Listy klinické logopedie 2022, 6(1):39-45 | DOI: 10.36833/lkl.2022.0142028

Alternative and Augmentative Communication in Amyotrophic Lateral Sclerosis Patients

Naděžda Lasotová1, Adam Betík2, Eva Vlčková2
1 Neurologická klinika Fakultní nemocnice Brno; Katedra speciální a inkluzivní pedagogiky, Pedagogická fakulta Masarykovy univerzity Brno, Česká republika
2 Neurologická klinika Fakultní nemocnice Brno; Lékařská fakulta Masarykovy univerzity Brno, Česká republika.

Amyotrophic Lateral Sclerosis (ALS) is a progressive neurodegenerative disease. Among others, dysarthria and dysphagia (i.e. bulbar dysfunction) represent common clinical manifestations of ALS. Gradual impairment or even loss of speech functions puts ALS patients in the position of serious candidates for the implementation of Alternative and Augmentative Communication (AAC). Regular follow-up with the assessment of speech functions and AAC recommendation and settings in the relevant cases provided by the Clinical Speech Therapist are recommended in all ALS patients, from the onset of the disease. Maintaining the possibility of communication and interaction with the family and friends throughout the disease significantly improves the quality of life of patients and their caregivers. The paper presents the results of the long-term follow-up of a group of 89 ALS patients with bulbar impairment, focused on the use of AAC and the timing of AAC onset. Almost one-half of our patients started to use AAC in the follow-up period. Not surprisingly, the AAC methods were used mainly by patients with severe dysarthria or anarthria. In the study sample, patients started to use AAC approximately 16 months after the onset of bulbar symptoms. However, the time to onset of AAC was significantly variable individually, and a few patients did not use any AAC methods, even in the interval of more than 8 years from the onset of clinical bulbar impairment.

Keywords: Amyotrophic Lateral Sclerosis, dysarthria, Augmentative and Alternative Communication, quality of life

Received: March 18, 2022; Revised: May 3, 2022; Accepted: May 8, 2022; Published: June 14, 2022  Show citation

ACS AIP APA ASA Harvard Chicago Chicago Notes IEEE ISO690 MLA NLM Turabian Vancouver
Lasotová N, Betík A, Vlčková E. Alternative and Augmentative Communication in Amyotrophic Lateral Sclerosis Patients. Listy klinické logopedie. 2022;6(1):39-45. doi: 10.36833/lkl.2022.014.
Download citation

References

  1. ANDERSEN, P. M., S. ABRAHAMS, G. D. BORASIO, M. de CARVALHO, A. CHIO, P. Van DAMME, O. HARDIMAN, K. KOLLEWE, K. E. MORRISON, S. PETRI, P.-F. PRADAT, V. SILANI, B. TOMIK, M. WASNER a M. WEBER, 2012. The EFNS task force on diagnosis and management of amyotrophic lateral sclerosis. EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS) - revised report of an EFNS task force. European journal of neurology. 19(3), s. 360-375. DOI:10.1111/j.1468-1331.2011.03501.x. Go to original source... Go to PubMed...
  2. BARRIGUINHA, C. I. F., M. T. do COMO MOURAO a J. MARTINS, 2017. Communication and swallowing difficulties in palliative patients: patients, families and/or caregivers perspective. Audiol., Commun. Res. 22:e1655. DOI:10.1590/2317-6431-2015-1655. ISSN 2317-6431. Go to original source...
  3. BEUKELMAN, D., S. FAGER a A. NORDNESS, 2011. Communication support for people with ALS. Neurology research international. 2011:714693, DOI: 10.1155/2011/714693. Go to original source... Go to PubMed...
  4. BUŽGOVÁ, R., M. BAR, P. BÁRTOVÁ, R. KOZÁKOVÁ, P. RESSNER, L. SIKOROVÁ a R. ZELENÍKOVÁ, 2017. Neuropaliativní a rehabilitační péče u pacientů v pokročilé fázi progresivních neurologických onemocnění. Cesk Slov Neurol N. 81(1), s. 17-23. DOI: 10.14735/amcsnn201717. Go to original source...
  5. BUŽGOVÁ, R., R. KOZÁKOVÁ, R. ZELENÍKOVÁ a L. SIKOROVÁ, 2018. Přehled dotazníků a škál hodnotících pacienty s amyotrofickou laterální sklerózou. Čas. Lék. čes. 157(1), s. 41-45.
  6. CREUTZFELDT, C. J., B. KLUGER, A. G. KELLY, M. LEMMON, D. Y. HWANG, N. B. GALIFIANAKIS, A. CARVER, M. KATZ, J. R. CURTIS a R. G. HOLLOWAY, 2018. Neuropalliative care. Priorities to move the field forward. Neurology. 31; 91(5), s. 217-226. DOI: 10.1212/WNL.0000000000005916. Go to original source... Go to PubMed...
  7. HANSON, E., K. YORKSTON a D. BRITTON, 2011. Dysarthria in amyotrophic lateral aclerosis: A systematic review of characteristics, speech treatment, and augmentative and alternative communication. Journal of medical speech-language pathology. 19(3), s. 12-30.
  8. LASOTOVÁ, N., M. DUBOVÁ, E. VLČKOVÁ a R. SLÁMOVÁ, 2020. Bulbární symptomy - dysfagie, poruchy řeči, slintání. In: BUŽGOVÁ, R., R. KOZÁKOVÁ et al. Základy paliativní péče v neurologii. Praha: Galén. ISBN 978- 80-7492-502-3.
  9. NICE. National Institute for Health and Care Excellence. 2016, last update 2019. Motor neuron disease: assessment and management. NICE giudeline [NG42]. [online] [cit. 2.3.2022]. Dostupné z: https://www.nice.org.uk/guidance/ng42
  10. PATTEE, G. L., E. K. PLOWMAN, K. L. FOCHT GARAND, J. COSTELLO, B.R. BROOKS, J. D. BERRY, R. A. SMITH, N. ATASSI, J. L. CHAPLIN, Y. YUNUSOVA, C. E. McILDUFF, E. YOUNG, E. A. MACKLIN, E. R. LOCATELLI, V. SILANI, D. HEITZMAN, J. WYMER, S. A. GOUTMAN, D.F. GELINAS, B. PERRY, P. NALIPINSKI, K. STIPANICIC, M. O´BRIEN, S. L. SULLIVAN, E. P. PIORO, G. GARGIULO a J. R. GREEN, 2019. Provisional best practices guidelines for the evaluation of bulbar dysfunction in amyotrophic lateral sclerosis. Muscle & nerve. 59(5), s. 531-536. DOI:10.1002/mus.26408. Go to original source... Go to PubMed...
  11. POLLENS, R., 2004. Role of the speech-language pathologist in palliative hospice care. Journal of Palliative Medicine.7(5), s. 694-702. DOI:10.1089/jpm.2004.7.694. Go to original source... Go to PubMed...
  12. POLLENS, R., 2012. Integrating speech-language pathology services in palliative end-of-life care. Top Lang Disorders 32(2), s. 137-148. DOI: 10.1097/TLD.0b013e3182543533. Go to original source...
  13. RIDZOŇ, P., 2020. Onemocnění motorického neuronu. In: BUŽGOVÁ, R., R. KOZÁKOVÁ et al. Základy paliativní péče v neurologii. Praha: Galén. ISBN 978- 80-7492-502-3.
  14. ROUBÍČKOVÁ, J., J. HEDÁNEK a A. STRÁNÍK, 2011. Test 3F: dysartrický profil. Praha: Galén. ISBN 978-80-7262-714-1.
  15. TOMIK, B. a R. J. GUILOFF, 2010. Dysarthria in amyotrophic lateral sclerosis: A review. Amyotrophic lateral sclerosis. 11, s. 4-15. DOI:10.3109/17482960802379004. Go to original source... Go to PubMed...
  16. VLČKOVÁ, E., 2016. Amyotrofická laterální skleróza. Neurol. praxi, 17(6), s. 362-365. DOI: 10.36290/neu.2016.076. Go to original source...

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0), which permits non-comercial use, distribution, and reproduction in any medium, provided the original publication is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.