目的 探讨超声引导下腹横肌平面阻滞（TAP）联合无阿片药全身麻醉（全麻）在腹腔镜子宫全切术中的应用效果。方法 选取武威市凉州医院2021年5月—2023年5月收治的60例择期行腹腔镜子宫全切术患者展开前瞻性研究，应用抽签法将其分为观察组与对照组，各30例。对照组患者实施常规阿片类药物全麻，观察组采用TAP联合无阿片药全身麻醉。对比两组患者入室后（T0）、切皮时（T1）、手术10 min后（T2）和手术结束即刻（T3）生命体征变化，麻醉后监测治疗室（PACU）恢复情况，术后1、4、8、12、24、48 h疼痛程度，最后对比其48 h内不良反应发生率。结果 两组T0、T1、T2、T3时间血氧饱和度（SpO2），T0、T3时间平均动脉压（MAP）、心率水平无明显变化，两组对比差异无统计学意义（P＞0.05），T1、T2时间对照组MAP、心率升高，观察组T1、T2的MAP、心率均低于对照组（P＜0.05）；观察组PACU停留时间、首次肛门排气时间明显低于对照组（P＜0.05）；观察组术后1、4、8、12、24、48 h活动时视觉模量表（VAS）评分与静息时VAS评分低于对照组（P＜0.05）；观察组术后48 h内不良反应发生率比对照组更低（P＜0.05）。结论 针对腹腔镜子宫全切术患者采取超声引下TAP联合无阿片药全麻可稳定患者术中生命体征，缩短患者术后恢复时间，减轻疼痛程度，且可降低术后48 h内不良反应发生率。
Objective To explore the application effect of ultrasound-guided transverse abdominis plane（TAP）block combined with opioid-free general anesthesia in laparoscopic total hysterectomy．Methods A prospective study was conducted in 60 patients who underwent selective laparoscopic total hysterectomy in Wuwei Liangzhou Hospital from May 2021 to May 2023．They were divided into a observation group and a control group using a lottery method，30 cases in each group．The control group received routine opioid general anaesthesia，while the observation group received TAP in combination with opioid-free general anaesthesia．Comparing the changes of vital signs after invasion（T0），skin cutting（T1），10 min after operating（T2），the end of surgery（T3），and condition in the post-anesthesia care unit（PACU）after anesthesia，the pain degree at 1 h，4 h，8 h，12 h，24 h and 48 h after surgery，and the incidence of adverse reactions within 48 h．Results There were no significant changes in blood SpO2，mean arterial pressure（MAP）and heart rate at T0，T1，T2 and T3 in both groups，and no significant difference between the two groups（P＞0.05）．MAP and heart rate increased in the control group at T1 and T2，while those in the observation group were lower than the control group（P＜0.05）．The observation group had significantly shorter PACU time and first anal exhaust time than the control group（P＜0.05）．VAS scores at 1 h，4 h，8 h，12 h，24 h and 48 h after surgery and VAS score at rest in the observation group were lower than in the control group（P＜0.05）．The incidence of adverse reactions within 48 h after surgery was lower in the observation group than in the control group（P＜0.05）．Conclusions Ultrasound guided TAP combined with opioid-free general anesthesia can stabilize intraoperative vital signs，shorten postoperative recovery time，alleviate postoperative pain，and reduce the incidence of anesthesia related adverse reactions within 48 hours for patients undergoing laparoscopic total hysterectomy．
目的 观察腹横肌平面阻滞复合七氟醚诱导喉罩全身麻醉在高危产妇剖宫产手术中的应用效果。方法 在2016年12月-2017年12月间,选取我院收治的80例高危产妇作为观察对象,均择期行剖宫产手术,依照随机数字表法分为观察组、对照组,每组产妇各40例。剖宫产手术的麻醉方式为,观察组采取双侧腹横肌平面阻滞后,七氟醚吸入诱导插入喉罩,对照组采取腰硬联合麻醉。观察比较两组的生命体征、手术持续时间、麻醉并发症发生率、新生儿Apgar 评分。结果 ①观察组T1~T3时段的平均动脉压、心率均低于对照组,（P<0.05）,有统计学意义。②观察组手术持续时间、麻醉并发症发生率、新生儿Apgar 评分与对照组比较,无差异,（P>0.05）。结论 腹横肌平面阻滞复合七氟醚诱导喉罩全身麻醉在高危产妇剖宫产手术中的应用效果较好,对产妇和胎儿影响小,麻醉平稳、苏醒快,麻醉风险低,值得应用。
目的 比较不同浓度罗哌卡因横纹肌阻滞应用于剖宫产术后镇痛的临床效果。方法 选取2015年3月—2016年3月于我院剖宫产的孕妇300例,随机分为A组、B组、C组,每组100例,A组产妇给予质量浓度为1.5 g/L的罗哌卡因1.5 mg/kg,B组产妇给予质量浓度为2 g/L的罗哌卡因1.5 mg/kg,C组产妇给予质量浓度为2.5 g/L的罗哌卡因1.5 mg/kg,同时给予所有产妇镇痛泵辅助镇痛。记录观察所有产妇术后6 h、12 h、24 h、36 h、48 h的疼痛视觉模拟评分(VAS)、镇痛泵按压次数、产妇对镇痛效果的满意程度以及腹横肌平面阻滞(TAP)不良反应发生情况。结果 B、C组产妇的VAS评分均低于A组产妇(P＜0.05),24 h后C组产妇的VAS评分低于B组产妇(P＜0.05);与B、C组产妇相比,A组产妇的镇痛泵按压次数更多,镇痛效果满意度较低(P＜0.05),同时B组产妇的镇痛泵按压次数多于C组产妇(P＜0.05);3组产妇均未出现术后不良反应。结论 使用质量浓度为2.5 g/L的罗哌卡因横纹肌阻滞进行剖宫产术后镇痛,效果显著、安全性较高,临床中可推广使用。
Objective To compare the clinical effects of different concentrations of ropivacaine for postoperative analgesia after cesarean section. Methods 300 cases of pregnant women undergoing cesarean section in our hospital from March 2015 to March 2016 were selected and were randomly divided into group A, group B and group C with 100 cases in each group. The patients in group A were given 0.15% ropivacaine 1.5 mg/kg, 0.20% ropivacaine 1.5 mg/kg in group B and 0.25% ropivacaine 1.5 mg/kg in group C, and at the same time all the pregnant women were given analgesic pump assisting analgesia. The pain visual analogue scales (VAS) of the pregnant women were recorded at 6 hours, 12 hours, 24 hours and 36 hours after cesarean section and the number of times of analgesia pressing pump were also recorded. The satisfaction degree of analgesic effect and the TAP occurrence of adverse reactions of the patients were also recorded. Results The VAS scores of group B and group C were lower than that of group A(P<0.05). 24 hours after cesarean section, the VAS score of group C was lower than that of group B (P<0.05). Compared with group B and C, the number of times of analgesia pressing pump in group A were more but the analgesic effect of satisfaction was lower (P<0.05), and at the same time the number of times of analgesia pressing pump in group B were more than those in group C (P<0.05). No adverse reactions were found in the three groups. Conclusion The treatment of using of 0.25% of ropivacaine for muscle block for postoperative analgesia after cesarean section is effective and safe, which may be widely used in clinical practice.
