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The Role of N-acetyl-L-Cysteine (NAC) as an Adjuvant to Opioid Treatment in Patients with Inadequately Controlled Chronic Neuropathic Pain

机译:N-乙酰基-L-半胱氨酸(NAC)作为阿片类药物治疗不良慢性控制性疼痛患者的作用

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摘要

Introduction. While opioid medications are commonly prescribed for management of neuropathic pain (NP), long-term use has been associated with increased risk for overdose, drug interactions and addiction. New strategies are necessary to better manage chronic pain, thereby reducing need for opioid medications and their associated adverse consequences. N-acetyl-L-cysteine (NAC), an over-the-counter supplement, has shown promise in the treatment of psychiatric and addictive disorders. In addition, NAC has shown promise for reducing physiological signs of NP in laboratory rat models, prompting this study.Purpose. The present study was an open-label clinical trial of NAC as an adjuvant to opioid treatment for poorly controlled, chronic NP. It examined whether 1200 mg NAC twice daily for 4 weeks was associated with: lower ratings of patient-reported pain; reductions in PRN opioid medication for breakthrough pain; and improvements in physical and mental health quality of life (QoL). The study also examined whether appraisal of pain impacts response to medication.Method. Participants were N=28 chronic NP patients who consented to study participation. This consisted of 2 baseline assessments, 4 weeks of NAC and 1 post-trial follow-up visit. The majority (N=17) dropped out or were excluded during baseline. Of the remaining participants, N = 11 started the study medication and N=10 completed the study, with daily recordings of pain severity ratings and use of PRN opioid medication. Small sample size limited analyses to qualitative case reviews and effect sizes.Results. Over 90% of participants receiving NAC completed the study. Case review found varied results. While 4 of 10 participants showed decrease in average pain ratings during NAC, estimated effect sizes for the whole sample were small, bordering on negligible (ω² from .003 to .027) as were those for PRN opioids (Partial Eta-Squared=.0003). Effect size for mental health QoL was medium (Cohenu27s d=.421). Conclusions. With N=10, findings must be interpreted with caution. Nonetheless, the study found some albeit small evidence supporting NAC for improving mental health QoL and pain ratings. Several participants reported improvements in pain and mental health domains while taking NAC. NAC was well tolerated with minimal side effects. Lessons from this study will inform design and implementation of future NAC studies.
机译:介绍。虽然阿片类药物通常被指定用于治疗神经性疼痛(NP),但长期使用与过量服用,药物相互作用和成瘾的风险增加有关。必须采取新的策略来更好地控制慢性疼痛,从而减少对阿片类药物的需求及其相关的不良后果。非处方药N-乙酰-L-半胱氨酸(NAC)在治疗精神病和成瘾性疾病方面显示出了希望。此外,NAC还显示出有望减少实验室大鼠模型中NP的生理征象的前景,从而推动了这项研究。本研究是NAC作为阿片类药物治疗不良控制的慢性NP佐剂的开放标签临床试验。它检查了1200毫克NAC每天两次,共4周是否与以下症状有关:患者报告的疼痛评分降低;减少用于突破性疼痛的PRN阿片类药物;以及改善身心健康的生活质量(QoL)。该研究还检查了疼痛评估是否会影响对药物的反应。参加者为同意参加研究的N = 28名慢性NP患者。这包括2项基线评估,4周NAC和1项试验后随访。在基线期间,大多数(N = 17)辍学或被排除在外。在其余参与者中,N = 11开始研究药物,N = 10完成研究,每天记录疼痛严重程度等级和使用PRN阿片类药物。小样本量限制了对定性病例审查和效果量的分析。接受NAC的参与者中有90%以上完成了研究。案例审查发现结果各异。尽管10名参与者中有4名在NAC期间平均疼痛等级降低,但整个样本的估计效应量很小,与PRN阿片类药物的效应值可忽略不计(ω²从.003到.027)(部分Eta平方= .0003) )。心理健康QoL的影响大小为中等(Cohen d27.d = .421)。结论。在N = 10时,必须谨慎解释发现。尽管如此,该研究发现,尽管有少量证据支持NAC改善心理健康QoL和疼痛等级。几位参与者报告了服用NAC期间在疼痛和心理健康方面的改善。 NAC具有良好的耐受性,且副作用极小。这项研究的经验教训将为将来NAC研究的设计和实施提供信息。

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    Moore Thomas B;

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