Effect of combined use of different dose of exmedetomidine and ultra-low dose naloxoneon postoperative hyperalgesia induced by remifentanil
10.3969/j.issn.1006-5725.2015.15.024
- VernacularTitle:不同剂量右美托咪定联合超低剂量纳洛酮对瑞芬太尼诱发的术后痛觉过敏的影响
- Author:
Suyun TAN
;
Shenghua XIAO
;
Zhijun WANG
;
Quanguo HAN
;
Yonghong LIU
;
Zhijian QIU
;
Zhaokai LU
- Publication Type:Journal Article
- Keywords:
Dexmedetomidine;
Naloxone;
Remifentanil;
Hyperalgesia
- From:
The Journal of Practical Medicine
2015;31(15):2486-2489
- CountryChina
- Language:Chinese
-
Abstract:
Obejective To explore the effect of combined use of dexmedetomidine and ultra-low dose naloxone on postoperative hyperalgesia induced by remifentanil. Method 80 ASA gradeⅠ-Ⅱ female patients who were scheduled to perform endoscopic sinus surgery (ESS) were randomly divided into four groups: purely remifentanil group (group R) and remifentanil plus different dosage dexmedetomidine and ultra-low dose naloxone group (group RDN1 ~ RDN3). Then the postoperative VAS on 30 min, 1 h, 2 h, 4 h, 8 h, 12 h and 24 h together with the firstpostoperative pain time , PCA press numbers , fentanyl usage and adverse reaction rate were recorded and evaluated. Results Average VAS of group R are higher than other groups in all 7 time points at the adjusted significant level of 0.0083, and group R > group RDN1 > group RDN2 > group RDN3, while differences between group RDN2 and RDN3 in all time points are not statistical significant.There is no difference between group RDN1 and group RDN2 inthe first postoperative pain time and the PCA press time at 1h after operation. Difference between group RDN2 and group RDN3 in the PCA press time at 24 h after operation was not significant, and the fentanyl usage of RDN groups are significantly less than group R. Conclusions Combined use of dexmedetomidine and ultra-low dose naloxone induced by remifentanil can improving patients′postoperative hyperalgesia , effect increase with the dose of dexmedetomidine increas , and the increasement is more sensitive in acute pain.