Cited by 39Amyotrophic Lateral Sclerosis ResearchNursing care and researchAssistive Technology in Communication and Mobility

Ventilator dependence and expressions of need: A study of patients with amyotrophic lateral sclerosis in Japan

Hirano, Yuko Mandai, Yamazaki, Yoshihiko, Shimizu, Junichi, Togari, Taisuke, Bryce, Thomas James·2006·Social Science & Medicine

Abstract

This research examined the experience of Amyotrophic Lateral Sclerosis (ALS) patients who depend on an invasive mechanical ventilator in Japan. We investigated their difficulties in expressing their needs, their desires and wishes, and their sources of support and happiness. We examined the relationship between these factors and patient demographics, and hope as an indicator of successful adaptation to the illness experience (assessed by the Herth Hope Index). Interview results guided the formation of an anonymous questionnaire distributed to patients by mail. We interviewed 27 patients and their families and surveyed 157 respondents with a questionnaire. Most patients experienced multiple categories of difficulties, which correlated with reduced hope. More severe physical symptoms correlated with more emotional and social difficulties. Notable findings included a high prevalence of unalleviated pain, fear or experience of ventilator difficulties, and fear of burdening others. Having more sources of psychosocial support and happiness was associated with greater hope. Living at home was associated with fewer social difficulties. No patients claimed additional sources of support without claiming family or professional caregiver support, suggesting their mediation may be crucial in maintaining other social connections. Users of computer communication reported more sources of support and happiness and less frustration from difficulty expressing themselves. The most common reported desires, following a cure for ALS, related to the happiness of the patients' families, and a desire not to burden them. We also found that invasive mechanical ventilation (IMV) had been initiated emergently in 30.1% of patients without patient or family consent. Our results provide an insight into the world of this challenged population, elucidating the difficulties they face, and clarifying the role of support and other factors in maintaining hope. We identify concrete areas to which increased attention should be directed in patient care.

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Crossref · 10.1016/j.socscimed.2005.08.015

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  • Initial lack of communication has been described as traumatic, often when there was a lack of support from qualified medical personnel approaching this delicate period.

    “The initial lack of communication has been described as traumatic [18] often when there was a lack of support from qualified medical personnel approaching this delicate period [19].”

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References 38 · Cited by 39

Authors
Hirano, Y. M., Yamazaki, Y., Shimizu, J., Togari, T., & Bryce, T. J.
Affiliations
  • The University of Tokyo (JP)
  • Tokyo Metropolitan University (JP)
Corresponding author
Hirano, Yuko Mandai
Venue
Social Science & Medicine
Publisher
Elsevier BV
Published
2006-03
Volume
62
Issue
6
Pages
1403-1413
ISSN
0277-9536 (ISSN-L)
OpenAlex
W2007687214
Cited by
39
References
38
Citations by year
2026: 1 · 2025: 2 · 2024: 1 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 3 · 2019: 3 · 2018: 1 · 2017: 3 · 2016: 1 · 2015: 1 · 2014: 2 · 2013: 4 · 2012: 1
FWCI
0.65
Type
journal article
Language
en
Open access
closed
Locations
  • Social Science & Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
Funders
Ministry of Education, Culture, Sports, Science and Technology
Topics
  • Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
  • Health Sciences › Health Professions › Pharmacy › Nursing care and research
  • Health Sciences › Health Professions › Occupational Therapy › Assistive Technology in Communication and Mobility
Keywords
amyotrophic lateral sclerosis, invasive mechanical ventilation, ventilator dependence, hope, psychosocial support, unmet needs, caregiver support, computer communication, living at home, social-emotional problems, pain, patient experience
MeSH terms
Adult, Aged, Amyotrophic Lateral Sclerosis, Demography, Female, Happiness, Humans, Japan, Male, Middle Aged, Pain, Quality of Health Care, Residence Characteristics, Respiration, Artificial, Social Support, Stress, Psychological

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