Li C S, Liu S F, Zhou Y, Lu X H
Department of Anesthesiology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou 450003, China.
Zhonghua Yi Xue Za Zhi. 2018 Dec 11;98(46):3778-3783. doi: 10.3760/cma.j.issn.0376-2491.2018.46.011.
To investigate the effects of dexmedetomidine on perioperative stress and postoperative pain in patients with radical resection of esophageal cancer under combined thoracoscope and laparoscope. In this prospective study, one hundred patients undergoing radical resection of esophageal cancer in Affiliated Cancer Hospital of Zhengzhou University from January 2016 to October 2017, were randomly divided into control group (group C) and dexmedetomidine group (group D), =50. All patients were anaesthetized (induced and maintained) with intravenous target-controlled infusion(TCl) of propofol and remifentanil, and intermittent intravenous injection of cisatracuriumbesylate. Bispectral index(BIS) was used to monitor the depth of anesthesia and maintained between 45-60 during operation.All patients received sufentanil (0.3 μg/kg) 30 min before the end of the operation and then received intravenous analgesia pump for postoperative patient controlled analgesia(PCA). Patients in group D received intravenous infusion of dexmedetomidine(1 μg/kg) 20 min before anesthesia induction, followed by intravenous pumping of dexmedetomidine(0.2 μg·kg(-1)·h(-1)) intraoperatively.Postoperative intravenous patient-controlled analgesia(PCA) was performed in all patients, with background doses of sufentanil 0.04 μg· kg(-1)·h(-1) for patients in group C, and sufentanil 0.025 μg·kg(-1)·h(-1) plus dexmedetomidine 0.1 μg· kg(-1)·h(-1) for patients in group D. The operation time, liquid input and output during operation, the number of PCA pressings after operation were recorded. At these time points: T(0)(the day before operation), T(1)(immediate before anesthesia induction), T(2)(1 h after emergence), T(3)(24 h after operation), T(4)(3 d after operation), T(5)(7 d after operation), T(6)(one month after operation), T(7)(3 months after operation) and T(8)(6 month after operation) , venous blood samples of patients were collected for detection of epinephrine, norepinephrine and corticosterone. The pain visual analogue scale(VSA) was used to assess pain levels in patients at T(2), T(3), T(4), T(5), T(6), T(7), T(8). The age, sex ratio, body mass index (BMI) and ASA grading ratio in two groups were not significantly different(all >0.05). There were no Significant differences in operation time, liquid input and blood output between group C and group D(all >0.05). Within 24 h after operation, the sufentanil consumption in group D[(35.86±8.65)μg]was significantly less than that in group C[(59.53±15.26) μg, =7.061, <0.05], and the number of PCA pressing in group D(2.15±1.38) was obviously less than that in group C(5.85±2.16, =4.971, <0.05). Compared with group C, serum norepinephrines in group D was significantly less (=13.276, 16.027, 14.319, 12.771, 12.296, respectively; all <0.05) at T(1), T(2), T(3), T(4), T(5).And there were no difference between these two groups at T(0), T(6), T(7), T(8)(all >0.05). Serum epinephrine in group D were significantly lower than them in group C at T(2), T(3), T(4), T(5) (=6.153, 8.774, 9.127, 8.409, respectively; all <0.05), but there were no difference between these two groups at T(0), T(1), T(6), T(7), T(8)(all >0.05). Serum corticosterone in group D were sharply less than them in group C at T(2), T(3), T(4), T(5) (=16.364, 15.306, 12.153, 12.592, respectively; all <0.05), but at T(0), T(1), T(6), T(7), T(8), there were no difference between these two groups (all >0.05). Compared with group C, the number of patients with postoperative pain(VAS score≥4) in group D was obviously less at T(6), T(7), T(8)(10 vs 20, 4 vs 12, 3 vs 10; χ(2)=4.762, 4.762, 4.332, respectively; all <0.05). Perioperative application of dexmedetomidine can effectively decrease the perioperative stress response, obviously cut down the perioperative opioid consumption, and prevent the transition from postoperative acute pain to chronic pain in patients with radical resection of esophageal cancer under combined thoracoscope and laparoscope.
探讨右美托咪定对胸腔镜与腹腔镜联合食管癌根治术患者围手术期应激及术后疼痛的影响。在这项前瞻性研究中,选取2016年1月至2017年10月在郑州大学附属肿瘤医院行食管癌根治术的100例患者,随机分为对照组(C组)和右美托咪定组(D组),每组50例。所有患者均采用丙泊酚和瑞芬太尼静脉靶控输注(TCI)诱导并维持麻醉,间断静脉注射苯磺顺阿曲库铵。采用脑电双频指数(BIS)监测麻醉深度,术中维持在45 - 60。所有患者在手术结束前30分钟静脉注射舒芬太尼(0.3μg/kg),术后接静脉镇痛泵行患者自控镇痛(PCA)。D组患者在麻醉诱导前20分钟静脉输注右美托咪定(1μg/kg),术中持续静脉泵注右美托咪定(0.2μg·kg⁻¹·h⁻¹)。所有患者术后均行静脉自控镇痛(PCA),C组患者舒芬太尼背景剂量为0.04μg·kg⁻¹·h⁻¹,D组患者舒芬太尼背景剂量为0.025μg·kg⁻¹·h⁻¹加右美托咪定0.1μg·kg⁻¹·h⁻¹。记录手术时间、术中液体出入量、术后PCA按压次数。于T(0)(术前1天)、T(1)(麻醉诱导前即刻)、T(2)(苏醒后1小时)、T(3)(术后24小时)、T(4)(术后3天)、T(5)(术后7天)、T(6)(术后1个月)、T(7)(术后3个月)、T(8)(术后6个月)采集患者静脉血样,检测肾上腺素、去甲肾上腺素和皮质酮。采用疼痛视觉模拟评分法(VSA)评估患者在T(2)、T(3)、T(4)、T(5)、T(6)、T(7)、T(8)时的疼痛程度。两组患者的年龄、性别比、体重指数(BMI)及ASA分级比例差异均无统计学意义(均>0.05)。C组和D组患者的手术时间、液体出入量差异均无统计学意义(均>0.05)。术后24小时内,D组舒芬太尼用量[(35.86±8.65)μg]明显少于C组[(59.53±15.26)μg,t = 7.061,P < 0.05],D组PCA按压次数(2.15±1.38)明显少于C组(5.85±2.16,t = 4.971,P < 0.05)。与C组比较,D组在T(1)、T(2)、T(3)、T(4)、T(5)时血清去甲肾上腺素水平明显降低(分别为t = 13.276、16.027、14.319、12.771、12.296;均P < 0.05),在T(0)、T(6)、T(7)、T(8)时两组差异无统计学意义(均>0.05)。D组在T(2)、T(3)、T(4)、T(5)时血清肾上腺素水平明显低于C组(分别为t = 6.153、8.774、9.127、8.409;均P < 0.05),在T(0)、T(1)、T(6)、T(7)、T(8)时两组差异无统计学意义(均>0.05)。D组在T(2)、T(3)、T(4)、T(5)时血清皮质酮水平明显低于C组(分别为t = 16.364、15.306、12.153、12.592;均P < 0.05),在T(0)、T(1)、T(6)、T(7)、T(8)时两组差异无统计学意义(均>0.05)。与C组比较,D组在T(6)、T(7)、T(8)时术后疼痛(VAS评分≥4)患者例数明显减少(分别为10例对20例、4例对12例、3例对10例;χ²分别 = 4.762、4.762、4.332;均P < 0.05)。围手术期应用右美托咪定可有效降低胸腔镜与腹腔镜联合食管癌根治术患者围手术期应激反应,明显减少围手术期阿片类药物用量,预防术后急性疼痛向慢性疼痛转化。