Background and Purpose: The increased care burden among home caregivers results in significant stress. This preliminary report aimed to evaluate the pediatric respiratory home caregivers’ burden and quality of life (QOL). Methods: This cross-sectional study used purposive sampling to prospectively recruit children re-ceiving pediatric respiratory home care and their caregivers. Eligible children were defined as children younger than 18 years who had used home ventilators for more than 30 days or who needed tracheostomy care. The Caregiver Care Burden Scale was used to investigate the caregivers’ physiological, psychological, social and economic burdens. QOL was assessed using a brief version of the QOL scale developed by the World Health Organization (WHOQOL-BREF). Results: A total of 102 pairs of chil-dren and caregivers were included. Caregivers’ mean age was 41.2±9.7 years, and 90% were mothers of home care children. Children’s demographic and clinical char-acteristics were: age 7.6±5.4 years, ventilator-dependent (n=96), tracheostomy (n=52), with major diagnoses of central nervous system disorders (44%) and neuromuscular dystrophy (23%). Social burden was the highest care burden, and the four care burden domains were all above 70%, indicating a medium level of care burden. Psychological QOL had the lowest score among the four QOL domains. Conclusions: Pediatric res-piratory home care is long-term, multidisciplinary, and highly-dependent. The overall care burden and QOL of home caregivers are at a medium level. Psychosocial support and focusing on caregivers’ needs and general health may reduce caregivers’ care burden, improve QOL and enhance family dynamics in pediatric respiratory home care.