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Development and validation of the Patient Experience with Treatment and Self-management (PETS): a patient-reported measure of treatment burden.

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Title: Development and validation of the Patient Experience with Treatment and Self-management (PETS): a patient-reported measure of treatment burden.
Authors: Eton, David, Yost, Kathleen, Lai, Jin-shei, Ridgeway, Jennifer, Egginton, Jason, Rosedahl, Jordan, Linzer, Mark, Boehm, Deborah, Thakur, Azra, Poplau, Sara, Odell, Laura, Montori, Victor, May, Carl, Anderson, Roger, Eton, David T (AUTHOR), Yost, Kathleen J (AUTHOR), Ridgeway, Jennifer L (AUTHOR), Egginton, Jason S (AUTHOR), Rosedahl, Jordan K (AUTHOR), Boehm, Deborah H (AUTHOR)
Source: Quality of Life Research. Feb2017, Vol. 26 Issue 2, p489-503. 15p.
Subjects: Treatment effectiveness, Medical records, Medical informatics, Customer satisfaction, Mental health, Quality of life, Health self-care
Abstract: Purpose: The purpose of this study was to develop and validate a new comprehensive patient-reported measure of treatment burden-the Patient Experience with Treatment and Self-management (PETS).Methods: A conceptual framework was used to derive the PETS with items reviewed and cognitively tested with patients. A survey battery, including a pilot version of the PETS, was mailed to 838 multi-morbid patients from two healthcare institutions for validation.Results: A total of 332 multi-morbid patients returned completed surveys. Diagnostics supported deletion and consolidation of some items and domains. Confirmatory factor analysis supported a domain model for scaling comprised of 9 factors: medical information, medications, medical appointments, monitoring health, interpersonal challenges, medical/healthcare expenses, difficulty with healthcare services, role/social activity limitations, and physical/mental exhaustion. Scales showed good internal consistency (α range 0.79-0.95). Higher PETS scores, indicative of greater treatment burden, were correlated with more distress, less satisfaction with medications, lower self-efficacy, worse physical and mental health, and lower convenience of healthcare (Ps < 0.001). Patients with lower health literacy, less adherence to medications, and more financial difficulties reported higher PETS scores (Ps < 0.01).Conclusion: A comprehensive patient-reported measure of treatment burden can help to better characterize the impact of treatment and self-management burden on patient well-being and guide care toward minimally disruptive medicine. [ABSTRACT FROM AUTHOR]
Copyright of Quality of Life Research is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: Development and validation of the Patient Experience with Treatment and Self-management (PETS): a patient-reported measure of treatment burden.
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  Data: &lt;searchLink fieldCode=&quot;JN&quot; term=&quot;%22Quality+of+Life+Research%22&quot;&gt;Quality of Life Research&lt;/searchLink&gt;. Feb2017, Vol. 26 Issue 2, p489-503. 15p.
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  Data: &lt;bold&gt;Purpose: &lt;/bold&gt;The purpose of this study was to develop and validate a new comprehensive patient-reported measure of treatment burden-the Patient Experience with Treatment and Self-management (PETS).&lt;bold&gt;Methods: &lt;/bold&gt;A conceptual framework was used to derive the PETS with items reviewed and cognitively tested with patients. A survey battery, including a pilot version of the PETS, was mailed to 838 multi-morbid patients from two healthcare institutions for validation.&lt;bold&gt;Results: &lt;/bold&gt;A total of 332 multi-morbid patients returned completed surveys. Diagnostics supported deletion and consolidation of some items and domains. Confirmatory factor analysis supported a domain model for scaling comprised of 9 factors: medical information, medications, medical appointments, monitoring health, interpersonal challenges, medical/healthcare expenses, difficulty with healthcare services, role/social activity limitations, and physical/mental exhaustion. Scales showed good internal consistency (α range 0.79-0.95). Higher PETS scores, indicative of greater treatment burden, were correlated with more distress, less satisfaction with medications, lower self-efficacy, worse physical and mental health, and lower convenience of healthcare (Ps&#160;&lt;&#160;0.001). Patients with lower health literacy, less adherence to medications, and more financial difficulties reported higher PETS scores (Ps&#160;&lt;&#160;0.01).&lt;bold&gt;Conclusion: &lt;/bold&gt;A comprehensive patient-reported measure of treatment burden can help to better characterize the impact of treatment and self-management burden on patient well-being and guide care toward minimally disruptive medicine. [ABSTRACT FROM AUTHOR]
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  Data: &lt;i&gt;Copyright of Quality of Life Research is the property of Springer Nature and its content may not be copied or emailed to multiple sites without the copyright holder&#39;s express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.&lt;/i&gt; (Copyright applies to all Abstracts.)
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