Evidence map›Paper›PMID 41225579›Full record

ArticleOrphanet journal of rare diseases2025

Pain assessment and treatment in patients with mucopolysaccharidoses: a French multicentric pediatric study.

Mélanie Blin, Marine Tardieu, Didier Lacombe, Magali Gorce, Léna Damaj, Magalie Barth, Delphine Genevaz, Sophie Vibet, François Labarthe

Abstract readMulticenter Study
In one paragraph

Article in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Mélanie BlinCentre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France.
Marine TardieuCentre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France.
Didier LacombeInserm U1211, Université de Bordeaux, Centre de Compétences Maladies Héréditaires du Métabolisme, CHU de Bordeaux, Bordeaux, France.
Magali GorceCentre de Référence Maladies Héréditaires du Métabolisme, CHU Toulouse, Toulouse, France.
Léna DamajCentre de Compétences Maladies Héréditaires du Métabolisme, CHU Rennes, Rennes, France.
Magalie BarthCentre de Compétences Maladies Héréditaires du Métabolisme, CHU Angers, Angers, France.
Delphine GenevazVaincre les Maladies Lysosomales (VML), Massy, France.
Sophie VibetCentre d'Évaluation et de Traitement de la Douleur, CHRU Tours, Tours, France.
François LabartheCentre de Référence Maladies Héréditaires du Métabolisme ToTeM, CHRU Tours, Tours, France. labarthe@univ-tours.fr.ORCID 0000-0001-9788-9667

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMucopolysaccharidoses (MPS) are a group of rare genetic lysosomal storage disorders with a wide spectrum of clinical severities. Chronic pain is frequent but difficult to assess. The aim of this study was to evaluate the detection and management of pain in pediatric MPS patients.

methodsPain-related data were retrospectively collected from the medical records of pediatric MPS patients from five French centers for inborn metabolic disorders. A national online survey was also conducted about the feelings of patients and/or their families and of healthcare professionals about the detection and management of pain in pediatric MPS patients.

resultsThe medical records of 48 patients with all subtypes of MPS were analyzed. Pain was frequent and recurrent in MPS patients (pain was reported in 94% of the patients), but it was undoubtedly difficult to assess. We observed important differences between (1) medical records demonstrating frequent assessment and treatment of pain, (2) feelings of patients or their families (53 questionnaires) reporting frequent pain, and (3) feelings of healthcare professionals (21 questionnaires) who were quite satisfied with their own practices, suggesting that the majority of patients were unpainful. We recommend a more systematic evaluation of pain, particularly for outpatients, with the use of adapted tools, notably in children with disabilities, and with a multidimensional approach to pain assessment and management. Caregiver training is also needed, and close collaboration with pain centers is encouraged.

conclusionA routine pain assessment protocol for MPS patients is required that covers the entire spectrum of pain and can be adapted for every type of patient, including those with neurocognitive and motor impairments.

Indexed as

MucopolysaccharidosesPainPain MeasurementAdolescentChildChild, PreschoolFemaleFranceHumansInfantMalePain ManagementRetrospective StudiesSurveys and QuestionnairesChildrenChronic painLysosomal storage diseasePractice assessment

Identifiers

PMID41225579
PMCPMC12613516

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.