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1.
Anesth Analg ; 88(3): 573-6, 1999 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10072008

RESUMO

UNLABELLED: We sought to determine whether spinal clonidine 50 microg prolongs the analgesia from the spinal administration of sufentanil 7.5 microg and bupivacaine 2.5 mg early in the first stage of labor. Thirty patients were randomized to receive a 2-mL spinal injection of sufentanil 7.5 microg + bupivacaine 2.5 mg with or without clonidine 50 microg using a combined spinal-epidural (CSE) technique. Pain, nausea, pruritus, sedation, motor block, blood pressure, and heart rate were assessed until the patient requested additional analgesia. Analgesia was significantly prolonged in patients who received spinal sufentanil + bupivacaine + clonidine (197 +/- 70 vs 132 +/- 39 min; P = 0.004). Pain scores and side effects, including motor block, sedation, and hypotension, were similar between groups. Spinal clonidine significantly prolongs labor analgesia from spinal sufentanil and bupivacaine without producing serious adverse side effects. IMPLICATIONS: We studied the effects of spinal clonidine administered with spinal sufentanil and bupivacaine on labor analgesia using a combined spinal-epidural technique and conclude that spinal clonidine significantly prolongs labor analgesia from spinal sufentanil and bupivacaine without producing serious adverse effects.


Assuntos
Analgesia Obstétrica/métodos , Analgésicos Opioides/administração & dosagem , Analgésicos/administração & dosagem , Anestésicos Locais/administração & dosagem , Bupivacaína/administração & dosagem , Clonidina/administração & dosagem , Sufentanil/administração & dosagem , Adulto , Analgésicos/efeitos adversos , Analgésicos Opioides/efeitos adversos , Anestésicos Locais/efeitos adversos , Bupivacaína/efeitos adversos , Clonidina/efeitos adversos , Sinergismo Farmacológico , Quimioterapia Combinada , Feminino , Humanos , Injeções Espinhais , Sufentanil/efeitos adversos
2.
Arch Otolaryngol ; 102(10): 621-6, 1976 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-971135

RESUMO

Brief-tone audiometry was administered to two groups of listeners. The first group consisted of five sophisticated subjects with normal hearing, who were tested under normal and simulated hearing-loss conditions. The second group consisted of five patients with true pseudohypacusis. Results under simulated and true pseudohypacusic conditions were similar, but were different from those obtained from the normal listeners under normal conditions, which further extends the diagnostic value of brief-tone audiometry.


Assuntos
Audiometria/métodos , Transtornos da Audição/diagnóstico , Estimulação Acústica , Limiar Auditivo , Humanos
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