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1.
PLoS One ; 8(12): e83370, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24358279

RESUMO

Spinal cord ischemia can lead to paralysis or paraparesis, but if detected early it may be amenable to treatment. Current methods use evoked potentials for detection of spinal cord ischemia, a decades old technology whose warning signs are indirect and significantly delayed from the onset of ischemia. Here we introduce and demonstrate a prototype fiber optic device that directly measures spinal cord blood flow and oxygenation. This technical advance in neurological monitoring promises a new standard of care for detection of spinal cord ischemia and the opportunity for early intervention. We demonstrate the probe in an adult Dorset sheep model. Both open and percutaneous approaches were evaluated during pharmacologic, physiological, and mechanical interventions designed to induce variations in spinal cord blood flow and oxygenation. The induced variations were rapidly and reproducibly detected, demonstrating direct measurement of spinal cord ischemia in real-time. In the future, this form of hemodynamic spinal cord diagnosis could significantly improve monitoring and management in a broad range of patients, including those undergoing thoracic and abdominal aortic revascularization, spine stabilization procedures for scoliosis and trauma, spinal cord tumor resection, and those requiring management of spinal cord injury in intensive care settings.


Assuntos
Tecnologia de Fibra Óptica/métodos , Monitorização Intraoperatória/métodos , Isquemia do Cordão Espinal/diagnóstico , Isquemia do Cordão Espinal/cirurgia , Animais , Modelos Animais de Doenças , Humanos , Fluxo Sanguíneo Regional , Ovinos , Análise Espectral/métodos , Medula Espinal/irrigação sanguínea , Traumatismos da Medula Espinal/complicações , Traumatismos da Medula Espinal/cirurgia , Isquemia do Cordão Espinal/etiologia , Isquemia do Cordão Espinal/patologia
2.
Biomed Opt Express ; 4(7): 978-94, 2013 Jul 01.
Artigo em Inglês | MEDLINE | ID: mdl-23847725

RESUMO

A pilot study explores relative contributions of extra-cerebral (scalp/skull) versus brain (cerebral) tissues to the blood flow index determined by diffuse correlation spectroscopy (DCS). Microvascular DCS flow measurements were made on the head during baseline and breath-holding/hyperventilation tasks, both with and without pressure. Baseline (resting) data enabled estimation of extra-cerebral flow signals and their pressure dependencies. A simple two-component model was used to derive baseline and activated cerebral blood flow (CBF) signals, and the DCS flow indices were also cross-correlated with concurrent Transcranial Doppler Ultrasound (TCD) blood velocity measurements. The study suggests new pressure-dependent experimental paradigms for elucidation of blood flow contributions from extra-cerebral and cerebral tissues.

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