加巴喷丁与普瑞巴林治疗慢性炎性脱髓鞘性多根神经病变。

American journal of neurodegenerative disease Pub Date : 2021-08-15 eCollection Date: 2021-01-01
Moulood Rayani, Behnaz Ansari, Sajad Asadi Boroujeni, Hossein Abdollahi Veshnavei, Keivan Basiri
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引用次数: 0

摘要

慢性炎症性脱髓鞘性多根神经病变(CIDP)是一种慢性自身免疫性脱髓鞘周围神经病变,可导致对称性肌肉无力、感觉缺陷、反射减退、慢性疲劳和生活质量下降(QoL)。本研究旨在探讨加巴喷丁与普瑞巴林对CIDP患者疼痛、睡眠障碍和生活质量的影响。方法:本临床试验选取40例确诊为CIDP的患者,随机分为加巴喷丁100 ~ 500mg (n=20)和普瑞巴林50 ~ 300mg (n=20)两组,两组联合文拉法辛37.5 mg。加巴喷丁/普瑞巴林的剂量根据患者对治疗的耐受性/反应进行调整。分别于干预后3个月、6个月、9个月和12个月填写视觉模拟量表(VAS)、匹兹堡睡眠质量问卷和简短健康问卷(SF-36),评估疼痛程度、睡眠质量和生活质量。伊朗临床试验登记处(IRCT)代码:IRCT20200217046523N16, https://fa.irct.ir/search/result?query=IRCT20200217046523N16.Results:加巴喷丁在疼痛严重程度(p值=0.004,r=0.287)、睡眠质量(p值p值=0.001,r=-0.378)和普瑞巴林(p值>0.05)方面显示剂量依赖性疗效。加巴喷丁与文拉法辛合用可显著改善睡眠质量(p值=0.009)和生活质量(p值=0.004),但可显著改善疼痛程度(p值=0.796)。普瑞巴林联合文拉法辛对普瑞巴林的疼痛(p值=0.046)、睡眠质量(p值p值>0.001)和生活质量(p值=0.03)均有统计学意义的改善。结论:在本研究中,与文拉法辛加巴喷丁相比,普瑞巴林与文拉法辛联合用药在控制CIDP的疼痛、睡眠质量和生活质量方面具有显著的优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gabapentin versus Pregabalin for management of chronic inflammatory demyelinating polyradiculoneuropathy.

Introduction: Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a chronic autoimmune demyelinating peripheral neuropathy that leads to symmetrical muscular weakness, sensory deficit, hyporeflexia, chronic fatigue, and impaired quality of life (QoL). The current study aims to investigate the effects of gabapentin versus pregabalin on pain, sleep disturbances, and QoL in CIDP patients.

Methods: This clinical trial was conducted on 40 patients diagnosed with CIDP randomly allocated to treatment with 100-500 mg gabapentin (n=20) or 50-300 mg pregabalin (n=20) both co-medicated with 37.5 mg venlafaxine. The dose of gabapentin/pregabalin was adjusted based on the patient's tolerability/response to the treatment. Visual analogue scale (VAS), Pittsburg Sleep Quality Questionnaire and Short Form Health Survey (SF-36) were filled at baseline, within three, six, nine and 12 months after the interventions to assess pain severity, sleep quality and QoL, respectively. The Iranian Registry of Clinical Trials (IRCT) code: IRCT20200217046523N16, https://fa.irct.ir/search/result?query=IRCT20200217046523N16.

Results: Gabapentin revealed a dose-dependent efficacy in pain severity (P-value =0.004, r=0.287), sleep quality (P-value <0.001, r=0.387) and QoL (P-value =0.001, r=-0.378), but pregabalin (P-value >0.05). Co-medication of gabapentin plus venlafaxine could significantly improve sleep quality (P-value =0.009) and QoL (P-value =0.004), but pain severity (P-value =0.796). Pregabalin plus venlafaxine showed statistically significant improvement in pain (P-value =0.046), sleep quality (P-value <0.001) and QoL (P-value <0.001). The comparison of the two medications revealed the superiority of pregabalin in pain relief (P-value >0.001) and QoL (P-value =0.03) to pregabalin.

Conclusion: Based on this study, the co-medication of pregabalin and venlafaxine led to remarkable superior outcomes compared to venlafaxine plus gabapentin in the management of pain, sleep quality, and QoL due to CIDP.

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