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Trends in Research Literature Describing Dysphagia in Motor Neuron Diseases (MND): A Scoping Review

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An Erratum to this article was published on 03 August 2017

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Abstract

Dysphagia in motor neuron diseases (MNDs) is highly complex, affecting all stages of swallowing and leading to impaired swallowing safety and efficiency. In order to explore the degree to which research is capturing the symptom of dysphagia in MND, we conducted a scoping review of the existing literature. The primary aims of this review were to identify common themes within the literature on dysphagia in MND, explore patterns and trends in research focus, and identify if any imbalances exist between the research themes related to dysphagia description and management. A comprehensive search strategy yielded 1690 unique articles for review. Following relevance screening, a total of 157 articles were included in the synthesis. Relevant data and keywords were extracted from each article and grouped into themes. Frequency estimates were calculated for each theme to identify trends across research literature. Swallowing impairment in MNDs is described in a variety of ways across current research. The most commonly reported theme was Aspiration/Penetration, mentioned in 73.2% of all included articles; a significant imbalance was identified between reports of swallowing safety and efficiency (p = 0.008). The most frequently reported theme related to dysphagia management was Enteral Nutrition, and very few studies have reported on the efficacy of Rehabilitation/Compensatory recommendations. It is suggested that researchers and clinicians remain mindful of imbalances and gaps in research, and aim to characterize dysphagia in MNDs in a comprehensive manner. Further research investigating discrete, measureable changes in swallowing pathophysiology would be beneficial to delineate the key factors contributing to impaired swallowing safety and efficiency.

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  • 03 August 2017

    An erratum to this article has been published.

References

  1. National Institute of Neurological Disorders and Stroke. Motor neuron diseases fact sheet. 2012. http://www.ninds.nih.gov/disorders/motor_neuron_diseases/detail_motor_neuron_diseases.htm. Accessed 25 Sept 2016.

  2. World Health Organization. International Statistical Classification of Diseases and Related Health Problems (10th Revision). 2015. http://apps.who.int/classifications/icd10/browse/2016/en. Accessed 14 Nov 2015.

  3. Karam C, Scelsa SN, MacGowan DJL. The clinical course of progressive bulbar palsy. Amyotroph. 2010;11(4):364–8. doi:10.3109/17482960903513159.

    Article  Google Scholar 

  4. Gordon PH, Cheng B, Katz IB, Pinto M, Hays AP, Mitsumoto H, Rowland LP. The natural history of primary lateral sclerosis. Neurology. 2006;66(5):647–53.

    Article  CAS  PubMed  Google Scholar 

  5. Al-Chalabi A, Hardiman O, Kiernan MC, Chiò A, Rix-Brooks B, van den Berg LH. Amyotrophic lateral sclerosis: moving towards a new classification system. Lancet Neurol. 2016;15(11):1182–94.

    Article  PubMed  Google Scholar 

  6. Swinnen B, Robberecht W. The phenotypic variability of amyotrophic lateral sclerosis. Nat Rev Neurol. 2014;10(11):661.

    Article  PubMed  Google Scholar 

  7. Miller RM, Britton D. Dysphagia in neuromuscular diseases. San Diego: Plural Publishing; 2011.

    Google Scholar 

  8. D’Amico E, Pasmantier M, Lee Y-W, Weimer L, Mitsumoto H. Clinical evolution of pure upper motor neuron disease/dysfunction (PUMND). Muscle Nerve. 2013;47(1):28–32. doi:10.1002/mus.23496.

    Article  PubMed  Google Scholar 

  9. Valadi N. Evaluation and management of amyotrophic lateral sclerosis. Prim Care. 2015;42(2):177–87. doi:10.1016/j.pop.2015.01.009.

    Article  PubMed  Google Scholar 

  10. Barber C. Management of bulbar symptoms in motor neurone disease: a community speech and language therapist perspective. Br J Neurosci Nurs. 2015;11(1):41–6.

    Article  Google Scholar 

  11. Borasio GD, Miller RG. Clinical characteristics and management of ALS. Semin Neurol. 2001;21(2):155–66.

    Article  CAS  PubMed  Google Scholar 

  12. Houseman G. Symptom management of the patient with amyotrophic lateral sclerosis: a guide for hospice nurses. J Hosp Palliat Nurs. 2008;10(4):207–15.

    Article  Google Scholar 

  13. Ruoppolo G, Schettino I, Frasca V, Giacomelli E, Prosperini L, Cambieri C, Roma R, Greco A, Mancini P, De Vincentiis M, Silani V, Inghilleri M. Dysphagia in amyotrophic lateral sclerosis: prevalence and clinical findings. Acta Neurol Scand. 2013;128(6):397–401. doi:10.1111/ane.12136.

    Article  CAS  PubMed  Google Scholar 

  14. Kuhnlein P, Gdynia HJ, Sperfeld AD, Lindner-Pfleghar B, Ludolph AC, Prosiegel M, Riecker A. Diagnosis and treatment of bulbar symptoms in amyotrophic lateral sclerosis. Nat Clin Pract Neurol. 2008;4(7):366–74. doi:10.1038/ncpneuro0853.

    Article  PubMed  Google Scholar 

  15. Robbins J. Swallowing in ALS and motor neuron disorders. Neurol Clin. 1987;5(2):213–29.

    CAS  PubMed  Google Scholar 

  16. Briani C, Marcon M, Ermani M, Costantini M, Bottin R, Iurilli V, Zaninotto G, Primon D, Feltrin G, Angelini C. Radiological evidence of subclinical dysphagia in motor neuron disease. J Neurol. 1998;245(4):211–6.

    Article  CAS  PubMed  Google Scholar 

  17. Szacka K, Potulska-Chromik A, Fronczewska-Wieniawska K, Spychaa A, Krolicki L, Kuma-Kozakiewicz M. Scintigraphic evaluation of mild to moderate dysphagia in motor neuron disease. Clin Nucl Med. 2016;41(4):e175–80. doi:10.1097/RLU.0000000000001162.

    Article  PubMed  Google Scholar 

  18. Leighton SE, Burton MJ, Lund WS, Cochrane GM. Swallowing in motor neurone disease. J R Soc Med. 1994;87(12):801–5.

    CAS  PubMed  PubMed Central  Google Scholar 

  19. Watanabe R, Iino M, Honda M, Sano J, Hara M. Primary lateral sclerosis. Neuropathology. 1997;17(3):220–4.

    Article  Google Scholar 

  20. Corcia P, Pradat PF, Salachas F, Bruneteau G, le Forestier N, Seilhean D, Hauw JJ, Meininger V. Causes of death in a post-mortem series of ALS patients. Amyotroph. 2008;9(1):59–62. doi:10.1080/17482960701656940.

    Article  Google Scholar 

  21. Levac D, Colquhoun H, O’Brien KK. Scoping studies: advancing the methodology. Implement Sci. 2010;5(1):69. doi:10.1186/1748-5908-5-69.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Pham MT, Rajić A, Greig JD, Sargeant JM, Papadopoulos A, McEwen SA. A scoping review of scoping reviews: advancing the approach and enhancing the consistency. Res Synth Methods. 2014;5(4):371–85.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Colquhoun HL, Levac D, O’Brien KK, Straus S, Tricco AC, Perrier L, Kastner M, Moher D. Scoping reviews: time for clarity in definition, methods, and reporting. J Clin Epidemiol. 2014;67(12):1291–4.

    Article  PubMed  Google Scholar 

  24. Arksey H, O’Malley L. Scoping studies: towards a methodological framework. Int J Soc Res Methodol. 2005;8(1):19–32. doi:10.1080/1364557032000119616.

    Article  Google Scholar 

  25. Viera AJ, Garrett JM. Understanding interobserver agreement: the kappa statistic. Fam Med. 2005;37(5):360.

    PubMed  Google Scholar 

  26. Tabor L, Gaziano J, Watts S, Robison R, Plowman EK. Defining swallowing-related quality of life profiles in individuals with amyotrophic lateral sclerosis. Dysphagia. 2016;31(3):376–82. doi:10.1007/s00455-015-9686-2.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Luchesi KF, Kitamua S, Mourao LF. Amyotrophic Lateral Sclerosis survival analysis: swallowing and non-oral feeding. NeuroRehabilitation. 2014;35(3):535–42. doi:10.3233/NRE-141149.

    CAS  PubMed  Google Scholar 

  28. Atsuta N, Watanabe H, Ito M, Tanaka F, Tamakoshi A, Nakano I, Aoki M, Tsuji S, Yuasa T, Takano H, Hayashi H, Kuzuhara S, Sobue G, Research Committee on the Neurodegenerative Diseases of J. Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis. J Neurol Sci. 2009;276(1–2):163–9. doi:10.1016/j.jns.2008.09.024.

    Article  PubMed  Google Scholar 

  29. Nakamori M, Hosomi N, Takaki S, Oda M, Hiraoka A, Yoshikawa M, Matsushima H, Ochi K, Tsuga K, Maruyama H, Izumi Y, Matsumoto M. Tongue thickness evaluation using ultrasonography can predict swallowing function in amyotrophic lateral sclerosis patients. Clin Neurophysiol. 2016;127(2):1669–74.

    Article  PubMed  Google Scholar 

  30. Strand EA, Miller RM, Yorkston KM, Hillel AD. Management of oral-pharyngeal dysphagia symptoms in amyotrophic lateral sclerosis. Dysphagia. 1996;11(2):129–39.

    Article  CAS  PubMed  Google Scholar 

  31. Lever TE, Simon E, Cox KT, Capra NF, O’Brien KF, Hough MS, Murashov AK. A mouse model of pharyngeal dysphagia in amyotrophic lateral sclerosis. Dysphagia. 2010;25(2):112–26. doi:10.1007/s00455-009-9232-1.

    Article  PubMed  Google Scholar 

  32. Luchesi KF, Kitamura S, Mourao LF. Higher risk of complications in odynophagia-associated dysphagia in amyotrophic lateral sclerosis. Arq Neuropsiquiatr. 2014;72(3):203–7.

    Article  PubMed  Google Scholar 

  33. Higo R, Tayama N, Nito T. Longitudinal analysis of progression of dysphagia in amyotrophic lateral sclerosis. Auris Nasus Larynx. 2004;31(3):247–54.

    Article  PubMed  Google Scholar 

  34. Baker L. Motor neurone disease: overview and case study—a community nursing perspective. Australas J Neurosci. 1997;10(2):6–9.

    Google Scholar 

  35. Cerero Lapiedra R, Moreno Lopez LA, Esparza Gomez GC. Progressive bulbar palsy: a case report diagnosed by lingual symptoms. J Oral Pathol Med. 2002;31(5):277–9.

    Article  CAS  PubMed  Google Scholar 

  36. Smith RO, Sands CJ, Goldberg NM, Massey RU, Gay JR. Injection of silicone lateral to a vocal cord in a patient with progressive bulbar palsy. Neurology. 1967;17(12):1217–8.

    Article  CAS  PubMed  Google Scholar 

  37. Talacko AA, Reade PC. Progressive bulbar palsy: a case report of a type of motor neuron disease presenting with oral symptoms. Oral Surg Oral Med Oral Pathol. 1990;69(2):182–4.

    Article  CAS  PubMed  Google Scholar 

  38. Beal MF, Richardson EP Jr. Primary lateral sclerosis: a case report. Arch Neurol. 1981;38(10):630–3.

    Article  CAS  PubMed  Google Scholar 

  39. Lo Re G, Galia M, La Grutta L, Russo S, Runza G, Taibbi A, D’Agostino T, Lo Greco V, Bartolotta TV, Midiri M, Cardinale AE, De Maria M, Lagalla R. Digital cineradiographic study of swallowing in patients with amyotrophic lateral sclerosis. Radiol Med (Torino). 2007;112(8):1173–87.

    Article  CAS  Google Scholar 

  40. Goeleven A, Robberecht W, Sonies B, Carbonez A, Dejaeger E. Manofluorographic evaluation of swallowing in amyotrophic lateral sclerosis and its relationship with clinical evaluation of swallowing. Amyotroph Lateral Scler. 2006;7(4):235–40.

    Article  PubMed  Google Scholar 

  41. Noh EJ, Park MI, Park SJ, Moon W, Jung HJ. A case of amyotrophic lateral sclerosis presented as oropharyngeal Dysphagia. J Neurogastroenterol Motil. 2010;16(3):319–22. doi:10.5056/jnm.2010.16.3.319.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Leder SB, Novella S, Patwa H. Use of fiberoptic endoscopic evaluation of swallowing (FEES) in patients with amyotrophic lateral sclerosis. Dysphagia. 2004;19(3):177–81.

    Article  PubMed  Google Scholar 

  43. Li S, Chen Q, Yu B, Xue K, Luo C, Xu Y, Gong Q, He C, Zhou D, He L, Yao D. Structural and functional changes mapped in the brains of amyotrophic lateral sclerosis patients with/without dysphagia: a pilot study. Amyotroph. 2009;10(5–6):280–7. doi:10.3109/17482960902893342.

    Article  Google Scholar 

  44. Paris G, Martinaud O, Petit A, Cuvelier A, Hannequin D, Roppeneck P, Verin E. Oropharyngeal dysphagia in amyotrophic lateral sclerosis alters quality of life. J Oral Rehabil. 2013;40(3):199–204. doi:10.1111/joor.12019.

    Article  CAS  PubMed  Google Scholar 

  45. Solazzo A, Del Vecchio L, Reginelli A, Monaco L, Sagnelli A, Monsorro M, Di Martino N, Tedeschi G, Grassi R. Search for compensation postures with videofluoromanometric investigation in dysphagic patients affected by amyotrophic lateral sclerosis. Radiol Med (Torino). 2011;116(7):1083–94. doi:10.1007/s11547-011-0698-1.

    Article  CAS  Google Scholar 

  46. Amin MR, Harris D, Cassel SG, Grimes E, Heiman-Patterson T. Sensory testing in the assessment of laryngeal sensation in patients with amyotrophic lateral sclerosis. Ann Otol Rhinol Laryngol. 2006;115(7):528–34.

    Article  PubMed  Google Scholar 

  47. D’Ottaviano FG, Linhares Filho TA, Andrade HM, Alves PC, Rocha MS. Fiberoptic endoscopy evaluation of swallowing in patients with amyotrophic lateral sclerosis. Rev Bras Otorrinolaringol (Engl Ed). 2013;79(3):349–53. doi:10.5935/1808-8694.20130061.

    Google Scholar 

  48. Bevan K, Griffiths MV. Chronic aspiration and laryngeal competence. J Laryngol Otol. 1989;103(2):196–9.

    Article  CAS  PubMed  Google Scholar 

  49. Bosma JF, Brodie DR. Disabilities of the pharynx in amyotrophic lateral sclerosis as demonstrated by cineradiography. Radiology. 1969;92(1):97–103.

    Article  CAS  PubMed  Google Scholar 

  50. Fattori B, Grosso M, Bongioanni P, Nacci A, Cristofani R, AlSharif A, Licitra R, Matteucci F, Rossi B, Rubello D, Ursino F, Mariani G. Assessment of swallowing by oropharyngoesophageal scintigraphy in patients with amyotrophic lateral sclerosis. Dysphagia. 2006;21(4):280–6.

    Article  PubMed  Google Scholar 

  51. Kawai S, Tsukuda M, Mochimatsu I, Enomoto H, Kagesato Y, Hirose H, Kuroiwa Y, Suzuki Y. A study of the early stage of Dysphagia in amyotrophic lateral sclerosis. Dysphagia. 2003;18(1):1–8.

    Article  PubMed  Google Scholar 

  52. Morimoto N, Yamashita T, Sato K, Kurata T, Ikeda Y, Kusuhara T, Murata N, Abe K. Assessment of swallowing in motor neuron disease and Asidan/SCA36 patients with new methods. J Neurol Sci. 2013;324(1–2):149–55. doi:10.1016/j.jns.2012.10.025.

    Article  PubMed  Google Scholar 

  53. Murono S, Hamaguchi T, Yoshida H, Nakanishi Y, Tsuji A, Endo K, Kondo S, Wakisaka N, Yamada M, Yoshizaki T. Evaluation of dysphagia at the initial diagnosis of amyotrophic lateral sclerosis. Auris Nasus Larynx. 2015;42(3):213–7. doi:10.1016/j.anl.2014.10.012.

    Article  PubMed  Google Scholar 

  54. Nozaki S, Sugishita S, Saito T, Umaki Y, Adachi K, Shinno S. Prolonged apnea/hypopnea during water swallowing in patients with amyotrophic lateral sclerosis. Rinsho Shinkeigaku. 2008;48(9):634–9.

    Article  PubMed  Google Scholar 

  55. Restivo DA, Casabona A, Nicotra A, Zappia M, Elia M, Romano MC, Alfonsi E, Marchese-Ragona R. ALS dysphagia pathophysiology: differential botulinum toxin response. Neurology. 2013;80(7):616–20. doi:10.1212/WNL.0b013e318281cc1b.

    Article  CAS  PubMed  Google Scholar 

  56. Rubin AD, Griffin GR, Hogikyan ND, Feldman EL. A new member of the multidisciplinary ALS team: the otolaryngologist. Amyotroph. 2012;13(2):229–32. doi:10.3109/17482968.2011.643898.

    Article  Google Scholar 

  57. Scott A, Heughan A. A review of dysphagia in four cases of motor neurone disease. Palliat Med. 1993;7(4 Suppl):41–7.

    Article  CAS  PubMed  Google Scholar 

  58. Silverstein A, Faegenburg D. Cineradiography of swallowing. observation in patients with lesions of brain stem, lower cranial nerves, or bulbar musculature. Arch Neurol. 1965;12:67–71.

    Article  CAS  PubMed  Google Scholar 

  59. Takasaki K, Umeki H, Enatsu K, Kumagami H, Takahashi H. Evaluation of swallowing pressure in a patient with amyotrophic lateral sclerosis before and after cricopharyngeal myotomy using high-resolution manometry system. Auris Nasus Larynx. 2010;37(5):644–7. doi:10.1016/j.anl.2010.02.003.

    Article  PubMed  Google Scholar 

  60. Teismann IK, Warnecke T, Suntrup S, Steinstrater O, Kronenberg L, Ringelstein EB, Dengler R, Petri S, Pantev C, Dziewas R. Cortical processing of swallowing in ALS patients with progressive dysphagia—a magnetoencephalographic study. PLoS ONE. 2011;6(5):e19987. doi:10.1371/journal.pone.0019987.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  61. Watts CR, Vanryckeghem M. Laryngeal dysfunction in amyotrophic lateral sclerosis: a review and case report. BMC Ear Nose Throat Disord. 2001;1:1–5. doi:10.1186/1472-6815-1-1.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Wright R, Jordan C. Videofluoroscopic evaluation of dysphagia in motor neurone disease with modified barium swallow. Palliat Med. 1997;11(1):44–8.

    Article  CAS  PubMed  Google Scholar 

  63. Kiuchi S, Sasaki J, Arai T, Suzuki T. Functional disorders of the pharynx and esophagus. Acta Otolaryngol Suppl (Stockh). 1969;256:1–30.

    Article  CAS  Google Scholar 

  64. Wada A, Kawakami M, Liu M, Otaka E, Nishimura A, Liu F, Otsuka T. Development of a new scale for dysphagia in patients with progressive neuromuscular diseases: the Neuromuscular Disease Swallowing Status Scale (NdSSS). J Neurol. 2015;262(10):2225–31. doi:10.1007/s00415-015-7836-y.

    Article  CAS  PubMed  Google Scholar 

  65. Plowman EK, Watts SA, Tabor L, Robison R, Gaziano J, Domer AS, Richter J, Vu T, Gooch C. Impact of expiratory strength training in amyotrophic lateral sclerosis. Muscle Nerve. 2016;54(1):48–53. doi:10.1002/mus.24990.

    Article  PubMed  PubMed Central  Google Scholar 

  66. Solazzo A, Monaco L, Vecchio LD, Reginelli A, Iacobellis F, Capasso R, Tamburrini S, Berritto D, Barillari MR, Monsurro MR, Di Martino N, Grassi R. Earliest videofluoromanometric pharyngeal signs of dysphagia in ALS patients. Dysphagia. 2014;29(5):539–44. doi:10.1007/s00455-014-9542-9.

    Article  PubMed  Google Scholar 

  67. Aydogdu I, Tanriverdi Z, Ertekin C. Dysfunction of bulbar central pattern generator in ALS patients with dysphagia during sequential deglutition. Clin Neurophysiol. 2011;122(6):1219–28. doi:10.1016/j.clinph.2010.11.002.

    Article  PubMed  Google Scholar 

  68. Ertekin C, Aydogdu I, Yuceyar N, Kiylioglu N, Tarlaci S, Uludag B. Pathophysiological mechanisms of oropharyngeal dysphagia in amyotrophic lateral sclerosis. Brain. 2000;123(Pt 1):125–40.

    Article  PubMed  Google Scholar 

  69. Higo R, Tayama N, Watanabe T, Nitou T. Videomanofluorometric study in amyotrophic lateral sclerosis. Laryngoscope. 2002;112(5):911–7.

    Article  PubMed  Google Scholar 

  70. MacDougall G, Wilson JA, Pryde A, Grant R. Analysis of the pharyngoesophageal pressure profile in amyotrophic lateral sclerosis. Otolaryngol Head Neck Surg. 1995;112(2):258–61.

    Article  CAS  PubMed  Google Scholar 

  71. Omari TI, Wiklendt L, Dinning P, Costa M, Rommel N, Cock C. Upper esophageal sphincter mechanical states analysis: a novel methodology to describe UES relaxation and opening. Front Syst Neurosci. 2014;8:241. doi:10.3389/fnsys.2014.00241.

    PubMed  Google Scholar 

  72. Ertekin C, Aydogdu I, Yuceyar N, Tarlaci S, Kiylioglu N, Pehlivan M, Celebi G. Electrodiagnostic methods for neurogenic dysphagia. Electroencephalogr Clin Neurophysiol. 1998;109(4):331–40.

    Article  CAS  PubMed  Google Scholar 

  73. Plowman EK, Watts SA, Tabor L, Robison R, Gaziano J, Domer AS, Richter J, Vu T, Gooch C. Impact of expiratory strength training in amyotrophic lateral sclerosis. Muscle and Nerve. 2016;. doi:10.1002/mus.24990.

    PubMed  PubMed Central  Google Scholar 

  74. Plowman EK, Watts SA, Robison R, Tabor L, Dion C, Gaziano J, Vu T, Gooch C. Voluntary cough airflow differentiates safe versus unsafe swallowing in amyotrophic lateral sclerosis. Dysphagia (0179051X). 2016;31(3):383–90. doi:10.1007/s00455-015-9687-1.

    Article  Google Scholar 

  75. Erdem NS, Karaali K, Unal A, Kizilay F, Ogus C, Uysal H. The interaction between breathing and swallowing in amyotrophic lateral sclerosis. Acta Neurol Belg. 2016;116(4):549–56. doi:10.1007/s13760-016-0643-0.

    Article  PubMed  Google Scholar 

  76. Easterling C, Antinoja J, Cashin S, Barkhaus PE. Changes in tongue pressure, pulmonary function, and salivary flow in patients with amyotrophic lateral sclerosis. Dysphagia. 2013;28(2):217–25. doi:10.1007/s00455-012-9436-7.

    Article  PubMed  Google Scholar 

  77. Kikutani T, Tamura F, Nishiwaki K. Case presentation: dental treatment with PAP for ALS patient. Int J Orofac Myol. 2006;32:32–5.

    Google Scholar 

  78. Umemoto G, Furuya H, Arahata H, Sugahara M, Sakai M, Tsuboi Y. Relationship between tongue thickness and tongue pressure in neuromuscular disorders. Neurol Clin Neurosci. 2016;4(4):142–5. doi:10.1111/ncn3.12058.

    Article  Google Scholar 

  79. Tamburrini S, Solazzo A, Sagnelli A, Del Vecchio L, Reginelli A, Monsorro M, Grassi R. Amyotrophic lateral sclerosis: sonographic evaluation of dysphagia. Radiol Med (Torino). 2010;115(5):784–93. doi:10.1007/s11547-010-0523-2.

    Article  CAS  Google Scholar 

  80. Carrión S, Cabré M, Monteis R, Roca M, Palomera E, Serra-Prat M, Rofes L, Clavé P. Oropharyngeal dysphagia is a prevalent risk factor for malnutrition in a cohort of older patients admitted with an acute disease to a general hospital. Clin Nutr. 2015;34(3):436–42. doi:10.1016/j.clnu.2014.04.014.

    Article  PubMed  Google Scholar 

  81. Rofes L, Arreola V, Almirall J, Cabre M, Campins L, Garcia-Peris P, Speyer R, Clave P. Diagnosis and management of oropharyngeal Dysphagia and its nutritional and respiratory complications in the elderly. Gastroenterol Res Pract. 2011;. doi:10.1155/2011/818979.

    PubMed  Google Scholar 

  82. Oliveira DL, Moreira EAM, de Freitas MB, Gonçalves JDA, Furkim AM, Clavé P. Pharyngeal residue and aspiration and the relationship with clinical/nutritional status of patients with oropharyngeal dysphagia submitted to videofluoroscopy. J Nutr Health Aging. 2017;21(3):336–341. doi:10.1007/s12603-016-0754-6.

  83. Fattori B, Siciliano G, Mancini V, Bastiani L, Bongioanni P, Caldarazzo Ienco E, Barillari MR, Romeo SO, Nacci A. Dysphagia in amyotrophic lateral sclerosis: relationships between disease progression and fiberoptic endoscopic evaluation of swallowing. Auris Nasus Larynx. 2016;. doi:10.1016/j.anl.2016.07.002.

    PubMed  Google Scholar 

  84. Cedarbaum JM, Stambler N, Malta E, Fuller C, Hilt D, Thurmond B, Nakanishi A. The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. J Neurol Sci. 1999;169(1–2):13–21. doi:10.1016/s0022-510x(99)00210-5.

    Article  CAS  PubMed  Google Scholar 

  85. Chio A, Finocchiaro E, Meineri P, Bottacchi E, Schiffer D. Safety and factors related to survival after percutaneous endoscopic gastrostomy in ALS. ALS Percutaneous Endoscopic Gastrostomy Study Group. Neurology. 1999;53(5):1123–5.

    Article  CAS  PubMed  Google Scholar 

  86. Desport JC, Preux PM, Truong CT, Courat L, Vallat JM, Couratier P. Nutritional assessment and survival in ALS patients. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000;1(2):91–6.

    Article  CAS  PubMed  Google Scholar 

  87. Mitsumoto H, Davidson M, Moore D, Gad N, Brandis M, Ringel S, Shefner JM, Strong MJ, Sufit R, Anderson FA, Echols C, Heiman-Patterson T, Paylor T, Huffnagles V, Murphy J, Lou JS, Tullar D, McClusky L, Damiano P, Miller R, Tkachenko I, Neville H, Blackwell KH, Oh S, Olney R, Mass J, Pascuzzi R, Michaels A, Pioro E, Andrews-Hinders D, Rosenfeld J, King R, Scelsa S, Shefner J, Lepsky T, Strong M, Rowe A, Sufit RL, Casey P. Percutaneous endoscopic gastrostomy (PEG) in patients with ALS and bulbar dysfunction. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003;4(3):177–85. doi:10.1080/14660820310011728.

    Article  CAS  PubMed  Google Scholar 

  88. Mazzini L, Corra T, Zaccala M, Mora G, Del Piano M, Galante M. Percutaneous endoscopic gastrostomy and enteral nutrition in amyotrophic lateral sclerosis. J Neurol. 1995;242(10):695–8.

    Article  CAS  PubMed  Google Scholar 

  89. Langmore SE, Kasarskis EJ, Manca ML, Olney RK. Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database Syst Rev. 2006;4:CD004030.

  90. Katzberg HD, Benatar M. Enteral tube feeding for amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database Syst Rev. 2011;1:CD004030. doi:10.1002/14651858.CD004030.pub3.

  91. Kasarskis EJ, Scarlata D, Hill R, Fuller C, Stambler N, Cedarbaum JM. A retrospective study of percutaneous endoscopic gastrostomy in ALS patients during the BDNF and CNTF trials. J Neurol Sci. 1999;169(1–2):118–25.

    Article  CAS  PubMed  Google Scholar 

  92. Chio A, Galletti R, Finocchiaro C, Righi D, Ruffino MA, Calvo A, Di Vito N, Ghiglione P, Terreni AA, Mutani R. Percutaneous radiological gastrostomy: a safe and effective method of nutritional tube placement in advanced ALS. J Neurol Neurosurg Psychiatry. 2004;75(4):645–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  93. Benstead T, Jackson-Tarlton C, Leddin D. Nutrition with gastrostomy feeding tubes for amyotrophic lateral sclerosis in Canada. Can J Neurolog Sci. 2016;43(6):796–800. doi:10.1017/cjn.2016.28.

    Article  Google Scholar 

  94. Nunes G, Santos CA, Grunho M, Fonseca J. Enteral feeding through endoscopic gastrostomy in amyotrophic lateral sclerosis patients. Nutr Hosp. 2016;33(5):561. doi:10.20960/nh.561.

    Article  PubMed  Google Scholar 

  95. Spataro R, Ficano L, Piccoli F, La Bella V. Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: effect on survival. J Neurol Sci. 2011;304(1–2):44–8. doi:10.1016/j.jns.2011.02.016.

    Article  PubMed  Google Scholar 

  96. Johnson J, Leigh PN, Shaw CE, Ellis C, Burman R, Al-Chalabi A. Eating-derived pleasure in amyotrophic lateral sclerosis as a predictor of non-oral feeding. Amyotroph. 2012;13(6):555–9. doi:10.3109/17482968.2012.704925.

    Article  Google Scholar 

  97. Wilson PS, Bruce-Lockhart FJ, Johnson AP. Videofluoroscopy in motor neurone disease prior to cricopharyngeal myotomy. Ann R Coll Surg Engl. 1990;72(6):375–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  98. Benditt JO. Respiratory complications of amyotrophic lateral sclerosis. Semin Respir Crit Care Med. 2002;23(3):239–47.

    Article  PubMed  Google Scholar 

  99. Wijesekera LC, Leigh PN. Amyotrophic lateral sclerosis. Orphanet J Rare Dis. 2009;. doi:10.1186/1750-1172-4-3.

    PubMed  PubMed Central  Google Scholar 

  100. Palovcak M, Mancinelli JM, Elman LB, McCluskey L. Diagnostic and therapeutic methods in the management of dysphagia in the ALS population: issues in efficacy for the out-patient setting. NeuroRehabilitation. 2007;22(6):417–23.

    PubMed  Google Scholar 

  101. Luchesi KF, Kitamura S, Mourao LF. Management of dysphagia in Parkinson’s disease and amyotrophic lateral sclerosis. CoDAS. 2013;25(4):358–64.

    Article  PubMed  Google Scholar 

  102. Escuro AA. Nutrition support in amyotrophic lateral sclerosis: from diagnosis through terminal phase. Support Line. 2012;34(2):8–19.

    Google Scholar 

  103. Greenwood DI. Nutrition management of amyotrophic lateral sclerosis. Nutr Clin Pract. 2013;28(3):392–9. doi:10.1177/0884533613476554.

    Article  PubMed  Google Scholar 

  104. Heffernan C, Jenkinson C, Holmes T, Feder G, Kupfer R, Leigh PN, McGowan S, Rio A, Sidhu P. Nutritional management in MND/ALS patients: an evidence based review. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004;5(2):72–83.

    Article  PubMed  Google Scholar 

  105. Hillel AD, Miller R. Bulbar amyotrophic lateral sclerosis: patterns of progression and clinical management. Head Neck. 1989;11(1):51–9.

    Article  CAS  PubMed  Google Scholar 

  106. Procaccini NJ, Nemergut EC. Percutaneous endoscopic gastrostomy in the patient with amyotrophic lateral sclerosis: risk vs benefit? Pract Gastroenterol. 2008;32(3):24–34.

    Google Scholar 

  107. Scott AG, Austin HE. Nasogastric feeding in the management of severe dysphagia in motor neurone disease. Palliat Med. 1994;8(1):45–9.

    Article  CAS  PubMed  Google Scholar 

  108. Silani V, Kasarskis EJ, Yanagisawa N. Nutritional management in amyotrophic lateral sclerosis: a worldwide perspective. J Neurol. 1998;245(Suppl 2):S13–19; discussion S29.

  109. Stavroulakis T, Baird WO, Baxter SK, Walsh T, Shaw PJ, McDermott CJ. Factors influencing decision-making in relation to timing of gastrostomy insertion in patients with motor neurone disease. BMJ support. 2014;4(1):57–63. doi:10.1136/bmjspcare-2013-000497.

    Article  Google Scholar 

  110. Stavroulakis T, Walsh T, Shaw PJ, McDermott CJ, Progas S. Gastrostomy use in motor neurone disease (MND): a review, meta-analysis and survey of current practice. Amyotroph Lateral Scler Frontotemporal Degener. 2013;14(2):96–104. doi:10.3109/17482968.2012.723722.

    Article  PubMed  Google Scholar 

  111. Perry A, Anderson K, Lean R, Cotton S. Elevation of the soft palate in speech and swallowing in normal female participants and females with motor neuron disease: an innovative procedure for measuring palatal elevation. Int J Lang Commun Disord. 2002;37(2):197–214.

    Article  PubMed  Google Scholar 

  112. Jesus P, Massoulard A, Marin B, Nicol M, Laplagne O, Baptiste A, Gindre-Poulvelarie L, Couratier P, Fraysse JL, Desport JC. First assessment at home of amyotrophic lateral sclerosis (ALS) patients by a nutrition network in the French region of Limousin. Amyotroph. 2012;13(6):538–43. doi:10.3109/17482968.2012.701309.

    Article  CAS  Google Scholar 

  113. Corcia P, Meininger V. Management of amyotrophic lateral sclerosis. Drugs. 2008;68(8):1037–48.

    Article  CAS  PubMed  Google Scholar 

  114. Elman LB, Houghton DJ, Wu G, Hurtig HI, Markowitz CE, McCluskey L. Palliative care in amyotrophic lateral sclerosis, Parkinson’s disease, and multiple sclerosis. J Palliat Med. 2007;10(2):433–57. doi:10.1089/jpm.2006.9978.

    Article  PubMed  Google Scholar 

  115. Kosseifi SG, Abdel Nour S, Roy TM, Byrd RP Jr, Alwani A. Respiratory failure in a 70-year-old veteran. South Med J. 2010;103(4):378–81. doi:10.1097/SMJ.0b013e3181d3ceaa.

    Article  PubMed  Google Scholar 

  116. Kidney D, Alexander M, Corr B, O’Toole O, Hardiman O. Oropharyngeal dysphagia in amyotrophic lateral sclerosis: neurological and dysphagia specific rating scales. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004;5(3):150–3.

    Article  PubMed  Google Scholar 

  117. Dworkin JP, Hartman DE. Progressive speech deterioration and dysphagia in amyotrophic lateral sclerosis: case report. Arch Phys Med Rehabil. 1979;60(9):423–5.

    CAS  PubMed  Google Scholar 

  118. Hansen A, Bedore B, Nickel E, Hanowski K, Tangen S, Goldish G. Elastic head support for persons with amyotrophic lateral sclerosis. J Rehabil Res Dev. 2014;51(2):297–303. doi:10.1682/JRRD.2013.03.0072.

    Article  PubMed  Google Scholar 

  119. Walshe M. Oropharyngeal dysphagia in neurodegenerative disease. J Gastroenterol Hepatol Res. 2014;3(10):1265–71. doi:10.6051/j.issn.2224-3992.2014.03.408-2.

    Google Scholar 

  120. Plowman EK. Is there a role for exercise in the management of bulbar dysfunction in amyotrophic lateral sclerosis? J Speech Lang Hear Res. 2015;58(4):1151–66.

    Article  PubMed  Google Scholar 

  121. Robison R. The impact of lingual resistance training in two individuals with amyotrophic lateral sclerosis: a case series. Thesis, University of South Florida, 2015.

  122. Mayberry JF, Atkinson M. Swallowing problems in patients with motor neuron disease. J Clin Gastroenterol. 1986;8:233–4.

    Article  CAS  PubMed  Google Scholar 

  123. Isaacs JD, Dean AF, Shaw CE, Al-Chalabi A, Mills KR, Leigh PN. Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder? J Neurol Neurosurg Psychiatry. 2007;78(7):750–3. doi:10.1136/jnnp.2006.098798.

    Article  PubMed  PubMed Central  Google Scholar 

  124. Setzen M, Cohen MA, Perlman PW, Belafsky PC, Guss J, Mattucci KF, Ditkoff M. The association between laryngopharyngeal sensory deficits, pharyngeal motor function, and the prevalence of aspiration with thin liquids. Otolaryngol Head Neck Surg. 2003;128(1):99–102.

    Article  PubMed  Google Scholar 

  125. Aviv JE, Sacco RL, Mohr JP, Thompson JL, Levin B, Sunshine S, Thomson J, Close LG. Laryngopharyngeal sensory testing with modified barium swallow as predictors of aspiration pneumonia after stroke. Laryngoscope. 1997;107(9):1254–60.

    Article  CAS  PubMed  Google Scholar 

  126. Rodriguez de Rivera FJ, Oreja Guevara C, Sanz Gallego I, San Jose Valiente B, Santiago Recuerda A, Gomez Mendieta MA, Arpa J, Diez Tejedor E. Outcome of patients with amyotrophic lateral sclerosis attending in a multidisciplinary care unit. Neurologia. 2011;26(8):455–60. doi:10.1016/j.nrl.2011.01.021.

    Article  CAS  PubMed  Google Scholar 

  127. Sancho J, Servera E, Díaz J, Marín J. Efficacy of mechanical insufflation-exsufflation in medically stable patients with amyotrophic lateral sclerosis. Chest. 2004;125(4):1400–5. doi:10.1378/chest.125.4.1400.

    Article  PubMed  Google Scholar 

  128. Sancho J, Servera E, Díaz J, Marín J. Predictors of ineffective cough during a chest infection in patients with stable amyotrophic lateral sclerosis. Am J Respir Crit Care Med. 2007;175(12):1266–71. doi:10.1164/rccm.200612-1841OC.

    Article  PubMed  Google Scholar 

  129. Miller RG, Jackson CE, Kasarskis EJ, England JD, Forshew D, Johnston W, Kalra S, Katz JS, Mitsumoto H, Rosenfeld J, Shoesmith C, Strong MJ, Woolley SC. Practice parameter update: The care of the patient with amyotrophic lateral sclerosis: Multidisciplinary care, symptom management, and cognitive/behavioral impairment (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2009;73(15):1227–33.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  130. Britton D, Benditt JO, Merati AL, Miller RM, Stepp CE, Boitano L, Hu A, Ciol MA, Yorkston KM. Associations between laryngeal and cough dysfunction in motor neuron disease with bulbar involvement. Dysphagia. 2014;29(6):637–46. doi:10.1007/s00455-014-9554-5.

    Article  PubMed  Google Scholar 

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Acknowledgements

The authors wish to thank Jessica Babineau, MLIS from the Toronto Rehabilitation Institute—University Health Network, for her work in defining and translating the initial search strategy. We also extend appreciation to Professor Heather Colquhoun from the University of Toronto, Rehabilitation Sciences Institute for her guidance with scoping review methodology. This work was supported in part by doctoral research funding provided by the University of Toronto, Rehabilitation Sciences Institute.

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Correspondence to Ashley A. Waito.

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The original version of this article was revised: The term “Dysphagia” under the ‘Discussion’ section was incorrectly published as “Fysphagia”. This has been corrected in this version.

An erratum to this article is available at https://doi.org/10.1007/s00455-017-9829-8.

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Waito, A.A., Valenzano, T.J., Peladeau-Pigeon, M. et al. Trends in Research Literature Describing Dysphagia in Motor Neuron Diseases (MND): A Scoping Review. Dysphagia 32, 734–747 (2017). https://doi.org/10.1007/s00455-017-9819-x

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