Exploring the multidimensional impact of caregiver burden in patients with inflammatory bowel disease
View abstract on PubMed
Summary
This summary is machine-generated.Caregivers of inflammatory bowel disease (IBD) patients face significant burden, linked to caregiver depression, anxiety, and daily care hours. Addressing this burden is crucial for both patient outcomes and caregiver well-being.
Area Of Science
- Gastroenterology and Hepatology
- Psychology
- Public Health
Background
- Inflammatory bowel disease (IBD) is a chronic condition requiring frequent medical attention.
- Family members often act as primary caregivers, experiencing substantial physical, psychological, and financial strain.
- Limited research exists on the burden faced by IBD caregivers.
Purpose Of The Study
- To assess the current state of caregiver burden in IBD.
- To identify factors contributing to caregiver burden in IBD.
- To provide a reference for evaluating and intervening in caregiver burden.
Main Methods
- A questionnaire survey was conducted with 236 IBD patients and their caregivers.
- Data collected included demographics, anxiety (SAS), depression (SDS), sleep quality (PSQI), and caregiver burden (CBI).
- Statistical analyses included correlation and multiple linear regression.
Main Results
- Caregiver burden (CBI) positively correlated with anxiety (SAS), depression (SDS), and poor sleep quality (PSQI).
- Increased caregiver burden was associated with higher caregiver depression and anxiety, longer caregiving duration, younger patient age, lower patient education, and greater disease severity.
- Female caregivers reported a higher burden than male caregivers.
Conclusions
- Caregivers of IBD patients experience significant and often underestimated burden.
- This burden adversely affects patient outcomes and caregiver well-being.
- Comprehensive support for IBD caregivers is essential from healthcare professionals and society.
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