Remote Electrical Neuromodulation for the Acute Treatment of Migraine in Patients with Chronic Migraine: An Open-Label Pilot Study

被引:19
|
作者
Nierenburg, Hida [1 ]
Vieira, Julio R. [1 ,2 ]
Lev, Nirit [3 ,4 ]
Lin, Tamar [5 ]
Harris, Dagan [5 ]
Vizel, Maya [5 ]
Ironi, Alon [5 ]
Lewis, Bryan [1 ]
Wright, Paul [1 ]
机构
[1] Nuvance Hlth, Div Neurol, Poughkeepsie, NY 12601 USA
[2] Albert Einstein Coll Med, Saul R Korey Dept Neurol, Bronx, NY 10467 USA
[3] Meir Med Ctr, Dept Neurol, Kefar Sava, Israel
[4] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[5] Theran Bioelect, Netanya, Israel
关键词
Acute migraine treatment; Chronic migraine; Consistency; Headache; Remote electrical neuromodulation; Medication overuse headache; Nerivio; NOXIOUS INHIBITORY CONTROLS; STIMULATION; PAIN; DISABILITY; CONSISTENCY; PLACEBO;
D O I
10.1007/s40122-020-00185-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction Remote electrical neuromodulation (REN) is a novel acute treatment of migraine. Upper arm peripheral nerves are stimulated to induce conditioned pain modulation (CPM)-an endogenous analgesic mechanism in which conditioning stimulation inhibits pain in remote body regions. The REN device (Nerivio(R), Theranica Bio-Electronics LTD., Israel) is FDA-authorized for acute treatment of migraine in adults who do not have chronic migraine. The current study assessed the consistency of response over multiple migraine attacks in people with chronic migraine who are typically characterized with severe pain intensity, high disability, and less robust response to triptans. Methods This was an open-label, single-arm, dual-center study conducted on adults with chronic migraine. Participants underwent a 4-week treatment phase in which they treated their migraine headaches with the device for 45 min within 1 h of attack onset. Pain levels were recorded at baseline, 2 h, and 24 h post-treatment. Efficacy outcomes (pain relief and pain-free responses at 2 h, sustained pain relief and sustained pain-free responses at 24 h) focused on intra-individual consistency of response across multiple attacks, which was defined as response in at least 50% of the treatments. Results Forty-two participants were enrolled, and 38 participants were evaluable for analyses; 73.7% (28/38) achieved pain relief at 2 h, 26.3% (10/38) were pain-free at 2 h, 84.4% (27/32) had sustained pain relief response at 24 h and 45.0% (9/20) had sustained pain relief response at 24 h in at least 50% of their treated attacks. The effects of REN on associated symptoms and improvement in function were also consistent. The incidence of device-related adverse events was low (1.8%). Conclusions REN used for a series of migraine attacks was effective and well tolerated across attacks. REN may offer a safe and effective non-pharmacological alternative for acute treatment in patients with chronic migraine.
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收藏
页码:531 / 543
页数:13
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