Use of noninvasive ventilation in patients with amyotrophic lateral sclerosis
Authors
Lechtzin, NoahWiener, Charles M.
Clawson, Lora
Davidson, Matthew C.
Anderson, Frederick A. Jr.
Gowda, Neelam
Diette, Gregory B.
UMass Chan Affiliations
Center for Outcomes ResearchDocument Type
Journal ArticlePublication Date
2004-03-19Keywords
AdolescentAdult
Age Factors
Aged
Aged, 80 and over
Amyotrophic Lateral Sclerosis
Cross-Sectional Studies
Demography
Female
Humans
Intermittent Positive-Pressure Ventilation
numerical data
Male
Middle Aged
Retrospective Studies
Sex Factors
Sickness Impact Profile
Social Support
Socioeconomic Factors
Survival Analysis
Time Factors
Treatment Outcome
Health Services Research
Metadata
Show full item recordAbstract
INTRODUCTION: Noninvasive positive pressure ventilation (NIPPV) is associated with improved survival in amyotrophic lateral sclerosis (ALS) and has been widely recommended. The extent of NIPPV use in ALS patients and the factors associated with its use have not been studied. METHODS: A cross-sectional study using the ALS Patient Care Database. Analyses were performed to assess the association of patient and care characteristics with use of ventilatory support. RESULTS: 1458 patients were studied. 15.6% used NIPPV and 2.1% used invasive mechanical ventilation. Patients who used NIPPV were significantly more likely to be male and have higher income than those who did not. They were also more likely to have a gastrostomy tube, lower vital capacity, more severe disease, bulbar involvement and poorer general health status as measured by the SF-12 and Sickness Impact Profile. Multivariate analysis revealed that lower FVC, higher income and use of gastrostomy tube were independently associated with use of NIPPV. CONCLUSIONS: NIPPV is used more than seven times as frequently as invasive ventilation in ALS patients. Patients who use NIPPV have more severe disease than those who do not use any respiratory intervention. Patients with lower income are less likely to use NIPPV, which raises concerns about disparities in the care of patients with ALS.Source
Amyotroph Lateral Scler Other Motor Neuron Disord. 2004 Mar;5(1):9-15. Link to article on publisher's siteDOI
10.1080/14660820310017335Permanent Link to this Item
http://hdl.handle.net/20.500.14038/27100PubMed ID
15204018Related Resources
Link to Article in PubMedae974a485f413a2113503eed53cd6c53
10.1080/14660820310017335