Pressure sensitivity and phenotypic changes in patients with suspected opioid-induced hyperalgesia being withdrawn from full mu agonists.

Journal of nature and science Pub Date : 2017-02-01
Ronald A Wasserman, Afton L Hassett, Steven E Harte, Jenna Goesling, Herbert L Malinoff, Daniel W Berland, Jennifer Zollars, Stephanie E Moser, Chad M Brummett
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Abstract

Objectives: To assess changes in phenotype and pressure sensitivity in patients with suspected opioid-induced-hyperalgesia (OIH) after transitioning to buprenorphine.

Methods: Twenty patients with suspected OIH were enrolled to transition to buprenorphine therapy. Patients completed validated self-report measures at baseline and at 1, 4, 8 weeks, and 6 months after initiation of buprenorphine along with quantitative sensory testing including measures of pressure pain threshold, pain tolerance and Pain 50 (a pain intensity rating).

Results: 20 patients were enrolled, 17 were treated with buprenorphine and 11 completed all assessment points. We found that after transitioning to buprenorphine, patients on higher opioid doses (≥100mg oral morphine equivalents) had significant improvements for some measures including decreased pain severity and fibromyalgia survey scores, fewer neuropathic pain features, less catastrophizing, fewer depressive symptoms, and improved functioning 1-week after transitioning to buprenorphine with an eventual return back to baseline. Although not statistically significant, patients on high dose opioids (≥100mg OME) also showed a trend of decreased pressure sensitivity 1-week after transitioning to buprenorphine with a gradual return back to baseline.

Conclusions: Our study is the first to look at pressure pain sensitivity in patients who were taking opioids and transitioned to buprenorphine. These results suggest that the patients most likely to benefit from buprenorphine therapy are those on higher doses. In addition, the eventual return back to baseline on measures of pain phenotype and pressure sensitivity suggests that buprenorphine may over time result in a return of the hyperalgesic effects of a full mu agonist.

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疑似阿片类药物致痛觉过敏患者停用全受体激动剂后的压力敏感性和表型变化。
目的:评估疑似阿片类药物致痛觉过敏(OIH)患者改用丁丙诺啡后表型和压力敏感性的变化。方法:选取20例疑似OIH患者转入丁丙诺啡治疗。患者在丁丙诺啡开始使用后的基线、1、4、8周和6个月完成了有效的自我报告测量,并进行了定量感觉测试,包括压痛阈值、疼痛耐受性和pain 50(疼痛强度评级)。结果:20例患者入组,17例患者接受丁丙诺啡治疗,11例患者完成所有评估点。我们发现,在过渡到丁丙诺啡后,服用高阿片类药物剂量(≥100mg口服吗啡当量)的患者在一些措施上有显著改善,包括疼痛严重程度和纤维肌痛调查评分降低,神经性疼痛特征减少,灾难化减少,抑郁症状减少,并且在过渡到丁丙诺啡后1周功能改善并最终恢复到基线。虽然没有统计学意义,但高剂量阿片类药物(≥100mg OME)患者在过渡到丁丙诺啡后1周也有降低压力敏感性的趋势,并逐渐恢复到基线水平。结论:我们的研究首次观察了服用阿片类药物并过渡到丁丙诺啡的患者的压痛敏感性。这些结果表明,最有可能从丁丙诺啡治疗中获益的患者是那些服用高剂量丁丙诺啡的患者。此外,疼痛表型和压力敏感性测量的最终回归基线表明,丁丙诺啡可能随着时间的推移导致全受体激动剂的超痛觉作用的回归。
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