Comparison of effects of Sufentanil plus Ropivacaine on postoperative epidural analgesia
Xiu Gong
Abstract
Xiu Gong
Abstract
Objective: To study the clinical effect and safety of Sufentanil combined with Ropivacaine in postoperative patients with epidural analgesia(EA). Methods: 60 patients(ages ranged between 56±12.3), ASA I-II, undergoing selective upper abdominal surgery under general anesthesia, were randomly divided into four groups. Ropivacaine 0.125% was used in group I, ropivacaine 0.125% plus sufentanil 0.25ug/ml in group II, ropivacaine 0.125% plus sufentanil 0.5ug/ml in group III and ropivacaine 0.125% plus sufentanil 0.75ug/ml in group IV. Postoperative analgesic effects,PEA pump usage, drug consumption and side effects,and visual analogue scales(VAS) were observed at 3,6,12 and 24 hr. Results: VAS and drug consumption in group III and IV within 24 hr were significantly lower than those in group I and II when patients were in the state of rest or coughing, respectively(P0.05); Pruritus incidence in the four groups was 0%,27.2%,54.5% and 63.6% in proper order,and there was significant difference between the four groups(P0.05). All the patients had no severe complications(such as respiratory depression). Conclusion: In this study, Sufentanil 0.5ug/ml with Ropivacaine 0.125% could be safe in PEA after UAS, which had the best analgesic effect in the four, with less side effects.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective: To study the clinical effect and safety of Sufentanil combined with Ropivacaine in postoperative patients with epidural analgesia(EA). Methods: 60 patients(ages ranged between 56±12.3), ASA I-II, undergoing selective upper abdominal surgery under general anesthesia, were randomly divided into four groups. Ropivacaine 0.125% was used in group I, ropivacaine 0.125% plus sufentanil 0.25ug/ml in group II, ropivacaine 0.125% plus sufentanil 0.5ug/ml in group III and ropivacaine 0.125% plus sufentanil 0.75ug/ml in group IV. Postoperative analgesic effects,PEA pump usage, drug consumption and side effects,and visual analogue scales(VAS) were observed at 3,6,12 and 24 hr. Results: VAS and drug consumption in group III and IV within 24 hr were significantly lower than those in group I and II when patients were in the state of rest or coughing, respectively(P0.05); Pruritus incidence in the four groups was 0%,27.2%,54.5% and 63.6% in proper order,and there was significant difference between the four groups(P0.05). All the patients had no severe complications(such as respiratory depression). Conclusion: In this study, Sufentanil 0.5ug/ml with Ropivacaine 0.125% could be safe in PEA after UAS, which had the best analgesic effect in the four, with less side effects.
Key concepts: Ropivacaine, Sufentanil, Medicine, Anesthesia, Analgesic, Visual analogue scale, Surgery