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Research Articles

Pulmonary function decline in amyotrophic lateral sclerosis

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Pages 54-61 | Received 04 Jan 2021, Accepted 22 Mar 2021, Published online: 04 Aug 2021

References

  • Miller RG, Jackson CE, Kasarskis EJ, England JD, Forshew D, Johnston W, et al.; Quality Standards Subcommittee of the American Academy of Neurology. Practice Parameter update: The care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the quality standards subcommittee of the American Academy of Neurology. Neurology 2009;73:1218–26.
  • Lo Coco D, Marchese S, Pesco MC, La Bella V, Piccoli F, Lo Coco A, et al. Non-invasive positive-pressure ventilation in ALS: predictors of tolerance and survival. Neurology 2006;67:761–5.
  • Kleopa KA, Sherman M, Neal B, Romano GJ, Heiman-Patterson T. Bipap improves survival and rate of pulmonary function decline in patients with ALS. J Neurol Sci. 1999;164:82–8.
  • Aboussouan LS, Khan SU, Banerjee M, Arroliga AC, Mitsumoto H. Objective measures of the efficacy of noninvasive positive-pressure ventilation in ALS. Muscle Nerve. 2001;24:403–9.
  • Lyall RA, Donaldson N, Fleming T, Wood C, Newsom-Davis I, Polkey MI, et al. A prospective study of quality of life in ALS patients treated with noninvasive ventilation. Neurology. 2001;57:153–6.
  • Newsome-Davis IC, et al. The effect of noninvasive positive pressure ventilation (NIPPV) on cognitive function in ALS: a prospective study. J Neurol Neurosurg Psychiatry. 2001;71:482–7.
  • Martin S, Trevor-Jones E, Khan S, Shaw K, Marchment D, Kulka A, et al. The benefit of evolving multidisciplinary care in ALS: a diagnostic cohort survival comparison. Amyotroph Lateral Scler Frontotemporal Degener. 2017;18:569–75.
  • Aboussouan LS, Mireles-Cabodevila E. Respiratory support in patients with amyotrophic lateral sclerosis. Respir Care. 2013;58:1555–8.
  • Andersen PM, Abrahams S, Borasio GD, de Carvalho M, Chio A, Van Damme P, et al. EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)-revised report of an EFNS task force. Eur J Neurol. 2012;19:360–75.
  • Heiman-Patterson TD, Cudkowicz ME, De Carvalho M, Genge A, Hardiman O, Jackson CE, et al. Understanding the use of NIV in ALS: results of an international ALS specialist survey. Amyotroph Lateral Scler Frontotemporal Degener. 2018; 19:331–41.
  • Jacobs TL, Brown DL, Baek J, Migda EM, Funckes T, Gruis KL. Trial of early noninvasive ventilation for ALS: A pilot placebo-controlled study. Neurology 2016;87:1878–83.
  • Vitacca M, Montini A, Lunetta C, Banfi P, Bertella E, De Mattia E, et al.; ALS RESPILOM Study Group. Impact of an early respiratory care programme with non-invasive ventilation adaptation in patients with amyotrophic lateral sclerosis. Eur J Neurol. 2018;25:556–e33.
  • Noah L, et al. Respiratory measures in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis Frontotemporal Degen 2018;19:321–30.
  • Kasarskis EJ, Mendiondo MS, Wells S, Malguizo MS, Thompson M, Healey M, et al.; ALS Nutrition/NIPPV Study Group. The ALS Nutrition/NIPPV Study: design, feasibility, and initial results. Amyotroph Lateral Scler. 2011;12:17–25.
  • Jackson C, De Carvalho M, Genge A, Heiman-Patterson T, Shefner JM, Wei J, et al. Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R. Amyotrophic Lateral Sclerosis Frontotemporal Degen. 2018;19:506–12.
  • Polla B, D'Antona G, Bottinelli R, Reggiani C. Respiratory muscle fibres: specialisation and plasticity. Thorax 2004;59:808–17.
  • Plowman EK, Tabor-Gray L, Rosado KM, Vasilopoulos T, Robison R, Chapin JL, et al. Impact of expiratory strength training in amyotrophic lateral sclerosis: Results of a randomized, sham-controlled trial. Muscle Nerve. 2019;59:40–6. Epub 2018 Nov 29. PMID: 29981250.