Nabilone as an Adjunctive to Gabapentin for Multiple Sclerosis-Induced Neuropathic Pain: A Randomized Controlled Trial

被引:75
作者
Turcotte, Dana [1 ]
Doupe, Malcolm [5 ]
Torabi, Mahmoud [7 ]
Gomori, Andrew [2 ]
Ethans, Karen [3 ]
Esfahani, Farid [6 ]
Galloway, Katie [4 ]
Namaka, Mike [1 ,3 ,8 ]
机构
[1] Univ Manitoba, Fac Pharm, Winnipeg, MB R3E 0T5, Canada
[2] Univ Manitoba, Dept Community Hlth Sci, Winnipeg, MB R3E 0T5, Canada
[3] Univ Manitoba, Dept Neurol, Fac Med, Winnipeg, MB R3E 0T5, Canada
[4] Univ Manitoba, Sect Phys Med & Rehabil, Winnipeg, MB R3E 0T5, Canada
[5] Univ Manitoba, Dept Stat, Winnipeg, MB R3E 0T5, Canada
[6] Univ Manitoba, Fac Med, Winnipeg, MB, Canada
[7] Manitoba Ctr Hlth Policy, Winnipeg, MB, Canada
[8] Winnipeg Clin, Winnipeg, MB, Canada
关键词
Chronic Pain; Controlled Trial; Gabapentin; Neuropathic Pain; Pain Management; Multiple Sclerosis; NECROSIS-FACTOR-ALPHA; DOUBLE-BLIND; OUTCOME MEASURES; PARALLEL-GROUP; SPINAL-CORD; CANNABINOIDS; EFFICACY; COMBINATION; VALIDATION; MECHANISMS;
D O I
10.1111/pme.12569
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BackgroundNeuropathic pain (NPP) is a chronic syndrome suffered by patients with multiple sclerosis (MS), for which there is no cure. Underlying cellular mechanisms involved in its pathogenesis are multifaceted, presenting significant challenges in its management. MethodsA randomized, double-blind, placebo-controlled study involving 15 relapsing-remitting MS patients with MS-induced NPP was conducted to evaluate nabilone combined with gabapentin (GBP). Eligible patients stabilized on GBP (1,800mg/day) with inadequate pain relief were recruited. Nabilone or placebo was titrated over 4 weeks (0.5mg/week increase) followed by 5-week maintenance of 1mg oral nabilone (placebo) twice daily. Primary outcomes included two daily patient-reported measures using a 100-mm visual analog scale (VAS), pain intensity (VAS(pain)), and impact of pain on daily activities (VAS(impact)). Hierarchical regression modeling was conducted on each outcome to determine if within-person pain trajectory differed across study groups, during 63-day follow-up. ResultsAfter adjustment for key patient-level covariates (e.g., age, sex, Expanded Disability Status Scale, duration of MS, baseline pain), a significant groupxtime(2) interaction term was reported for both the VAS(pain) (P<0.01) and VAS(impact) score (P<0.01), demonstrating the adjusted rate of decrease for both outcomes was statistically greater in nabilone vs placebo study group. No significant difference in attrition rates was noted between treatments. Nabilone was well tolerated, with dizziness/drowsiness most frequently reported. ConclusionNabilone as an adjunctive to GBP is an effective, well-tolerated combination for MS-induced NPP. The results of this study identify a novel therapeutic combination for use in this population of patients predisposed to tolerability issues that may otherwise prevent effective pain management.
引用
收藏
页码:149 / 159
页数:11
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