2010Chinese Journal of New Clinical MedicineRequires access

Application of sufentanil combined with ropivacaine for obstetric epidural analgesia in the cesarean section patients

Shiqin Chen

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Abstract

Objective To explore the application of sufentanil combined with ropivacaine for obstetric epidural analgesia in the cesarean section patient controlled epidural analgesia ( PCEA) .Methods Ninety cases of cesarean section were randomly divided into three groups with spinal-epidural anesthesia, i.e.group A, group B and group C.There were 30 cases in each group.The patients received 0.2 μg/ml sufentanil combined with 0.125% ropivacaine in group A, 0.4 μg/ml sufentanil combined with 0.125% ropivacaine in group B and 0.6 μg/ml sufentanil combined with 0.125% ropivacaine in group C, respectively.Postoperative PCEA were performed through loading dose (5 ml) + continuous dose (3 ml/h) + PCA dose (1 ml/times).The data were analyzed on the VAS scoring of incision pain,uterine pain in the period of 0~3,3~6,6~12,12~24 h postoperatively and the incidence of adverse reactions such as nausea, vomiting, itching, motor block, lethargy, respiratory depression in the period of 0 ~24 h postoperatively.Results The incision pain VAS score and contraction VAS pain score decreased with sufentanil concentration increasing.The defference between Group B, group C and Group A had statistic significance ( P 0.05).The defference between Group B and group C had not statistic significance ( P 0.05 ).The rate of adverse reactions in the nausea and the incidence of itching increased with sufentanil concentration increasesing.The defference between Group C and group B, Group A had statistic significance (P 0.05).The defference between Group B and group A had not statistic significance ( P 0.05 ) .The incidence rate of vomiting, motor block, lethargy had not statistic significance ( P 0.05 ) among the three group.No respiratory depression happened.Conclusion In the cesarean section PCEA, 0.4 μg/ml sufentanil combined with 0.125% ropivacaine can get better analgesic effect and less side effects.

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What this paper is about

Objective To explore the application of sufentanil combined with ropivacaine for obstetric epidural analgesia in the cesarean section patient controlled epidural analgesia ( PCEA) .Methods Ninety cases of cesarean section were randomly divided into three groups with spinal-epidural anesthesia, i.e.group A, group B and group C.There were 30 cases in each group.The patients received 0.2 μg/ml sufentanil combined with 0.125% ropivacaine in group A, 0.4 μg/ml sufentanil combined with 0.125% ropivacaine in group B and 0.6 μg/ml sufentanil combined with 0.125% ropivacaine in group C, respectively.Postoperative PCEA were performed through loading dose (5 ml) + continuous dose (3 ml/h) + PCA dose (1 ml/times).The data were analyzed on the VAS scoring of incision pain,uterine pain in the period of 0~3,3~6,6~12,12~24 h postoperatively and the incidence of adverse reactions such as nausea, vomiting, itching, motor block, lethargy, respiratory depression in the period of 0 ~24 h postoperatively.Results The incision pain VAS score and contraction VAS pain score decreased with sufentanil concentration increasing.The defference between Group B, group C and Group A had statistic significance ( P 0.05).The defference between Group B and group C had not statistic significance ( P 0.05 ).The rate of adverse reactions in the nausea and the incidence of itching increased with sufentanil concentration increasesing.The defference between Group C and group B, Group A had statistic significance (P 0.05).The defference between Group B and group A had not statistic significance ( P 0.05 ) .The incidence rate of vomiting, motor block, lethargy had not statistic significance ( P 0.05 ) among the three group.No respiratory depression happened.Conclusion In the cesarean section PCEA, 0.4 μg/ml sufentanil combined with 0.125% ropivacaine can get better analgesic effect and less side effects.

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Available abstract

Objective To explore the application of sufentanil combined with ropivacaine for obstetric epidural analgesia in the cesarean section patient controlled epidural analgesia ( PCEA) .Methods Ninety cases of cesarean section were randomly divided into three groups with spinal-epidural anesthesia, i.e.group A, group B and group C.There were 30 cases in each group.The patients received 0.2 μg/ml sufentanil combined with 0.125% ropivacaine in group A, 0.4 μg/ml sufentanil combined with 0.125% ropivacaine in group B and 0.6 μg/ml sufentanil combined with 0.125% ropivacaine in group C, respectively.Postoperative PCEA were performed through loading dose (5 ml) + continuous dose (3 ml/h) + PCA dose (1 ml/times).The data were analyzed on the VAS scoring of incision pain,uterine pain in the period of 0~3,3~6,6~12,12~24 h postoperatively and the incidence of adverse reactions such as nausea, vomiting, itching, motor block, lethargy, respiratory depression in the period of 0 ~24 h postoperatively.Results The incision pain VAS score and contraction VAS pain score decreased with sufentanil concentration increasing.The defference between Group B, group C and Group A had statistic significance ( P 0.05).The defference between Group B and group C had not statistic significance ( P 0.05 ).The rate of adverse reactions in the nausea and the incidence of itching increased with sufentanil concentration increasesing.The defference between Group C and group B, Group A had statistic significance (P 0.05).The defference between Group B and group A had not statistic significance ( P 0.05 ) .The incidence rate of vomiting, motor block, lethargy had not statistic significance ( P 0.05 ) among the three group.No respiratory depression happened.Conclusion In the cesarean section PCEA, 0.4 μg/ml sufentanil combined with 0.125% ropivacaine can get better analgesic effect and less side effects.

Key concepts: Medicine, Sufentanil, Ropivacaine, Anesthesia, Nausea, Vomiting, Itching, Group B

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Application of sufentanil combined with ropivacaine for obstetric epidural analgesia in the cesarean section patients — Research Paper | ScholarLens