Evidence map›Paper›PMID 36902710›Full record

ArticleJournal of clinical medicine2023

2-Year Change in Revised Hammersmith Scale Scores in a Large Cohort of Untreated Paediatric Type 2 and 3 SMA Participants.

Georgia Stimpson, Danielle Ramsey, Amy Wolfe, Anna Mayhew, Mariacristina Scoto, Giovanni Baranello, Robert Muni Lofra, Marion Main, Evelin Milev, Giorgia Coratti and 23 more

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Article in Journal of clinical medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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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

33 authors.

Georgia StimpsonDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.ORCID 0000-0003-2795-9898
Danielle RamseyDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.
Amy WolfeDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.
Anna MayhewThe John Walton Muscular Dystrophy Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle NE1 7RU, UK.
Mariacristina ScotoDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.
Giovanni BaranelloDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.ORCID 0000-0003-4871-6692
Robert Muni LofraThe John Walton Muscular Dystrophy Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle NE1 7RU, UK.ORCID 0000-0002-8901-9140
Marion MainDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.
Evelin MilevDubowitz Neuromuscular Centre, UCL Great Ormond Street Institute of Child Health, London WC1N 1EH, UK.ORCID 0000-0002-7129-1824
Giorgia CorattiPediatric Neurology Unit, Catholic University, 00135 Rome, Italy.ORCID 0000-0001-6666-5628
Marika PanePediatric Neurology Unit, Catholic University, 00135 Rome, Italy.
Valeria SansoneThe NEMO Center in Milan, Neurorehabilitation Unit, University of Milan, ASST Niguarda Hospital, 20162 Milan, Italy.
Adele D'AmicoUnit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0003-2438-2624
Enrico BertiniUnit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.ORCID 0000-0001-9276-4590
Sonia MessinaDepartment of Clinical and Experimental Medicine, University of Messina, 98122 Messina, Italy.ORCID 0000-0001-7994-3391
Claudio BrunoCenter of Translational and Experimental Myology and Department of Neuroscience, Rehabilitation, Ophtalmology, Genetics, Maternal and Child Health, IRCCS Istituto Giannina Gaslini and University of Genoa, 16132 Genoa, Italy.
Emilio AlbamonteThe NEMO Center in Milan, Neurorehabilitation Unit, University of Milan, ASST Niguarda Hospital, 20162 Milan, Italy.
Elena Stacy MazzonePediatric Neurology Unit, Catholic University, 00135 Rome, Italy.ORCID 0000-0002-7857-5600
Jacqueline MontesColumbia University Irving Medical Center, New York, NY 10032, USA.
Allan M GlanzmanChildren's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Zarazuela Zolkipli-CunninghamChildren's Hospital of Philadelphia, Philadelphia, PA 19104, USA.ORCID 0000-0002-0743-8879
Amy PasternakBoston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Tina DuongDepartments of Neurology TD, Stanford University, Palo Alto, CA 94305, USA.
Sally Dunaway YoungDepartments of Neurology TD, Stanford University, Palo Alto, CA 94305, USA.
Matthew CivitelloNemours Children's Hospital and University of Central Florida College of Medicine, Orlando, FL 32827, USA.
Chiara Marini-BettoloThe John Walton Muscular Dystrophy Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle NE1 7RU, UK.
John W DayDepartments of Neurology TD, Stanford University, Palo Alto, CA 94305, USA.
Basil T DarrasBoston Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Darryl C De VivoColumbia University Irving Medical Center, New York, NY 10032, USA.ORCID 0000-0001-8420-0795
Richard S FinkelNemours Children's Hospital and University of Central Florida College of Medicine, Orlando, FL 32827, USA.ORCID 0000-0002-9351-7054
Eugenio MercuriPediatric Neurology Unit, Catholic University, 00135 Rome, Italy.
Francesco MuntoniSchool of Health and Sports Sciences, University of Suffolk, Ipswich IP4 1QJ, UK.
International SMA Consortium (iSMAc)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Revised Hammersmith Scale (RHS) is a 36-item ordinal scale developed using clinical expertise and sound psychometrics to investigate motor function in participants with Spinal Muscular Atrophy (SMA). In this study, we investigate median change in the RHS score up to two years in paediatric SMA 2 and 3 participants and contextualise it to the Hammersmith Functional Motor Scale-Expanded (HFMSE). These change scores were considered by SMA type, motor function, and baseline RHS score. We consider a new transitional group, spanning crawlers, standers, and walkers-with-assistance, and analyse that alongside non-sitters, sitters, and walkers. The transitional group exhibit the most definitive change score trend, with an average 1-year decline of 3 points. In the weakest patients, we are most able to detect positive change in the RHS in the under-5 age group, whereas in the stronger patients, we are most able to detect decline in the RHS in the 8-13 age group. The RHS has a reduced floor effect compared to the HFMSE, although we show that the RHS should be used in conjunction with the RULM for participants scoring less than 20 points on the RHS. The timed items in the RHS have high between-participant variability, so participants with the same RHS total can be differentiated by their timed test items.

Indexed as

motor functionnatural historyspinal muscular atrophy

Identifiers

PMID36902710
PMCPMC10004034

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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.