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Spotlight on cervical vagus nerve stimulation for the treatment of primary headache disorders: a review

机译:聚焦颈迷走神经刺激治疗原发性头痛疾病的研究进展

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Objectives: Cervical noninvasive vagus nerve stimulation (nVNS) emerged as an adjunctive neuromodulation approach for primary headache disorders with limited responsiveness to pharmacologic and behavioral treatment. This narrative review evaluates the safety and efficacy of invasive and noninvasive peripheral nerve stimulation of the cervical branch of the vagal nerve (afferent properties) for primary headache disorders (episodic/chronic migraine [EM/CM] and cluster headache [ECH/CCH]) and provides a brief summary of the preclinical data on the possible mechanism of action of cervical vagus nerve stimulation (VNS) and trigemino-nociceptive head pain transmission. Materials and methods: A systematic search of published data was performed in PubMed for randomized controlled trials (RCTs) and prospective cohort clinical studies assessing the efficacy/safety and cost-effectiveness of cervical VNS in primary headache disorders and related preclinical studies. Results: Three RCTs were identified for ECH/CCH (ACT-1, ACT-2 and PREVA), one RCT for migraine (EVENT) and several prospective cohort studies and retrospective analyses for both headache disorders. In ACT-1, a significantly higher response rate, a higher pain-free rate and a decrease in mean attack duration were found in nVNS-treated ECH/CCH patients compared to sham stimulation. ACT-2 confirmed these findings (e.g., significantly higher pain-free attacks, pain severity decline and increased responder-rate [defined as ≥50% reduction]). The PREVA study demonstrated the superiority of adjunctive nVNS to standard care alone and observed a significantly higher attack reduction ( p =0.02) and responder rate (defined as ≥50% reduction). For CM, the EVENT study assessed a significantly higher frequency of decline in the open-label phase. Mostly transient mild/moderate adverse events were recorded, and no severe device-related adverse events occurred. Conclusion: Cervical nVNS represents a novel, safe and efficient adjunctive treatment option for primary headache disorders. In particular, preliminary observations suggest enhanced nVNS responsiveness in favor of episodic subtypes (EM and ECH). However, preclinical studies are urgently warranted to dissect the mechanism of action.
机译:目的:宫颈无创迷走神经刺激(nVNS)作为一种辅助性神经调节方法出现,用于原发性头痛疾病,对药物和行为治疗的反应有限。这篇叙述性评论评估了迷走神经颈支的有创和无创周围神经刺激(原发性/慢性偏头痛[EM / CM]和丛集性头痛[ECH / CCH])的安全性和有效性(迷走性)并简要概述了临床上的临床数据,这些数据涉及宫颈迷走神经刺激(VNS)和三叉神经痛伤害性头疼传递的可能作用机制。材料和方法:在PubMed中对公开数据进行系统搜索,以评估随机对照试验(RCT)和前瞻性队列临床研究,以评估子宫颈VNS在原发性头痛疾病中的功效/安全性和成本效益以及相关的临床前研究。结果:确定了3个针对ECH / CCH的RCT(ACT-1,ACT-2和PREVA),1个针对偏头痛的RCT(EVENT)以及针对这两种头痛疾病的若干前瞻性队列研究和回顾性分析。与假刺激相比,在ACT-1中,nVNS治疗的ECH / CCH患者的应答率,无痛率更高,平均发作持续时间缩短。 ACT-2证实了这些发现(例如,无痛发作明显增加,疼痛严重程度降低和应答率增加(定义为≥50%降低))。 PREVA研究证明了辅助性nVNS优于单纯的标准治疗,并观察到明显降低了发作率(p = 0.02)和缓解率(定义为≥50%)。对于CM,EVENT研究评估了开放标签阶段显着较高的下降频率。记录的大部分是短暂的轻度/中度不良事件,没有发生与设备相关的严重不良事件。结论:宫颈nVNS代表了一种针对原发性头痛疾病的新颖,安全,有效的辅助治疗选择。特别是,初步观察结果表明,增强的nVNS响应性有利于情节性亚型(EM和ECH)。但是,迫切需要进行临床前研究来剖析其作用机理。

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