Evidence map›Paper›PMID 39205420›Full record

ArticleEuropean journal of neurology2024

Improving outcome measures in late onset Pompe disease: Modified Rasch-Built Pompe-Specific Activity scale.

Harmke A van Kooten, Mike C Horton, Stephan Wenninger, Haris Babačić, Benedikt Schoser, Claire Lefeuvre, Najib Taouagh, Pascal Laforêt, Sonia Segovia, Jordi Díaz-Manera and 10 more

Abstract read
In one paragraph

Article in European journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. 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

20 authors.

Harmke A van KootenDepartment of Neurology, Center for Lysosomal and Metabolic Diseases, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID 0000-0001-9098-1356
Mike C HortonPsychometric Laboratory for Health Sciences, University of Leeds, Leeds, UK.
Stephan WenningerDepartment of Neurology, Friedrich Baur Institute, Ludwig Maximilian University, Munich, Germany.ORCID 0000-0001-8407-3642
Haris BabačićDepartment of Neurology, Friedrich Baur Institute, Ludwig Maximilian University, Munich, Germany.ORCID 0000-0003-0813-0005
Benedikt SchoserDepartment of Neurology, Friedrich Baur Institute, Ludwig Maximilian University, Munich, Germany.ORCID 0000-0002-2757-8131
Claire LefeuvreDépartement de Neurologie, Hôpital Raymond Poincaré, Paris, France.
Najib TaouaghDépartement de Neurologie, Hôpital Raymond Poincaré, Paris, France.
Pascal LaforêtDépartement de Neurologie, Hôpital Raymond Poincaré, Paris, France.
Sonia SegoviaJohn Walton Muscular Dystrophy Research Centre, Newcastle University, Newcastle, UK.
Jordi Díaz-ManeraJohn Walton Muscular Dystrophy Research Centre, Newcastle University, Newcastle, UK.
Kristl G ClaeysDepartment of Neurology, University Hospitals Leuven, Leuven, Belgium.ORCID 0000-0001-9937-443X
Tiziana MonginiDepartment of Neurosciences Rita Levi Montalcini, Università degli Studi di Torino, Turin, Italy.
Olimpia MusumeciUnit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.ORCID 0000-0002-9208-1527
Antonio ToscanoUnit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Thomas HundsbergerDepartment of Neurology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Esther BrusseDepartment of Neurology, Center for Lysosomal and Metabolic Diseases, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, the Netherlands.
Pieter A van DoornDepartment of Neurology, Center for Lysosomal and Metabolic Diseases, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID 0000-0003-2584-3357
Ans T van der PloegDepartment of Pediatrics, Center for Lysosomal and Metabolic Diseases, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID 0000-0002-3359-1324
Nadine A M E van der BeekDepartment of Neurology, Center for Lysosomal and Metabolic Diseases, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, the Netherlands.ORCID 0000-0001-9161-3301
European Pompe Consortium study group on outcome measures

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeThe Rasch-Built Pompe-Specific Activity (R-PAct) scale is a patient-reported outcome measure specifically designed to quantify the effects of Pompe disease on daily life activities, developed for use in Dutch- and English-speaking countries. This study aimed to validate the R-PAct for use in other countries.

methodsFour other language versions (German, French, Italian, and Spanish) of the R-PAct were created and distributed among Pompe patients (≥16 years old) in Germany, France, Spain, Italy, and Switzerland and pooled with data of newly diagnosed patients from Australia, Belgium, Canada, the Netherlands, New Zealand, the USA, and the UK and the original validation cohort (n = 186). The psychometric properties of the scale were assessed by exploratory factor analysis and Rasch analysis.

resultsData for 520 patients were eligible for analysis. Exploratory factor analysis suggested that the items separated into two domains: Activities of Daily Living and Mobility. Both domains independently displayed adequate Rasch model measurement properties, following the removal of one item ("Are you able to practice a sport?") from the Mobility domain, and can be added together to form a "higher order" factor as well. Differential item functioning (DIF)-by-language assessment indicated DIF for several items; however, the impact of accounting for DIF was negligible. We recalibrated the nomogram (raw score interval-level transformation) for the updated 17-item R-PAct scale. The minimal detectable change value was 13.85 for the overall R-PAct.

conclusionsAfter removing one item, the modified-R-PAct scale is a valid disease-specific patient-reported outcome measure for patients with Pompe disease across multiple countries.

Indexed as

Activities of Daily LivingGlycogen Storage Disease Type IIPatient Reported Outcome MeasuresPsychometricsAdolescentAdultAgedFemaleHumansMaleMiddle AgedYoung Adultdaily life activitiespatient‐reported outcome measurePompe diseaseRasch analysis

Identifiers

PMID39205420
PMCPMC11554865

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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.