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The perspective of Polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study)

INTRODUCTION: A widely accepted treat-to-target strategy for rheumatoid arthritis (RA) requires the patient’s perspective in making treatment decisions. However, data on treatment preferences and expectations of Polish patients with RA are scarce. The aim of the study was to determine the satisfacti...

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Autores principales: Stajszczyk, Marcin, Świerkowska, Grażyna, Smolik, Katarzyna, Domysławska, Izabela, Charkiewicz, Karol, Samborski, Włodzimierz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634413/
https://www.ncbi.nlm.nih.gov/pubmed/37970121
http://dx.doi.org/10.5114/reum/171625
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author Stajszczyk, Marcin
Świerkowska, Grażyna
Smolik, Katarzyna
Domysławska, Izabela
Charkiewicz, Karol
Samborski, Włodzimierz
author_facet Stajszczyk, Marcin
Świerkowska, Grażyna
Smolik, Katarzyna
Domysławska, Izabela
Charkiewicz, Karol
Samborski, Włodzimierz
author_sort Stajszczyk, Marcin
collection PubMed
description INTRODUCTION: A widely accepted treat-to-target strategy for rheumatoid arthritis (RA) requires the patient’s perspective in making treatment decisions. However, data on treatment preferences and expectations of Polish patients with RA are scarce. The aim of the study was to determine the satisfaction with treatment and the nature of therapeutic preferences and expectations of Polish patients with moderate to severe RA. MATERIAL AND METHODS: Fifty-two adult Polish patients with moderately to highly active RA were asked to complete patient-reported outcomes and patient-provided information questionnaires. Additionally, patient sociodemographic and clinical data and information on patient current and planned treatment strategies were collected. RESULTS: The mean global assessment of patient satisfaction with treatment was 64.1 ±24.6, below the level of indicating satisfaction. Rheumatoid arthritis negatively impacted patients’ lives, resulting in a 37.8% impairment of work efficiency and 45% impairment of total activity. Primary treatment expectations for patients were lasting relief of RA symptoms, reduced pain and swelling in joints, increased flexibility of joints, and general improvement of arthritis. The most acceptable potential side effect was weight gain and the least acceptable were increases in the risk of cardiovascular disease, infection, and malignancies. The rapid onset of the drug effect (up to 1 week) was a preference of 48.1% of patients. Access to internet health resources was important for 44.2% of patients, but the median total eHealth literacy score in the study population was 24.0 (interquartile range: 20.5–28.0, range 8–37), which means low digital health literacy (DHL). CONCLUSIONS: Understanding these treatment preferences and expectations of patients with RA is essential for clinical practitioners to facilitate shared treatment decision-making. Digital health literacy data suggest the need of further improvement.
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spelling pubmed-106344132023-11-15 The perspective of Polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study) Stajszczyk, Marcin Świerkowska, Grażyna Smolik, Katarzyna Domysławska, Izabela Charkiewicz, Karol Samborski, Włodzimierz Reumatologia Original Paper INTRODUCTION: A widely accepted treat-to-target strategy for rheumatoid arthritis (RA) requires the patient’s perspective in making treatment decisions. However, data on treatment preferences and expectations of Polish patients with RA are scarce. The aim of the study was to determine the satisfaction with treatment and the nature of therapeutic preferences and expectations of Polish patients with moderate to severe RA. MATERIAL AND METHODS: Fifty-two adult Polish patients with moderately to highly active RA were asked to complete patient-reported outcomes and patient-provided information questionnaires. Additionally, patient sociodemographic and clinical data and information on patient current and planned treatment strategies were collected. RESULTS: The mean global assessment of patient satisfaction with treatment was 64.1 ±24.6, below the level of indicating satisfaction. Rheumatoid arthritis negatively impacted patients’ lives, resulting in a 37.8% impairment of work efficiency and 45% impairment of total activity. Primary treatment expectations for patients were lasting relief of RA symptoms, reduced pain and swelling in joints, increased flexibility of joints, and general improvement of arthritis. The most acceptable potential side effect was weight gain and the least acceptable were increases in the risk of cardiovascular disease, infection, and malignancies. The rapid onset of the drug effect (up to 1 week) was a preference of 48.1% of patients. Access to internet health resources was important for 44.2% of patients, but the median total eHealth literacy score in the study population was 24.0 (interquartile range: 20.5–28.0, range 8–37), which means low digital health literacy (DHL). CONCLUSIONS: Understanding these treatment preferences and expectations of patients with RA is essential for clinical practitioners to facilitate shared treatment decision-making. Digital health literacy data suggest the need of further improvement. Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie 2023-10-06 2023 /pmc/articles/PMC10634413/ /pubmed/37970121 http://dx.doi.org/10.5114/reum/171625 Text en Copyright: © 2023 Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji w Warszawie https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Stajszczyk, Marcin
Świerkowska, Grażyna
Smolik, Katarzyna
Domysławska, Izabela
Charkiewicz, Karol
Samborski, Włodzimierz
The perspective of Polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study)
title The perspective of Polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study)
title_full The perspective of Polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study)
title_fullStr The perspective of Polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study)
title_full_unstemmed The perspective of Polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study)
title_short The perspective of Polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the SENSE study)
title_sort perspective of polish patients with rheumatoid arthritis – treatment expectations, patient-reported outcomes, and digital literacy (the sense study)
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10634413/
https://www.ncbi.nlm.nih.gov/pubmed/37970121
http://dx.doi.org/10.5114/reum/171625
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