Tracheostomy and invasive mechanical ventilation in amyotrophic lateral sclerosis: Decision-making factors and survival analysis

Clinical Neurology

Volumn 56, Issue 4, 2016, Pages 241-247

  Kimura, Fumiharu ^a  

^a OSAKA MEDICAL COLLEGE   (Japan)

Author keywords

ALSFRS R; NIPPV; Preserved lower motor neuron function; Prognosis; Respite

Indexed keywords

AGED; AMYOTROPHIC LATERAL SCLEROSIS; ARTIFICIAL VENTILATION; CONTROLLED STUDY; HOME CARE; HUMAN; INVASIVE MECHANICAL VENTILATION; MAJOR CLINICAL STUDY; MOTOR PERFORMANCE; NONINVASIVE VENTILATION; PATIENT DECISION MAKING; REVIEW; SURVIVAL; SURVIVAL ANALYSIS; TRACHEOSTOMY; VENTILATED PATIENT; CLINICAL DECISION MAKING; DISEASE COURSE; MORTALITY; PROGNOSIS; SEVERITY OF ILLNESS INDEX; STATISTICS AND NUMERICAL DATA; TIME FACTOR; TRACHEOTOMY; TRENDS; UTILIZATION;

AMYOTROPHIC LATERAL SCLEROSIS; CLINICAL DECISION-MAKING; DISEASE PROGRESSION; HUMANS; NONINVASIVE VENTILATION; PROGNOSIS; RESPIRATION, ARTIFICIAL; SEVERITY OF ILLNESS INDEX; SURVIVAL ANALYSIS; TIME FACTORS; TRACHEOTOMY;

EID: 84964998631     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: 10.5692/clinicalneurol.cn-000837     Document Type: Review

References (36)

1. 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;118:707-719.
2. Brooks BR. Natural history of ALS: symptoms, strength, pulmonary function, and disability. Neurology 1996;47:71-81.
3. Hayashi H. Ventilatory support: Japanese experience. J Neurol Sci 1997;152:97-100.
4. Sancho J, Servera E, Díaz JL, et al. Home tracheotomy mechanical ventilation in patients with amyotrophic lateral sclerosis: causes, complications and 1-year survival. Thorax 2011;66:948-952.
5. Tagami M, Kimura F, Nakajima H, et al. Tracheostomy and invasive ventilation in Japanese ALS patients: Decision-making and survival analysis: 1990-2010. J Neurol Sci 2014;344:158-164.
6. Miller RG, Rosenberg JA, Gelinas DF, et al. 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;52:1311-1323.
7. Miller RG, Munsat TL, Swash M, et al. Consensus guidelines for the design and implementation of clinical trials in ALS. World Federation of Neurology committee on Research. J Neurol Sci 1999;169:2-12.
8. Campbell JC, Ikegami N. Long-term care insurance comes to Japan. Health Aff (Millwood) 2000;19:26-39.
9. Furuta N, Makioka K, Fujita Y, et al. Changes in the clinical features of amyotrophic lateral sclerosis in rural Japan. Intern Med 2013;52:1691-1696.
10. Atsuta N, Watanabe H, Ito M, et al. Research Committee on the Neurodegenerative Diseases of Japan. Age at onset influences on wide-ranged clinical features of sporadic amyotrophic lateral sclerosis. J Neurol Sci 2009;276:163-169.
11. Horiuchi S. Major causes of the rapid longevity extension in postwar Japan. Jpn J Popul 2011;9:162-171.
12. Kimura F. Increased incidence of deep venous thrombosis in ALS. Neurology 2007;68:2046-2047.
13. Kimura F, Ishida S, Furutama D, et al. Wheelchair economy class syndrome in amyotrophic lateral sclerosis. Neuromuscul Disord 2006;16:204-207.
14. Spataro R, Bono V, Marchese S, et al. Tracheostomy mechanical ventilation in patients with amyotrophic lateral sclerosis: clinical features and survival analysis. J Neurol Sci 2012;323:66-70.
15. Stoller JK, Xu M, Mascha E, et al. Long-term outcomes for patients discharged from a long-term hospital-based weaning unit. Chest 2003;124:1892-1899.
16. Vianello A, Arcaro G, Palmieri A, 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.
17. Chiò A, Calvo A, Ghiglione P, et al. PARALS. Tracheostomy in amyotrophic lateral sclerosis: a 10-year population-based study in Italy. J Neurol Neurosurg Psychiatry 2010;81:1141-1143.
18. Tollefsen E, Midgren B, Bakke P, et al. Amyotrophic lateral sclerosis: gender differences in the use of mechanical ventilation. Eur J Neurol 2010;17:1352-1357.
19. Atkins L, Brown RG, Leigh PN, et al. Marital relationships in amyotrophic lateral sclerosis. Amyotroph Lateral Scler 2010;11: 344-350.
20. Fujimura-Kiyono C, Kimura F, Ishida S, et al. Onset and spreading patterns of lower neuron involvements predict survival in sporadic amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry 2011;82:1244-1249.
21. Kimura F, Fujimura C, Ishida S, et al. Progression rate of ALSFRS-R at time of diagnosis predicts survival time in ALS. Neurology 2006;66:265-267.
22. Borasio GD, Gelinas DF, Yanagisawa N. Mechanical ventilation in amyotrophic lateral sclerosis: a cross-cultural perspective. J Neurol 1998;245:7-12.
23. Lee CT, Chiu YW, Wang KC, et al. Riluzole and prognostic factors in amyotrophic lateral sclerosis long-term and short-term survival: a population-based study of 1149 cases in Taiwan. J Epidemiol 2013;23:35-40.
24. Bae JS, Hong YH, Baek W, et al. Korean ALS/MND Research Group. Current status of the diagnosis and management of amyotrophic lateral sclerosis in Korea: a multi-center cross-sectional study. J Clin Neurol 2012;8:293-300.
25. Neudert C, Oliver D, Wasner M, et al. The course of the terminal phase in patients with amyotrophic lateral sclerosis. J Neurol 2001;248:612-616.
26. Miller RG, Jackson CE, Kasarskis EJ, 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;73:1218-1226.
27. Moss AH, Casey P, Stocking CB, et al. Home ventilation for amyotrophic lateral sclerosis patients: outcomes, costs, and patient, family, and physician attitudes. Neurology 1993;43:438-443.
28. Lechtzin N, Wiener CM, Clawson L, et al. ALS CARE Study Group. Use of noninvasive ventilation in patients with amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord 2004;5:9-15.
29. Ritsma BR, Berger MJ, Charland DA, et al. NIPPV: prevalence, approach and barriers to use at Canadian ALS centres. Can J Neurol Sci 2010;37:54-60.
30. Gonzalez-Bermejo J. Indications and equipment needs for ventilatory support in amyotrophic lateral sclerosis. Rev Neurol (Paris) 2006;162:4S320-4S322.
31. Dreyer P, Lorenzen CK, Schou L, et al. 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;15:62-67.
32. Sancho J, Servera E, Díaz JL, et al. Home tracheotomy mechanical ventilation in patients with amyotrophic lateral sclerosis: causes, complications and 1-year survival. Thorax 2011;66:948-952.
33. Christodoulou G, Goetz R, Ogino M, et al. Opinions of Japanese and American ALS caregivers regarding tracheostomy with invasive ventilation (TIV). Amyotroph Lateral Scler 2015;17: 47-54.
34. Rabkin J, Ogino M, Goetz R, et al. Japanese and American ALS patient preferences regarding TIV (tracheostomy with invasive ventilation): a cross-national survey. Amyotroph Lateral Scler Frontotemporal Degener 2014;15:185-191.
35. Dreyer PS, Felding M, Klitnæs CS, et al. Withdrawal of invasive home mechanical ventilation in patients with advanced amyotrophic lateral sclerosis: ten years of Danish experience. J Palliat Med 2012;15:205-209.
36. Vianello A, Concas A. Tracheostomy ventilation in ALS: a Japanese bias. J Neurol Sci 2014;344:3-4.