Health-related quality of life, self-reported impairments and activities of daily living in relation to muscle function in post-polio syndrome
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Published:2020-07-16
Issue:1
Volume:4
Page:
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ISSN:2509-8020
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Container-title:Journal of Patient-Reported Outcomes
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language:en
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Short-container-title:J Patient Rep Outcomes
Author:
Gocheva VanyaORCID, Hafner Patricia, Orsini Anna-Lena, Schmidt Simone, Schaedelin Sabine, Rueedi Nicole, Rubino-Nacht Daniela, Weber Peter, Fischer Dirk
Abstract
Abstract
Background
The symptoms of post-polio syndrome (PPS) and its resulting disabilities can affect quality of life and the ability to perform daily activities. No study has comprehensively analysed how various patient-reported outcome measures (PROMs) are associated with objectively assessed physical function in patients with PPS.
Aim
To investigate health-related quality of life (HRQOL), self-reported impairments and activities of daily living during 6 months and evaluate their association with clinical muscle function outcomes in individuals with PPS.
Methods
Twenty-seven patients with PPS were included in the study. At baseline and 6 months, patients were administered PROMs measuring HRQOL (WHOQOL-BREF), self-reported impairments related to PPS (SIPP-RS) and activities of daily living (IBM-FRS). Clinical muscle function outcomes included 6 min walking distance (6MWD) and motor function measure (MFM).
Results
There were no changes in self-reported impairments (25.52 to 24.93, p = 0.40), activities of daily living (33.89 to 33.30, p = 0.20), 6MWD (391.52 to 401.85, p = 0.30) and MFM (83.87 to 85.46, p = 0.14) during 6 months, while the HRQOL psychological health decreased during this period (76.85 to 72.38, p = 0.05). A strong association was found between activities of daily living and clinical muscle function outcomes (6MWD: ß = 0.02, 95% CI: 0.02;0.03, t = 6.88, p < 0.01; MFM: ß = 0.25, 95% CI: 0.17;0.33, t = 6.69, p < 0.01). Self-reported impairments and HRQOL domains were not associated with the clinical muscle outcomes.
Conclusions
Study findings indicate that objectively measured walking and motor abilities do not reflect patient’s perspectives of their HRQOL and impairment due to PPS. More research is needed to assess changes over time and capture clinically meaningful changes in individuals with PPS and to increase the understanding of how the patient’s perspective of disability measured by PROMs is related to objectively measured walking and motor abilities.
Trial registration
ClinicalTrials.gov Identifier (NCT02801071) registered June 15, 2016.
Funder
the Lorenzo-Piaggio Foundation
Publisher
Springer Science and Business Media LLC
Subject
Health Information Management,Health Informatics
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