Impact of the COVID-19 pandemic on a cohort of ALS patients in Catalonia

Recasens, B. Bertran; Panades, Mónica Povedano; Rubio, Miguel A.

doi:10.1016/j.nrleng.2020.12.001

Cited by 1 publication

(1 citation statement)

References 8 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Patient management, such as routine check-ups, has been limited in 2020 and 2021 because of the COVID-19 pandemic, which has made it more important to manage patients at home with thorough professionalism. [ 7 ].…”

Section: Introductionmentioning

confidence: 99%

Family Caregiver Suffering in Caring for Patients with Amyotrophic Lateral Sclerosis in Korea

Kim

Chu

2021

IJERPH

View full text Add to dashboard Cite

The purpose of this study was to describe the meaning of the suffering experience of Korean ALS family caregivers. This is a descriptive phenomenological study that included ten participants using convenience sampling with maximum variation in a tertiary hospital in Seoul, South Korea. Colaizzi’s data analysis method was used to inductively determine themes and formulate meanings. The three main themes derived from analysis were: “frustration with seeing a patient suffering”, “burnout at the cost of a life of dedication”, and “desperate need for help”. Caregivers experience high levels of suffering, which can come in various forms depending on the circumstances of the particular patient and family. Especially, distress from seeing a loved one suffering was another aspect of suffering in Korean ALS caregivers, reflecting strong family ties. At the same time, patients are in desperate need of help and support from their families. Thus, it is essential to provide care to lessen the causes of distress and meet the needs of not only patients, but also caregivers through family-centered care to improve overall quality of life for all involved.

show abstract

Section: Introductionmentioning

confidence: 99%