bone Cement ◽  
Interbody Fusion ◽  
In Vitro Study ◽  
Axial Rotation ◽  
Vitro Study ◽  
Implant Design ◽  
Lateral Bending ◽  
Content Type ◽  
Fine Print

Object. The aim of this in vitro study was to determine the influence of simulated postoperative neck movements on the stabilizing effect and subsidence of four different anterior cervical interbody fusion devices. Emphasis was placed on the relation between subsidence and spinal stability. Methods. The flexibility of 24 human cervical spine specimens was tested before and directly after being stabilized with a WING, BAK/C, AcroMed I/F cage, or with bone cement in standard flexibility tests under 50 N axial preload. Thereafter, 700 pure moment loading cycles (± 2 Nm) were applied in randomized directions to simulate physiological neck movements. Additional flexibility tests in combination with measurements of the subsidence depth were conducted after 50, 100, 200, 300, 500, and 700 loading cycles. In all four groups, simulated postoperative neck movements caused an increase of the range of motion (ROM) ranging from 0.4 to 3.1° and of the neutral zone from 0.1 to 4.2°. This increase in flexibility was most distinct in extension followed by flexion, lateral bending, and axial rotation. After cyclic loading, ROM tended to be lower in the group fitted with AcroMed cages (3.3° in right lateral bending, 3.5° in left axial rotation, 7.8° in flexion, 8.3° in extension) and in the group in which bone cement was applied (5.4°, 2.5°, 7.4°, and 8.8°, respectively) than in those fixed with the WING (6.3°, 5.4°, 9.7°, and 6.9°, respectively) and BAK cages (6.2°, 4.5°, 10.2°, and 11.6°, respectively). Conclusions. Simulated repeated neck movements not only caused an increase of the flexibility but also subsidence of the implants into the adjacent vertebrae. The relation between flexibility increase and subsidence seemed to depend on the implant design: subsiding BAK/C cages partially supported stability whereas subsiding WING cages and AcroMed cages did not.

Bioabsorbable anterior lumbar plate fixation in conjunction with cage-assisted anterior interbody fusion

2002 ◽  
Vol 97 (4) ◽  
pp. 447-455 ◽  
Author(s):  
Denis J. DiAngelo ◽  
Jeffrey L. Scifert ◽  
Scott Kitchel ◽  
G. Bryan Cornwall ◽  
Bobby J. McVay
Keyword(s):  
Interbody Fusion ◽  
Plate Fixation ◽  
Axial Rotation ◽  
Biomechanical Study ◽  
Local Motion ◽  
Content Type ◽  
Flexion Extension ◽  
Spine Model ◽  
Fine Print

Object. An in vitro biomechanical study was conducted to determine the effects of anterior stabilization on cage-assisted lumbar interbody fusion biomechanics in a multilevel human cadaveric lumbar spine model. Methods. Three spine conditions were compared: harvested, bilateral multilevel cages (CAGES), and CAGES with bioabsorbable anterior plates (CBAP), tested under flexion—extension, lateral bending, and axial rotation. Measurements included vertebral motion, applied load, and bending/rotational moments. Application of anterior fixation decreased local motion and increased stiffness of the instrumented levels. Clinically, this spinal stability may serve to promote fusion. Conclusions. Coupled with the bioabsorbability of the plating material, the bioabsorbable anterior lumbar plating system is considered biomechanically advantageous.

Cerebrovascular characterization of clazosentan, the first nonpeptide endothelin receptor antagonist clinically effective for the treatment of cerebral vasospasm. Part I: Inhibitory effect on endothelinA receptor—mediated contraction

2005 ◽  
Vol 102 (6) ◽  
pp. 1101-1107 ◽  
Author(s):  
Hartmut Vatter ◽  
Michael Zimmermann ◽  
Veronika Tesanovic ◽  
Andreas Raabe ◽  
Lothar Schilling ◽  
...  
Keyword(s):  
Receptor Antagonist ◽  
Cerebral Vasospasm ◽  
Isometric Force ◽  
Inhibitory Effect ◽  
Affinity Constant ◽  
Dependent Manner ◽  
Content Type ◽  
The Right ◽  
Fine Print

Object. The central role of endothelin (ET)—1 in the development of cerebral vasospasm after subarachnoid hemorrhage is indicated by the successful treatment of this vasospasm in several animal models by using selective ETA receptor antagonists. Clazosentan is a selective ETA receptor antagonist that provides for the first time clinical proof that ET-1 is involved in the pathogenesis of cerebral vasospasm. The aim of the present investigation was, therefore, to define the pharmacological properties of clazosentan that affect ETA receptor—mediated contraction in the cerebrovasculature. Methods. Isometric force measurements were performed in rat basilar artery (BA) ring segments with (E+) and without (E−) endothelial function. Concentration effect curves (CECs) were constructed by cumulative application of ET-1 or big ET-1 in the absence or presence of clazosentan (10−9, 10−8, and 10−7 M). The inhibitory potency of clazosentan was determined by the value of the affinity constant (pA2). The CECs for contraction induced by ET-1 and big ET-1 were shifted to the right in the presence of clazosentan in a parallel dose-dependent manner, which indicates competitive antagonism. The pA2 values for ET-1 were 7.8 (E+) and 8.6 (E−) and the corresponding values for big ET-1 were 8.6 (E+) and 8.3 (E−). Conclusions. The present data characterize clazosentan as a potent competitive antagonist of ETA receptor—mediated constriction of the cerebrovasculature by ET-1 and its precursor big ET-1. These functional data may also be used to define an in vitro profile of an ET receptor antagonist with a high probability of clinical efficacy.

Antitumor effects of antiprogesterones on human meningioma cells in vitro and in vivo

1994 ◽  
Vol 80 (3) ◽  
pp. 527-534 ◽  
Author(s):  
Yasuhiro Matsuda ◽  
Keiichi Kawamoto ◽  
Katsuzo Kiya ◽  
Kaoru Kurisu ◽  
Kazuhiko Sugiyama ◽  
...  
Keyword(s):  
Marked Reduction ◽  
Tumor Volume ◽  
Collagen Gel ◽  
Antitumor Effects ◽  
Histological Changes ◽  
Content Type ◽  
The Relationship ◽  
Fine Print

✓ The presence of the progesterone receptor (PR) in meningioma tissue has been confirmed by previous investigations. Studies have shown that the antiprogesterone drug, mifepristone, is a potent agent that inhibits the growth of cultured meningioma cells and reduces the size of meningiomas in experimental animal models and humans. However, these studies have not fully examined the relationship between the antitumor effects of an antiprogesterone agent and the expression of the PR. The present study examined the antitumor effects of mifepristone and a new potent antiprogesterone agent, onapristone; a correlation between the antitumor effects of these antiprogesterones and the presence of PR's in meningiomas in vitro and in vivo was also investigated. Meningioma tissue surgically removed from 13 patients was used in this study. In the in vitro arm of the study, mifepristone and onapristone exhibited cytostatic and cytocidal effects against cultured meningioma cells, regardless of the presence or absence of PR's; however, three PR-negative meningiomas showed no response to any dose of mifepristone and/or onapristone. In the in vivo arm, meningioma cells, embedded in a collagen gel, were implanted into the renal capsules of nude mice. Antiprogesterone treatment resulted in a marked reduction of the tumor volume regardless of the presence or absence of PR's. No histological changes in the meningioma cells suggestive of necrosis or apoptosis were detected in any of the mice treated with antiprogesterones. These findings suggest that mifepristone and onapristone have an antitumor effect against meningioma cells via the PR's and/or another receptor, such as the glucocorticoid receptor.

Neoplastic and pharmacological influence on the permeability of an in vitro blood-brain barrier

1995 ◽  
Vol 82 (6) ◽  
pp. 1053-1058 ◽  
Author(s):  
Paul A. Grabb ◽  
Mark R. Gilbert
Keyword(s):  
Endothelial Cell ◽  
Rat Brain ◽  
Phospholipase A ◽  
Cell Permeability ◽  
Capillary Endothelium ◽  
Brain Capillary ◽  
Content Type ◽  
Endothelial Cell Permeability ◽  
Fine Print

✓ The authors investigated the effects of glioma cells and pharmacological agents on the permeability of an in vitro blood-brain barrier (BBB) to determine the following: 1) whether malignant glia increase endothelial cell permeability; 2) how glucocorticoids affect endothelial cell permeability in the presence and absence of malignant glia; and 3) whether inhibiting phospholipase A2, the enzyme that releases arachidonic acid from membrane phospholipids, would reduce any malignant glioma—induced increase in endothelial cell permeability. Primary cultures of rat brain capillary endothelium were grown on porous membranes; below the membrane, C6, 9L rat glioma, T98G human glioblastoma, or no cells (control) were cocultured. Dexamethasone (0.1 µM), bromophenacyl bromide (1.0 µM), a phospholipase A2 inhibitor, or nothing was added to culture media 72 hours prior to assaying the rat brain capillary endothelium permeability. Permeability was measured as the flux of radiolabeled sucrose across the rat brain capillary endothelium monolayer and then calculated as an effective permeability coefficient (Pe). When neither dexamethasone nor bromophenacyl bromide was present, C6 cells reduced the Pe significantly (p < 0.05), whereas 9L and T98G cells increased Pe significantly (p < 0.05) relative to rat brain capillary endothelium only (control). Dexamethasone reduced Pe significantly for all cell preparations (p < 0.05). The 9L and T98G cell preparations coincubated with dexamethasone had the lowest Pe of all cell preparations. The Pe was not affected in any cell preparation by coincubation with bromophenacyl bromide (p > 0.45). These in vitro BBB experiments showed that: 1) malignant glia, such as 9L and T98G cells, increase Pe whereas C6 cells probably provide an astrocytic influence by reducing Pe; 2) dexamethasone provided significant BBB “tightening” effects both in the presence and absence of glioma cells; 3) the in vivo BBB is actively made more permeable by malignant glia and not simply because of a lack of astrocytic induction; 4) tumor or endothelial phospholipase A2 activity is probably not responsible for glioma-induced increased in BBB permeability; and 5) this model is useful for testing potential agents for BBB protection and for studying the pathophysiology of tumor-induced BBB disruption.

Impairment of helper T-cell function and lymphokineactivated killer cytotoxicity following severe head injury

1991 ◽  
Vol 75 (5) ◽  
pp. 766-773 ◽  
Author(s):  
Keith B. Quattrocchi ◽  
Edmund H. Frank ◽  
Claramae H. Miller ◽  
Asim Amin ◽  
Bernardo W. Issel ◽  
...  
Keyword(s):  
T Cell ◽  
Head Injury ◽  
Severe Head Injury ◽  
Cell Cytotoxicity ◽  
Content Type ◽  
Lak Cell ◽  
Head Injured ◽  
Injured Patients ◽  
Fine Print

✓ Infection is a major complication of severe head injury, occurring in 50% to 75% of patients who survive to hospitalization. Previous investigations of immune activity following head injury have demonstrated suppression of helper T-cell activation. In this study, the in vitro production of interferon-gamma (INF-γ), interleukin-1 (IL-1), and interleukin-2 (IL-2) was determined in 25 head-injured patients following incubation of peripheral blood lymphocytes (PBL's) with the lymphocyte mitogen phytohemagglutinin (PHA). In order to elucidate the functional status of cellular cytotoxicity, lymphokine-activated killer (LAK) cell cytotoxicity assays were performed both prior to and following incubation of PBL's with IL-2 in five patients with severe head injury. The production of INF-γ and IL-2 by PHA-stimulated PBL's was maximally depressed within 24 hours of injury (p < 0.001 for INF-γ, p = 0.035 for IL-2) and partially normalized within 21 days of injury. There was no change in the production of IL-1. When comparing the in vitro LAK cell cytotoxicity of PBL's from head-injured patients and normal subjects, there was a significant depression in LAK cell cytotoxicity both prior to (p = 0.010) and following (p < 0.001) incubation of PBL's with IL-2. The results of this study indicate that IL-2 and INF-γ production, normally required for inducing cell-mediated immunity, is suppressed following severe head injury. The failure of IL-2 to enhance LAK cell cytotoxicity suggests that factors other than decreased IL-2 production, such as inhibitory soluble mediators or suppressor lymphocytes, may be responsible for the reduction in cellular immune activity following severe head injury. These findings may have significant implications in designing clinical studies aimed at reducing the incidence of infection following severe head injury.

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