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Respiratory function of people with amyotrophic lateral sclerosis and caregiver distress level: a correlational study

DOI: 10.1186/1751-0759-6-14

Keywords: Quality of life, Bio-psycho-social interaction, Amyotrophic lateral sclerosis, Non-invasive ventilation, Health care, Caregivers

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Abstract:

A cross-sectional study was conducted to investigate respiratory issues (PCF and FVC) and the perception of social support of ALS patients. Caregivers filled questionnaires about trait anxiety, depression, and burden of care. Forty ALS patients and their caregivers were recruited.FVC and PCF were positively related to patient perception of social support and negatively related to caregiver anxiety, depression, and burden.The distress of ALS caregivers is related to patient respiratory issues. The first and more intuitive explanation emphasizes the impact that the patient’s clinical condition has with respect to the caregiver. However, it is possible to hypothesize that if caregivers feel psychologically better, their patient’s quality of life improves and that a condition of greater well-being and relaxation could also increase ventilatory capacity. Furthermore, care management could be carried out more easily by caregivers who pay more attention to the patient's respiratory needs.Patient perception of social support and caregiver distress are related to respiratory issues in ALS.

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