RETRACTED: Effect of perioperative infusion of Dexmedetomidine combined with Sufentanil on quality of postoperative analgesia in patients undergoing laparoscopic nephrectomy: a CONSORT-prospective, randomized, controlled trial (Retracted Article)

被引:3
|
作者
Song, Fuxi [1 ]
Ye, Chunmiao [2 ]
Qi, Feng [3 ]
Zhang, Ping [2 ]
Wang, Xuexiang [4 ]
Lue, Yanfeng [5 ]
Fernandez-Escobar, Alejandro [6 ]
Zheng, Chao [2 ]
Li, Liang [2 ]
机构
[1] Shandong Univ, Hosp 2, Dept Anaesthesiol, 247 Beiyuan St, Jinan 250033, Shandong, Peoples R China
[2] Shandong Univ, Hosp 2, Dept Breast Surg, 247 Beiyuan St, Jinan 250033, Shandong, Peoples R China
[3] Shandong Univ, Qilu Hosp, Dept Anaesthesiol, 107 Wenhua West Rd, Jinan 250012, Shandong, Peoples R China
[4] Shandong Univ, Inst Translat Med, Hosp 2, 247 Beiyuan St, Jinan 250033, Shandong, Peoples R China
[5] Shandong Univ, Dept Anoproctol, Hosp 2, 247 Beiyuan St, Jinan 250033, Shandong, Peoples R China
[6] Univ Toronto, Translat Res Program, 27 Kings Coll Circle, Toronto, ON M5S 1A1, Canada
来源
BMC ANESTHESIOLOGY | 2018年 / 18卷
基金
中国国家自然科学基金;
关键词
Dexmedetomidine; Sufenanil; Postoperative analgesia; Flatus; Defecation; INTRATHECAL CLONIDINE; CHRONIC PAIN; MANAGEMENT; MORPHINE; RAT; PREVENTION; MIDAZOLAM; ETIOLOGY; SEDATION; SURGERY;
D O I
10.1186/s12871-018-0608-3
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BackgroundPostoperative pain is one of the most common symptoms after surgery, which brings physical discomfort to patients. In addition, it may cause a series of complications, and even affect the long-term quality of life. The purpose of this prospective, randomized, double-blinded, controlled trial is to investigate the efficacy and safety of dexmedetomidine combined with sufentanil to attenuate postoperative pain in patients after laparoscopic nephrectomy.MethodsNinety patients undergoing laparoscopic nephrectomy were randomized into three groups: the control (sufentanil 0.02g/kg/h, Group C), sufentanil plus low dose of dexmedetomidine (0.02g/kg/h each, Group D1), and sufentanil plus high dose of dexmedetomidine (0.04g/kg/h, Group D2). The patient-controlled analgesia was programmed to deliver a bolus dose of 0.5ml, followed by an infusion of 2ml/h and a lockout time of 10min. The primary goal was to calculate the cumulative amount of self-administered sufentanil; the secondary goals were to estimate pain intensity using the numerical rating scale (NRS), level of sedation, the first bowel movement, concerning adverse effects as well as duration of postoperative hospital stay.ResultsThe total consumption of sufentanil in group D1 and D2 were significantly lower than in group C during the first 8h after surgery (P<0.05), whereas there were no statistically significant differences (P>0.05) between group D1 and D2. Compared with group C, the NRS scores at rest during first 8h after surgery were significantly lower in group D1 (P<0.05). The NRS scores, neither at rest nor with movement, show statistically significant differences between group D1 and D2 at each time point following surgery (P>0.05). The time to first flatus was shorter in group D1 compared with the control group (P<0.05). In addition, compared with group C, group D1 and D2 had a shorter time for first defecation (P<0.05).ConclusionsDexmedetomidine combined with sufentanil showed better postoperative analgesia without adverse effects, as well as facilitated bowel movements for patients undergoing laparoscopic nephrectomy.Trial registrationWe registered this study in a Chinese Clinical Trial Registry (ChiCTR) centre on Dec 23 2015 and received the registration number: ChiCTR-IPR-15007628.
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页数:10
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