Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-28T02:01:38.520Z Has data issue: false hasContentIssue false

NIPPV: Prevalence, Approach and Barriers to Use at Canadian ALS Centres

Published online by Cambridge University Press:  02 December 2014

Benjamin R. Ritsma
Affiliation:
Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario, Canada
Michael J. Berger
Affiliation:
Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario, Canada School of Kinesiology, Faculty of Health Sciences, The University of Western Ontario, London, Ontario, Canada
David A. Charland
Affiliation:
Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario, Canada
Michael A. Khoury
Affiliation:
Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario, Canada
Joel T. Phillips
Affiliation:
Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario, Canada
Michael J. Quon
Affiliation:
Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario, Canada
Michael J. Strong*
Affiliation:
Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario, Canada Department of Clinical Neurological Sciences, The University of Western Ontario, London, Ontario, Canada
Valerie M. Schulz
Affiliation:
Schulich School of Medicine & Dentistry, The University of Western Ontario, London, Ontario, Canada Department of Anesthesia & Perioperative Medicine, The University of Western Ontario, London, Ontario, Canada
*
Room C7-120, UH-LHSC, 339 Windermere Road, London, Ontario, N6A 5A5, Canada.
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Objective:

The purpose of this study was to evaluate Canadian amyotrophic lateral sclerosis (ALS) centres with respect to: 1) the prevalence of Non-invasive positive pressure ventilation (NIPPV) and invasive mechanical ventilation via tracheostomy (TV) utilization, 2) the approach to NIPPV use, focusing upon the currently employed initiation criteria and 3) the barriers influencing NIPPV administration.

Methods:

A descriptive survey research design aimed to obtain quantitative data and open-ended responses from an active physician at each of the 15 multidisciplinary Canadian ALS centres.

Results:

The principal findings of this study were: 1) NIPPV and TV are used in 18.3% and 1.5% of patients at Canadian ALS centres, respectively, 2) symptoms of respiratory insufficiency, namely orthopnea (clinical significance rated at 9.00/10 ± 1.48), dyspnea (8.27 ± 1.95) and morning headache (7.55 ± 1.21) are the most significant indicators for NIPPV initiation, 3) the primary barriers to NIPPV utilization are patient intolerance (70% of centres) and inaccessibility of respirologists and ventilation technologists (50% of centres).

Conclusions:

Variability in NIPPV use has an impact upon the management of Canadian ALS patients. The establishment of more definitive NIPPV initiation criteria, emphasizing respiratory symptoms, and the attenuation of barriers to NIPPV use should be targeted so as to ensure optimal care for all ALS patients.

Objectif:

Le but de cette étude était d’examiner dans les centres canadiens de traitement de la SLA : 1) la prévalence de NIPPV (ventilation non invasive en pression positive) et de l’utilisation de la ventilation mécanique avec trachéotomie (VT); 2) l’approche à l’utilisation de NIPPV ciblant les critères utilisés actuellement pour la commencer et 3) les freins à son utilisation.

Méthodes:

Nous avons utilisé un plan d’enquête descriptive dont le but était d’obtenir des données quantitatives et des réponses ouvertes des médecins pratiquant dans chacun des 15 centres multidisciplinaires canadiens de traitement de la SLA.

Résultats:

Les constatations principales de cette étude sont les suivantes : 1) la NIPPV et la VT sont utilisées respectivement chez 18,3% et 1,5% des patients des centres canadiens de traitement de la SLA; 2) les symptômes d’insuffisance respiratoire, soit l’orthopnée (évaluée au point de vue clinique à 9,00/10 ± 1,48), la dyspnée (8,27 ± 1,95) et la céphalée matinale (7,55 ± 1,21) sont les indicateurs les plus importants pour le début d’une NIPPV; 3) Les principales entraves à l’utilisation de la NIPPV sont l’intolérance du patient (70% des centres) et l’absence de pneumologues et de techniciens en assistance respiratoire (50% des centres).

Conclusions:

La variabilité de l’utilisation de la NIPPV a un impact sur le traitement des patients canadiens atteints de SLA. Afin d’assurer la prise en charge optimale de tous les patients atteints de SLA, il faudra procéder à l’élaboration de critères de référence plus précis pour débuter la NIPPV en mettant l’emphase sur les symptômes respiratoires et tenter d’atténuer les barrières à son utilisation.

Type
Research Article
Copyright
Copyright © The Canadian Journal of Neurological 2010

References

1. Andersen, PM, Borasio, GD, Dengler, R, Hardiman, O, Kollewe, K, Leigh, PN, et al. 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(4):195213.CrossRefGoogle ScholarPubMed
2. Miller, RG, Rosenberg, JA, Gelinas, DF, Mitsumoto, H, Newman, D, Sufit, R, 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(7):131123.CrossRefGoogle Scholar
3. Aboussouan, LS, Khan, SU, Banerjee, M, Arroliga, AC, Mitsumoto, H. Objective measures of the efficacy of noninvasive positive-pressure ventilation in amyotrophic lateral sclerosis. Muscle Nerve. 2001; 24(3):4039.Google Scholar
4. Aboussouan, LS, Khan, SU, Meeker, DP, Stelmach, K, Mitsumoto, H. Effect of noninvasive positive-pressure ventilation on survival in amyotrophic lateral sclerosis. Ann Intern Med. 1997; 127(6):4503.Google Scholar
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(1):828.Google Scholar
6. Lo Coco, D, Marchese, S, Pesco, MC, La Bella, V, Piccoli, F, Lo Coco, A. Noninvasive positive-pressure ventilation in ALS: predictors of tolerance and survival. Neurology. 2006; 67(5):7615.Google Scholar
7. Pinto, AC, Evangelista, T, Carvalho, M, Alves, MA, Sales Luis, ML. Respiratory assistance with a non-invasive ventilator (Bipap) in MND/ALS patients: survival rates in a controlled trial. J Neurol Sci. 1995; 129 Suppl: 1926.CrossRefGoogle ScholarPubMed
8. 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 randomised controlled trial. Lancet Neurol. 2006; 5(2):1407.Google Scholar
9. Bourke, SC, Williams, TL, Bullock, RE, Gibson, GJ, Shaw, PJ. Non-invasive ventilation in motor neuron disease: current UK practice. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002; 3(3):1459.Google Scholar
10. Borasio, GD, Shaw, PJ, Hardiman, O, Ludolph, AC, Sales Luis, ML, Silani, V. Standards of palliative care for patients with amyotrophic lateral sclerosis: results of a European survey. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001; 2 (3):15964.Google Scholar
11. Melo, J, Homma, A, Iturriaga, E, Frierson, L, Amato, A, Anzueto, A, et al. Pulmonary evaluation and prevalence of non-invasive ventilation in patients with amyotrophic lateral sclerosis: a multicenter survey and proposal of a pulmonary protocol. J Neurol Sci. 1999; 169(1-2):1147.Google Scholar
12. Cedarbaum, JM, Stambler, N. Disease status and use of ventilatory support by ALS patients. BDNF Study Group. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001; 2(1):1922.Google Scholar
13. Bradley, WG, Anderson, F, Gowda, N, Miller, RG. 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(4):2404.Google Scholar
14. Jackson, CE, Lovitt, S, Gowda, N, Anderson, F, Miller, RG. Factors correlated with NPPV use in ALS. Amyotroph Lateral Scler. 2006; 7(2):805.Google Scholar
15. Lechtzin, N, Wiener, CM, Clawson, L, Davidson, MC, Anderson, F, Gowda, N, et al. Use of noninvasive ventilation in patients with amyotrophic lateral sclerosis. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004; 5(1):915.Google Scholar
16. Borasio, GD, Gelinas, DF, Yanagisawa, N. Mechanical ventilation in amyotrophic lateral sclerosis: a cross-cultural perspective. J Neurol. 1998; 245 Suppl 2:S712; discussion S29.Google Scholar
17. Bourke, SC, Gibson, GJ. Non-invasive ventilation in ALS: current practice and future role. Amyotroph Lateral Scler Other Motor Neuron Disord. 2004; 5(2):6771.Google Scholar
18. Sivak, ED, Shefner, JM, Mitsumoto, H, Taft, JM. The use of non-invasive positive pressure ventilation (NIPPV) in ALS patients. A need for improved determination of intervention timing. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001; 2 (3):13945.Google Scholar
19. Lechtzin, N, Scott, Y, Busse, AM, Clawson, LL, Kimball, R, Wiener, CM. Early use of non-invasive ventilation prolongs survival in subjects with ALS. Amyotroph Lateral Scler. 2007; 8(3):1858.Google Scholar
20. Pinto, A, de Carvalho, M, Evangelista, T, Lopes, A, Sales-Luis, L. Nocturnal pulse oximetry: a new approach to establish the appropriate time for non-invasive ventilation in ALS patients. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003; 4 (1):315.CrossRefGoogle ScholarPubMed
21. Heiman-Patterson, TD, Miller, RG. NIPPV: a treatment for ALS whose time has come. Neurology. 2006; 67(5):7367.Google Scholar
22. Hillberg, RE, Johnson, DC. Noninvasive ventilation. N Engl J Med. 1997; 337(24):174652.Google Scholar
23. Shoesmith, CL, Strong, MJ. Amyotrophic lateral sclerosis: update for family physicians. Can Fam Physician. 2006; 52(12):15639.Google ScholarPubMed
24. Mitchell, JD, Borasio, GD. Amyotrophic lateral sclerosis. Lancet. 2007; 369(9578):203141.CrossRefGoogle ScholarPubMed
25. Bourke, SC, Bullock, RE, Williams, TL, Shaw, PJ, Gibson, GJ. Noninvasive ventilation in ALS: indications and effect on quality of life. Neurology. 2003; 61(2):1717.Google Scholar
26. Lechtzin, N, Wiener, CM, Shade, DM, Clawson, L, Diette, GB. Spirometry in the supine position improves the detection of diaphragmatic weakness in patients with amyotrophic lateral sclerosis. Chest. 2002; 121(2):43642.Google Scholar
27. Farrero, E, Prats, E, Povedano, M, Martinez-Matos, JA, Manresa, F, Escarrabill, J. Survival in amyotrophic lateral sclerosis with home mechanical ventilation: the impact of systematic respiratory assessment and bulbar involvement. Chest. 2005; 127 (6):21328.CrossRefGoogle ScholarPubMed
28. Gelinas, D. Respiratory complications of amyotrophic lateral sclerosis: symptoms, signs, diagnosis and treatment. Continuum: lifelong learning in neurology. 2002; 8(4):11024.Google Scholar
29.Health Canada. Canadian Health Act - Annual Report 2006-07. Ottawa: Heath Canada; 2007. p. 1.Google Scholar