Marmura Michael J, Lin Tamar, Harris Dagan, Ironi Alon, Rosen Noah L
Jefferson Headache Center, Thomas Jefferson University, Philadelphia, PA, United States.
Theranica Bio-Electronics Ltd., Netanya, Israel.
Front Neurol. 2020 Apr 7;11:226. doi: 10.3389/fneur.2020.00226. eCollection 2020.
A recent randomized controlled study showed that 66.7% (66/99) and 37.4% (37/99) of people undergoing remote electrical neuromodulation (REN), a novel non-pharmacological migraine treatment, achieve pain relief and pain freedom, respectively, at 2 h post-treatment. The participants who completed the 6-weeks double-blind phase of this study were offered to participate in an open-label extension (OLE) with an active REN device. This study investigated the clinical use of REN, focusing on its potential in reducing the use of acute migraine medications. The parent study for this open-label extension (OLE) was a randomized, double-blind, sham-controlled study of acute treatment conducted on 296 participants enrolled at 12 sites in the USA and Israel. This study included a run-in phase, in which migraine attacks were treated with usual care, and an 8-weeks double-blind treatment phase. One hundred sixty participants continued in an 8-weeks OLE phase in which they could incorporate a REN device into their usual care. Medication use rate (percentage of participants who treated their attacks only with REN and avoided medications in all their attacks) and pain outcomes at 2 h post-treatment were compared between the OLE and the run-in phase in a within-subject design. The analyses were performed on 117 participants with episodic migraine. During the OLE, 89.7% of the participants treated their attacks only with REN and avoided medications in all their attacks compared with 15.4% in the run-in phase ( < 0.0001). The rates of pain relief and pain-free in at least 50% of the treatments at 2 h post-treatment were comparable (pain relief: 58.1% in the run-in phase and 57.3% in the OLE, = 0.999; pain-free: 23.1% in the run-in vs. 30.8% in the OLE, = 0.175). REN may reduce the use of acute migraine medications. Thus, incorporating REN into usual care may reduce the risk for medication overuse headache (MOH). Future studies should evaluate whether REN reduces the use of acute migraine medications in a population at risk for MOH.
最近一项随机对照研究表明,接受远程电神经调节(REN,一种新型非药物偏头痛治疗方法)的患者中,分别有66.7%(66/99)和37.4%(37/99)在治疗后2小时实现了疼痛缓解和疼痛消失。完成该研究6周双盲阶段的参与者被邀请参加一项使用活性REN设备的开放标签扩展(OLE)研究。本研究调查了REN的临床应用,重点关注其在减少急性偏头痛药物使用方面的潜力。这项开放标签扩展(OLE)研究的母研究是一项针对在美国和以色列12个地点招募的296名参与者进行的急性治疗随机、双盲、假对照研究。该研究包括一个导入期,在此期间偏头痛发作采用常规治疗,以及一个为期8周的双盲治疗期。160名参与者继续进入为期8周的OLE阶段,在此期间他们可以将REN设备纳入其常规治疗中。在一项受试者内设计中,比较了OLE阶段和导入期的药物使用率(仅使用REN治疗发作且在所有发作中均避免使用药物的参与者百分比)以及治疗后2小时的疼痛结果。对117名发作性偏头痛患者进行了分析。在OLE阶段,89.7%的参与者仅使用REN治疗发作且在所有发作中均避免使用药物,而在导入期这一比例为15.4%(<0.0001)。治疗后2小时至少50%的治疗中疼痛缓解和疼痛消失的比例相当(疼痛缓解:导入期为58.1%,OLE阶段为57.3%,P = 0.999;疼痛消失:导入期为23.1%,OLE阶段为30.8%,P = 0.175)。REN可能会减少急性偏头痛药物的使用。因此,将REN纳入常规治疗可能会降低药物过度使用性头痛(MOH)的风险。未来的研究应评估REN是否能减少有MOH风险人群中急性偏头痛药物的使用。