Evidence map›Paper›PMID 38818282›Full record

ArticleWorld journal of hepatology2024

Characteristics of patients with Wilson disease in the United States: An insurance claims database study.

Thomas Daniel-Robin, Pradeep Kumar, Bernard Benichou, Jean-Philippe Combal

Abstract read
In one paragraph

Article in World journal of hepatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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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

2 citing papers in PubMed.

  1. Article
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4 · The record

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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

4 authors.

Thomas Daniel-RobinVivet Therapeutics, Paris 75008, France.
Pradeep KumarClarivate, Noida 201301, Uttar Pradesh, India.
Bernard BenichouVivet Therapeutics, Paris 75008, France.
Jean-Philippe CombalVivet Therapeutics, Paris 75008, France. jpcombal@vivet-therapeutics.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWilson disease (WD) is a progressive, potentially fatal degenerative disease affecting the liver and central nervous system. Given its low prevalence, collecting data on large cohorts of patients with WD is challenging. Comprehensive insurance claims databases provide powerful tools to collect retrospective data on large numbers of patients with rare diseases.

aimTo describe patients with WD in the United States, their treatment and clinical outcome, using a large insurance claims database.

methodsThis retrospective, longitudinal study was performed in the Clarivate Real-World Data Product database

resultsOverall, 5376 patients with an ICD-10 diagnostic code for WD were identified. The mean age at inclusion was 41.2 years and 52.0% were men. A specific WD treatment was documented for 885 patients (15.1%), although the number of patients taking zinc salts may be underestimated due to over the counter purchase. At inclusion, the mean age of patients with a documented treatment was 36.6 ± 17.8 years

conclusionPatients treated for WD in the United States had an excess early mortality compared with the American population. These findings indicate that there is a significant unmet need for effective treatment for WD in the United States.

Indexed as

Copper chelatorsMortalityTreatmentUnited StatesWilson diseaseZinc acetate

Identifiers

PMID38818282
PMCPMC11135267

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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.