TY - JOUR
T1 - The caregiver burden of idiopathic inflammatory myopathies
AU - Brady, Parker
AU - Hernandez, Roberto Sergio
AU - Salter, Amber
AU - Hua, Catherine
AU - Wilson, Lynn
AU - Lubinus, Manuel
AU - Hu, Yuan Pai
AU - Nandakumar, Dhruv
AU - Bhashyam, Abhiram R.
AU - Bhai, Salman
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2025.
PY - 2025
Y1 - 2025
N2 - Purpose: The purpose of this cross-sectional study was to determine the prevalence of caregiver burden (CB) in caregivers of patients with idiopathic inflammatory myopathies (IIM). Methods: An anonymous survey was distributed worldwide to caregivers of myositis patients through Myositis Support and Understanding in May 2022. CB was measured using the Zarit Burden Interview. The survey also gathered caregiver demographic, financial, and insurance information as well as patient demographic and disease information. Results: Overall, 75.8% of caregivers had at least mild to moderate CB. 39.2% reported not being affected financially by their caregiving responsibilities. A positive effect was found between CB and time since diagnosis, disability level, and financial hardship. A negative effect was found with CB and caregiver age. No association was found between IIM type and CB. Conclusion: CB is a common experience among caregivers of all types of IIM patients. Future research can use our results to generate viable hypothesis about CB in myositis. They should also seek to further understand what contributed to CB in this population. Clinicians should also be attuned to the needs of caregivers tending to long-term myositis patients, especially caregivers of more disabled patients, older caregivers, and individuals financially challenged by caregiving.
AB - Purpose: The purpose of this cross-sectional study was to determine the prevalence of caregiver burden (CB) in caregivers of patients with idiopathic inflammatory myopathies (IIM). Methods: An anonymous survey was distributed worldwide to caregivers of myositis patients through Myositis Support and Understanding in May 2022. CB was measured using the Zarit Burden Interview. The survey also gathered caregiver demographic, financial, and insurance information as well as patient demographic and disease information. Results: Overall, 75.8% of caregivers had at least mild to moderate CB. 39.2% reported not being affected financially by their caregiving responsibilities. A positive effect was found between CB and time since diagnosis, disability level, and financial hardship. A negative effect was found with CB and caregiver age. No association was found between IIM type and CB. Conclusion: CB is a common experience among caregivers of all types of IIM patients. Future research can use our results to generate viable hypothesis about CB in myositis. They should also seek to further understand what contributed to CB in this population. Clinicians should also be attuned to the needs of caregivers tending to long-term myositis patients, especially caregivers of more disabled patients, older caregivers, and individuals financially challenged by caregiving.
KW - Caregiver burden
KW - Dermatomyositis
KW - Idiopathic inflammatory myopathies
KW - Inclusion body myositis
KW - Myositis
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U2 - 10.1007/s11136-025-03953-8
DO - 10.1007/s11136-025-03953-8
M3 - Article
C2 - 40138115
AN - SCOPUS:105001502235
SN - 0962-9343
JO - Quality of Life Research
JF - Quality of Life Research
ER -