Family-Related Quality of Life and Burden in Caregivers of Patients with Chronic Skin Diseases

The study assessed the prevalence of burnout and its impact on the quality of life among 213 caregivers of patients with chronic skin diseases, specifically vitiligo, psoriasis, and alopecia areata. It found that 29.5% of caregivers lacked sufficient time due to caregiving duties, with those caring for psoriasis and vitiligo patients most affected. Additionally, 37.1% experienced stress balancing caregiving with other responsibilities, particularly for psoriasis and alopecia areata patients. Caregivers of psoriasis patients faced the highest burden. The study highlighted a positive correlation between caregiver burden and factors such as age, caregiving duration, and disease severity. It concluded that caregivers of patients with chronic skin conditions face significant burdens that negatively impact their quality of life, emphasizing the need for better support systems.