Brennan T J, Umali E F, Zahn P K
Department of Anesthesia, The University of Iowa, Iowa City 52242-1079, USA.
Anesthesiology. 1997 Dec;87(6):1517-28. doi: 10.1097/00000542-199712000-00031.
Preclinical studies in experimental animals suggest that preemptive analgesia may improve postoperative pain management. The beneficial effects of preemptive analgesia appear less remarkable clinically. The purpose of this study is to examine the effect of pre- and post-incision administration of intrathecal bupivacaine and intrathecal morphine in a rat model for postoperative pain.
Rats with intrathecal catheters were anesthetized with halothane, and the surgical field was prepared. A saline vehicle or the test drug was administered 15 min before an incision was made in the plantar aspect of the hindpaw or after the incision was completed. After recovery, mechanical hyperalgesia to punctate and nonpunctate stimuli was measured. Rats were tested on the day of surgery for the first 5 h and each day for 6 days.
In saline vehicle-treated rats, the median withdrawal threshold decreased from 522 mN to 54 mN or less, and the response frequency to pressure from application of the plastic disc increased from 0 +/- 0% to 96 +/- 12% or greater after incision. Hyperalgesia was persistent through 2 days after surgery and then gradually returned toward preincision values over the next 4 days. Pre- or postincision administration of either intrathecal morphine or intrathecal bupivacaine reduced hyperalgesia on the day of surgery; at all subsequent times, there were no differences between the saline vehicle groups and the drug treatment groups. There were never any significant differences between pre- and postincision treatments.
Early reduction in pain behaviors either by pre- or postincision management had no impact on subsequent measures of hyperalgesia in this model. These results agree with a number of clinical studies and suggest that incisional pain may be initiated and maintained differently than pain in other models.
对实验动物的临床前研究表明,超前镇痛可能改善术后疼痛管理。然而,超前镇痛在临床上的有益效果似乎并不显著。本研究的目的是在大鼠术后疼痛模型中,研究鞘内注射布比卡因和鞘内注射吗啡在切口前和切口后给药的效果。
将带有鞘内导管的大鼠用氟烷麻醉,并准备手术区域。在大鼠后爪足底切口前15分钟或切口完成后,给予生理盐水或受试药物。恢复后,测量对点状和非点状刺激的机械性痛觉过敏。在手术当天的前5小时对大鼠进行测试,并在随后的6天每天进行测试。
在生理盐水处理的大鼠中,切口后,中位撤针阈值从522 mN降至54 mN或更低,对塑料盘施加压力的反应频率从0 +/- 0%增加到96 +/- 12%或更高。痛觉过敏在术后持续2天,然后在接下来的4天逐渐恢复到切口前的值。鞘内注射吗啡或鞘内注射布比卡因在切口前或切口后给药均可在手术当天减轻痛觉过敏;在所有后续时间,生理盐水组和药物治疗组之间没有差异。切口前和切口后治疗之间从未有任何显著差异。
在该模型中,通过切口前或切口后处理早期减轻疼痛行为,对随后的痛觉过敏测量没有影响。这些结果与许多临床研究一致,表明切口痛的引发和维持方式可能与其他模型中的疼痛不同。