Ziadni Maisa, Chen Abby L, Krishnamurthy Parthasarathy, Flood Pamela, Stieg Richard L, Darnall Beth D
Division of Pain Medicine, Department of Anesthesiology, Perioperative and Pain Medicine, Stanford University School of Medicine, Palo Alto, CA, USA.
Department of Marketing and Entrepreneurship, CT Bauer College of Business, University of Houston, Houston, TX, USA.
Pain Rep. 2020 Sep 17;5(5):e851. doi: 10.1097/PR9.0000000000000851. eCollection 2020 Sep-Oct.
We previously reported promising results for a 4-month patient-centered voluntary opioid tapering study. Key questions remain about the durability of effects and possible risks after opioid reduction. We provide the longest follow-up data to date for prospective opioid tapering: 2- to 3-year follow-up for pain intensity and daily opioid use in a subset of patients from our original 4-month opioid tapering study.
Twenty-three patients (44% of original sample) responded to contact attempts through telephone and reported their average pain intensity and current opioid use. Opioid doses were converted to morphine equivalent daily dose (MEDD). Data were analyzed within a repeated-measures model where time (baseline, 4 months, and 2-3 years) was the within-subject factor.
Among reachable patients, the effect of time on change in MEDD from baseline to 4 months to 2 to 3 years was significant. Since baseline, 20 (95%) of the current sample reduced MEDD, and 15 (71%) further reduced MEDD at 2- to 3-year follow-up. There was no effect of time on change in pain intensity from baseline to 4 months to 2 to 3 years. Since baseline, 11 (52%) of the current sample reported pain reduction, and 12 (57%) reported reduced pain from the 4-month follow-up to the 2- to 3-year follow-up. Five (24%) reported increased pain intensity.
Study findings reveal continued MEDD reduction and enduring pain stability 2 to 3 years after a patient-centered voluntary opioid tapering program for a substantial fraction of patients. Notably, we were not able to verify current opioid use through medical records and were limited by self-report.
我们之前报告了一项为期4个月的以患者为中心的自愿阿片类药物减量研究取得了令人鼓舞的结果。关于阿片类药物减量后效果的持久性和可能的风险,关键问题仍然存在。我们提供了迄今为止前瞻性阿片类药物减量最长的随访数据:对我们最初为期4个月的阿片类药物减量研究中的一部分患者进行了2至3年的疼痛强度和每日阿片类药物使用情况的随访。
23名患者(占原始样本的44%)通过电话回应了联系尝试,并报告了他们的平均疼痛强度和当前阿片类药物使用情况。阿片类药物剂量转换为吗啡当量日剂量(MEDD)。数据在重复测量模型中进行分析,其中时间(基线、4个月和2至3年)是受试者内因素。
在可联系到的患者中,从基线到4个月再到2至3年,时间对MEDD变化的影响显著。自基线以来,当前样本中的20名(95%)患者降低了MEDD,15名(71%)患者在2至3年随访时进一步降低了MEDD。从基线到4个月再到2至3年,时间对疼痛强度变化没有影响。自基线以来,当前样本中的11名(52%)患者报告疼痛减轻,12名(57%)患者报告从4个月随访到2至3年随访疼痛减轻。5名(24%)患者报告疼痛强度增加。
研究结果显示,在以患者为中心的自愿阿片类药物减量计划实施2至3年后,相当一部分患者的MEDD持续降低,疼痛保持稳定。值得注意的是,我们无法通过医疗记录核实当前的阿片类药物使用情况,且受自我报告的限制。