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July 29, 2024Disability and Rehabilitation

Amyotrophic lateral sclerosis in Argentina: unveiling the burden of treatment through patient and caregiver perspectives

Juan Pedro Alonso Natalí Ini Agustina Villarejo María Belizán Javier Roberti

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Abstract

Purpose To examine the burden of treatment (BoT) experienced by people with Amyotrophic Lateral Sclerosis (ALS) in Argentina.

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Cite This Study

Alonso et al. (2024) studied this question.

synapsesocial.com/papers/68e5ea43b6db64358757f4ba https://doi.org/10.1080/09638288.2024.2385732

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Impact of treatment burden on medication adherence and quality of life in amyotrophic lateral sclerosis: a prospective multicentre studyCohort Study · 2026
2The burden of care: Health and wellbeing of informal caregivers of people with amyotrophic lateral sclerosisCross-Sectional Study · 2026
3The economic burden of amyotrophic lateral sclerosis for patients and families: a survey on out-of-pocket expenses and income loss in FranceOriginal Research · 2026
4Clinical features and quality of life of patients with amyotrophic lateral sclerosis at a specialized care service in Salvador-BA2024
5Quality of life and care burden of people living with amyotrophic lateral sclerosis who need home-based medical care in Korea and their family caregivers2025

More related papers

Patients’ and caregivers’ perception of multidimensional and palliative care in amyotrophic lateral sclerosis – protocol of a German multicentre study2024
Amyotrophic lateral sclerosis in Colombia: a population-based study of incidence and socioeconomic determinants2025
P.065 Understanding treatment barriers and adherence among people living with amyotrophic lateral sclerosis2024

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