Background: Neurogenic dysphagia is one of the most frequent and prognostically relevant neurological deficits in a variety of disorders, such as stroke, parkinsonism and advanced neuromuscular diseases. Flexible endoscopic evaluation of swallowing (FEES) is now probably the most frequently used tool for objective dysphagia assessment in Germany. It allows evaluation of the efficacy and safety of swallowing, determination of appropriate feeding strategies and assessment of the efficacy of different swallowing manoeuvres. The literature furthermore indicates that FEES is a safe and well-tolerated procedure. In spite of the huge demand for qualified dysphagia diagnostics in neurology, a systematic FEES education has not yet been established.

Results: The structured training curriculum presented in this article aims to close this gap and intends to enforce a robust and qualified FEES service. As management of neurogenic dysphagia is not confined to neurologists, this educational programme is applicable to other clinicians and speech-language therapists with expertise in dysphagia as well.

Conclusion: The systematic education in carrying out FEES across a variety of different professions proposed by this curriculum will help to spread this instrumental approach and to improve dysphagia management.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766659PMC
http://dx.doi.org/10.1186/s12909-016-0587-3DOI Listing

Publication Analysis

Top Keywords

neurogenic dysphagia
12
flexible endoscopic
8
endoscopic evaluation
8
evaluation swallowing
8
swallowing fees
8
training curriculum
8
dysphagia
7
fees
6
swallowing
4
fees neurogenic
4

Similar Publications

[Analysis of clinical characteristics of amyotrophic lateral sclerosis patients initially diagnosed with abnormal laryngeal function].

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi

December 2024

Department of Voice Medicine, Zhongshan Hospital of Xiamen University, School of Medicine, Xiamen Key Laboratory of Voice Medicine, Xiamen361004, China.

To study the laryngeal functional characteristics of patients with amyotrophic lateral sclerosis (ALS)disease diagnosed at the voice clinic. A retrospective analysis(case series study) was conducted on the laryngeal functional characteristics of 7 patients [2 males, 5 females, age ranged from 43 to 76(60.85±13.

View Article and Find Full Text PDF

Study on the predictive value of APACHE II score and neurogenic dysphagia in carbapenem-resistant Klebsiella pneumoniae.

Medicine (Baltimore)

December 2024

Department of Pulmonary and Critical Care Medicine, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Hefei, Anhui Province, China.

Article Synopsis
  • Carbapenem-resistant Klebsiella pneumoniae (CRKP) is a growing global clinical challenge, making early identification of high-risk patients crucial for controlling infection spread and improving treatment.
  • A study involving 152 patients classified them into carbapenem-resistant and non-resistant groups, findings indicated that patients with CRKP had higher APACHE II scores and neurogenic dysphagia, both significant risk factors.
  • A new predictive model utilizing APACHE II scores and neurogenic dysphagia showed improved risk classification, successfully reclassifying over 24% of individuals into a higher risk category for CRKP infection.
View Article and Find Full Text PDF
Article Synopsis
  • The study investigates how the examination of cranial nerves (CN) can help analyze swallowing efficiency by assessing facial-oral integrity in patients with neurogenic dysphagia.
  • A total of 96 dysphagic patients were evaluated through the Yale Pharyngeal Residue Severity Rating Scale and the Penetration-Aspiration Scale during a Fiberoptic Endoscopic Evaluation of Swallowing.
  • Results showed that specific CN impairments could predict different types of pharyngeal residue, aiding clinicians in understanding swallowing issues and planning targeted interventions effectively.
View Article and Find Full Text PDF

Very early and severe presentation of Triple A syndrome - case report and review of the literature.

Front Endocrinol (Lausanne)

October 2024

Department of Pediatrics, Faculty of Medicine and University, Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.

Article Synopsis
  • Triple A syndrome (TAS), also known as Allgrove syndrome, is a rare genetic disorder characterized by three main symptoms: alacrima (lack of tears), achalasia (difficulty swallowing), and adrenal insufficiency.
  • The disorder is caused by mutations in the ALADIN gene located on chromosome 12q13, affecting protein transport within cells and leading to various neurological issues in many patients.
  • A case study details an infant who showed severe symptoms of TAS at just six months, resulting in complications like neurogenic bladder and acute pancreatitis, leading to a fatal outcome by 25 months, highlighting the importance of early diagnosis and awareness of the syndrome's variability.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!