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1.
J Korean Med Sci ; 31(9): 1485-90, 2016 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-27510395

RESUMO

We aimed to compare fentanyl, remifentanil and dexmedetomidine with respect to hemodynamic stability, postoperative pain control and achievement of sedation at the postanesthetic care unit (PACU). In this randomized double-blind study, 90 consecutive total laparoscopic hysterectomy patients scheduled for elective surgery were randomly assigned to receive fentanyl (1.0 µg/kg) over 1 minute followed by a 0.4 µg/kg/hr infusion (FK group, n = 30), or remifentanil (1.0 µg/kg) over 1 minute followed by a 0.08 µg/kg/min infusion (RK group, n = 30), or dexmedetomidine (1 µg/kg) over 10 minutes followed by a 0.5 µg/kg/hr infusion (DK group, n = 30) initiating at the end of main procedures of the operation to the time in the PACU. A single dose of intravenous ketorolac (30 mg) was given to all patients at the end of surgery. We respectively evaluated the pain VAS scores, the modified OAA/S scores, the BIS, the vital signs and the perioperative side effects to compare the efficacy of fentanyl, remifentanil and dexmedetomidine. Compared with other groups, the modified OAA/S scores were significantly lower in DK group at 0, 5 and 10 minutes after arrival at the PACU (P < 0.05), whereas the pain VAS and BIS were not significantly different from other groups. The blood pressure and heart rate in the DK group were significantly lower than those of other groups at the PACU (P < 0.05). DK group, at sedative doses, had the better postoperative hemodynamic stability than RK group or FK group and demonstrated a similar effect of pain control as RK group and FK group with patient awareness during sedation in the PACU. (World Health Organization registry, KCT0001524).


Assuntos
Analgésicos Opioides/administração & dosagem , Dexmedetomidina/administração & dosagem , Fentanila/administração & dosagem , Dor Pós-Operatória/tratamento farmacológico , Piperidinas/administração & dosagem , Adolescente , Adulto , Analgésicos Opioides/efeitos adversos , Pressão Sanguínea , Dexmedetomidina/efeitos adversos , Método Duplo-Cego , Feminino , Fentanila/efeitos adversos , Frequência Cardíaca , Hemodinâmica/fisiologia , Humanos , Hipotensão/etiologia , Laparoscopia , Masculino , Pessoa de Meia-Idade , Náusea/etiologia , Manejo da Dor , Piperidinas/efeitos adversos , Remifentanil , Adulto Jovem
2.
J Korean Med Sci ; 31(1): 125-30, 2016 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-26770048

RESUMO

Transurethral resection has been the gold standard in the operative management of benign prostatic hyperplasia and bladder tumor; however, it is associated with several complications that may cause patient discomfort. We evaluated the usefulness of continuous infusion of dexmedetomidine on emergence agitation, hemodynamic status, and recovery profiles in patients undergoing elective surgery by a randomized clinical trial. Sixty patients aged 30 to 80 yr who were scheduled for elective transurethral resection under general anesthesia were included in this study. Participants were randomly assigned to two groups (control group, group C; dexmedetomidine group, group D). A total of 60 male patients were enrolled in this study and randomly assigned to group C (n=30) or group D (n=30). The quality of emergence in group D was marked by a significantly lower incidence of emergence agitation than in group C (P=0.015). Patients in group D therefore felt less discomfort induced by the indwelling Foley catheter than those in group C (P=0.022). No statistically significant differences were found between the two groups with respect to side effects including bradycardia (P=0.085), hypotension (P=0.640), and postoperative nausea and vomiting (P=0.389). Our study showed that intraoperative dexmedetomidine infusion effectively reduced the incidence and intensity of emergence agitation and catheter-induced bladder discomfort without delaying recovery time and discharge time, thus providing smooth emergence during the recovery period in patients undergoing transurethral resection (Clinical Trial Registry No. KT0001683).


Assuntos
Dexmedetomidina/uso terapêutico , Hipnóticos e Sedativos/uso terapêutico , Hiperplasia Prostática/cirurgia , Agitação Psicomotora/tratamento farmacológico , Ressecção Transuretral da Próstata , Adulto , Idoso , Idoso de 80 Anos ou mais , Pressão Sanguínea , Bradicardia/etiologia , Dexmedetomidina/efeitos adversos , Hemodinâmica , Humanos , Hipnóticos e Sedativos/efeitos adversos , Hipotensão/etiologia , Masculino , Pessoa de Meia-Idade , Náusea/etiologia , Vômito/etiologia
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