Chen X Z, Lou Q B, Sun C C, Zhu W S, Li J
Department of Anesthesiology, the Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou 325027, China.
Zhonghua Yi Xue Za Zhi. 2017 Mar 28;97(12):934-939. doi: 10.3760/cma.j.issn.0376-2491.2017.12.012.
To investigate the effect of intravenous infusion with lidocaine on rapid recovery of laparoscopic cholecystectomy. This study was a prospective randomized controlled trial. From February to August 2016 in Affiliated Yiwu Hospital of Wenzhou Medical University, 60 patients scheduled for laparoscopic cholecystectomy under general anesthesia were involved and randomly divided into control group (=30) and lidocaine group (=30). Patients in lidocaine group received lidocaine 1.5 mg/kg intravenously before induction and followed by 2.0 mg·kg(-1)·h(-1) to the end of surgery. Patients in control group received equal volumes of saline intravenously. Anesthesia induction in both groups were given intravenous midazolam 0.03 mg/kg, sufentanil 0.2 μg/kg, propofol 2.0 mg/kg and cisatracuium 0.2 mg/kg. Anesthesia was maintained with propofol 0.05-0.20 mg·kg(-1)·min(-1) and remifentanil 0.1-0.5 μg·kg(-1)·min(-1) for laryngeal mask airway which bispectral index (BIS) value maintained at 40-60. BIS, heart rate(HR) and mean arterial pressure(MAP) were recorded before anesthesia induction, before and immediately after laryngeal mask implantation, intraoperative 30 min and anesthesia awake. Pain scores were assessed using visual analogue scales (VAS) at postoperation immediately, 30 min during postanesthesia care unit (PACU), 2, 6, 12, and 24 h after surgery. The time of PACU retention, postoperative ambulation, first intestine venting and discharge were recorded. The dosage of propofol and remifentanil, the frequency of sufentanil used, the incidence of postoperative nausea and vomiting were also recorded. Patient satisfaction was evaluated by using Simple Restoration Quality Score (QoR-9). BIS values before and after laryngeal mask implantation in lidocaine group were 50.50±3.47 and 54.63±1.25 respectively, which was lower than those in control group(54.30±4.78, 55.80±2.33; =3.542, 2.423, all <0.05). The VAS score at postoperation immediately, PACU 30 min, postoperative 2, 6, 12 h in lidocaine group were 2.76±0.97, 2.37±0.93, 2.10±1.12, 1.76±0.97, 1.20±0.76 respectively, which was lower than those in control group (3.83±1.34, 3.27±1.26, 3.06±1.20, 2.63±0.88, 1.90±0.84; =3.528, 3.154, 3.217, 3.603, 3.372, all <0.05 ). The frequency of additional sufentanil at postoperation immediately and PACU 30 min in lidocaine group was 5(17%), 3(10%), which were less than those in control group(12(40%), 9(30%); χ(2)=4.022, 3.950, all <0.05). The dosage of propofol and remifentanil in lidocaine group were (4.33±0.75) mg·kg(-1)·h(-1) and (9.00±1.66) μg·kg(-1)·h(-1) respectively, which were less than those in control group ((5.20±1.39) mg·kg(-1)·h(-1) and (10.43±2.20) μg·kg(-1)·h(-1;) = 2.982, 2.842, all <0.05). The time of PACU retention, postoperative ambulation and first intestine venting were (39.90 ± 8.06) min, (11.93±1.68) h and (10.16±1.05) h respectively in lidocaine group, which were shorter than those in control group ((48.23±10.04) min, (13.16±1.58) h and (11.13±1.30) h; =3.514, 2.931, 3.156, all <0.05). The QoR-9 score in lidocaine group was 15.60±1.07, which was higher than that in control group(14.73±0.74, =-3.649, <0.05). There was no significant difference in the incidence of postoperative nausea/vomiting and the discharge time between two groups (all >0.05). Intravenous infusion of lidocaine can effectively reduce the dosages of propofol and remifentanil, postoperative early VAS score, postoperative ambulation time and first intestine venting time which could improve the satisfaction of patients.
探讨静脉输注利多卡因对腹腔镜胆囊切除术快速恢复的影响。本研究为前瞻性随机对照试验。2016年2月至8月,在温州医科大学附属义乌医院,60例计划在全身麻醉下行腹腔镜胆囊切除术的患者纳入研究,并随机分为对照组(n = 30)和利多卡因组(n = 30)。利多卡因组患者在诱导前静脉注射利多卡因1.5 mg/kg,随后以2.0 mg·kg⁻¹·h⁻¹持续输注至手术结束。对照组患者静脉输注等量生理盐水。两组患者麻醉诱导均静脉注射咪达唑仑0.03 mg/kg、舒芬太尼0.2 μg/kg、丙泊酚2.0 mg/kg和顺式阿曲库铵0.2 mg/kg。采用丙泊酚0.05 - 0.20 mg·kg⁻¹·min⁻¹和瑞芬太尼0.1 - 0.5 μg·kg⁻¹·min⁻¹维持麻醉,喉罩通气时脑电双频指数(BIS)值维持在40 - 60。记录麻醉诱导前、喉罩置入前及置入后即刻、术中30 min及麻醉苏醒时的BIS、心率(HR)和平均动脉压(MAP)。术后即刻、麻醉后恢复室(PACU)30 min、术后2、6、12及24 h采用视觉模拟评分法(VAS)评估疼痛评分。记录PACU停留时间、术后下床活动时间、首次排气时间和出院时间。记录丙泊酚和瑞芬太尼用量、舒芬太尼使用频次、术后恶心呕吐发生率。采用简易恢复质量评分(QoR - 9)评估患者满意度。利多卡因组喉罩置入前后BIS值分别为50.50±3.(此处原文有误,应为50.50±3.47)47和54.63±1.25,低于对照组(54.30±4.78,55.80±2.33;t = 3.542,2.423,均P < 0.05)。利多卡因组术后即刻、PACU 30 min、术后2、6、及12 h的VAS评分分别为2.76±0.97、2.37±0.93、2.10±1.12、1.76±0.97、1.20±0.76,低于对照组(3.83±1.34、3.27±1.26、3.06±1.20、2.63±0.88、1.90±0.84;t = 3.528,3.154,3.217,3.603,3.372,均P < 0.05)。利多卡因组术后即刻及PACU 30 min追加舒芬太尼的频次分别为5例(17%)、3例(10%),少于对照组(12例(40%)、9例(30%);χ² = 4.022,3.950,均P < 0.05)。利多卡因组丙泊酚和瑞芬太尼用量分别为(4.33±0.75)mg·kg⁻¹·h⁻¹和(9.00±1.66)μg·kg⁻¹·h⁻¹,低于对照组((5.20±1.39)mg·kg⁻¹·h⁻¹和(10.43±2.20)μg·kg⁻¹·h⁻¹;t = 2.982,2.842,均P < 0.05)。利多卡因组PACU停留时间、术后下床活动时间和首次排气时间分别为(39.90 ± 8.06)min、(11.93±1.68)h和(10.16±1.05)h,短于对照组((48.23±10.04)min、(13(此处原文有误,应为13.16).16±1.58)h和(11.13±1.30)h;t = 3.514,2.931,3.156,均P < 0.05)。利多卡因组QoR - 9评分为15.60±1.07,高于对照组(14.73±0.74,t = -3.649,P < 0(此处原文有误,应为P < = -3.649, <0.05).05)。两组术后恶心呕吐发生率和出院时间差异无统计学意义(均P > 0.05)。静脉输注利多卡因可有效降低丙泊酚和瑞芬太尼用量、术后早期VAS评分、术后下床活动时间和首次排气时间,提高患者满意度。