Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
Anesth Analg ; 128(6): 1154-1159, 2019 06.
Artículo en Inglés | MEDLINE | ID: mdl-31094782

RESUMEN

BACKGROUND: Apneic oxygenation via the oral route using a buccal device extends the safe apnea time in most but not all obese patients. Apneic oxygenation techniques are most effective when tracheal oxygen concentrations are maintained >90%. It remains unclear whether buccal oxygen administration consistently achieves this goal and whether significant risks of hypercarbia or barotrauma exist. METHODS: We conducted a randomized trial of buccal or sham oxygenation in healthy, nonobese patients (n = 20), using prolonged laryngoscopy to maintain apnea with a patent airway until arterial oxygen saturation (SpO2) dropped <95% or 750 seconds elapsed. Tracheal oxygen concentration, tracheal pressure, and transcutaneous carbon dioxide (CO2) were measured throughout. The primary outcome was maintenance of a tracheal oxygen concentration >90% during apnea. RESULTS: Buccal patients were more likely to achieve the primary outcome (P < .0001), had higher tracheal oxygen concentrations throughout apnea (mean difference, 65.9%; 95% confidence interval [CI], 62.6%-69.3%; P < .0001), and had a prolonged median (interquartile range) apnea time with SpO2 >94%; 750 seconds (750-750 seconds) vs 447 seconds (405-525 seconds); P < .001. One patient desaturated to SpO2 <95% despite 100% tracheal oxygen. Mean tracheal pressures were low in the buccal (0.21 cm·H2O; SD = 0.39) and sham (0.56 cm·H2O; SD = 1.25) arms; mean difference, -0.35 cm·H2O; 95% CI, 1.22-0.53; P = .41. CO2 accumulation during early apnea before any study end points were reached was linear and marginally faster in the buccal arm (3.16 vs 2.82 mm Hg/min; mean difference, 0.34; 95% CI, 0.30-0.38; P < .001). Prolonged apnea in the buccal arm revealed nonlinear CO2 accumulation that declined over time and averaged 2.22 mm Hg/min (95% CI, 2.21-2.23). CONCLUSIONS: Buccal oxygen administration reliably maintains high tracheal oxygen concentrations, but early arterial desaturation can still occur through mechanisms other than device failure. Whereas the risk of hypercarbia is similar to that observed with other approaches, the risk of barotrauma is negligible. Continuous measurement of advanced physiological parameters is feasible in an apneic oxygenation trial and can assist with device evaluation.


Asunto(s)
Administración Bucal , Apnea/terapia , Dióxido de Carbono/análisis , Oxígeno/uso terapéutico , Respiración Artificial/instrumentación , Adolescente , Adulto , Anciano , Manejo de la Vía Aérea/métodos , Anestesiología/métodos , Femenino , Humanos , Intubación Intratraqueal/métodos , Laringoscopía , Modelos Lineales , Masculino , Persona de Mediana Edad , Terapia por Inhalación de Oxígeno , Respiración Artificial/métodos , Tráquea , Adulto Joven
2.
Neuroreport ; 14(1): 47-50, 2003 Jan 20.
Artículo en Inglés | MEDLINE | ID: mdl-12544829

RESUMEN

Previous studies suggest that estrogen treatment protects nigrostriatal dopaminergic neurons, but have not examined whether the changes in estrogen levels during estrous cycle can influence the susceptibility of these neurons to neurotoxins. Here we show that the loss of dopaminergic neurons in the substantia nigra was greater in animals lesioned at diestrus (low estrogen) using 6-hydroxydopamine or buffered iron chloride, when compared with animals lesioned at proestrus (high estrogen). Lesioning at diestrus with 6-hydroxydopamine reduced the striatal dopamine content, whereas the dopamine content was preserved in animals lesioned at proestrus. The density of the dopamine transporter, upon which 6-hydroxydopamine toxicity is dependent, was lower when circulating estrogen was high. These results thus support a neuroprotectory role for estrogen.


Asunto(s)
Dopamina/metabolismo , Estrógenos/fisiología , Ciclo Estral/efectos de los fármacos , Glicoproteínas de Membrana , Proteínas de Transporte de Membrana/metabolismo , Proteínas del Tejido Nervioso/metabolismo , Trastornos Parkinsonianos/prevención & control , Sustancia Negra/metabolismo , Ácido 3,4-Dihidroxifenilacético/análisis , Animales , Cloruros , Diestro , Proteínas de Transporte de Dopamina a través de la Membrana Plasmática , Estradiol/análisis , Femenino , Compuestos Férricos/toxicidad , Radicales Libres , Ácido Homovanílico/análisis , Inyecciones , Fármacos Neuroprotectores , Neurotoxinas/toxicidad , Oxidopamina/toxicidad , Trastornos Parkinsonianos/inducido químicamente , Proestro , Ratas , Ratas Wistar , Sustancia Negra/patología
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA