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1.
Clin Spine Surg ; 30(10): 433-438, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-29088012

RESUMO

Lateral atlantoaxial osteoarthritis (AAOA), or C1-C2 lateral mass arthritis (LMA), is an unfamiliar degenerative cervical disease with a clinical presentation that markedly differs from subaxial spondylosis. The prevalence of LMA in the nonsurgical outpatient setting is 4%. Risk factors include age and occupation. The typical patient is between 50 and 90 years old, presents with upper cervical or occipital pain, has limited rotation, and has pain provocation during passive rotation to the affected side. Pain stems from degeneration of the lateral C1-C2 articulation and may be referred or radicular, through the greater occipital nerve. Although there is no consensus on diagnostic work-up, the disease is classically seen on the open-mouth odontoid radiograph. Computerized tomography, magnetic resonance imaging, bone scan, and diagnostic injections are also useful. Initial treatment is conservative, and upwards of two-thirds of LMA patients obtain lasting relief with noninvasive measures and injections. In patients with severe, recalcitrant pain, limited C1-C2 fusion offers satisfactory and reliable relief. The goals of this review article are to provide a synthesis of the literature on LMA, to offer a treatment approach to LMA, and to identify problems with the current state of knowledge on LMA.


Assuntos
Articulação Atlantoaxial/cirurgia , Vértebras Cervicais/cirurgia , Osteoartrite/cirurgia , Idoso , Idoso de 80 Anos ou mais , Humanos , Pessoa de Meia-Idade , Osteoartrite/epidemiologia , Resultado do Tratamento
2.
Spine J ; 13(8): 877-81, 2013 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23523442

RESUMO

BACKGROUND CONTEXT: Posterior spine fusion is associated with significant intra- and postoperative blood losses. When referring to the total blood loss during spine surgery, the standard is to measure the intraoperative bleeding plus the postoperative drainage. This ignores the "hidden" blood loss that was found to be significant in other fields of surgery. PURPOSE: The purpose of this study was to examine whether posterior spine fusion carries a substantial hidden blood loss. STUDY DESIGN/SETTING: A prospective study. PATIENT SAMPLE: We prospectively studied 114 patients undergoing instrumented posterior spinal fusion at one center between January 2011 and April 2011. OUTCOME MEASURES: Total blood loss, visible blood loss, and hidden blood loss. METHODS: For each patient, the hidden blood loss was calculated by deducting the observed perioperative blood loss from the calculated total blood loss based on the hematocrit changes. We compared the percentage of the hidden blood loss out of the total blood loss for primary versus revision posterior spine fusion. RESULTS: Primary decompression and posterior fusion patients had a mean total true loss of 1,439 mL. Their calculated hidden loss was 600 mL, 42% of the total loss. After revision posterior spinal fusion surgery, the mean total blood loss was 1,606 mL. The mean visible loss was 975 mL, and the mean hidden loss was 631 mL, 39% of the total loss. Thus, there was no statistical difference in the hidden blood loss between primary and revision posterior spinal fusion surgeries (p>.05). We did not find a significant difference in the percentage of the hidden blood loss between patients who underwent one, two, or three or more levels of surgery. CONCLUSIONS: After posterior spinal fusion, there may be a large amount of the hidden blood loss.


Assuntos
Perda Sanguínea Cirúrgica , Descompressão Cirúrgica/efeitos adversos , Vértebras Lombares/cirurgia , Fusão Vertebral/efeitos adversos , Vértebras Torácicas/cirurgia , Idoso , Descompressão Cirúrgica/métodos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Período Pós-Operatório , Estudos Prospectivos , Reoperação , Fusão Vertebral/instrumentação , Fusão Vertebral/métodos
3.
J Spinal Disord Tech ; 20(3): 248-54, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17473648

RESUMO

STUDY DESIGN: Case report with forensic failure analysis. OBJECTIVE: To determine the failure modes of 3 explanted 70:30 PLDLA Mystique (Medtronic Sofamor Danek, Memphis, TN) graft containment plates retrieved from revision surgery for early device failure. SUMMARY OF BACKGROUND DATA: To reduce the problems of stress-shielding and radiopacity associated with metallic systems, bioabsorbable polymers have been used in anterior cervical discectomy and fusion procedures. Degradation of mechanical properties in vivo is a major concern when using bioabsorbable systems. Three of 6 patients who underwent anterior cervical discectomy with instrumented fusion, using Mystique graft containment systems experienced early failure requiring revision to alternate hardware. METHODS: Devices were retrieved after failure and analyzed by light microscopy and environmental scanning electron microscopy. Simulations were performed with an unused plating system to induce damage for comparison with the retrieved devices. A detailed case review was performed to identify possible sources of extraordinary loading or damage. RESULTS: One plating system failed at 6 weeks postimplantation due to fatigue fracture of the screws. Crack initiation sites were identified at the interface of the thread root and mold line of the screw. Another plating system failed at 16 weeks postimplantation due to the coalescence of radial microcracking between holes in the plate, leading to catastrophic failure of the plate. The final plating system failed during the implantation surgery, when the screw fractured in torsion. CONCLUSIONS: Stress concentrations at the screw head-shaft interface and thread-shaft interface reduce the fatigue performance of bioabsorbable screws. Hydrolysis of the polymer may also play a role in the reduction of resistance to crack initiation and propagation.


Assuntos
Implantes Absorvíveis/efeitos adversos , Vértebras Cervicais/cirurgia , Discotomia/efeitos adversos , Fixadores Internos/efeitos adversos , Complicações Pós-Operatórias/etiologia , Fusão Vertebral/efeitos adversos , Implantes Absorvíveis/normas , Adulto , Parafusos Ósseos/efeitos adversos , Parafusos Ósseos/normas , Vértebras Cervicais/diagnóstico por imagem , Vértebras Cervicais/patologia , Discotomia/instrumentação , Discotomia/métodos , Falha de Equipamento , Análise de Falha de Equipamento/métodos , Feminino , Humanos , Fixadores Internos/normas , Disco Intervertebral/cirurgia , Deslocamento do Disco Intervertebral/cirurgia , Microscopia Eletrônica de Varredura , Pessoa de Meia-Idade , Plásticos/efeitos adversos , Plásticos/normas , Polímeros/efeitos adversos , Polímeros/normas , Complicações Pós-Operatórias/patologia , Complicações Pós-Operatórias/fisiopatologia , Radiografia , Fusão Vertebral/instrumentação , Fusão Vertebral/métodos , Estresse Mecânico , Fatores de Tempo
4.
J Nucl Cardiol ; 9(5): 523-33, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12360133

RESUMO

We review evidence for integrated effects of the signals that promote cardiac growth and remodeling and that modify the processes of excitation-contraction coupling. We have focused on integration of alterations in myofilament function with cell growth on the basis of genetic linkage analysis demonstrating that sarcomeric mutations are causal in hypertrophic cardiomyopathies. This evidence argues strongly for a path of communication between the intrinsic functional changes associated with a sarcomeric protein mutation and nuclear events. Our hypothesis is that this communication is also essential to the transduction of extrinsic signals leading to hypertrophy and failure. Understanding this network of signaling pathways is certain to lead to better diagnostic and treatment approaches to heart failure.


Assuntos
Citoesqueleto de Actina/fisiologia , Coração/crescimento & desenvolvimento , Modelos Biológicos , Contração Miocárdica/fisiologia , Miocárdio/metabolismo , Transdução de Sinais/fisiologia , Cardiomegalia/fisiopatologia , Expressão Gênica , Regulação da Expressão Gênica , Humanos , Modelos Químicos , Modelos Moleculares , Miócitos Cardíacos/fisiologia , Proteínas Quinases/metabolismo
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