dc.contributor | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-05-27T11:22:49Z | |
dc.date.available | 2014-05-27T11:22:49Z | |
dc.date.created | 2014-05-27T11:22:49Z | |
dc.date.issued | 2008-03-01 | |
dc.identifier | Revista da Associacao Medica Brasileira, v. 54, n. 2, p. 110-115, 2008. | |
dc.identifier | 0104-4230 | |
dc.identifier | http://hdl.handle.net/11449/70329 | |
dc.identifier | 10.1590/S0104-42302008000200011 | |
dc.identifier | S0104-42302008000200011 | |
dc.identifier | 2-s2.0-45849096058 | |
dc.identifier | 2-s2.0-45849096058.pdf | |
dc.identifier | 8223546475724058 | |
dc.identifier | 8745358989680600 | |
dc.identifier | 0000-0002-2323-9159 | |
dc.description.abstract | BACKGROUND. This study aimed to evaluate clinical characteristics of epidural anesthesia performed with 0.75% ropivacaine associated with dexmedetomidine. METHODS. Forty patients scheduled for hernia repair or varicose vein surgeries under epidural anesthesia participated in this study. They were assigned to: Control Group (n = 20), 0.75% ropivacaine, 20 ml (150 mg); and Dexmedetomidine Group (n = 20), 0.75% ropivacaine, 20 ml (150 mg), plus dexmedetomidine, 1 μg.kg -1. The following variables were studied: total analgesic block onset time, upper level of analgesia, analgesic and motor block duration time, intensity of motor block, state of consciousness, hemodynamics, postoperative analgesia and incidence of side-effects. RESULTS. Epidural dexmedetomidine did not affect onset time or upper level of anesthesia (p > 0.05) however it prolonged sensory and motor block duration time (p < 0.05) and postoperative analgesia (p < 0.05), and also resulted in a more intense motor block, 1 (p < 0.05). Values of bispectral index were lower in Dexmedetomidine Group (p < 0.05). There was no difference in incidence of hypotension and bradycardia (p > 0.05). Occurrence of side-effects (shivering, vomiting and SpO 2 < 90%) was low and similar between groups (p > 0.05). CONCLUSION. There is clear synergism between epidural dexmedetomidine and ropivacaine, further this drug association does not bring about additional morbidity. | |
dc.language | por | |
dc.relation | Revista da Associação Médica Brasileira | |
dc.relation | 0.736 | |
dc.relation | 0,265 | |
dc.rights | Acesso aberto | |
dc.source | Scopus | |
dc.subject | Analgesics | |
dc.subject | Anesthetic techniques | |
dc.subject | Anesthetics | |
dc.subject | Dexmedetomidine | |
dc.subject | Epidural block | |
dc.subject | Ropivacaine | |
dc.subject | alpha adrenergic receptor stimulating agent | |
dc.subject | amide | |
dc.subject | dexmedetomidine | |
dc.subject | local anesthetic agent | |
dc.subject | ropivacaine | |
dc.subject | adolescent | |
dc.subject | adult | |
dc.subject | chi square distribution | |
dc.subject | clinical trial | |
dc.subject | controlled clinical trial | |
dc.subject | controlled study | |
dc.subject | double blind procedure | |
dc.subject | drug potentiation | |
dc.subject | epidural anesthesia | |
dc.subject | female | |
dc.subject | human | |
dc.subject | inguinal hernia | |
dc.subject | leg | |
dc.subject | male | |
dc.subject | middle aged | |
dc.subject | nerve block | |
dc.subject | nonparametric test | |
dc.subject | randomized controlled trial | |
dc.subject | time | |
dc.subject | Adolescent | |
dc.subject | Adrenergic alpha-Agonists | |
dc.subject | Adult | |
dc.subject | Amides | |
dc.subject | Anesthesia, Epidural | |
dc.subject | Anesthetics, Local | |
dc.subject | Chi-Square Distribution | |
dc.subject | Double-Blind Method | |
dc.subject | Drug Synergism | |
dc.subject | Female | |
dc.subject | Hernia, Inguinal | |
dc.subject | Humans | |
dc.subject | Lower Extremity | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Nerve Block | |
dc.subject | Statistics, Nonparametric | |
dc.subject | Time Factors | |
dc.subject | Young Adult | |
dc.title | Efeito sinérgico entre a dexmedetomidina e a ropivacaína 0,75% na anestesia peridural | |
dc.type | Artículos de revistas | |