Lynch Mary, Moulin Dwight, Perez Jordy
Anesthesia, Pain Management and Perioperative Medicine, Psychiatry and Pharmacology, Dalhousie University, Halifax, Nova Scotia, Canada.
Department of Clinical Neurological Sciences, Western University, London, Ontario, Canada.
Can J Pain. 2019 Oct 22;3(1):180-189. doi: 10.1080/24740527.2019.1660575. eCollection 2019.
: Accumulating evidence has identified a number of advantages for methadone over other opioids for the treatment of chronic pain including: agonist action at both μ and δ opioid receptors, -methyl-d-aspartate (NMDA) antagonist activity and the ability to inhibit the reuptake of monoamines. It was hypothesized that with these three mechanisms of action methadone might be a good option for the treatment of neuropathic pain. : This was a double-blind randomized controlled trial comparing methadone to controlled-release morphine. The primary objective was to determine whether methadone is clinically inferior versus noninferior to morphine as an analgesic. : We attempted recruitment at three academic pain centers over a 3-year period. In the end only 14 participants were able to be recruited; 5 withdrew and only 9 completed the trial. This study was underpowered. All participants showed a mean reduction in pain intensity according to the Numeric Rating Scale for Pain Intensity (morphine 5.86 to 4.38, methadone 6.11 to 4.5) and reported pain relief compared to pretreatment, but the sample size was too small for statistical analysis. : Reasons for challenges in recruitment included tight inclusion and exclusion criteria and high participant burden. In addition, there was significant heterogeneity of patients between the three sites, leading to differences in reasons for exclusion. This included seemingly disparate reasons at the different sites, including few participants who were methadone naïve vs. avoidance or fear of opioids. In the end, we were unable to answer the question of the study.
越来越多的证据表明,与其他阿片类药物相比,美沙酮在治疗慢性疼痛方面具有许多优势,包括:对μ和δ阿片受体的激动作用、N-甲基-D-天冬氨酸(NMDA)拮抗剂活性以及抑制单胺再摄取的能力。据推测,凭借这三种作用机制,美沙酮可能是治疗神经性疼痛的一个不错选择。
这是一项双盲随机对照试验,将美沙酮与缓释吗啡进行比较。主要目的是确定美沙酮作为镇痛药在临床上是否比吗啡差或不劣于吗啡。
我们在3年时间里尝试在三个学术疼痛中心进行招募。最终仅招募到14名参与者;5人退出,只有9人完成了试验。这项研究的样本量不足。根据疼痛强度数字评定量表,所有参与者的疼痛强度均有平均降低(吗啡从5.86降至4.38,美沙酮从6.11降至4.5),并且与治疗前相比均报告疼痛得到缓解,但样本量太小无法进行统计分析。
招募面临挑战的原因包括严格的纳入和排除标准以及参与者负担过重。此外,三个地点的患者存在显著异质性,导致排除原因存在差异。这包括不同地点看似不同的原因,包括初用美沙酮的参与者较少与对阿片类药物的回避或恐惧。最终,我们无法回答该研究的问题。