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1.
Orthopedics ; 44(1): e36-e42, 2021 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-33289849

RESUMO

Bicortical drilling of the clavicle is associated with risk of iatrogenic damage from plunging given the close proximity of neurovascular structures. This study determined plunge depth during superior-to-inferior clavicle drilling using a standard drill vs drill-sensing technology. Two orthopedic surgeons drilled 10 holes in a fresh cadaveric clavicle with drill-sensing technology in freehand mode (functions as standard orthopedic drill) and another 10 holes with drill-sensing technology in bicortical mode (drill motor stops when the second cortex is breached and depth is measured in real time). The drill-measured depths were compared with computed tomography-measured depths. Distances to the neurovascular structures were also measured. The surgeons' plunge depths were compared using an independent t test. With freehand (standard) drilling, the mean plunge depth was 8.8 mm. For surgeon 1, the range was 5.6 to 15.8 mm (mean, 10.9 mm). For surgeon 2, the range was 3.3 to 11.0 mm (mean, 6.4 mm). The surgeons' plunge depths were significantly different. In bicortical mode, the drill motor stopped when the second cortex was penetrated. Drill-measured depths were verified by computed tomography scan, with a mean difference of 0.8 mm. Mean distances from the clavicle to the neurovascular structures were 15.5 mm for the subclavian vein, 18.0 mm for the subclavian artery, and 8.0 mm for the brachial plexus. Plunge depths differed between surgeons. However, both surgeons' plunge depths were greater than distances to the neurovascular structures, indicating a risk of injury due to plunging. Although a nonspinning drill bit may still cause soft tissue damage, drill-sensing technology may decrease the risk of penetrating soft tissue structures due to plunging. [Orthopedics. 2021;44(1):e36-e42.].


Assuntos
Plexo Braquial/lesões , Clavícula/cirurgia , Complicações Intraoperatórias/etiologia , Procedimentos Ortopédicos/efeitos adversos , Artéria Subclávia/lesões , Veia Subclávia/lesões , Humanos , Procedimentos Ortopédicos/métodos
2.
J Spinal Disord Tech ; 25(4): 190-5, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21423052

RESUMO

STUDY DESIGN: Clinical case series. OBJECTIVE: To show the efficacy of prophylactic inferior vena cava (IVC) filters in preventing venous thromboembolic event (VTE) in high-risk patients undergoing major spinal surgery. SUMMARY OF BACKGROUND DATA: Patients undergoing major spinal surgery are at increased risk for VTEs. Recent studies have shown IVC filters are effective in preventing clinically significant pulmonary embolism (PE), but have not documented the frequency of all emboli prevented. METHODS: Patients undergoing major spinal surgery from 2006 to 2009, having IVC filters placed for VTE prophylaxis, were reviewed. Patients with 2 or more risk factors for VTE were included and their perioperative courses were reviewed for PE and device-related complications. Cavograms obtained at the time of attempted filter retrieval identified intercepted emboli. The rates of intercepted emboli and clinical PEs were compared with those of similar populations undergoing similar procedures. RESULTS: Approximately 17% of patients had entrapped thrombus present at attempted filter retrieval. An additional 17% of filters were unable to be retrieved due to change in position within the IVC. No patients experienced symptomatic PE. One patient developed a deep vein thrombus requiring pharmacologic treatment and another patient developed superficial phlebitis. There were no complications related to IVC filter use. CONCLUSIONS: These findings show that the decreased rate of PE observed in this and other series is likely because of the use of IVC filters, rather than sampling bias inherent when studying a relatively rare problem. The safety of IVC filters in this population is also confirmed. The observed rate of clinical PE is consistent with other published series. Emboli intercepted by filters may more accurately estimate clinically significant emboli prevented. Therefore, cavograms may prove to be a valuable method of assessing the efficacy of these devices in future studies.


Assuntos
Embolia Pulmonar/prevenção & controle , Coluna Vertebral/cirurgia , Filtros de Veia Cava , Adulto , Segurança de Equipamentos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fatores de Risco , Resultado do Tratamento
3.
J Cell Physiol ; 222(3): 612-24, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19927303

RESUMO

Development is punctuated by morphogenetic rearrangements of epithelial tissues, including detachment of motile cells during epithelial-mesenchymal transition (EMT). Dramatic actin rearrangements occur as cell-cell junctions are dismantled and cells become independently motile during EMT. Characterizing dynamic actin rearrangements and identifying actin machinery driving these rearrangements is essential for understanding basic mechanisms of cell-cell junction remodeling. Using immunofluorescence and live cell imaging of scattering MDCK cells we examine dynamic actin rearrangement events during EMT and demonstrate that zyxin-VASP complexes mediate linkage of dynamic medial actin networks to adherens junction (AJ) membranes. A functional analysis of zyxin in EMT reveals its role in regulating disruption of actin membrane linkages at cell-cell junctions, altering cells' ability to fully detach and migrate independently during EMT. Expression of a constitutively active zyxin mutant results in persistent actin-membrane linkages and cell migration without loss of cell-cell adhesion. We propose zyxin functions in morphogenetic rearrangements, maintaining collective migration by transducing individual cells' movements through AJs, thus preventing the dissociation of individual migratory cells.


Assuntos
Actinas/metabolismo , Junções Aderentes/metabolismo , Movimento Celular , Transdiferenciação Celular , Proteínas do Citoesqueleto/metabolismo , Células Epiteliais/metabolismo , Mesoderma/metabolismo , Animais , Adesão Celular , Moléculas de Adesão Celular/metabolismo , Linhagem Celular , Forma Celular , Proteínas do Citoesqueleto/genética , Cães , Imunofluorescência , Fator de Crescimento de Hepatócito/metabolismo , Mesoderma/citologia , Proteínas dos Microfilamentos/metabolismo , Microscopia de Fluorescência , Microscopia de Vídeo , Mutação , Fosfoproteínas/metabolismo , Interferência de RNA , Fatores de Tempo
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