Literature DB >> 31672715

Dying of amyotrophic lateral sclerosis: Health care use and cost in the last year of life.

Jocelyn Zwicker1, Danial Qureshi2, Robert Talarico2, Pierre Bourque2, Mary Scott2, Nicolas Chin-Yee2, Peter Tanuseputro2.   

Abstract

OBJECTIVE: To describe health care service utilization and cost for decedents with and without amyotrophic lateral sclerosis (ALS) in the last year of life.
METHODS: Using linked health administrative data, we conducted a retrospective, population-based cohort study of Ontario, Canada, decedents from 2013 to 2015. We examined demographic data, rate of utilization, and cost of health care services in the last year of life.
RESULTS: We identified 283,096 decedents in Ontario, of whom 1,212 (0.42%) had ALS. Decedents with ALS spent 3 times as many days in an intensive care unit (ICU) (mean 6.3 vs 2.1, p < 0.001), and twice as many days using complex continuing care (mean 12.7 vs 6.0, p < 0.001) and home care (mean 99.1 vs 41.3, p < 0.001). A greater percentage of decedents with ALS received palliative home care (44% vs 20%, p < 0.001) and palliative physician home visits (40% vs 18%, p < 0.001) than decedents without ALS. Among decedents with ALS, a palliative physician home visit in the last year of life was associated with reduced adjusted odds of dying in hospital (odds ratio 0.65, 95% confidence interval 0.48-0.89) and fewer days spent in the ICU. Mean cost of care in the last year of life was greater for those with ALS ($68,311.98 vs $55,773.48, p < 0.001).
CONCLUSIONS: In this large population-based cohort of decedents, individuals with ALS spent more days in the ICU, received more community-based services, and incurred higher costs of care in the last year of life. A palliative care physician home visit was associated with improved end of life outcomes; however, the majority of patients with ALS did not access such services.
© 2019 American Academy of Neurology.

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Year:  2019        PMID: 31672715     DOI: 10.1212/WNL.0000000000008582

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  7 in total

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Journal:  Neurol Clin Pract       Date:  2022-02

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4.  Activities of Daily Living and Associated Costs in the Most Widespread Neurodegenerative Diseases: A Systematic Review.

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5.  Caregivers' View of Socio-Medical Care in the Terminal Phase of Amyotrophic Lateral Sclerosis-How Can We Improve Holistic Care in ALS?

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6.  Amyotrophic lateral sclerosis care in Saudi Arabia: A survey of providers' perceptions.

Authors:  Ahmad R Abuzinadah; Aysha A AlShareef; Abdullah AlKutbi; Ahmed K Bamaga; Ali Alshehri; Hussein Algahtani; Edward Cupler; Mohammed H Alanazy
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7.  Healthcare Utilisation and Satisfaction with Care in Patients with Amyotrophic Lateral Sclerosis - An Observational Study.

Authors:  Marie Kierkegaard; Kristina Gottberg; Sverker Johansson; Susanne Littorin; Petter Sandstedt; Charlotte Ytterberg; Lotta Widén Holmqvist
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  7 in total

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