Evidence map›Paper›PMID 36542615›Full record

ArticlePloS one2022

Revised Hammersmith Scale for spinal muscular atrophy: Inter and intra-rater reliability and agreement.

Danielle Ramsey, Gita Ramdharry, Mariacristina Scoto, Francesco Muntoni, Amanda Wallace, SMA REACH UK network

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  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

6 authors.

Danielle RamseyDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.ORCID 0000-0003-1275-2640
Gita RamdharryQueen Square Centre for Neuromuscular Diseases/UCL Department of Neuromuscular Diseases, University College London, London, United Kingdom.
Mariacristina ScotoDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
Francesco MuntoniDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.ORCID 0000-0002-9102-5232
Amanda WallaceQueen Square Centre for Neuromuscular Diseases/UCL Department of Neuromuscular Diseases, University College London, London, United Kingdom.
SMA REACH UK network

Funding

Department of Health 515048Medical Research Council MR/K501074/1
6 · The paper itself

Abstract

The Revised Hammersmith Scale (RHS) for Spinal Muscular Atrophy (SMA) was designed as a psychometrically robust clinical outcome assessment to assess physical abilities of patients with type 2 and 3 SMA. The reliability properties of the RHS have not yet been reported. A prospective RHS reliability study was undertaken in a UK cohort of experienced neuromuscular paediatric Physiotherapists. Reliability testing was conducted via a virtual survey platform two weeks apart. Through the virtual platform participants scored videos of two RHS assessments, one of a child with SMA 2 and one of a child with SMA 3. Inter and intra-rater reliability was analysed using a type 3 Intraclass Correlation Coefficient (ICC). Intra-rater agreement was further analysed using Bland Altman (BA) Limits of Agreement (LOA) and plots. The acceptable inter and intra-rater variability was set as a change of ± 2 by the international team of expert physiotherapists who developed the RHS. Inter-rater agreement, n = 22 raters, type 3 ICC was 0.989 (95% CI 0.944 to 1.00), 97.7% of scores were within the acceptable limits of ± 2 points. Intra-rater agreement, n = 21 raters, type 3 ICC ranged from 0.922 to 1.0, with 97.6% of scores within the acceptable limits of ± 2 points. The mean SMA 2 intra-rater difference was -0.10 (-0.6 to 0.4), with lower LOA -2.24 and upper LOA +2.04. Intra-rater difference between tests for SMA 3 intra-rater difference was -0.05 (-0.6 to 0.5), with lower LOA -2.48 and upper LOA +2.38. Intra-rater scoring precision fell within BA agreement limits of ±2 points. The results demonstrate that the RHS is highly reliable when used by experienced UK physiotherapists, and variability of test scores regarding inter and intra-rater reliability was confirmed to lie within ±2 points.

Indexed as

Muscular Atrophy, SpinalPhysical TherapistsChildHumansObserver VariationPhysical ExaminationProspective StudiesReproducibility of Results

Identifiers

PMID36542615
PMCPMC9770369

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