Abstract

BackgroundAs family caregivers of patients undergoing hematopoietic cell transplantation have multifaceted caregiving responsibilities (such as medical, household, financial) of long duration, they also have multiple physical, social, psychological, and informational needs.ObjectiveThis study explored the prevalence of electronic health record patient portal use by family caregivers for managing both their own and their hematopoietic cell transplantation care recipient’s health, as well as potential factors associated with portal use.MethodsAn electronic caregiver health survey, first developed via cognitive interviewing methods of hematopoietic cell transplantation caregivers, was distributed nationally (in the United States) by patient advocacy organizations to family caregivers of hematopoietic cell transplantation patients. It was used to assess self-reported caregiver demographics, caregiving characteristics, depression and anxiety with the Patient Health Questionnaire–4, coping with the Brief COPE, and caregiver portal use to manage care recipient’s and their own health.ResultsWe found that 77% of respondents (720/937) accessed electronic health record patient portals for their care recipients, themselves, or both. Multivariate models indicated use of care recipient electronic health record portals by caregivers was more likely with young, White, married, low-income caregivers caring for a parent, residing with the care recipient, and experiencing more caregiver depression. Caregiver use of their own electronic health record portal was more likely with young, White, high-income caregivers caring for a parent and experiencing chronic medical conditions of their own. Partially due to multicollinearity, anxiety and coping did not contribute independently to this model.ConclusionsFindings from the survey could open avenues for future research into caregiver use of technology for informational support or intervention, including wearables and mobile health.International Registered Report Identifier (IRRID)RR2-10.2196/4918

Highlights

  • Caregivers of Patients Undergoing Hematopoietic Cell TransplantationHematopoietic cell transplantation is a high-risk but potentially curative therapy for life-threatening blood diseases [1,2,3]

  • Building on inpatient and outpatient interviews, we developed a survey to be distributed nationally to family caregivers of hematopoietic cell transplantation patients—the National Caregiver Health Survey [3,16,17]

  • This study of more than 900 caregivers from a national US sample is the largest published sample of hematopoietic cell transplantation caregivers surveyed to date focused on caregivers’ use of their own and their care recipients’ health portal [3,24,25,31]

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Summary

Introduction

Caregivers of Patients Undergoing Hematopoietic Cell TransplantationHematopoietic cell transplantation is a high-risk but potentially curative therapy for life-threatening blood diseases [1,2,3]. Hematopoietic cell transplantation patients require a committed informal family caregiver or care partner (relative or friend) to provide unpaid assistance for long durations [4]. Patients undergoing hematopoietic cell transplantation require caregiving for an extended time, and demands vary based on stage of disease at diagnosis, treatment intensity, and possible treatment complications [4]. Caregiving has been described as a rewarding and positive experience; ensuring quality of life among caregivers of hematopoietic cell transplantation patients requires broad consideration of their physical, social, psychological, and spiritual demands and needs [4]. As family caregivers of patients undergoing hematopoietic cell transplantation have multifaceted caregiving responsibilities (such as medical, household, financial) of long duration, they have multiple physical, social, psychological, and informational needs

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