瑞马唑仑复合芬太尼在无痛胃镜检查中的应用效果

Application effect of remimazolam combined with fentanyl in painless gastroscopy

  • 摘要:
    目的 探讨瑞马唑仑复合芬太尼在无痛胃镜检查中的有效性及最佳剂量。
    方法 选取拟行无痛胃镜检查患者200例为研究对象,随机分为R1组(0.05 mg芬太尼复合瑞马唑仑0.20 mg/kg组)、R2组(0.05 mg芬太尼复合瑞马唑仑0.30 mg/kg组)、R3组(0.05 mg芬太尼复合瑞马唑仑0.40 mg/kg组)和C组(0.05 mg芬太尼复合丙泊酚2.00 mg/kg, 对照组),每组50例。比较4组患者一般资料; 比较检查前(T0)、进镜时(T1)、进镜后2 min(T2)、进镜后4 min(T3)时的心率(HR)、平均动脉压(MAP)、镇静成功率以及胃镜检查时间、苏醒时间、离院时间和不良反应发生情况。
    结果 4组患者一般资料比较,差异无统计学意义(P > 0.05)。与C组比较, R1组镇静成功率降低,检查时间延长,苏醒时间缩短,体动及呛咳的发生率增加,差异有统计学意义(P < 0.05); R1组、R2组、R3组低血压、低氧血症与注射痛发生率均下降, R3组呃逆发生率升高,差异有统计学意义(P < 0.05)。与R1组比较, R2组、R3组镇静成功率升高,体动与呛咳的发生率下降,差异有统计学意义(P < 0.05)。与R3组比较,R2组苏醒时间、离院时间缩短,差异有统计学意义(P < 0.05)。与C组比较, R1组、R2组、R3组在T1时的HR、MAP升高,差异有统计学意义(P < 0.05); 与R1组比较, R2、R3组在T1时的HR、MAP降低,差异有统计学意义(P < 0.05); 组内比较时, R1组T1时的MAP、HR高于其他时点, C组T1时的MAP低于其他时点,差异有统计学意义(P < 0.05)。结论0.30 mg/kg瑞马唑仑复合0.05 mg芬太尼镇静成功率高,对循环和呼吸系统的影响小,术中不良反应发生率低,效果最佳。

     

    Abstract:
    Objective To investigate the effectiveness and optimal dose of remimazolam combined with fentanyl in painless gastroscopy.
    Methods  A total of 200 patients who planned to undergo painless gastroscopy were selected as study objects. They were randomly divided into R1 group (0.05 mg fentanyl combined with remimazolam 0.20 mg/kg group), R2 group (0.05 mg fentanyl combined with remimazolam 0.30 mg/kg group), R3 group (0.05 mg fentanyl combined with remimazolam 0.40 mg/kg group) and C group (0.05 mg fentanyl combined with propofol 2.00 mg/kg, control group), with 50 cases in each group. General data of the four groups were compared; heart rate (HR), mean arterial pressure (MAP), success rate of sedation, time to gastroscopy, time to recovery, time to leave hospital and incidence of adverse reactions were compared before examination (T0), at admission (T1), 2 min after admission (T2) and 4 min after admission (T3).
    Results  There was no statistical significance in the general data of the four groups (P > 0.05). Compared with the group C, the success rate of sedation in the R1 group was significantly decreased, the time of examination was significantly prolonged, the time of recovery was significantly shortened, and the incidence of body movement and cough was significantly increased (P < 0.05); the incidence rates of hypotension, hypoxemia and injection pain in the R1, R2 and R3 groups were significantly decreased, while the incidence of hiccup in the R3 group was significantly increased (P < 0.05). Compared with the R1 group, the success rates of sedation in the R2 and R3 groups were significantly increased, and the incidence of body movement and cough was significantly decreased (P < 0.05). Compared with the R3 group, the time to wake up and time to leave hospital in the R2 group were significantly shortened (P < 0.05). Compared with group C, HR and MAP in R1, R2 and R3 groups were significantly increased at T1 (P < 0.05); compared with the R1 group, HR and MAP in the R2 and R3 groups at T1 were significantly decreased (P < 0.05); the MAP and HR at T1 in the R1 group were significantly higher than those at other time points; the MAP of the C group at T1 was significantly lower than that at other time points (P < 0.05). Conclusion 0.30 mg/kg remazolam combined with 0.05 mg fentanyl has high success rate of sedation, little influence on circulation and respiratory system, low incidence of intraoperative adverse reactions, and the best effect.

     

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