1. Pharyngeal electrical stimulation for neurogenic dysphagia following stroke, traumatic brain injury or other causes: Main results from the PHADER cohort study
- Author
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Leopold Saltuari, Michael Schuttler, Elke Pucks-Faes, Lisa J Woodhouse, Philip M.W. Bath, Anushka Warusevitane, Ernst Walther, Christian Ledl, for Phader Investigators, Markus Koestenberger, Lisa F Everton, Rainer Dziewas, Suzanne Ragab, Claus G Haase, Alicja Raginis-Zborowska, Milan R. Vosko, Satish Mistry, Shaheen Hamdy, Juergen Herzog, Johanna de Broux, Sonja Suntrup-Krueger, Rudolf Likar, and Christof Bocksrucker
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Traumatic brain injury ,medicine.medical_treatment ,Medizin ,01 natural sciences ,03 medical and health sciences ,Medicine, General & Internal ,0302 clinical medicine ,Tracheotomy ,Pharyngeal electrical stimulation ,Interquartile range ,Decannulation ,General & Internal Medicine ,medicine ,030212 general & internal medicine ,0101 mathematics ,Stroke ,lcsh:R5-920 ,Science & Technology ,POSTSTROKE ,business.industry ,010102 general mathematics ,General Medicine ,Dysphagia ,medicine.disease ,Confidence interval ,Ventilation ,Anesthesia ,Breathing ,medicine.symptom ,lcsh:Medicine (General) ,business ,Life Sciences & Biomedicine ,Research Paper ,Cohort study - Abstract
BACKGROUND: Neurogenic dysphagia is common and has no definitive treatment. We assessed whether pharyngeal electrical stimulation (PES) is associated with reduced dysphagia. METHODS: The PHAryngeal electrical stimulation for treatment of neurogenic Dysphagia European Registry (PHADER) was a prospective single-arm observational cohort study. Participants were recruited with neurogenic dysphagia (comprising five groups - stroke not needing ventilation; stroke needing ventilation; ventilation acquired; traumatic brain injury; other neurological causes). PES was administered once daily for three days. The primary outcome was the validated dysphagia severity rating scale (DSRS, score best-worst 0-12) at 3 months. FINDINGS: Of 255 enrolled patients from 14 centres in Austria, Germany and UK, 10 failed screening. At baseline, mean (standard deviation) or median [interquartile range]: age 68 (14) years, male 71%, DSRS 11·4 (1·7), time from onset to treatment 32 [44] days; age, time and DSRS differed between diagnostic groups. Insertion of PES catheters was successfully inserted in 239/245 (98%) participants, and was typically easy taking 11·8 min. 9 participants withdrew before the end of treatment. DSRS improved significantly in all dysphagia groups, difference in means (95% confidence intervals, CI) from 0 to 3 months: stroke (n = 79) -6·7 (-7·8, -5·5), ventilated stroke (n = 98) -6·5 (-7·6, -5·5); ventilation acquired (n = 35) -6·6 (-8·4, -4·8); traumatic brain injury (n = 24) -4·5 (-6·6, -2·4). The results for DSRS were mirrored for instrumentally assessed penetration aspiration scale scores. DSRS improved in both supratentorial and infratentorial stroke, with no difference between them (p = 0·32). In previously ventilated participants with tracheotomy, DSRS improved more in participants who could be decannulated (n = 66) -7·5 (-8·6, -6·5) versus not decannulated (n = 33) -2·1 (-3·2, -1·0) (p
- Published
- 2020
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