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鞘内注射吗啡治疗癌痛会导致耐受性的产生吗?

Does intrathecal morphine in the treatment of cancer pain induce the development of tolerance?

作者信息

Sallerin-Caute B, Lazorthes Y, Deguine O, Francés B, Verdié J C, Charlet J P, Bastide R

机构信息

Department of Neurosurgery, Faculty of Pharmaceutic Sciences, Paul Sabatier University, Toulouse, France.

出版信息

Neurosurgery. 1998 Jan;42(1):44-9; discussion 49-50. doi: 10.1097/00006123-199801000-00009.

Abstract

OBJECTIVE

This retrospective study was designed to investigate whether chronic lumbar intrathecal administration of morphine leads to the development of opioid tolerance in patients suffering from intractable cancer pain.

METHODS

Between 1978 and 1995, 159 patients with refractory cancer pain were treated with intrathecal morphine in our Multidisciplinary Pain Center. The treatment consisted of preservative-free morphine administered through an access port as a single bolus. In this series of patients (n = 159), the daily doses of intrathecal morphine were determined as a function of duration of follow-up.

RESULTS

The mean follow-up period was 95 days (range, 5-909 d), the mean starting daily dose of intrathecal morphine was 2.69 mg (range, 1-7.5 mg), and the mean terminal dose was 7.82 mg (range, 1-80 mg). The results demonstrated that only a moderate increase in daily dose of intrathecal morphine was required during the course of treatment (a two- to threefold increase for a 3-mo period). Furthermore, the dose increment was similar for patients followed up for more or less than 60 days. This increase did not result in any central opioid-related side effects, and the pain was managed satisfactorily.

CONCLUSION

The requirement for a moderate increase in intrathecal opioid doses reflects the development of tolerance but did not limit the patients' ability to obtain adequate analgesia during the course of their painful disease.

摘要

目的

本回顾性研究旨在调查慢性鞘内注射吗啡是否会导致顽固性癌痛患者产生阿片类药物耐受性。

方法

1978年至1995年间,我们的多学科疼痛中心对159例难治性癌痛患者进行了鞘内注射吗啡治疗。治疗采用通过接入端口单次推注无防腐剂吗啡。在这组患者(n = 159)中,鞘内吗啡的每日剂量根据随访时间确定。

结果

平均随访期为95天(范围5 - 909天),鞘内吗啡的平均起始每日剂量为2.69毫克(范围1 - 7.5毫克),平均终末剂量为7.82毫克(范围1 - 80毫克)。结果表明,治疗过程中仅需鞘内吗啡每日剂量适度增加(3个月内增加两到三倍)。此外,随访时间或多或少超过60天的患者剂量增加相似。这种增加未导致任何与阿片类药物相关的中枢性副作用,且疼痛得到了满意的控制。

结论

鞘内阿片类药物剂量适度增加反映了耐受性的产生,但并未限制患者在疼痛疾病过程中获得充分镇痛的能力。

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