The effects of inflammatory bowel disease on caregivers: significant burden and loss of productivity

• Published in: BMC health services research 2020-06, Vol.20 (1), p.556-556, Article 556
• Main Authors: Zand, Aria, Kim, Brian J, van Deen, Welmoed K, Stokes, Zachary, Platt, Anya, O'Hara, Shelby, Khong, Harrison, Hommes, Daniel W
• Format: Article
• Language: English
• Subjects: Absenteeism; Absenteeism (Labor); Adaptation, Psychological; Adult; Aged; Analysis; Caregiver; Caregiver burden; Caregivers; Caregivers - psychology; Chronic illnesses; Cost of Illness; Cross-Sectional Studies; Demographics; Efficiency; Female; Health services; Humans; Inflammatory bowel disease; Inflammatory Bowel Diseases - nursing; Inflammatory Bowel Diseases - psychology; Male; Medical research; Middle Aged; Pain; Patients; Presenteeism; Productivity; Prospective Studies; Quality of Life; Questionnaires; Regression analysis; Remission (Medicine); Surveys and Questionnaires; Ulcerative colitis; Work Performance
• ISSN: 1472-6963; 1472-6963
• DOI: 10.1186/s12913-020-05425-w

Caregiver burden is the emotional, physical, practical, and/or financial burden associated with taking care of a patient with a chronic condition. Limited literature on caregiver burden in Inflammatory Bowel Diseases (IBD) has accounted for some predictors, but its effect on work productivity (absenteeism and presenteeism) is unknown. In a prospective study, patients and their respective caregivers were surveyed from November 2015 until July 2017. Data on demographics, work productivity, quality of life, disease activity, caregiver burden and productivity were collected. The burden on caregivers was assessed and associations between caregiver productivity and caregiver burden were analyzed. Additionally, predictors for caregiver burden were identified. One hundred two IBD patients and their respective caregiver were included. In total, 39% of IBD caregivers experienced burden. Caregivers with burden experienced significantly more absenteeism and presenteeism (65 and 85% respectively). Furthermore, 51% of caregivers felt that they should be doing more for their care recipient and felt they could do a better job at caregiving. Predictors of burden included race/ethnicity, history of fistulas, diagnosis of ulcerative colitis, higher caregiver education, and hours spent caregiving. Caregivers with burden had significantly more productivity decrease compared to those without burden. Additionally, the majority of caregivers feel they should be providing more and better care for their recipients. The development of strategies to address caregiver's distress and perceived burden when caring for IBD patients is warranted.