Combined electrical stimulation and exercise for swallow rehabilitation post-stroke: a pilot randomized control trial

被引:51
作者
Sproson, Lise [1 ]
Pownall, Sue [2 ]
Enderby, Pam [3 ]
Freeman, Jenny [4 ]
机构
[1] Sheffield Teaching Hosp NHS Fdn Trust, NIHR Devices Dign HTC, Sheffield S10 2JF, S Yorkshire, England
[2] Sheffield Teaching Hosp NHS Fdn Trust, Speech & Language Therapy Dept, Sheffield, S Yorkshire, England
[3] Univ Sheffield, Sch Hlth & Related Res, Western Bank, Sheffield, S Yorkshire, England
[4] Univ Leeds, Fac Med & Hlth, Leeds, W Yorkshire, England
关键词
dysphagia; stroke; electrical stimulation; randomized controlled trial; rehabilitation; STROKE PATIENTS; OROPHARYNGEAL DYSPHAGIA; NMES; DIAGNOSIS; THERAPY;
D O I
10.1111/1460-6984.12359
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100103 [病原生物学]; 100213 [耳鼻咽喉科学];
摘要
BackgroundDysphagia is common after stroke, affecting up to 50% of patients initially. It can lead to post-stroke pneumonia, which causes 30% of stroke-related deaths, a longer hospital stay and poorer health outcomes. Dysphagia care post-stroke generally focuses on the management of symptoms, via modified oral intake textures and adapted posture, rather than direct physical rehabilitation of the swallowing function. Transcutaneous neuromuscular electrical stimulation (NMES) is a promising rehabilitation technology that can be used to stimulate swallowing; however, findings regarding efficacy have been conflicting. AimsThis pilot randomized controlled study involving three UK sites compared the efficacy of the Ampcare Effective Swallowing Protocol (ESP), combining NMES with swallow-strengthening exercises, with usual care in order to clarify evidence on NMES in the treatment of dysphagia post-stroke. A further objective was to pilot recruitment procedures and outcome measures in order to inform the design of a full-scale trial. Methods & ProceduresThirty patients were recruited and randomized into either (1) usual speech and language therapy dysphagia care; or (2) Ampcare ESP, receiving treatment 5 days/week for 4 weeks. Outcome measures included: the Functional Oral Intake Scale (FOIS), the Rosenbek Penetration-Aspiration Scale (PAS) and patient-reported outcomes (Swallow Related Quality of LifeSWAL-QOL). Outcomes & ResultsThirty patients were recruited; 15 were randomized to the Ampcare ESP intervention arm and 15 to usual care. A greater proportion (75%, or 9/12) of patients receiving Ampcare ESP improved compared with 57% (or 8/14) of the usual-care group. Patients receiving Ampcare ESP also made clinically meaningful change (a comparative benefit of 1.5 on the FOIS, and on the PAS: 1.35 for diet and 0.3 for fluids) compared with usual care. The intervention group also reported much better outcome satisfaction. Conclusions & ImplicationsThe pilot demonstrated successful recruitment, treatment safety and tolerability and clinically meaningful outcome improvements, justifying progression to a fully powered study. It also showed clinically meaningful treatment trends for the Ampcare ESP intervention.
引用
收藏
页码:405 / 417
页数:13
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