Evidence map›Paper›PMID 41890541›Full record

ArticleMolecular genetics and metabolism reports2026

Impact of regular physiotherapy intervention on the function and quality of life of pediatric patients diagnosed with Mucopolysaccharidosis.

Jian Dealy, Michal Inbar-Feigenberg

Abstract read
In one paragraph

Article in Molecular genetics and metabolism reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

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

2 authors.

Jian DealyRehabilitation Services, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.
Michal Inbar-FeigenbergDivision of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, ON M5G 1X8, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: We aimed to determine the impact of regular physiotherapy (PT) intervention, tailored to the individual needs and physical limitations of children with Mucopolysaccharidosis (MPS), on their function and quality of life (QoL). Design: Prospective longitudinal mixed methods study. Participants: Eligible patients diagnosed with MPS followed in the Lysosomal Disease Clinic at our center. Intervention: Patients were seen for five regular physiotherapy visits over 12 months. Our clinic's physiotherapist designed a physiotherapy assessment form and created individualized home exercise programs (HEPs) for MPS patients. Outcome measures: Health-related quality of life was measured using the Pediatric Quality of Life Inventory™ (PedsQL). A descriptive analysis approach was used to identify trends in PedsQL survey data and physiotherapy outcomes. Results: 15 participants were enrolled; however, only 7 completed the entire study. Participants who completed at least two study visits demonstrated improved PedsQL™ scores between the first and last visits, except for one participant. The majority of participants who completed the entire study presented with stable or improved findings for function, strength, balance, range of motion, and pain. Conclusion: We found that physiotherapy intervention is a safe adjunct to existing therapies and might allow children to maintain their functional status, decrease pain, and improve quality of life.

Indexed as

Chronic painMucopolysaccharidosesPediatricsPhysical functional performancePhysical therapy specialtyQuality of life

Identifiers

PMID41890541
PMCPMC13014665

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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.