Toby Helliwell t.helliwell@keele.ac.uk
The availability of health information to patients with newly diagnosed polymyalgia rheumatica: results from the PMR Cohort study
Helliwell, Toby; Hider, Samantha; Mallen, Christian; Muller, Sara
Authors
Samantha Hider s.hider@keele.ac.uk
Christian Mallen c.d.mallen@keele.ac.uk
Sara Muller s.muller@keele.ac.uk
Abstract
Aim
To assess the provision of information to, and seeking of, information by patients newly diagnosed with polymyalgia rheumatica (PMR) in primary care.
Background
Polymyalgia rheumatica (PMR) is an inflammatory rheumatological condition of older people than can be treated with long-term oral glucocorticoids. Management usually requires the patient to understand the potential complications of treatment and the disease, as well as involvement in reducing treatment dose. This may be complex for patients to understand.
Method
Data are taken from the baseline phase of the PMR Cohort study, which recruited newly diagnosed patients with PMR from UK primary care. Participants provided information on their PMR symptoms, general health and sociodemographics. They also completed items regarding information provision by their doctor at diagnosis, its usefulness and their own search for information.
Findings
652 people responded to the baseline survey. 399 (62.7%) had received written information from their doctor. 237 (98%) found it useful. 265 (42.9%) would have liked more information and 311 (48.4%) sought out more information. Those who were not given information and did not seek it out tended to be older and have poorer internet access.
Information provided at diagnosis to patients with PMR is useful, but more than a third did not receive any. This is concerning when PMR requires self-management and vigilance for red flags. Doctors should make use of the resources already available to them to support patients and should specifically ensure that these are available to more elderly patients and those without internet access.
Citation
Helliwell, T., Hider, S., Mallen, C., & Muller, S. (2018). The availability of health information to patients with newly diagnosed polymyalgia rheumatica: results from the PMR Cohort study. Primary Health Care Research and Development, https://doi.org/10.1017/S1463423618000543
Acceptance Date | Jul 4, 2018 |
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Publication Date | Aug 8, 2018 |
Journal | Primary Health Care Research and Development |
Print ISSN | 1463-4236 |
Publisher | Cambridge University Press |
DOI | https://doi.org/10.1017/S1463423618000543 |
Keywords | polymyalgia rheumatica, survey, glucocorticoids, patient and public involvement, information |
Publisher URL | https://doi.org/10.1017/S1463423618000543 |
Files
20180806_Tshimologo PCHRD.docx
(30 Kb)
Document
Publisher Licence URL
https://creativecommons.org/licenses/by-nc/4.0/
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