Sökning: "caregiver burden"

Visar resultat 21 - 25 av 31 avhandlingar innehållade orden caregiver burden.

  1. 21. Health-related quality of life in persons with Parkinson's disease. Aspects of symptoms, caregiving and sense of coherence

    Författare :Marianne Caap-Ahlgren; Geriatrik; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; SOC; PDQ-8 and 39; SF-36; GDS; insomnia; caregiving; Parkinson s disease; health-related quality of life; Neurology; neuropsychology; neurophysiology; Neurologi; neuropsykologi; neurofysiologi; Gerontology; Gerontologi;

    Sammanfattning : Abstract Aims: The aim of this thesis was to investigate how the impact of Parkinson’s disease, a chronic neurodegenerative disorder, influences the person’s health-related quality of life. The aim was also to investigate nursing assessment and management of Parkinson’s in elderly persons. LÄS MER

  3. 22. The health economics of Duchenne muscular dystrophy

    Författare :Erik Landfeldt; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :;

    Sammanfattning : Duchenne muscular dystrophy (DMD) is a rare neuromuscular disease characterized by progressive muscle degeneration resulting in loss of independent ambulation, serious multisystem complications, and a mean life expectancy at birth of about 25 years. Several therapies are on the horizon for DMD and it has thus become urgent to better understand the health economic context of the disease to enable assessments of cost-effectiveness and inform decisions regarding reimbursement of new health technologies. LÄS MER

  4. 23. Quality of life in family caregivers to persons with breast cancer in Iran : methodological and clinical aspects

    Författare :Sedigheh Khanjari; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :quality of life;

    Sammanfattning : Background: In Iran, cancer is the third cause of death and breast cancer is the most common cancer among women. Nursing care should focus on the entire family (and not only the patient) as one unit of care. LÄS MER

  5. 24. Disability and health-related quality of life in patients with amyotrophic lateral sclerosis, and caregiving experience from the perspective of next of kin

    Författare :Petter Sandstedt; Karolinska Institutet; Karolinska Institutet; []
    Nyckelord :;

    Sammanfattning : Background: Amyotrophic lateral sclerosis (ALS) is a degenerative motor neuron disease leading to progressive muscle weakness resulting in respiratory failure and death. The average survival time from diagnosis is two to three years. The use of tracheostomy invasive ventilation (TIV) may, however, prolong life by several years. LÄS MER

  7. 25. Self-harm - hovering between hope and despair : experiences and interactions in a health care context

    Författare :Britt-Marie Lindgren; Ulla Hällgren Graneheim; Sture Åström; Agneta Berg; Umeå universitet; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; discursive psychology; experiences; hope; hopelessness; interactions; narratives; phenomenological hermeneutics; psychiatric nursing; qualitative content analysis; self-harm; berättelser; diskurspsykologi; fenomenologisk hermeneutik; hopp; hopplöshet; interaktion; kvalitativ innehållsanalys; psykiatrisk omvårdnad; självskada; upplevelser; omvårdnadsforskning med medicinsk inriktning; Caring Sciences;

    Sammanfattning : Background The definition of self-harm used in this project is repeated, impulsive behaviour causing tissue damage, yet not intended as a suicide attempt. Instead of wishing to die, the person who self-harms wishes to be relieved from anxiety. LÄS MER