Pharyngeal electrical stimulation in amyotrophic lateral sclerosis: a pilot study

医学 吞咽 吞咽困难 肌萎缩侧索硬化 口咽吞咽困难 吸入性肺炎 四分位间距 不利影响 生活质量(医疗保健) 咽肌 内科学 麻醉 物理疗法 外科 肺炎 护理部 疾病
作者
Christine Herrmann,Falk Schradt,Beate Lindner-Pfleghar,Joachim Schuster,Albert C. Ludolph,Johannes Dorst
出处
期刊:Therapeutic Advances in Neurological Disorders [SAGE Publishing]
卷期号:15: 17562864211068394-17562864211068394 被引量:15
标识
DOI:10.1177/17562864211068394
摘要

Background: Patients with amyotrophic lateral sclerosis (ALS) suffer from dysphagia that increases the risk for aspiration, pneumonia and weight loss. Pharyngeal electrical stimulation (PES) is a therapeutic technique that applies electric stimuli to the patient’s pharynx in order to improve swallowing based on the principle of cortical plasticity and reorganization. Previous studies have demonstrated positive effects in patients with various neurological diseases. Objective: This study was initiated to investigate the effect of PES on swallowing function in patients with ALS. Methods: In all, 20 ALS patients with severe dysphagia [characterized by a Penetration Aspiration Scale (PAS) of at least 4 in thin liquid] were randomized to receive either PES for 10 min at 3 consecutive days in addition to Standard Logopaedic Therapy (SLT) or SLT alone. Swallowing function was evaluated by Fiberoptic Endoscopic Evaluation of Swallowing (FEES) at five timepoints: at baseline, 1 day, 4 days, 3 weeks and 3 months after treatment. Primary endpoint was the severity of penetrations or aspirations as classified by PAS. Secondary endpoints were adverse events, dysphagia-related quality of life, Swallowing Quality of Life (SWAL-QOL), Dysphagia Severity Rating Scale (DSRS), residues, leaking, ALS Functional Rating Scale Revised (ALSFRS-R), and the performance in Clinical Evaluation of Swallowing (CES). The trial is registered under the name of ‘Pharyngeal Electrical Stimulation in Amyotrophic Lateral Sclerosis’ with ClinialTrials.gov, number NCT03481348 ( https://clinicaltrials.gov/ct2/show/NCT03481348 ). Results: Both groups combined showed a significant improvement ( p = 0.003) of median Total-PAS from 3.6 [interquartile range (IQR) = 2.9–5.0] at baseline to 2.3 (IQR = 1.8–4.0) 1 day after treatment. During subsequent study visits, PAS increased again but remained below baseline. PES and control group did not differ significantly 1 day after intervention ( p = 0.32). Similar effects were found in the majority of secondary endpoints. Interpretation: The findings suggest that PES may not provide an additional positive effect on swallowing function in ALS. SLT seems to yield at least short-term positive effects on swallowing function and swallowing-specific life quality in ALS. Registration: ClinialTrials.gov: NCT03481348
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