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1.
Acta cir. bras ; 29(10): 675-680, 10/2014. tab
Article in English | LILACS | ID: lil-725290

ABSTRACT

PURPOSE: To evaluate the pain on injection of propofol via different combinations of fentanyl, sufentanil or remifentanil in gastrointestinal endoscopy. METHODS: Total 439 patients were randomly allocated into 6 groups. Propofol & fentanil (PF) group received 1 μg/kg fentanyl, propofol & sufentanil (PS) group received 0.1 μg/kg sufentanil and propofol & remifentanyl (PR) group received 1 μg/kg remifentanyl prior to administration of 1-2 mg/kg of propofol. The propofol & half-fentanil (Pf) group, propofol & half-sufentanil (Ps) group and propofol & half-remifentanyl (Pr) group were given 0.5 μg/kg fentanyl, 0.05 μg/kg sufentanil and 0.5 μg/kg remifentanyl, respectively and later administrated 1-2 mg/kg propofol. All patients were monitored for the blood pressure (MAP), heart rate (HR), and oxygen saturation (SpO2). Additionally, the pain intensity was assessed using a 4-point verbal rating scale (VRS) by professional doctors. RESULTS: The incidence of pain due to propofol injection in Ps group (33.8%) was significantly lower than other 5 groups. The heart rate (HR) and mean arterial pressure (MAP) were maintained within the normal limits in all six groups and there was no hypotension or bradycardia encountered during the study period. CONCLUSION: Propofol and sufentanil group was the most suitable program for painless gastroscopy. .


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Analgesics, Opioid/administration & dosage , Endoscopy, Gastrointestinal/methods , Hypnotics and Sedatives/adverse effects , Pain/prevention & control , Propofol/adverse effects , Drug Combinations , Fentanyl/administration & dosage , Heart Rate/drug effects , Hypnotics and Sedatives/administration & dosage , Injections, Intravenous/adverse effects , Pain Measurement , Pain/chemically induced , Piperidines/administration & dosage , Propofol/administration & dosage , Reproducibility of Results , Severity of Illness Index , Sufentanil/administration & dosage , Time Factors , Treatment Outcome
2.
Acta cir. bras ; 29(1): 66-70, 01/2014. tab, graf
Article in English | LILACS | ID: lil-697551

ABSTRACT

To investigate a saddle anesthesia with different doses of chloroprocaine in perianal surgery. METHODS: Total 60 Patients aged 18-75 years (Anesthesiologists grade I or II) scheduled to receive perianal surgery. Patients using saddle anesthesia were randomized to group A, group B and group C with the same concentration (0.5%) chloroprocaine with different doses 1.0 mL, 0.8 mL and 0.6 mL, respectively. Systolic blood pressure (SBP), diastolic blood pressure (DBP), heart rate (HR) and the sensory and motor block were recorded to evaluate the anesthesia effect of chloroprocaine in each group. RESULTS: The duration of sensory block of group C is shorter than those of group A and B. The maximum degree of motor block is observed (group C: 0 level, group A: III level; and group B: I level) after 15 minutes. Besides, there was a better anesthetic effect in group B than group A and group C, such as walking after saddle anesthesia. However, there is also no significant difference of blood pressure decreasing in these three groups. CONCLUSION: It's worth to employ a saddle anesthesia with appropriate doses of chloroprocaine in clinical perianal surgery.


Subject(s)
Animals , General Surgery/methods , Perineum/anatomy & histology , Urinary Retention , Anesthesiology/methods
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