Unknown

Dataset Information

0

Dexmedetomidine Added to Sufentanil Patient-Controlled Intravenous Analgesia Relieves the Postoperative Pain after Cesarean Delivery: A Prospective Randomized Controlled Multicenter Study.


ABSTRACT: This study evaluated the efficacy and safety of dexmedetomidine in intravenous patient-controlled analgesia (PCA) after cesarean delivery. This multicenter study enrolled 208 subjects who were scheduled for selective cesarean delivery from 9 research centers. Patients received 0.5?ug/kg dexmedetomidine (study group) or normal saline (control group) after delivery and an intravenous PCA pump after surgery (100??g sufentanil +300??g dexmedetomidine for the study group, 100??g sufentanil for the control group, background infusion: 1?ml/h, bolus dose: 2?ml and lock time: 8?min). The sufentanil consumption, pain scores, rescue analgesia, sedation scores, analgesic satisfaction, the incidence of postoperative nausea and vomiting (PONV) and the first passage of flatus were recorded within 24?h after surgery. The sufentanil consumption in the study group was significantly lower than that in the control group (p?=?0.004). Compared with the control group, the study group had lower pain scores (p?

SUBMITTER: Nie Y 

PROVIDER: S-EPMC6028483 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Dexmedetomidine Added to Sufentanil Patient-Controlled Intravenous Analgesia Relieves the Postoperative Pain after Cesarean Delivery: A Prospective Randomized Controlled Multicenter Study.

Nie Yuyan Y   Tu Weifeng W   Shen Xiaofeng X   Yu Weifeng W   Yu Yonghao Y   Song Xingrong X   Wang Shiduan S   Luo Ailin A   Cao Minghui M   Wu Xinmin X   Huang Shaoqiang S  

Scientific reports 20180702 1


This study evaluated the efficacy and safety of dexmedetomidine in intravenous patient-controlled analgesia (PCA) after cesarean delivery. This multicenter study enrolled 208 subjects who were scheduled for selective cesarean delivery from 9 research centers. Patients received 0.5 ug/kg dexmedetomidine (study group) or normal saline (control group) after delivery and an intravenous PCA pump after surgery (100 μg sufentanil +300 μg dexmedetomidine for the study group, 100 μg sufentanil for the co  ...[more]

Similar Datasets

| S-EPMC7751695 | biostudies-literature
| S-EPMC10520140 | biostudies-literature
| S-EPMC4234007 | biostudies-literature
| S-EPMC10657160 | biostudies-literature
| S-EPMC6990885 | biostudies-literature
| S-EPMC5784834 | biostudies-literature
| S-EPMC6192643 | biostudies-literature
| S-EPMC9354301 | biostudies-literature
| S-EPMC7305826 | biostudies-literature
| S-EPMC11012364 | biostudies-literature