Harvey Richard L, Smith Richard, Bathula Rajaram, Everton Lisa, Rup Nicole, Saver Jeff, Martin-Harris Bonnie, Dziewas Rainer, Mistry Satish, Hamdy Shaheen, Bath Philip
Brain Innovation Center, Shirley Ryan Ability Lab, Chicago, Illinois USA.
Stroke Neurorehabilitation, St Anthony Hospital, CommonSpirit, Lakewood, Colorado USA.
J Rehabil Med. 2025 Sep 5;57:jrm43538. doi: 10.2340/jrm.v57.43538.
To assess the efficacy of pharyngeal electrical stimulation in improving dysphagia post-stroke.
A randomized, sham-controlled, blinded multicentre clinical trial.
SUBJECTS/PATIENTS: Seventeen patients with acute ischaemic or haemorrhagic stroke experiencing dysphagia, indicated by a penetration aspiration scale score of 4-8 on videofluoroscopy.
Sites enrolled 3 open-label roll-in participants and then randomized subsequent participants to either stimulation or sham treatment. Study interventions were delivered for 10 min daily over 3 consecutive days. Prior to data lock the primary outcome was modified to the change in dysphagia severity rating scale from pre-treatment to end of follow-up period. Secondary outcomes included penetration-aspiration scale score assessed via videofluoroscopy 48 h after final treatment and functional oral intake scale, measured at 7, 14, and 83 days post-randomization.
The trial was halted early due to low recruitment, with 15 participants receiving active stimulation and 2 receiving sham treatment. Active stimulation significantly reduced dysphagia severity at day 83 (difference: -4, p = 0.027). Improvements were observed in diet and supervision subscales, and functional oral intake scores. Of those treated, 67% were discharged home, with no serious adverse events attributable to the intervention noted in either group.
Pharyngeal electrical stimulation was safe and associated with reduced dysphagia severity in stroke patients, warranting further validation in larger studies.
评估咽部电刺激改善中风后吞咽困难的疗效。
一项随机、假对照、双盲多中心临床试验。
受试者/患者:17例急性缺血性或出血性中风且伴有吞咽困难的患者,其吞咽造影检查的渗透误吸量表评分为4 - 8分。
各研究点先纳入3名开放标签的导入期参与者,然后将后续参与者随机分为刺激组或假治疗组。研究干预每天进行10分钟,连续进行3天。在数据锁定前,主要结局指标修改为从治疗前到随访期末吞咽困难严重程度评定量表的变化。次要结局指标包括在最后一次治疗后48小时通过吞咽造影检查评估的渗透误吸量表评分,以及在随机分组后第7、14和83天测量的功能性经口摄食量表评分。
由于招募人数少,试验提前终止,15名参与者接受了主动刺激,2名接受了假治疗。主动刺激在第83天显著降低了吞咽困难的严重程度(差异:-4,p = 0.027)。在饮食和监督子量表以及功能性经口摄食评分方面均有改善。接受治疗的患者中,67%出院回家,两组均未发现与干预相关的严重不良事件。
咽部电刺激对中风患者是安全的,且与吞咽困难严重程度降低相关,值得在更大规模的研究中进一步验证。