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Improved opioid analgesic effect following opioid dose reduction.阿片类药物剂量减少后阿片类镇痛效果改善。
Pain Med. 2008 Sep;9(6):724-7. doi: 10.1111/j.1526-4637.2008.00501.x.
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A differential diagnosis of hyperalgesia, toxicity, and withdrawal from intrathecal morphine infusion.鞘内注射吗啡引起痛觉过敏、毒性反应及戒断反应的鉴别诊断。
Anesth Analg. 2007 Dec;105(6):1816-9, table of contents. doi: 10.1213/01.ane.0000290338.39037.38.
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Enhanced postoperative sensitivity to painful pressure stimulation after intraoperative high dose remifentanil in patients without significant surgical site pain.在无明显手术部位疼痛的患者中,术中使用高剂量瑞芬太尼后术后对疼痛性压力刺激的敏感性增强。
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Opioid tolerance and hyperalgesia in chronic pain patients after one month of oral morphine therapy: a preliminary prospective study.慢性疼痛患者口服吗啡治疗1个月后的阿片类药物耐受性和痛觉过敏:一项初步前瞻性研究。
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Oral opioid administration and hyperalgesia in patients with cancer or chronic nonmalignant pain.癌症或慢性非恶性疼痛患者口服阿片类药物与痛觉过敏
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接受阿片类药物治疗的受试者定量感觉测试结果发生改变。

Altered quantitative sensory testing outcome in subjects with opioid therapy.

作者信息

Chen Lucy, Malarick Charlene, Seefeld Lindsey, Wang Shuxing, Houghton Mary, Mao Jianren

机构信息

MGH Center for Translational Pain Research, Department of Anesthesia and Critical Care, WACC 324, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

出版信息

Pain. 2009 May;143(1-2):65-70. doi: 10.1016/j.pain.2009.01.022. Epub 2009 Feb 23.

DOI:10.1016/j.pain.2009.01.022
PMID:19237249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2680088/
Abstract

Preclinical studies have suggested that opioid exposure may induce a paradoxical decrease in the nociceptive threshold, commonly referred as opioid-induced hyperalgesia (OIH). While OIH may have implications in acute and chronic pain management, its clinical features remain unclear. Using an office-based quantitative sensory testing (QST) method, we compared pain threshold, pain tolerance, and the degree of temporal summation of the second pain in response to thermal stimulation among three groups of subjects: those with neither pain nor opioid therapy (group 1), with chronic pain but without opioid therapy (group 2), and with both chronic pain and opioid therapy (group 3). We also examined the possible correlation between QST responses to thermal stimulation and opioid dose, opioid treatment duration, opioid analgesic type, pain duration, or gender in group 3 subjects. As compared with both group 1 (n=41) and group 2 (n=41) subjects, group 3 subjects (n=58) displayed a decreased heat pain threshold and exacerbated temporal summation of the second pain to thermal stimulation. In contrast, there were no differences in cold or warm sensation among three groups. Among clinical factors, daily opioid dose consistently correlated with the decreased heat pain threshold and exacerbated temporal summation of the second pain in group 3 subjects. These results indicate that decreased heat pain threshold and exacerbated temporal summation of the second pain may be characteristic QST changes in subjects with opioid therapy. The data suggest that QST may be a useful tool in the clinical assessment of OIH.

摘要

临床前研究表明,接触阿片类药物可能会导致痛觉阈值出现反常下降,这通常被称为阿片类药物诱导的痛觉过敏(OIH)。虽然OIH可能对急性和慢性疼痛管理有影响,但其临床特征仍不明确。我们采用基于门诊的定量感觉测试(QST)方法,比较了三组受试者对热刺激的疼痛阈值、疼痛耐受度以及第二痛觉的时间总和程度:既无疼痛也未接受阿片类药物治疗的受试者(第1组)、患有慢性疼痛但未接受阿片类药物治疗的受试者(第2组),以及患有慢性疼痛且接受阿片类药物治疗的受试者(第3组)。我们还研究了第3组受试者对热刺激的QST反应与阿片类药物剂量、阿片类药物治疗持续时间、阿片类镇痛药物类型、疼痛持续时间或性别的可能相关性。与第1组(n = 41)和第2组(n = 41)受试者相比,第3组受试者(n = 58)的热痛阈值降低,对热刺激的第二痛觉时间总和加剧。相比之下,三组之间在冷觉或温觉方面没有差异。在临床因素中,第3组受试者的每日阿片类药物剂量始终与热痛阈值降低和第二痛觉时间总和加剧相关。这些结果表明,热痛阈值降低和第二痛觉时间总和加剧可能是接受阿片类药物治疗受试者QST的特征性变化。数据表明,QST可能是OIH临床评估中的一种有用工具。