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Electronic Health Record Portal Use by Family Caregivers of Patients Undergoing Hematopoietic Cell Transplantation: United States National Survey Study
BACKGROUND: As 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. OBJECTIVE: This study e...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JMIR Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8086639/ https://www.ncbi.nlm.nih.gov/pubmed/33687332 http://dx.doi.org/10.2196/26509 |
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author | Gupta, Vibhuti Raj, Minakshi Hoodin, Flora Yahng, Lilian Braun, Thomas Choi, Sung Won |
author_facet | Gupta, Vibhuti Raj, Minakshi Hoodin, Flora Yahng, Lilian Braun, Thomas Choi, Sung Won |
author_sort | Gupta, Vibhuti |
collection | PubMed |
description | BACKGROUND: As 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. OBJECTIVE: This 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. METHODS: An 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. RESULTS: We 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. CONCLUSIONS: Findings 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 |
format | Online Article Text |
id | pubmed-8086639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | JMIR Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-80866392021-05-07 Electronic Health Record Portal Use by Family Caregivers of Patients Undergoing Hematopoietic Cell Transplantation: United States National Survey Study Gupta, Vibhuti Raj, Minakshi Hoodin, Flora Yahng, Lilian Braun, Thomas Choi, Sung Won JMIR Cancer Original Paper BACKGROUND: As 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. OBJECTIVE: This 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. METHODS: An 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. RESULTS: We 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. CONCLUSIONS: Findings 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 JMIR Publications 2021-03-09 /pmc/articles/PMC8086639/ /pubmed/33687332 http://dx.doi.org/10.2196/26509 Text en ©Vibhuti Gupta, Minakshi Raj, Flora Hoodin, Lilian Yahng, Thomas Braun, Sung Won Choi. Originally published in JMIR Cancer (http://cancer.jmir.org), 09.03.2021. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Cancer, is properly cited. The complete bibliographic information, a link to the original publication on http://cancer.jmir.org/, as well as this copyright and license information must be included. |
spellingShingle | Original Paper Gupta, Vibhuti Raj, Minakshi Hoodin, Flora Yahng, Lilian Braun, Thomas Choi, Sung Won Electronic Health Record Portal Use by Family Caregivers of Patients Undergoing Hematopoietic Cell Transplantation: United States National Survey Study |
title | Electronic Health Record Portal Use by Family Caregivers of Patients Undergoing Hematopoietic Cell Transplantation: United States National Survey Study |
title_full | Electronic Health Record Portal Use by Family Caregivers of Patients Undergoing Hematopoietic Cell Transplantation: United States National Survey Study |
title_fullStr | Electronic Health Record Portal Use by Family Caregivers of Patients Undergoing Hematopoietic Cell Transplantation: United States National Survey Study |
title_full_unstemmed | Electronic Health Record Portal Use by Family Caregivers of Patients Undergoing Hematopoietic Cell Transplantation: United States National Survey Study |
title_short | Electronic Health Record Portal Use by Family Caregivers of Patients Undergoing Hematopoietic Cell Transplantation: United States National Survey Study |
title_sort | electronic health record portal use by family caregivers of patients undergoing hematopoietic cell transplantation: united states national survey study |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8086639/ https://www.ncbi.nlm.nih.gov/pubmed/33687332 http://dx.doi.org/10.2196/26509 |
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