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鞘内注射吗啡镇痛的药代动力学方面

Pharmacokinetic aspects of intrathecal morphine analgesia.

作者信息

Nordberg G, Hedner T, Mellstrand T, Dahlström B

出版信息

Anesthesiology. 1984 May;60(5):448-54. doi: 10.1097/00000542-198405000-00010.

Abstract

Fifteen patients undergoing thoracotomy were given 0.25 or 0.50 mg morphine intrathecally (L2-L3 or L3-L4) for an analgetic and pharmacokinetic study. Administration of morphine at the end of the operation resulted in a highly variable duration of analgesia ranging from 1-20.5 and 1-40 h for the 0.25 and 0.50 mg groups, respectively. Calculation of cumulative consumption pattern of additional analgesics given im indicated a dose-related analgesia lasting around 12 h. Morphine concentrations in the CSF were high and dose dependent. Thus, at 1 h, CSF concentrations (means +/- SEM) were 4,228 +/- 361 ng/ml and 10,447 +/- 1,538 ng/ml for the 0.25 and 0.50-mg groups, respectively. The plasma concentrations generally were very low, i.e., under 1 ng/ml. For the 0.50 and 0.25 mg groups, the terminal elimination half-life in CSF was 175 +/- 9 min and 196 +/- 13 min, respectively: the volume of CSF distribution was 0.88 +/- 0.16 ml X kg-1 and 1.06 +/- 0.17 ml X kg-1, respectively: and the clearance from CSF was 2.81 +/- 0.41 microliter X kg-1 X min-1 and 3.41 +/- 0.55 microliter X kg-1 X min-1, respectively (means +/- SEM). The study indicates that the significant pharmacokinetic parameter related to the long duration of analgesia after intrathecal morphine administration probably is the high CSF concentrations found, since the rate of elimination from CSF is similar to what is reported for morphine in plasma. Furthermore, modulation of nociceptive input in the thoracic region also may be achieved by lumbar administration, but a slower onset should be anticipated.

摘要

15名接受开胸手术的患者在L2-L3或L3-L4节段接受了鞘内注射0.25或0.50毫克吗啡的镇痛和药代动力学研究。手术结束时给予吗啡,0.25毫克组和0.50毫克组的镇痛持续时间差异很大,分别为1至20.5小时和1至40小时。静脉注射额外镇痛药的累积消耗模式计算表明,剂量相关的镇痛作用持续约12小时。脑脊液中的吗啡浓度很高且与剂量相关。因此,在1小时时,0.25毫克组和0.50毫克组的脑脊液浓度(平均值±标准误)分别为4228±361纳克/毫升和10447±1538纳克/毫升。血浆浓度通常非常低,即低于1纳克/毫升。对于0.50毫克组和0.25毫克组,脑脊液中的终末消除半衰期分别为175±9分钟和196±13分钟;脑脊液分布容积分别为0.88±0.16毫升·千克⁻¹和1.06±0.17毫升·千克⁻¹;脑脊液清除率分别为2.81±0.41微升·千克⁻¹·分钟⁻¹和3.41±0.55微升·千克⁻¹·分钟⁻¹(平均值±标准误)。该研究表明,鞘内注射吗啡后镇痛持续时间长的重要药代动力学参数可能是所发现的高脑脊液浓度,因为脑脊液中的消除速率与血浆中吗啡的报道相似。此外,通过腰部给药也可以实现对胸部伤害性输入的调节,但预计起效较慢。

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