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Swallowing assessment in myotonic dystrophy type 1 using fiberoptic endoscopic evaluation of swallowing (FEES)

Authors :
Nel Roodenburg
Walmari Pilz
Frederik W.R. Wesseling
Bernd Kremer
Catharina G. Faber
Rob J.C.G. Verdonschot
Laura W. J. Baijens
Valéria Lima Passos
RS: CAPHRI School for Public Health and Primary Care
Radiotherapie
RS: CAPHRI - Design and analysis of studies in health sciences
RS: MHeNs - R1 - Cognitive Neuropsychiatry and Clinical Neuroscience
FHML Methodologie & Statistiek
Klinische Neurowetenschappen
KNO
Emergency Medicine
Source :
Neuromuscular Disorders, 24(12), 1054-1062. Elsevier Science, Neuromuscular Disorders, 24(12), 1054-1062. Elsevier Ltd.
Publication Year :
2014

Abstract

This study describes the swallowing function of patients with myotonic dystrophy type 1 (DM1) and the effect of bolus consistency on swallowing in this group. The aim of the study is twofold: (a) to identify which (and to what extent) swallowing variables change for DM1 patients relative to healthy control subjects and (b) to examine whether the degree of oropharyngeal dysphagia is associated with disease severity. Forty-five consecutive DM1 patients and ten healthy subjects underwent a swallowing assessment, at Maastricht University medical Center in the Netherlands. The assessment included a standardized fiberoptic endoscopic evaluation of swallowing (FEES) protocol using different bolus consistencies. Clinical severity of the disease was assessed using the muscular impairment rating scale (MIRS). Significant differences were found between patients and controls for all FEES variables. The magnitude of these differences depended on the bolus consistency. The odds of a more pathological swallowing outcome increased significantly with higher MIRS levels. In conclusion, swallowing function is found to be significantly altered in DM1 patients. The results emphasize the importance of conducting a detailed swallowing assessment in all patients, even those with mild muscle weakness. (C) 2014 Elsevier B.V. All rights reserved.

Details

ISSN :
09608966
Volume :
24
Issue :
12
Database :
OpenAIRE
Journal :
Neuromuscular Disorders
Accession number :
edsair.doi.dedup.....a64bba095badfa537a056d8b0e726ee4
Full Text :
https://doi.org/10.1016/j.nmd.2014.06.002