[蛛网膜下给药丁卡因联合小剂量吗啡或纳布啡用于脊髓麻醉的镇痛效果]。

M L Lin
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引用次数: 0

摘要

对60例ASA身体状态为I级或II级的患者进行蛛网膜下腔给药丁卡因联合小剂量吗啡或纳布啡腰麻的镇痛效果评价。将葡萄糖溶液(10%)加入0.4 mg吗啡或0.4 mg纳布啡中,使其总容积为2 ml,采用双盲、随机方式在鞘内注射丁卡因。生命体征、感觉水平、运动阻滞、疼痛评分和副作用在前15分钟每2分钟记录一次,然后在15、30、45、60分钟和每隔30分钟记录一次,直到患者主诉疼痛。记录前24 h的副作用和阿片类药物需用量。对照组完全镇痛(从注射到首次报告疼痛的时间)持续180 +/- 51.6 min,添加0.4 mg纳布啡组持续238 +/- 71 min,添加0.4 mg吗啡组持续250 +/- 74 min (p < 0.05)。纳布啡组和吗啡组的有效镇痛(从注射到第一次阿片类药物需求的时间)也比对照组增加。在使用纳布啡或吗啡时,两组患者在完全或有效镇痛方面没有差异。结果表明,在高压压丁卡因中加入0.4 mg纳布啡或吗啡可提高术中镇痛质量,并可持续至术后。纳布啡组不良反应明显小于吗啡组。
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[The analgesic effect of subarachnoid administration of tetracaine combined with low dose morphine or nalbuphine for spinal anesthesia].

The analgesic effect of subarachnoid administration of tetracaine combined with low dose morphine or nalbuphine for spinal anesthesia was evaluated in 60 ASA physical status class I or II patients. Dextrose solution (10%) was added to 0.4 mg morphine or 0.4 mg nalbuphine to make a total volume of 2 ml, which was injected intrathecally with tetracaine in a double-blind, randomized fashion. Vital signs, sensory level, motor block, pain score, and side effects were recorded every 2 min for the first 15 min and then at 15, 30, 45, and 60 min and at 30-min intervals until the patient complained of pain. Side effects and opioid requirements were recorded for the first 24 h. Complete analgesia (time from injection to first report of pain) lasted 180 +/- 51.6 min in the control group and increased to 238 +/- 71 min in group with addition of 0.4 mg nalbuphine, 250 +/- 74 min in group with addition of 0.4 mg morphine (p less than 0.05). The effective analgesia (time from injection to first opioid requirement) also increased in groups of nalbuphine and morphine than the control group. No differences in complete or effective analgesia was found between groups in the presence of nalbuphine or morphine. Results indicate that the addition of 0.4 mg nalbuphine or morphine to hyperbaric tetracaine for spinal anesthesia improves the quality of intraoperative analgesia and can last into the postoperative period. Side effects were less in nalbuphine group than with morphine group.

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