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Factors in Patient Empowerment: A Survey of an Online Patient Research Network

BACKGROUND: Providers and healthcare organizations have begun recognizing the importance of patient empowerment as a driver of patient-centered care. Unfortunately, most studies have investigated empowerment with single diseases. Identifying factors of empowerment across conditions and populations w...

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Autores principales: Chiauzzi, Emil, DasMahapatra, Pronabesh, Cochin, Elisenda, Bunce, Mikele, Khoury, Raya, Dave, Purav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107186/
https://www.ncbi.nlm.nih.gov/pubmed/27155887
http://dx.doi.org/10.1007/s40271-016-0171-2
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author Chiauzzi, Emil
DasMahapatra, Pronabesh
Cochin, Elisenda
Bunce, Mikele
Khoury, Raya
Dave, Purav
author_facet Chiauzzi, Emil
DasMahapatra, Pronabesh
Cochin, Elisenda
Bunce, Mikele
Khoury, Raya
Dave, Purav
author_sort Chiauzzi, Emil
collection PubMed
description BACKGROUND: Providers and healthcare organizations have begun recognizing the importance of patient empowerment as a driver of patient-centered care. Unfortunately, most studies have investigated empowerment with single diseases. Identifying factors of empowerment across conditions and populations would enable a greater understanding of this construct. OBJECTIVE: The purpose of this study was to understand empowerment in relation to health information-seeking, interactions with providers and peers, and healthcare access in chronic disease patients. This study also sought to identify key empowerment factors and their association with patient characteristics. METHODS: Participants were recruited through PatientsLikeMe, an online research platform where patients share their personal and medical history data. Patients completed an online survey that assessed self-reported health behavior (e.g. knowledge-seeking, experiences with healthcare providers, and peer interactions) and healthcare access. An exploratory factor analysis identified key empowerment domains. Domain level sum scores and sum of all domains (total score) were compared across patient characteristics and diseases. RESULTS: Overall, 3988 participants were included in the study, with the majority actively involved in their healthcare, but many cited difficulties with matching their treatment goals with those of their physician (34 %) and spending sufficient time with the physician (36 %). Factor analysis identified two domains—Positive Patient–Provider Interaction, and Knowledge and Personal Control—that explained >60 % of the overall variance in the observed variables. Mean total empowerment scores for patients with a primary complaint of Parkinson’s disease (61.8) and multiple sclerosis (60.3) were significantly greater than fibromyalgia (55.3) and chronic fatigue syndrome (54.8). Patients who were older, male, more educated, and insured also reported significantly greater levels of empowerment. CONCLUSIONS: The two domains of empowerment identified in this study are consistent with previous studies, but the differences in empowerment levels across diseases suggest a need for further studies on disease-related attributes of empowerment. Future research should examine the pathways for empowerment, as well as the relationship between empowerment domains and clinical outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40271-016-0171-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-51071862016-11-29 Factors in Patient Empowerment: A Survey of an Online Patient Research Network Chiauzzi, Emil DasMahapatra, Pronabesh Cochin, Elisenda Bunce, Mikele Khoury, Raya Dave, Purav Patient Original Research Article BACKGROUND: Providers and healthcare organizations have begun recognizing the importance of patient empowerment as a driver of patient-centered care. Unfortunately, most studies have investigated empowerment with single diseases. Identifying factors of empowerment across conditions and populations would enable a greater understanding of this construct. OBJECTIVE: The purpose of this study was to understand empowerment in relation to health information-seeking, interactions with providers and peers, and healthcare access in chronic disease patients. This study also sought to identify key empowerment factors and their association with patient characteristics. METHODS: Participants were recruited through PatientsLikeMe, an online research platform where patients share their personal and medical history data. Patients completed an online survey that assessed self-reported health behavior (e.g. knowledge-seeking, experiences with healthcare providers, and peer interactions) and healthcare access. An exploratory factor analysis identified key empowerment domains. Domain level sum scores and sum of all domains (total score) were compared across patient characteristics and diseases. RESULTS: Overall, 3988 participants were included in the study, with the majority actively involved in their healthcare, but many cited difficulties with matching their treatment goals with those of their physician (34 %) and spending sufficient time with the physician (36 %). Factor analysis identified two domains—Positive Patient–Provider Interaction, and Knowledge and Personal Control—that explained >60 % of the overall variance in the observed variables. Mean total empowerment scores for patients with a primary complaint of Parkinson’s disease (61.8) and multiple sclerosis (60.3) were significantly greater than fibromyalgia (55.3) and chronic fatigue syndrome (54.8). Patients who were older, male, more educated, and insured also reported significantly greater levels of empowerment. CONCLUSIONS: The two domains of empowerment identified in this study are consistent with previous studies, but the differences in empowerment levels across diseases suggest a need for further studies on disease-related attributes of empowerment. Future research should examine the pathways for empowerment, as well as the relationship between empowerment domains and clinical outcomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s40271-016-0171-2) contains supplementary material, which is available to authorized users. Springer International Publishing 2016-05-07 2016 /pmc/articles/PMC5107186/ /pubmed/27155887 http://dx.doi.org/10.1007/s40271-016-0171-2 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research Article
Chiauzzi, Emil
DasMahapatra, Pronabesh
Cochin, Elisenda
Bunce, Mikele
Khoury, Raya
Dave, Purav
Factors in Patient Empowerment: A Survey of an Online Patient Research Network
title Factors in Patient Empowerment: A Survey of an Online Patient Research Network
title_full Factors in Patient Empowerment: A Survey of an Online Patient Research Network
title_fullStr Factors in Patient Empowerment: A Survey of an Online Patient Research Network
title_full_unstemmed Factors in Patient Empowerment: A Survey of an Online Patient Research Network
title_short Factors in Patient Empowerment: A Survey of an Online Patient Research Network
title_sort factors in patient empowerment: a survey of an online patient research network
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107186/
https://www.ncbi.nlm.nih.gov/pubmed/27155887
http://dx.doi.org/10.1007/s40271-016-0171-2
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