Department of Anesthesiology, Mayo Clinic College of Medicine, Rochester, Minnesota 55902, USA.
Pain Med. 2010 Nov;11(11):1587-98. doi: 10.1111/j.1526-4637.2010.00962.x. Epub 2010 Oct 1.
The purpose of this study was to investigate the associations between morphine equivalent dose and heat pain (HP) perception in patients with chronic pain undergoing opioid tapering in the context of a multidisciplinary rehabilitation program.
Prospective design.
Multidisciplinary pain rehabilitation center.
The cohort included 109 patients using opioids (female 52%) who met inclusion criteria, and were consecutively admitted from March 2007 to June 2008.
Three-week outpatient multidisciplinary rehabilitation program that incorporates opioid tapering.
Using a standardized quantitative sensory test (QST) method of levels, standardized values of HP perception were obtained one day following program admission and following completion of the opioid taper at program dismissal.
At admission, the mean morphine equivalent dose was 192 mg/day. Univariate linear regression analysis showed that greater baseline morphine equivalent dose was associated (P = 0.040) with lower, or more hyperalgesic, values of HP 5-0.5, which is a standardized measure of HP perception. The dose dependent association retained significance (P = 0.029) after adjusting for pain severity, pain duration and pain diagnosis. Tapering of greater morphine equivalent dosages was associated (P = 0.001) with lower values of HP 5-0.5. The association retained significance (P = 0.001) after adjusting for pain severity, pain duration, pain diagnosis, opioid withdrawal symptoms, and time between completion of the taper and performance of the dismissal QST.
The use of a validated QST method of levels and standardized values of HP 5-0.5 may expand the methodological approaches available for investigating the clinical effects of opioids on HP perception.
本研究旨在探讨在多学科康复计划背景下,慢性疼痛患者接受阿片类药物逐渐减量过程中,吗啡等效剂量与热痛(HP)感知之间的相关性。
前瞻性设计。
多学科疼痛康复中心。
该队列纳入了符合纳入标准、2007 年 3 月至 2008 年 6 月期间连续入院的 109 名使用阿片类药物的患者(女性占 52%)。
为期 3 周的门诊多学科康复计划,包括阿片类药物逐渐减量。
在入院时,平均吗啡等效剂量为 192mg/天。单变量线性回归分析显示,基线时较高的吗啡等效剂量与较低(即更痛觉过敏)的 HP5-0.5 标准化值相关(P=0.040),这是 HP 感知的标准化测量方法。在调整疼痛严重程度、疼痛持续时间和疼痛诊断后,剂量相关的相关性仍然具有统计学意义(P=0.029)。更大剂量的吗啡等效药物逐渐减量与 HP5-0.5 的较低值相关(P=0.001)。在调整疼痛严重程度、疼痛持续时间、疼痛诊断、阿片类药物戒断症状以及完成减量和进行出院 QST 之间的时间后,这种相关性仍然具有统计学意义(P=0.001)。
使用验证过的 QST 水平方法和标准化的 HP5-0.5 值可能会扩展研究阿片类药物对 HP 感知的临床效果的方法学方法。