Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Más filtros










Base de datos
Intervalo de año de publicación
2.
Reg Anesth Pain Med ; 26(2): 100-4, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11251131

RESUMEN

BACKGROUND AND OBJECTIVES: To quantify the motor threshold current of a needle following elicitation of paresthesia during axillary brachial plexus block (ABPB). METHODS: This is a prospective, observational study of ABPB in 72 patients. Having elicited paresthesia, the minimum current required to produce a motor response was noted. The development and success of the block were subsequently followed. RESULTS: Nineteen blocks were excluded (18 because of arterial puncture and 1 blocked needle). Of the remaining 53 blocks, 41 (77%) produced a motor response at 0.5 mA or less. The median current was 0.17 mA (range, 0.03 to 3.3 mA). The site of initial paresthesia and subsequent motor response were related in 43 (81%) of cases. CONCLUSIONS: A needle position causing paresthesia produced a motor response at 0.5 mA or less in 77% of cases studied. This current may, therefore, be a reasonable threshold to aim for when performing an ABPB.


Asunto(s)
Axila , Plexo Braquial , Bloqueo Nervioso , Parestesia , Anestésicos Locales , Brazo , Estimulación Eléctrica , Potenciales Evocados Motores , Humanos , Lidocaína , Persona de Mediana Edad , Músculo Esquelético/inervación , Bloqueo Nervioso/métodos , Parestesia/etiología , Estudios Prospectivos , Umbral Sensorial
3.
J Med Chem ; 14(12): 1193-7, 1971 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-5116233

RESUMEN

PIP: The synthesis of a series of triphenylethlenes with CF(3) groups placed directly on the ethylene carbon is described, and the postcoital and uterotropic activities of these 1-trifluoromethyl-1,2,2-triphenylethylenes are determined. The parent compound and 3 substituted analogs were prepared by the stepwise replacement of the vinylic F atoms of hexafluoropropene with aryl groups from ArLi reagents. The postcoital antifertility and uterotrophic activities in the rat were determined by treating rats with induced precocious puberty with the synthesized compounds for 6 days after mating occurred. The most potent compound of this series was trans-p-methyoxy-alpha-phenyl-alpha'-(trifluoromethyl) stilbene.^ieng


Asunto(s)
Anticonceptivos Orales/síntesis química , Etilenos/síntesis química , Administración Oral , Animales , Compuestos de Bencilo/administración & dosificación , Compuestos de Bencilo/síntesis química , Compuestos de Bencilo/farmacología , Anticonceptivos Orales/administración & dosificación , Anticonceptivos Orales/farmacología , Anticonceptivos Poscoito/síntesis química , Etilenos/administración & dosificación , Etilenos/farmacología , Femenino , Fertilidad/efectos de los fármacos , Flúor , Espectroscopía de Resonancia Magnética , Masculino , Ratas , Ratas Endogámicas , Relación Estructura-Actividad , Estirenos/administración & dosificación , Estirenos/síntesis química , Estirenos/farmacología , Factores de Tiempo , Útero/efectos de los fármacos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA
...