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The impact of the COVID-19 pandemic on health-related quality of life of cancer patients in British Columbia Izadi-Najafabadi, Sara; McTaggart-Cowan, Helen; Halperin, Ross; Lambert, Leah Kimberley; Mitton, Craig, 1972-; Peacock, Stuart
Abstract
Background: The COVID-19 pandemic resulted in unprecedented changes to cancer care in many countries, impacting cancer patients’ lives in numerous ways. This study examines the impact of changes in cancer care on patient’s health-related quality of life (HRQL), which is a key outcome in cancer care. The study aims to estimate patients’ self-reported HRQL before and during the pandemic and identify predictive factors for their physical and mental wellbeing. Method: The study employed the large-scale Outpatient Cancer Care (OCC) Patient Experience Survey, including the Veterans RAND 12-Item Health Survey, to evaluate cancer patients’ experiences and HRQL before (January to May 2020) and during the COVID-19 pandemic (May to July 2021). Paired t-tests were conducted to compare differences in Physical Component Scores (PCS) and Mental Component Scores (MCS) before and during the pandemic. Multivariable linear regressions were employed to investigate the factors (sociodemographic, clinical, and patient reported experience) influencing PCS and MCS during the pandemic. Results: PCS decreased significantly during the pandemic, while MCS remained stable. Lower PCS contributors included older age, more telehealth visits, self-reported hospitalization, and a longer time since the last cancer diagnosis. Higher PCS was associated with urban residence, higher MCS during the pandemic, and perceived active Healthcare Provider (HCP) involvement. For MCS, lower scores related to female gender and more telehealth visits, while higher scores were associated with being white, higher education, high MCS before the pandemic, and perceived active HCP involvement. Conclusion: The OCC Patient Experience Survey provides a unique patient level data set measuring HRQL pre- and post- the onset of the COVID-19 pandemic. The study highlights challenges faced by cancer patients during the pandemic, with a significant reduction in PCS. However, the stability in MCS suggests effective coping mechanisms. Sociodemographic, clinical, and telehealth-related variables play a complex role in shaping both PCS and MCS. Perceived HCP involvement emerges as a crucial factor correlating with higher PCS and MCS. Navigating the post-pandemic era necessitates interventions fortifying patient-provider relationships, optimizing healthcare support systems, such as telehealth services, and prioritizing mental-well-being given its impact on both PCS and MCS.
Item Metadata
Title |
The impact of the COVID-19 pandemic on health-related quality of life of cancer patients in British Columbia
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Creator | |
Contributor | |
Publisher |
Springer International Publishing
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Date Issued |
2024-08-23
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Description |
Background: The COVID-19 pandemic resulted in unprecedented changes to cancer care in many countries,
impacting cancer patients’ lives in numerous ways. This study examines the impact of changes in cancer care on
patient’s health-related quality of life (HRQL), which is a key outcome in cancer care. The study aims to estimate
patients’ self-reported HRQL before and during the pandemic and identify predictive factors for their physical and
mental wellbeing.
Method: The study employed the large-scale Outpatient Cancer Care (OCC) Patient Experience Survey, including
the Veterans RAND 12-Item Health Survey, to evaluate cancer patients’ experiences and HRQL before (January to May
2020) and during the COVID-19 pandemic (May to July 2021). Paired t-tests were conducted to compare differences
in Physical Component Scores (PCS) and Mental Component Scores (MCS) before and during the pandemic.
Multivariable linear regressions were employed to investigate the factors (sociodemographic, clinical, and patient reported experience) influencing PCS and MCS during the pandemic.
Results: PCS decreased significantly during the pandemic, while MCS remained stable. Lower PCS contributors
included older age, more telehealth visits, self-reported hospitalization, and a longer time since the last cancer
diagnosis. Higher PCS was associated with urban residence, higher MCS during the pandemic, and perceived active
Healthcare Provider (HCP) involvement. For MCS, lower scores related to female gender and more telehealth visits,
while higher scores were associated with being white, higher education, high MCS before the pandemic, and
perceived active HCP involvement.
Conclusion: The OCC Patient Experience Survey provides a unique patient level data set measuring HRQL pre- and
post- the onset of the COVID-19 pandemic. The study highlights challenges faced by cancer patients during the
pandemic, with a significant reduction in PCS. However, the stability in MCS suggests effective coping mechanisms.
Sociodemographic, clinical, and telehealth-related variables play a complex role in shaping both PCS and MCS.
Perceived HCP involvement emerges as a crucial factor correlating with higher PCS and MCS. Navigating the post-pandemic era necessitates interventions fortifying patient-provider relationships, optimizing healthcare support
systems, such as telehealth services, and prioritizing mental-well-being given its impact on both PCS and MCS.
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Subject | |
Genre | |
Type | |
Language |
eng
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Date Available |
2024-10-25
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Provider |
Vancouver : University of British Columbia Library
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Rights |
Attribution 4.0 International (CC BY 4.0)
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DOI |
10.14288/1.0447134
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URI | |
Affiliation | |
Citation |
Journal of Patient-Reported Outcomes. 2024 Aug 23;8(1):100
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Publisher DOI |
10.1186/s41687-024-00759-z
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Peer Review Status |
Reviewed
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Scholarly Level |
Faculty; Researcher
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Copyright Holder |
The Author(s)
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Rights URI | |
Aggregated Source Repository |
DSpace
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Item Media
Item Citations and Data
Rights
Attribution 4.0 International (CC BY 4.0)