Dose-response of ropivacaine administered caudally to children undergoing surgical procedures under sedation with midazolam.

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
F Tonatiu Aguirre-Garay, Rosario García, Alejandro A Nava-Ocampo
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引用次数: 3

Abstract

1. In a double-blind randomized controlled design, 50 children were allocated to receive bupivacaine 0.25% or ropivacaine 0.25%, 0.32%, 0.40% or 0.50% by caudal block. 2. Caudal block was performed after induction of anaesthesia with 2-5% sevoflurane, atropine 10 microg/kg and midazolam 100-300 microg/kg. During the surgical procedure, patients were maintained under spontaneous ventilation and no intravenous or inhalatory anaesthetic agent was administered. For transoperative sedation, midazolam 100-300 microg/kg was administered every 0.5-1.0 h. Transoperative cardiovascular response, postoperative analgesia and local and systemic complications were evaluated. 3. Groups were similar (P > 0.05) in sex, age, weight and in the time elapsed from caudal block to the beginning of the surgical procedure. The surgical time was significantly lower in the ropivacaine 0.25% group. The duration of analgesia was 24 h with ropivacaine 0.25% and approximately 10 h in the other four groups (P < 0.001). Linear regression analysis revealed a significant relationship between the postoperative analgesic period produced by ropivacaine and the surgical time (r = -0.48, two-sided P = 0.002). Systolic and diastolic blood pressures remained in the physiologically normal range for the duration of the transoperative period. Vomiting was present in only one patient receiving ropivacaine 0.50%. 4. In children, the duration of analgesia produced by caudal block with ropivacaine may be affected by surgical time. At surgical times of 0.5-1 h, ropivacaine 0.25% produced at least 24 h postoperative analgesia. At similar surgical times, ropivacaine 0.32%, 0.40% and 0.50% produced similar analgesic times to bupivacaine 0.25%.

在咪达唑仑镇静下,罗哌卡因对外科手术患儿的尾侧剂量反应。
1. 在双盲随机对照设计中,50名儿童被分配接受布比卡因0.25%或罗哌卡因0.25%、0.32%、0.40%或0.50%的尾侧阻断。2. 2-5%七氟醚、阿托品10微克/千克、咪达唑仑100-300微克/千克诱导麻醉后行尾侧阻滞。在手术过程中,患者保持自发通气,不使用静脉或吸入麻醉剂。对于术中镇静,每0.5-1.0 h给予咪达唑仑100-300微克/千克。评估术中心血管反应、术后镇痛以及局部和全身并发症。3.各组在性别、年龄、体重以及从尾侧阻滞到手术开始的时间上差异无统计学意义(P > 0.05)。罗哌卡因0.25%组手术时间明显缩短。0.25%罗哌卡因组的镇痛时间为24 h,其余4组的镇痛时间约为10 h (P < 0.001)。线性回归分析显示罗哌卡因术后镇痛时间与手术时间有显著相关(r = -0.48,双侧P = 0.002)。收缩压和舒张压在手术期间保持在生理正常范围内。只有1例服用0.50%罗哌卡因的患者出现呕吐。4. 在儿童中,罗哌卡因尾侧阻滞产生的镇痛持续时间可能受手术时间的影响。在0.5-1 h的手术时间内,0.25%的罗哌卡因产生至少24 h的术后镇痛。在相似的手术时间,0.32%、0.40%和0.50%的罗哌卡因与0.25%的布比卡因产生相似的镇痛时间。
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来源期刊
Clinical and Experimental Pharmacology and Physiology
Clinical and Experimental Pharmacology and Physiology PHARMACOLOGY & PHARMACY-PHYSIOLOGY
自引率
0.00%
发文量
128
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
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