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Subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers

App-based technologies could enhance patient and caregiver communication and provide alerts that potentially reducing readmissions. However, the burden of App alerts needs to be optimized to reduce provider burnout. AIM: The purpose of this study was to determine subjective and objective burden of u...

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Autores principales: Shaw, Jawaid, Acharya, Chathur, Albhaisi, Somaya, Fagan, Andrew, McGeorge, Sara, White, Melanie B., Lachar, Jatinder, Olson, Jessica, Olofson, Amy, Bergstrom, Lori, Kamath, Patrick S., Bajaj, Jasmohan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988316/
https://www.ncbi.nlm.nih.gov/pubmed/36706194
http://dx.doi.org/10.1097/HC9.0000000000000030
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author Shaw, Jawaid
Acharya, Chathur
Albhaisi, Somaya
Fagan, Andrew
McGeorge, Sara
White, Melanie B.
Lachar, Jatinder
Olson, Jessica
Olofson, Amy
Bergstrom, Lori
Kamath, Patrick S.
Bajaj, Jasmohan S.
author_facet Shaw, Jawaid
Acharya, Chathur
Albhaisi, Somaya
Fagan, Andrew
McGeorge, Sara
White, Melanie B.
Lachar, Jatinder
Olson, Jessica
Olofson, Amy
Bergstrom, Lori
Kamath, Patrick S.
Bajaj, Jasmohan S.
author_sort Shaw, Jawaid
collection PubMed
description App-based technologies could enhance patient and caregiver communication and provide alerts that potentially reducing readmissions. However, the burden of App alerts needs to be optimized to reduce provider burnout. AIM: The purpose of this study was to determine subjective and objective burden of using the Patient Buddy App, a health information technology (HIT) on providers in a randomized multicenter trial, who completed a semi-quantitative Likert scale survey regarding training procedures, data and privacy concerns, follow-up details, and technical support. This randomized multicenter trial recruits cirrhosis inpatients and their caregivers, and randomizes them into standard-of-care, HIT (communication only via App) and HIT+visits (App+phone calls/visits) for 30 days after discharge. The alerts are monitored by providers through a central iPad. The reason(s) and number of alerts were recorded as the objective burden. A total of 1442 messages were sent as alerts from the 103 dyads (patient + caregiver) (n=206) randomized to HIT arms. The most common messages related to Hepatic Encephalopathy (HE) (high or low bowel movement=50% or orientation tests=37%). Twelve providers completed the surveys reflecting the following themes—92% and 100%, felt adequately trained and confident about educating the patients and caregivers before roll out of App and had no concerns related to data and privacy; 70%, felt that appropriate time was spent on pursuing reason for data not being logged; 60% each, had issues with availability of adequate technical support and connectivity. CONCLUSION: The Patient Buddy App randomized multicenter trial till date shows an overall favorable rating regarding training procedures/education, privacy concerns, and ease of message follow-up, from providers. However, it is important to gauge and address subjective and objective burdens of monitoring human resources in current and future HIT studies to avoid burnout and to ensure successful study completion.
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spelling pubmed-99883162023-03-16 Subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers Shaw, Jawaid Acharya, Chathur Albhaisi, Somaya Fagan, Andrew McGeorge, Sara White, Melanie B. Lachar, Jatinder Olson, Jessica Olofson, Amy Bergstrom, Lori Kamath, Patrick S. Bajaj, Jasmohan S. Hepatol Commun Original Articles App-based technologies could enhance patient and caregiver communication and provide alerts that potentially reducing readmissions. However, the burden of App alerts needs to be optimized to reduce provider burnout. AIM: The purpose of this study was to determine subjective and objective burden of using the Patient Buddy App, a health information technology (HIT) on providers in a randomized multicenter trial, who completed a semi-quantitative Likert scale survey regarding training procedures, data and privacy concerns, follow-up details, and technical support. This randomized multicenter trial recruits cirrhosis inpatients and their caregivers, and randomizes them into standard-of-care, HIT (communication only via App) and HIT+visits (App+phone calls/visits) for 30 days after discharge. The alerts are monitored by providers through a central iPad. The reason(s) and number of alerts were recorded as the objective burden. A total of 1442 messages were sent as alerts from the 103 dyads (patient + caregiver) (n=206) randomized to HIT arms. The most common messages related to Hepatic Encephalopathy (HE) (high or low bowel movement=50% or orientation tests=37%). Twelve providers completed the surveys reflecting the following themes—92% and 100%, felt adequately trained and confident about educating the patients and caregivers before roll out of App and had no concerns related to data and privacy; 70%, felt that appropriate time was spent on pursuing reason for data not being logged; 60% each, had issues with availability of adequate technical support and connectivity. CONCLUSION: The Patient Buddy App randomized multicenter trial till date shows an overall favorable rating regarding training procedures/education, privacy concerns, and ease of message follow-up, from providers. However, it is important to gauge and address subjective and objective burdens of monitoring human resources in current and future HIT studies to avoid burnout and to ensure successful study completion. Lippincott Williams & Wilkins 2023-01-27 /pmc/articles/PMC9988316/ /pubmed/36706194 http://dx.doi.org/10.1097/HC9.0000000000000030 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Association for the Study of Liver Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Articles
Shaw, Jawaid
Acharya, Chathur
Albhaisi, Somaya
Fagan, Andrew
McGeorge, Sara
White, Melanie B.
Lachar, Jatinder
Olson, Jessica
Olofson, Amy
Bergstrom, Lori
Kamath, Patrick S.
Bajaj, Jasmohan S.
Subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers
title Subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers
title_full Subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers
title_fullStr Subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers
title_full_unstemmed Subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers
title_short Subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers
title_sort subjective and objective burden on providers from a multicenter app-based study of patients with cirrhosis and caregivers
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988316/
https://www.ncbi.nlm.nih.gov/pubmed/36706194
http://dx.doi.org/10.1097/HC9.0000000000000030
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