首页|瑞马唑仑与右美托咪定用于老年腰椎手术患者的临床研究

瑞马唑仑与右美托咪定用于老年腰椎手术患者的临床研究

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目的 比较甲苯磺酸瑞马唑仑注射剂和盐酸右美托咪定注射液用于老年腰椎手术患者的临床疗效及安全性.方法 将行腰椎手术老年患者按队列法分为对照组和试验组.于麻醉诱导前的10 min,对照组通过微量注射泵泵注1.0μg·kg-1右美托咪定,试验组静脉推注0.2 mg·kg-1瑞马唑仑.在麻醉诱导后,对照组右美托咪定速率调整为0.5 μg·kg-1·h-1持续泵注,试验组瑞马唑仑速率调整为0.5 mg·kg-1·h-1持续泵注,2组均于手术结束前1 h停止泵注.2组患者的静脉诱导药均为舒芬太尼+依托咪酯+罗库溴铵,麻醉维持用药均为丙泊酚+瑞芬太尼.比较2组患者的苏醒质量、围术期血流动力学、炎症指标,以及不良事件的发生情况.结果 试验组和对照组分别入组53例和58例.试验组和对照组的意识恢复时间分别为(6.83±4.53)和(6.86±3.71)min,拔管时间分别为(8.62±5.92)和(8.81±5.23)min,麻醉后监测治疗室停留时间分别为(38.36±6.80)和(39.36±6.27)min,在统计学上差异均无统计学意义(均P>0.05).在手术开始后1 h,试验组和对照组的平均动脉压分别为(71.91±5.15)和(68.88±4.84)mmHg,心率分别为(68.51±5.62)和(61.93±5.88)次/分;在手术结束时,试验组和对照组的平均动脉压分别为(73.08±5.78)和(70.74±6.25)mmHg,心率分别为(69.49±5.15)和(64.91±7.84)次/分,在统计学上差异均有统计学意义(均P<0.05).术毕拔管后,试验组和对照组的C反应蛋白分别为(20.78±2.17)和(21.86±2.63)mg·L-1,肿瘤坏死因子-α 分别为(64.55±5.96)和(70.55±5.14)pg·mL-1,白细胞介素-6分别为(107.79±6.94)和(114.66±6.00)pg·mL-1,在统计学上差异均有统计学意义(均P<0.05).2组患者的不良事件均以谵妄、苏醒延迟,术后低氧血症、术后恶心呕吐为主,2组患者的上述不良事件发生率比较,在统计学上差异均无统计学意义(均P>0.05).结论 与右美托咪定相比,瑞马唑仑不影响老年腰椎手术患者的苏醒质量,对血流动力学影响较小,同时能显著降低炎症水平,且不增加术后不良事件的发生率.
Clinical trial of remimazolam and dexmedetomidine in the treatment of elderly patients undergoing lumbar spine surgery
Objective To compare the clinical efficacy and safety of remimazolam injection and dexmedetomidine injection in the treatment of elderly patients undergoing lumbar surgery.Methods Elderly patients undergoing lumbar surgery were divided into treatment and control groups according to the cohort method.At 10 minutes before anesthesia induction,the control group was given 1.0 µg·kg-1 dexmedetomidine via a microinjection pump,while 0.2 mg·kg-1 remimazolam was injected intravenously in the experimental group.Then after anesthesia induction,the rate of dexmedetomidine in the control group was adjusted to 0.5 μg·kg-1·h-1.The rate of remazolam in the experimental group was adjusted to 0.5 mg·kg-1·h-1.Both groups stopped pumping 1 hour before the end of the operation.The intravenous induction drugs of two groups were sufentanyl+etomidate+rocuronium,and the anesthesia maintenance drugs were propofol+remifentanil.The awakening quality,perioperative hemodynamics,inflammatory indicators and adverse events were compared between two groups.Results Fifty-three patients were enrolled in the treatment group,and 58 patients were enrolled in the control group.The extubation time of treatment and control groups was(6.83±4.53)and(6.86±3.71)min;the consciousness recovery time was(8.62±5.92)and(8.81±5.23)min;postanesthesia care unit stay time was(38.36±6.80)and(39.36±6.27)min,the differences were not statistically significant(all P>0.05).At 1 h after the start of the surgery,the mean arterial pressure values of treatment and control groups were(71.91±5.15)and(68.88±4.84)mmHg,heart rates were(68.51±5.62)and(61.93±5.88)beat·min-1;at the end of the procedure,the mean arterial pressure values of treatment and control groups were(73.08±5.78)and(70.74±6.25)mmHg,heart rates were(69.49±5.15)and(64.91±7.84)beat·min-1;the differences were statistically significant(all P<0.05).After extubation,C-reactive protein levels of treatment and control groups were(20.78±2.17)and(21.86±2.63)mg·L-1;tumor necrosis factor-α levels were(64.55±5.96)and(70.55±5.14)pg·mL-1;interleukin-6 levels were(107.79±6.94)and(114.66±6.00)pg·mL-1;there were statistically significant of above indexes between two groups(all P<0.05).The main adverse events in both groups were delirium,delayed awakening,postoperative hypoxemia and postoperative nausea and vomiting,and there were no significant differences in the incidences of adverse events between two groups(all P>0.05).Conclusion Compared with dexmedetomidine,rimazzolam does not affect the quality of patients'recovery,with little influence on hemodynamics of elderly patients undergoing lumbar surgery,and reduces the level of inflammation without increasing the incidence of postoperative adverse events.

remimazolam injectiondexmedetomidine injectionlumbar surgeryelderly patientsafety evaluation

李国芳、宋昱

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首都医科大学附属北京潞河医院麻醉科,北京 101149

徐州医科大学附属医院麻醉科,江苏徐州 221006

瑞马唑仑注射剂 右美托咪定注射液 腰椎手术 老年患者 安全性评价

2024

中国临床药理学杂志
中国药学会

中国临床药理学杂志

CSTPCD北大核心
影响因子:1.91
ISSN:1001-6821
年,卷(期):2024.40(7)
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