Family caregivers of people with Amyotrophic Lateral Sclerosis (ALS), most often spouses, are likely to become depressed and feel burdened//, but that’s not the case for the people they are caring for, according to a study.
“Since there’s evidence a caregiver’s mental status greatly influences ALS patients, these findings show a family caregiver’s physical and psychological condition should not be overlooked when planning ALS care,” said study author Adriano Chio, MD, with the University of Torino in Torino, Italy, and a member of the American Academy of Neurology.
Researchers interviewed 31 ALS patient-caregiver couples at the beginning and end of a nine-month study. Couples were tested for depression and quality of life. Researchers also examined a caregiver’s feeling of burden, along with a patient’s self-perceived burden.
The study found a significant increase of burden and depression among caregivers over the nine months, while depression, quality of life, and self-perceived burden remained virtually unchanged among people with ALS.
Mild to moderate depression among caregivers jumped from 9.7 percent to 19.3 percent. Feeling burdened increased 11 percent among caregivers, with the most common complaint being not enough time for oneself. Quality of life scores dropped slightly among caregivers.
Chio says several factors may have contributed to the steadiness among quality of life and depression in people with ALS, including a patient’s acceptance of the deadly disease, or possibly cognitive impairment.
The study also found while quality of life was higher in caregivers than in patients at the beginning of the study, quality of life was higher in patients by the end. “ALS is considered a family disease, meaning that it involves every member of the patient’s entourage. Interventions specifically designed to enhance effective communication between patients and caregivers might improve the psyPage: 1 2 Related medicine news :1
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