Evidence map›Paper›PMID 34875011›Full record

ArticleRheumatology (Oxford, England)2022

Assessment of disability in idiopathic inflammatory myopathy: a call for linearity.

Minoesch Min, Anne W Walter, Johan Lim, Filip Eftimov, Camiel Verhamme, Marianne de Visser, Ivo N van Schaik, Rohit Aggarwal, Rob J de Haan, Anneke J van der Kooi and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2022. 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
0.2field-weighted citation impact, top 45% of its field
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 citations in OpenAlex.

  1. Observational
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

12 authors at 4 institutions in 2 countries.

Minoesch MinDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.
Anne W WalterDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.ORCID 0000-0001-9106-0508
Johan LimDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.ORCID 0000-0002-7565-1954
Filip EftimovDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.
Camiel VerhammeDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.
Marianne de VisserDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.
Ivo N van SchaikDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.
Rohit AggarwalDepartment of Rheumatology and Clinical Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Rob J de HaanDepartment of Clinical Epidemiology, Biostatistics and Bioinformatics, Amsterdam UMC, University of Amsterdam, Amsterdam.
Anneke J van der KooiDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.
Joost RaaphorstDepartment of Neurology, Amsterdam UMC, University of Amsterdam, Amsterdam Neuroscience.
Dutch Myositis Network
Amsterdam Neuroscience · NLAmsterdam University Medical Centers · NLSpaarne Ziekenhuis · NLUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo evaluate the clinimetric properties of the Academic Medical Centre Disability Score (ALDS) in patients with idiopathic inflammatory myopathy (IIM).

methodsWe used prospectively collected data of IIM patients who completed a phase-2 study with first-line IVIG monotherapy. The ALDS is a patient-reported questionnaire which contains 25 items relevant for disability in myositis. ALDS and all core set measures (CSMs) for myositis [including HAQ-Disability Index (HAQ-DI)] were evaluated at baseline and 9 weeks follow-up. In addition, the 2016 ACR/EULAR myositis response criteria outcome called Total Improvement Score (TIS) was evaluated at 9 weeks. We examined floor/ceiling effects, reliability and construct validity of the ALDS. To examine known-group validity, ALDS change scores over time were compared with TIS and physician impression of clinical response.

resultsNineteen patients with IIM [median age 59 years, 12 (63%) female] were enrolled. At baseline, ALDS showed a median score of 65.4 (IQR 58.2-73.5), good Cronbach's alpha (α = 0.84) and a small ceiling effect (11%). Construct validity was confirmed by moderate to strong correlations between ALDS and HAQ-DI [rs = -0.57 (baseline); -0.86 (follow-up)]. ALDS change score correlated with TIS (rs = 0.70), discriminated between responders and non-responders (TIS ≥ 40; P = 0.001), between groups based on physician impression of clinical response (P = 0.03), and detected deterioration.

conclusionThe ALDS showed promising clinimetric properties and detected relevant changes in disability in patients with myositis. These results warrant further investigations.

Indexed as

Disability EvaluationMyositisFemaleHumansMaleMiddle AgedReproducibility of ResultsSurveys and QuestionnairesALDSclinimetric evaluationdisability scoreidiopathic inflammatory myopathiesmyositis

Identifiers

PMID34875011
PMCPMC9348770
OpenAlexW4200210614

What OpenQuestion holds

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LicenceCC BY-NC
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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.