Predictors of impaired communication in amyotrophic lateral sclerosis patients with tracheostomy-invasive ventilation

References

• Radunovic A, Annane D, Rafiq MK, Mustfa N. Mechanical ventilation for amyotrophic lateral sclerosis/motor neuron disease. Cochrane Database Syst Rev. 2013;3: CD004427.
   Google Scholar
• Cazzolli PA, Oppenheimer EA. Home mechanical ventilation for amyotrophic lateral sclerosis: nasal compared to tracheostomy-intermittent positive pressure ventilation. J Neurol Sci. 1996;139:123–8.
   PubMed Web of Science ®Google Scholar
• Moss AH, Oppenheimer EA, Casey P, Cazzolli PA, Roos RP, Stocking CB, et al. Patients with amyotrophic lateral sclerosis receiving long-term mechanical ventilation. Advance care planning and outcomes. Chest. 1996;110:249–55.
   PubMed Web of Science ®Google Scholar
• Cazzolli PA. The perspective of family and caregivers. In: Ambrosino N, Goldstein R, editors. Ventilatory Support for Chronic Respiratory Failure. New York: Informa Healthcare USA; 2008. pp 480–500.
   Google Scholar
• Nakayama Y, Ogura A, Matsuda C. Physical outcomes of patients with amyotrophic lateral sclerosis using long-term home mechanical ventilation. Jpn J Intract Illness Nurs. 2010;14:179–93 (Article in Japanese).
   Google Scholar
• Atsuta N, Watanabe H, Ito M, Tanaka F, Tamakoshi A, Nakano I, et al. Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis. J Neurol Sci. 2009;276:163–9.
   PubMed Web of Science ®Google Scholar
• Beukelman D, Fager S, Nordness A. Communication support for people with ALS. Neurol Res Int. 2011;2011: 714693.
   PubMedGoogle Scholar
• Kawata A, Mizoguchi K, Hayashi H. A nationwide survey of ALS patients on trachoestomy-positive pressure ventilation (TPPV) who developed a totally lockedin state (TLS) in Japan. Rinsho Shinkeigaku. 2008;48:476–80 (Article in Japanese).
   PubMedGoogle Scholar
• Hayashi H, Kato S. Total manifestations of amyotrophic lateral sclerosis. ALS in the totally lockedin state. J Neurol Sci. 1989;93:19–35.
   PubMed Web of Science ®Google Scholar
• Hayashi H, Oppenheimer EA. ALS patients on TPPV. Totally locked-in state, neurologic findings and ethical implications . Neurology. 2003;61:135–7.
   PubMed Web of Science ®Google Scholar
• Cipresso P, Carelli L, Solca F, Meazzi D, Meriggi P, Poletti B, et al. The use of P300-based BCIs in amyotrophic lateral sclerosis: from augmentative and alternative communication to cognitive assessment. Brain Behav. 2012;2:479–98.
   PubMed Web of Science ®Google Scholar
• McCane LM, Sellers EW, McFarland DJ, Mak JN, Carmack CS, Zeitlin D, et al. Brain-computer interface (BCI) evaluation in people with amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15:207–15.
   PubMed Web of Science ®Google Scholar
• Nakayama Y, Matsuda C, Ogura A, Haraguchi M, Mochizuki Y, Nakamura Y, et al. The usability of an electroencephalography-based communication device ‘neuro-communicator’ and nursing intervention for severely neurological or neuromuscular disorders. Jpn J Intract Illness Nurs. 2013;17:187–203 (Article in Japanese).
   Google Scholar
• Hayashi K, Mochizuki Y, Nakayama Y, Shimizu T, Kawata A, Nagao M, et al. Communication disorder in amyotrophic lateral sclerosis after ventilation: a proposal of staging and a study of predictive factor. Rinsho Shinkeigaku. 2013;53: 98–103 (Article in Japanese).
   PubMedGoogle Scholar
• Chiò A, Logroscino G, Hardiman O, Swingler R, Mitchell D, Beghi E, et al. Prognostic factors in ALS: a critical review. Amyotroph Lateral Scler. 2009; 10:310–23.
   PubMed Web of Science ®Google Scholar
• Kollewe K, Mauss U, Krampfl K, Petri S, Dengler R, Mohammadi B. ALSFRS-R score and its ratio: a useful predictor for ALS progression. J Neurol Sci. 2008; 275:69–73.
   PubMed Web of Science ®Google Scholar
• Pinto S, Pinto A, Carvalho DM. Do bulbar-onset amyotrophic lateral sclerosis patients have an earlier respiratory involvement than spinal-onset amyotrophic lateral sclerosis patients? Eura Medicophys. 2007;43:505–9.
   PubMedGoogle Scholar
• Paganoni S, Deng J, Jaffa M, Cudkowicz ME, Wills AM. Body mass index, not dyslipidemia, is an independent predictor of survival in amyotrophic lateral sclerosis. Muscle Nerve. 2011;44:20–4.
   PubMed Web of Science ®Google Scholar
• Shimizu T, Nagaoka U, Nakayama Y, Kawata A, Kugimoto C, Kuroiwa Y, et al. Reduction rate of body mass index predicts prognosis for survival in amyotrophic lateral sclerosis: a multicenter study in Japan. Amyotroph Lateral Scler. 2012;13: 363–6.
   PubMed Web of Science ®Google Scholar
• Watanabe H, Atsuta N, Nakamura R, Hirakawa A, Watanabe H, Ito M, et al. Factors affecting longitudinal functional decline and survival in amyotrophic lateral sclerosis patients. Amyotroph Lateral Scler Frontotemporal Degener. 2014; Early Online.
   PubMed Web of Science ®Google Scholar
• Rabkin JG, Albert SM, Tider T, Del Bene ML, O’Sullivan I, Rowland LP, et al. Predictors and course of elective long-term mechanical ventilation: a prospective study of ALS patients. Amyotroph Lateral Scler. 2006;7:86–95.
   PubMed Web of Science ®Google Scholar
• Lo Coco D, Marchese S, La Bella V, Piccoli T, Lo Coco A. The amyotrophic lateral sclerosis functional rating scale predicts survival time in amyotrophic lateral sclerosis patients on invasive mechanical ventilation. Chest. 2007;132:64–9.
   PubMed Web of Science ®Google Scholar
• Vianello A, Arcaro G, Palmieri A, Ermani M, Braccioni F, Gallan F, et al. Survival and quality of life after tracheostomy for acute respiratory failure in patients with amyotrophic lateral sclerosis. J Crit Care. 2011;26:329.e7–14.
   PubMed Web of Science ®Google Scholar
• Spataro R, Bono V, Marchese S, La Bella V. Tracheostomy mechanical ventilation in patients with amyotrophic lateral sclerosis: clinical features and survival analysis. J Neurol Sci. 2012;323:66–70.
   PubMed Web of Science ®Google Scholar
• Sanjuán LP, Valiño Ló P, Ricoy GJ, Verea H. Amyotrophic Lateral Sclerosis: Impact of Pulmonary Follow-Up and Mechanical Ventilation on Survival. A Study of 114 Cases. Arch Bronconeumol. 2014;50:509–13.
   PubMed Web of Science ®Google Scholar
• Dreyer P, Lorenzen CK, Schou L, Felding M. Survival in ALS with home mechanical ventilation non-invasively and invasively: a 15-year cohort study in west Denmark. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15:62–7.
   PubMed Web of Science ®Google Scholar
• Tagami M, Kimura F, Nakajima H, Ishida S, Fujiwara S, Doi Y, et al. Tracheostomy and invasive ventilation in Japanese ALS patients: decision-making and survival analysis: 1990–2010. J Neurol Sci. 2014;344:158–64.
   PubMed Web of Science ®Google Scholar
• Veronese S, Valle A, Chiò A, Calvo A, Oliver D. The last months of life of people with amyotrophic lateral sclerosis in mechanical invasive ventilation: a qualitative study. Amyotroph Lateral Scler Frontotemporal Degener. 2014;15: 499–504.
   PubMed Web of Science ®Google Scholar
• Wicks P, Massagli MP, Wolf C, Heywood J. Measuring function in advanced ALS: validation of ALSFRS-EX extension items. Eur J Neurol. 2009;16:353–9.
   PubMed Web of Science ®Google Scholar
• Hayashi H, Kato S, Kawada T, Tsubaki T. Amyotrophic lateral sclerosis: oculomotor function in patients in respirators. Neurology. 1987;37:1431–2.
   PubMed Web of Science ®Google Scholar
• Shaunak S, Orrell RW, O’Sullivan E, Hawken MB, Lane RJ, Henderson L, et al. Oculomotor function in amyotrophic lateral sclerosis: evidence for frontotemporal impairment. Ann Neurol. 1995;38:38–44.
   PubMed Web of Science ®Google Scholar
• Sharma R, Hicks S, Berna CM, Kennard C, Talbot K, Turner MR. Oculomotor dysfunction in amyotrophic lateral sclerosis: a comprehensive review. Arch Neurol. 2011;68:857–61.
   PubMed Web of Science ®Google Scholar
• Shimizu T, Kawata A, Kato S, Hayashi M, Takamoto K, Hayashi K, et al. Autonomic failure in ALS with a novel SOD1 gene mutation. Neurology. 2000;54:1534–7.
   PubMed Web of Science ®Google Scholar
• Brettschneider J, Arai K, Del Tredici K, Toledo JB, Robinson JL, Lee EB, et al. TDP-43 pathology and neuronal loss in amyotrophic lateral sclerosis spinal cord. Acta Neuropathol. 2014;128:423–37.
   PubMed Web of Science ®Google Scholar
• Ludolph AC, Brettschneider J. TDP-43 in amyotrophic lateral sclerosis: is it a prion disease? Eur J Neurol. 2015; 22:753–61.
   PubMed Web of Science ®Google Scholar