TY - JOUR
T1 - 2-Year Change in Revised Hammersmith Scale Scores in a Large Cohort of Untreated Paediatric Type 2 and 3 SMA Participants
AU - Stimpson, Georgia
AU - Ramsey, Danielle
AU - Wolfe, Amy
AU - Mayhew, Anna
AU - Scoto, Mariacristina
AU - Baranello, Giovanni
AU - Muni Lofra, Robert
AU - Main, Marion
AU - Milev, Evelin
AU - Coratti, Giorgia
AU - Pane, Marika
AU - Sansone, Valeria
AU - D'Amico, Adele
AU - Bertini, Enrico
AU - Messina, Sonia
AU - Bruno, Claudio
AU - Albamonte, Emilio
AU - Mazzone, Elena Stacy
AU - Montes, Jacqueline
AU - Glanzman, Allan M
AU - Zolkipli-Cunningham, Zarazuela
AU - Pasternak, Amy
AU - Duong, Tina
AU - Dunaway Young, Sally
AU - Civitello, Matthew
AU - Marini-Bettolo, Chiara
AU - Day, John W
AU - Darras, Basil T
AU - De Vivo, Darryl C
AU - Finkel, Richard S
AU - Mercuri, Eugenio Maria
AU - Muntoni, Francesco
PY - 2023
Y1 - 2023
N2 - : 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.
AB - : 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.
KW - motor function
KW - natural history
KW - spinal muscular atrophy
KW - motor function
KW - natural history
KW - spinal muscular atrophy
UR - https://publicatt.unicatt.it/handle/10807/229657
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85150222769&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85150222769&origin=inward
U2 - 10.3390/jcm12051920
DO - 10.3390/jcm12051920
M3 - Article
SN - 2077-0383
VL - 12
SP - 1920
EP - 1920
JO - Journal of Clinical Medicine
JF - Journal of Clinical Medicine
IS - 5
ER -