ALS with respiratory onset: Clinical features and effects of non-invasive ventilation on the prognosis

References

• Haverkamp LJ, Appel V, Appel SH. Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction. Brain. 1995;118:707–19.
   PubMed Web of Science ®Google Scholar
• Stambler N, Charatan M, Cedarbaum JM. Prognostic indicators of survival in ALS. ALS CNTF Treatment Study Group. Neurology. 1998;50:66–72.
   PubMed Web of Science ®Google Scholar
• Traynor BJ, Zhang H, Shefner JM, Schoenfeld D, Cudkowicz ME, NEALS Consortium. Functional outcome measures as clinical trial endpoints in ALS. Neurology. 2004;63:1933–5.
   PubMed Web of Science ®Google Scholar
• Czaplinski A, Yen AA, Appel SH. Forced vital capacity (FVC) as an indicator of survival and disease progression in an ALS clinic population. J Neurol Neurosurg Psychiatry. 2006;77:390–2.
   PubMed Web of Science ®Google Scholar
• Corcia P, Pradat PF, Salachas F, Bruneteau G, Forestier N, Seilhean D, . Causes of death in a post mortem series of ALS patients. Amyotroph Lateral Scler. 2008;9:59–62.
   PubMed Web of Science ®Google Scholar
• Miller RG, Rosenberg JA, Gelinas DF, Mitsumoto H, Newman D, Sufit R, . Practice parameter: the care of the patient with amyotrophic lateral sclerosis (an evidence based review): report of the Quality Standards Subcommittee of the American Academy of Neurology, ALS Practice Parameters Task Force. Neurology. 1999;52:1311–23.
   PubMed Web of Science ®Google Scholar
• Bradley WG, Anderson F, Gowda N, Miller RG, ALS CARE Study Group. Changes in the management of ALS since the publication of the AAN ALS Practice Parameter 1999. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004;5:240–4.
   PubMed Web of Science ®Google Scholar
• Andersen PM, Borasio GD, Dengler R, Hardiman O, Kollewe K, Leigh PN, , the EALSC Working Group. Good practice in the management of amyotrophic lateral sclerosis: clinical guidelines. An evidence based review with good practice points. EALSC Working Group. Amyotroph Lateral Scler. 2007;8:195–213.
   PubMed Web of Science ®Google Scholar
• Shoesmith CL, Findlater K, Rowe A, Strong MJ. Prognosis of amyotrophic lateral sclerosis with respiratory onset. J Neurol Neurosurg Psychiatry. 2007;78:629–31.
   PubMed Web of Science ®Google Scholar
• Chen R, Grand’Maison F, Strong MJ, Ramsay DA, Bolton CF. Motor neuron disease presenting as acute respiratory failure: a clinical and pathological study. J Neurol Neurosurg Psychiatry. 1996;60:455–8.
   PubMed Web of Science ®Google Scholar
• de Carvalho M, Matias T, Coelho F, Evangelista T, Pinto A, Luis ML. Motor neuron disease presenting with respiratory failure. J Neurol Sci. 1996;139 (Suppl):117–22.
   PubMedGoogle Scholar
• Scelsa SN, Yakubov B, Salzman SH. Dyspnoea-fasciculation syndrome: early respiratory failure in ALS with minimal motor signs. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002;3:239–43.
   PubMed Web of Science ®Google Scholar
• Czapliński A, Strobel W, Gobbi C, Steck AJ, Fuhr P, Leppert D. Respiratory failure due to bilateral diaphragm palsy as an early manifestation of ALS. Med Sci Monit. 2003;9:S34–6.
   Google Scholar
• Bourke SC, Bullock RE, Williams TL, Shaw PJ, Gibson GJ. Non-invasive ventilation in ALS: indications and effect on quality of life. Neurology. 2003;61:171–7.
   PubMed Web of Science ®Google Scholar
• Bourke SC, Tomlinson M, Williams TL, Bullock RE, Shaw PJ, Gibson GJ. Effects of non-invasive ventilation on survival and quality of life in patients with amyotrophic lateral sclerosis: a randomized controlled trial. Lancet Neurol. 2006;5:140–7.
   PubMed Web of Science ®Google Scholar
• Peysson S, van den Berghe N, Philit F, Vial C, Petitjean T, Bouhour F, . Factors predicting survival following noninvasive ventilation in amyotrophic lateral sclerosis. Eur Neurol. 2008;59:164–71.
   PubMed Web of Science ®Google Scholar
• Brooks BR, Miller RG, Swash M, Munsat TL, World Federation of Neurology Research Group on Motor Neuron Diseases. El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2000;1:293–9.
   PubMed Web of Science ®Google Scholar
• Armon C. Epidemiology of ALS/motor neuron disease. Shaw PJ, Strong MJ, Blue Books of Practical Neurology: Motor Neuron Disorders. Philadelphia: Elsevier. 2003;167–205.
   Google Scholar
• de Carvalho M, Pinto S, Swash M. Association of paraspinal and diaphragm denervation in ALS. Amyotroph Lateral Scler. 2009:1–4. [Epub ahead of print]
   PubMedGoogle Scholar
• Mateen FJ, Sorenson EJ, Daube JR. Strength, physical activity, and fasciculations in patients with ALS. Amyotroph Lateral Scler. 2008;9:120–1.
   PubMed Web of Science ®Google Scholar
• Silani V, Kasarskis EJ, Yanagisawa N. Nutritional management in amyotrophic lateral sclerosis: a worldwide perspective. J Neurol. 1998;245(Suppl 2):S13–9, discussion S29.
   Google Scholar
• Desport JC, Preux PM, Truong TC, Vallat JM, Sautereau D, Couratier P. Nutritional status is a prognostic factor for survival in ALS patients. Neurology. 1999;53:1059–63.
   PubMed Web of Science ®Google Scholar
• Bouteloup C, Desport JC, Clavelou P, Guy N, Derumeaux-Burel H, Ferrier A, Couratier P. Hypermetabolism in ALS patients: an early and persistent phenomenon. J Neurol. 2009;256:1236–42.
   PubMed Web of Science ®Google Scholar
• Meyrignac C, Poirier J, Degos JD. Amyotrophic lateral sclerosis presenting with respiratory insufficiency as the primary complaint. Clinicopathological study of a case. Eur Neurol. 1985;24:115–20.
   PubMedGoogle Scholar
• Perez T. Amyotrophic lateral sclerosis (ALS): evaluation of respiratory function. Rev Neurol (Paris). 2006;162 (Suppl 2):S188–94.
   Google Scholar
• Lyall RA, Donaldson N, Polkey MI, Leigh PN, Moxham J. Respiratory muscle strength and ventilatory failure in amyotrophic lateral sclerosis. Brain. 2001;124:2000–13.
   PubMed Web of Science ®Google Scholar
• Pinto S, Turkman A, Pinto A, Swash M, de Carvalho M. Predicting respiratory insufficiency in amyotrophic lateral sclerosis: the role of phrenic nerve studies. Clin Neurophysiol. 2009;120:941–6.
   PubMed Web of Science ®Google Scholar