2009Journal of Gannan Medical UniversityRequires access

Clinical Study of Patient-controlled Analgesia with Intravenous Sufentanil after Cesarean Section

Yao Hong

Open publisher page 0 citations

Abstract

Objective:To evaluate the efficacy and safety of patient-controlled analgesia with intravenous sufentanil after cesarean section.Methods: Sixty ASAⅠor Ⅱpatients who will receive cesarean section were randomized into 2 groups: receive patient-controlled analgesia with intravenous sufentanil(group S) or tramadol(group T) after cesarean section.VAS,blood pressure,heart rate and side effects were recorded on 4,8,12,24 and 48 minutes after the operation.Results: VAS scores were significantly lower in group S than in group T(P0.05).There was no significant difference in BP,HR,and side effects between the two groups(P0.05).Conclusion: Patient-controlled analgesia with intravenous sufentanil after cesarean section provides good and safe postoperative analgesia.

About this research paper

What this paper is about

Objective:To evaluate the efficacy and safety of patient-controlled analgesia with intravenous sufentanil after cesarean section.Methods: Sixty ASAⅠor Ⅱpatients who will receive cesarean section were randomized into 2 groups: receive patient-controlled analgesia with intravenous sufentanil(group S) or tramadol(group T) after cesarean section.VAS,blood pressure,heart rate and side effects were recorded on 4,8,12,24 and 48 minutes after the operation.Results: VAS scores were significantly lower in group S than in group T(P0.05).There was no significant difference in BP,HR,and side effects between the two groups(P0.05).Conclusion: Patient-controlled analgesia with intravenous sufentanil after cesarean section provides good and safe postoperative analgesia.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective:To evaluate the efficacy and safety of patient-controlled analgesia with intravenous sufentanil after cesarean section.Methods: Sixty ASAⅠor Ⅱpatients who will receive cesarean section were randomized into 2 groups: receive patient-controlled analgesia with intravenous sufentanil(group S) or tramadol(group T) after cesarean section.VAS,blood pressure,heart rate and side effects were recorded on 4,8,12,24 and 48 minutes after the operation.Results: VAS scores were significantly lower in group S than in group T(P0.05).There was no significant difference in BP,HR,and side effects between the two groups(P0.05).Conclusion: Patient-controlled analgesia with intravenous sufentanil after cesarean section provides good and safe postoperative analgesia.

Key concepts: Medicine, Sufentanil, Anesthesia, Heart rate, Tramadol, Patient-controlled analgesia, Blood pressure, Surgery

Related papers

Back to paper searchBrowse research topicsOriginal source
Clinical Study of Patient-controlled Analgesia with Intravenous Sufentanil after Cesarean Section — Research Paper | ScholarLens