Literature DB >> 35848032

Congenital or Early Developing Neuromuscular Diseases Affecting Feeding, Swallowing and Speech - A Review of the Literature from January 1998 to August 2021.

Lotta Sjögreen1, Lisa Bengtsson1.   

Abstract

BACKGROUND: The knowledge about the impact of oral motor impairment in neuromuscular diseases (NMDs) is limited but increasing.
OBJECTIVE: The aim of this review was to collect and compile knowledge on how muscle weakness in congenital or early developing NMDs directly or indirectly affects feeding, swallowing, speech and saliva control.
METHODS: A literature search was performed in PubMed from January 1, 1998, to August 31, 2021. The keywords "feeding", "dysphagia", "swallowing", "dysarthria", "speech", "drooling" and "sialorrhea" were used in combination with "paediatric neuromuscular disease" or specific diagnoses.
RESULTS: Sixty-five studies were selected for the review, 33 focused on feeding and swallowing, 11 on speech, four on a combination of feeding, swallowing, saliva control or speech and 17 general descriptions. Most of the studies reported on patients with a disorder affecting muscles. These studies show that muscle weakness and impaired motility affecting the muscles innervated by the cranial nerves may influence feeding, swallowing, and speech, and that respiratory function, general health and neurodevelopmental delay also influence these functions. Feeding impairment and breathing difficulties are common in NMDs. Lifesaving interventions such as tube feeding and ventilatory support are common in severe cases.
CONCLUSIONS: Feeding impairment, dysphagia and dysarthria are prevalent in NMDs with congenital or early age of onset. Feeding and swallowing has been studied more than speech and saliva control. More children with NMD survive thanks to new treatment options and it is therefore urgent to follow up how these therapies may impact the development of feeding, swallowing, and speech.

Entities:  

Keywords:  Neuromuscular disease; dysarthria; dysphagia; feeding; speech; swallowing

Mesh:

Year:  2022        PMID: 35848032      PMCID: PMC9535595          DOI: 10.3233/JND-210772

Source DB:  PubMed          Journal:  J Neuromuscul Dis


  104 in total

1.  Orofacial dysfunction in children and adolescents with myotonic dystrophy.

Authors:  Lotta Sjögreen; Monica Engvall; Anne-Berit Ekström; Anette Lohmander; Stavros Kiliaridis; Már Tulinius
Journal:  Dev Med Child Neurol       Date:  2007-01       Impact factor: 5.449

2.  Bulbar Problems Self-Reported by Children and Adults with Spinal Muscular Atrophy.

Authors:  A M B van der Heul; C A Wijngaarde; R I Wadman; F Asselman; M T A van den Aardweg; B Bartels; I Cuppen; E Gerrits; L H van den Berg; W L van der Pol; L van den Engel-Hoek
Journal:  J Neuromuscul Dis       Date:  2019

Review 3.  Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.

Authors:  David J Birnkrant; Katharine Bushby; Carla M Bann; Susan D Apkon; Angela Blackwell; David Brumbaugh; Laura E Case; Paula R Clemens; Stasia Hadjiyannakis; Shree Pandya; Natalie Street; Jean Tomezsko; Kathryn R Wagner; Leanne M Ward; David R Weber
Journal:  Lancet Neurol       Date:  2018-02-03       Impact factor: 44.182

Review 4.  Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care.

Authors:  Eugenio Mercuri; Richard S Finkel; Francesco Muntoni; Brunhilde Wirth; Jacqueline Montes; Marion Main; Elena S Mazzone; Michael Vitale; Brian Snyder; Susana Quijano-Roy; Enrico Bertini; Rebecca Hurst Davis; Oscar H Meyer; Anita K Simonds; Mary K Schroth; Robert J Graham; Janbernd Kirschner; Susan T Iannaccone; Thomas O Crawford; Simon Woods; Ying Qian; Thomas Sejersen
Journal:  Neuromuscul Disord       Date:  2017-11-23       Impact factor: 4.296

5.  Congenital stridor with feeding difficulty as a presenting symptom of Dok7 congenital myasthenic syndrome.

Authors:  Chris G Jephson; Nikki A Mills; Matthew C Pitt; David Beeson; Annie Aloysius; Francesco Muntoni; Stephanie A Robb; C Martin Bailey
Journal:  Int J Pediatr Otorhinolaryngol       Date:  2010-06-15       Impact factor: 1.675

Review 6.  Recent advances in respiratory care for neuromuscular disease.

Authors:  Anita K Simonds
Journal:  Chest       Date:  2006-12       Impact factor: 9.410

Review 7.  Treatment for swallowing difficulties (dysphagia) in chronic muscle disease.

Authors:  M Hill; T Hughes; C Milford
Journal:  Cochrane Database Syst Rev       Date:  2004

8.  Oropharyngeal dysphagia in infants and children with infantile Pompe disease.

Authors:  Harrison N Jones; Carolyn W Muller; Min Lin; Suhrad G Banugaria; Laura E Case; Jennifer S Li; Gwendolyn O'Grady; James H Heller; Priya S Kishnani
Journal:  Dysphagia       Date:  2009-09-10       Impact factor: 3.438

Review 9.  Interventions for dysphagia in long-term, progressive muscle disease.

Authors:  Katherine Jones; Robert D S Pitceathly; Michael R Rose; Susan McGowan; Marguerite Hill; Umesh A Badrising; Tom Hughes
Journal:  Cochrane Database Syst Rev       Date:  2016-02-09

10.  Analysis of voice quality in patients with late-onset Pompe disease.

Authors:  Krzysztof Szklanny; Ryszard Gubrynowicz; Katarzyna Iwanicka-Pronicka; Anna Tylki-Szymańska
Journal:  Orphanet J Rare Dis       Date:  2016-07-15       Impact factor: 4.123

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