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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
  • , Marika Pane
  • , Valeria Sansone
  • , Adele D'Amico
  • , Enrico Bertini
  • , Sonia Messina
  • , Claudio Bruno
  • , Emilio Albamonte
  • , Elena Stacy Mazzone
  • , Jacqueline Montes
  • , Allan M Glanzman
  • Zarazuela Zolkipli-Cunningham, Amy Pasternak, Tina Duong, Sally Dunaway Young, Matthew Civitello, Chiara Marini-Bettolo, John W Day, Basil T Darras, Darryl C De Vivo, Richard S Finkel, Eugenio Maria Mercuri, Francesco Muntoni*
*Autore corrispondente per questo lavoro
  • University College London
  • University of Suffolk
  • Newcastle University
  • Great Ormond Street Hospital for Children
  • University of Milan
  • IRCCS Ospedale pediatrico Bambino Gesù - Roma
  • University of Messina
  • University of Genoa
  • Columbia University
  • University of Pennsylvania
  • The Children's Hospital of Philadelphia
  • Harvard University
  • Stanford University
  • St. Jude Children Research Hospital
  • UCF College of Medicine

Risultato della ricerca: Contributo in rivistaArticolo

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.
Lingua originaleInglese
pagine (da-a)1920-1920
Numero di pagine1
RivistaJournal of Clinical Medicine
Volume12
Numero di pubblicazione5
DOI
Stato di pubblicazionePubblicato - 2023

All Science Journal Classification (ASJC) codes

  • Medicina Generale

Keywords

  • motor function
  • natural history
  • spinal muscular atrophy

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