An exploratory aerodigestive swallowing study in the chronic respiratory disease, Idiopathic Pulmonary Fibrosis.
Date
2024-07
Authors
Journal Title
Journal ISSN
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Publisher
Newcastle university
Abstract
Abstract
Introduction: Dysphagia occurs in various respiratory conditions, leading to an
elevated risk of pulmonary complications due to aspiration. In Idiopathic Pulmonary
Fibrosis (IPF), reflux-associated aspiration and dysregulated lung microbiome are
implicated in the disease pathophysiology, but there is limited research on swallowing
dysfunction in IPF.
Aim: The overall aim of this research project is to explore swallowing in patients
diagnosed with IPF including perceived changes in their ability to eat and drink.
Methods and results: Four studies were conducted using different research designs.
The first study aimed to describe the perception of swallowing and oropharyngeal
swallowing physiology and safety using the ten-item Eating Assessment Tool (EAT
10) and the Videofluoroscopy Swallow Study (VFSS) (n:10). The results showed an
increased self-reporting of dysphagia symptoms and a range of swallowing
dysfunction, including aspiration into an unprotected airway. The second study
assessed swallowing safety and performance using the Water Swallow Test (WST)
(n:33). The study identified signs of penetration and/or aspiration and indicated that
swallow performance may be influenced by gender and age. IPF patients
demonstrated lower swallow performance compared with age- and sex-matched
individuals without dysphagia. The WST can be conducted online effectively in
community and hospital clinics. The third study described IPF patients’ perceptions of
swallowing dysfunction, laryngopharyngeal reflux and laryngeal hypersensitivity
symptoms using three validated questionnaires: EAT-10, Reflux Symptoms Index
(RSI), and Newcastle Laryngeal Hypersensitivity Questionnaire (LHQ) (n:40). The
study revealed that a considerable proportion of patients experience symptoms like
swallowing difficulties, laryngopharyngeal reflux and discomfort in the larynx. The
fourth study explored the lived eating and drinking experience for IPF patients using
qualitative interviews (n:14). The interviews highlighted those patients who
experienced eating and drinking changes impacting them physically, emotionally and
socially. They employed various coping strategies and expressed a strong desire for
knowledge about these changes in their lived experiences.
Conclusion: Swallowing dysfunction is a prevalent issue among patients diagnosed
with IPF.
Description
Keywords
Idiopathic pulmonary fibrosis, breathing, upper airway, respiratory physiology, breathing and swallowing coordination, aspiration