Evidence map›Paper›PMID 40847294›Full record

ArticleBMC public health2025

Understanding the experience of prescription charges in people living with parkinson's disease: a focus group study.

Megan Rose Readman, Ayomide Oluseye, Lisa Jane Brighton, Megan Polden, Ian Fairman, Ian Parkinson, Caroline Parkinson, Clarissa Giebel

Abstract read
In one paragraph

Article in BMC public health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Megan Rose ReadmanDepartment of Primary Care and Mental Health, The University of Liverpool, Liverpool, UK. m.readman@liverpool.ac.uk.
Ayomide OluseyeFaculty of Wellbeing, Education and Language Studies, The Open University, Milton Keynes, UK.
Lisa Jane BrightonCicely Saunders Institute of Palliative Care, Policy and Rehabilitation, King's College London, London, UK.
Megan PoldenDepartment of Primary Care and Mental Health, The University of Liverpool, Liverpool, UK.
Ian FairmanNIHR Applied Research Collaboration North West Coast, Liverpool, UK.
Ian ParkinsonNIHR Applied Research Collaboration North West Coast, Liverpool, UK.
Caroline ParkinsonNIHR Applied Research Collaboration North West Coast, Liverpool, UK.
Clarissa GiebelDepartment of Primary Care and Mental Health, The University of Liverpool, Liverpool, UK.

Funding

Economic and Social Research Council ES/X005259/1Economic and Social Research Council ES/X007375/1Economic Social Research Council ES/X004082/1
6 · The paper itself

Abstract

backgroundIn England, people aged > 60 are typically required to pay for their prescriptions. Whilst exemption criteria enable people living with specified long-term health conditions to receive free prescriptions, Parkinson's disease is omitted from this list. People with Parkinson's are often reliant upon medications, and evidence suggests that medical fees can reduce quality of life and medicine adherence. We, therefore, aimed to explore the impact of prescription charges on people with Parkinson's and their family care partners (caregivers).

methodsThis is a qualitative focus group study with people with Parkinson's and caregivers. Focus groups were semi-structured and conducted online. Participants were recruited through opportunity sampling. Eligible participants were adults aged 18 and over living in England who either (1) had a diagnosis of Idiopathic Parkinson's Disease or (2) provided unpaid care for someone with Parkinson's, including parents, adult children, siblings, or close friends. Data was analysed using reflexive thematic analysis within a critical realist paradigm.

resultsFive focus groups were conducted with people with Parkinson's (n = 12) and caregivers (n = 12). All focus groups comprised both people with Parkinson's and caregivers. Thematic analysis identified three overarching themes: (1) The financial toll of medication and its ripple effects; (2) Lack of inclusion and support; and (3) Difficulties of seeking support. People affected by Parkinson's disagreed with current policy and suggestions of per-prescription charge re-evaluation were expressed.

conclusionsPrescription charges have multifaceted negative impacts on people affected by Parkinson's. Current prescription charge policies, including their exemption criteria, should be reviewed, alongside initiatives to raise awareness of existing financial support systems, such as pre-payment certificates. REGISTRATION: Study protocol and analysis strategy are pre-registered on Open Science Framework ( https://osf.io/y8ve5/ ).

Indexed as

CaregiversParkinson DiseasePrescription FeesAdultAgedAged, 80 and overEnglandFemaleFocus GroupsHumansMaleMiddle AgedQualitative ResearchParkinson’s diseasePrescription charge policyPrescriptionsPublic health

Identifiers

PMID40847294
PMCPMC12372227

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.