Almeida Raquel A, Lauretti Gabriela R, Mattos Anita L
Hospital das Clínicas, Department of Biomechanics, Medicine and Rehabilitation, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Brazil.
Anesthesiology. 2003 Feb;98(2):495-8. doi: 10.1097/00000542-200302000-00031.
The purpose of this study was to determine whether combination of 1-5 microg intrathecal neostigmine would enhance analgesia from a fixed intrathecal dose of morphine.
A total of 60 patients undergoing gynecologic surgery were randomized to one of five groups. Patients received 15 mg bupivacaine plus 2 ml of the test drug intrathecally (saline, 100 microg morphine, or 1-5 microg neostigmine). The control group received spinal saline as the test drug. The morphine group received spinal morphine as test drug. The morphine + 1 microg neostigmine group received spinal morphine and 1 microg neostigmine. The morphine + 2.5 microg neostigmine group received spinal morphine and 2.5 microg neostigmine. Finally, the morphine + 5 microg neostigmine group received spinal morphine and 5 microg neostigmine.
The groups were demographically similar. The time to first rescue analgesic (minutes) was longer for all patients who received intrathecal morphine combined with 1-5 microg neostigmine (median, 6 h) compared with the control group (median, 3 h) (P < 0.02). The morphine group (P < 0.05) and the groups that received the combination of 100 microg intrathecal morphine combined with neostigmine (P < 0.005) required less rescue analgesics in 24 h compared with the control group. The incidence of perioperative adverse effects was similar among groups (P > 0.05).
The addition of 1-5 microg spinal neostigmine to 100 microg morphine doubled the duration to first rescue analgesic in the population studied and decreased the analgesic consumption in 24 h, without increasing the incidence of adverse effects. The data suggest that low-dose spinal neostigmine may improve morphine analgesia.
本研究旨在确定鞘内注射1 - 5微克新斯的明与固定剂量鞘内吗啡联合使用是否能增强镇痛效果。
总共60例接受妇科手术的患者被随机分为五组之一。患者鞘内注射15毫克布比卡因加2毫升试验药物(生理盐水、100微克吗啡或1 - 5微克新斯的明)。对照组接受鞘内生理盐水作为试验药物。吗啡组接受鞘内吗啡作为试验药物。吗啡 + 1微克新斯的明组接受鞘内吗啡和1微克新斯的明。吗啡 + 2.5微克新斯的明组接受鞘内吗啡和2.5微克新斯的明。最后,吗啡 + 5微克新斯的明组接受鞘内吗啡和5微克新斯的明。
各组在人口统计学上相似。与对照组(中位数为3小时)相比,所有接受鞘内吗啡联合1 - 5微克新斯的明的患者首次补救镇痛时间(分钟)更长(中位数为6小时)(P < 0.02)。与对照组相比,吗啡组(P < 0.05)以及接受100微克鞘内吗啡联合新斯的明的组(P < 0.005)在24小时内所需的补救镇痛药更少。各组围手术期不良反应的发生率相似(P > 0.05)。
在100微克吗啡中添加1 - 5微克鞘内新斯的明,在所研究的人群中使首次补救镇痛的持续时间加倍,并在24小时内减少了镇痛药的消耗量,且未增加不良反应的发生率。数据表明低剂量鞘内新斯的明可能改善吗啡的镇痛效果。