Evidence map›Paper›PMID 41592027›Full record

ArticlePloS one2026

The socioeconomic impact of inherited retinal dystrophies (IRDs) in Belgium: A cost-of-illness study.

Ine Vandersmissen, Janice Geers, Tom Denee, Salla Oinasmaa, Dagmar Hoeben, Xinyi Zhang, Burcak Aydin, Simone Cheung, Lorenzo Billiet, Inge Joniau and 3 more

Abstract read
In one paragraph

Article in PloS one, 2026. 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

13 authors.

Ine VandersmissenJohnson & Johnson, Beerse, Belgium.ORCID https://orcid.org/0009-0003-6741-5104
Janice GeersJohnson & Johnson, Beerse, Belgium.
Tom DeneeJohnson & Johnson, Breda, The Netherlands.
Salla OinasmaaJohnson & Johnson, Espoo, Finland.
Dagmar HoebenJohnson & Johnson, Beerse, Belgium.
Xinyi ZhangHealth Economics and Outcomes Research, Monitor Deloitte, Brussels, Belgium.
Burcak AydinHealth Economics and Outcomes Research, Monitor Deloitte, Brussels, Belgium.
Simone CheungHealth Economics and Social Policy, Deloitte Access Economics, Melbourne, Victoria, Australia.
Lorenzo BillietLicht en Liefde, Varsenare, Belgium.ORCID https://orcid.org/0000-0001-8389-9311
Inge JoniauDepartment of Ophthalmology, Ghent University Hospital, Ghent, Belgium.
Avril DalyRetina International, Dublin, Ireland.
Steven SimoensDepartment of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium.
Bart P LeroyDepartment of Ophthalmology, Ghent University Hospital, Ghent, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionInherited retinal diseases (IRDs) are a diverse group of vision-threatening conditions caused by genetic mutations, affecting over 5.5 million people globally. These diseases have profound impact on patients, families and society. However, there is a lack of comprehensive data on their prevalence, economic burden, and societal costs. This information gap hinders effective decision-making, and the allocation of resources needed for research, treatment, and patient support, ultimately compromising care and outcomes.

objectiveTo quantify the societal burden of IRDs in Belgium in 2023.

methodsThis cost-of-illness study estimated the total costs of the 11 most prevalent IRDs in Belgium. A survey of Belgian IRD patients collected primary data on disease burden, health resource utilization, productivity, and care-related expenses. Additionally, data on prevalence and health system costs were based on a literature review from PubMed and the Cochrane Library.

resultsPatients reported a substantial impact on daily activities (96%), mental health (81%), and 78% reported having received genetic testing. IRDs impose a significant economic burden in Belgium, with an average annual cost of €37,228 per patient and a total cumulative burden of €129.4 million. Indirect non-healthcare costs represented the largest proportion (84%), followed by direct healthcare costs (12%), mainly from rehabilitation, and direct non-healthcare costs (4%). Indirect costs included significant productivity losses of €77.7 million and an informal care burden of €31.3 million. Government support programmes accounted for €4.9 million annually.

conclusionThis study highlights the substantial clinical and economic burden of IRDs on Belgian society. Therefore, it is important to continue investing in research and development, as well as to consider the substantial societal impact of these conditions in decision-making and shaping policy changes for Belgium. Future investments informed by these findings can contribute to decreasing the burden on society and enhance the well-being, inclusion and productivity of patients and caregivers.

Indexed as

Cost of IllnessRetinal DystrophiesAdultAgedBelgiumFemaleHealth Care CostsHumansMaleMiddle AgedPrevalenceSocioeconomic Factors

Identifiers

PMID41592027
PMCPMC12843553

What OpenQuestion holds

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LicenceCC BY
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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.