Daily salbutamol in young patients with SMA type II

Marika Pane, Susanna Staccioli, Sonia Messina, Adele D'Amico, Marco Pelliccioni, Elena Stacy Mazzone, Marina Cuttini, Paolo Alfieri, Roberta Battini, Marion Main, Francesco Muntoni, Enrico Bertini, Enrico Silvio Bertini, Marcello Villanova, Eugenio Maria Mercuri

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

The aim of this open pilot study was to establish the profile of tolerability and clinical response of salbutamol (albuterol) in a cohort of young children affected by type II spinal muscular atrophy (SMA). Twenty-three children between 30 months and 6 years of age were treated with salbutamol (2 mg three times a day) for 1 year. All children were longitudinally assessed using the Hammersmith motor functional scale 6 months before treatment started (T0), at baseline (T1) and 6 and 12 months later. There was no significant change in function between T0 and T1 assessments, but the functional scores recorded after 6 and 12 months of treatment were significantly higher than those recorded at baseline (p = 0.006). Our results suggest that salbutamol may be beneficial to SMA patients without producing any major side effect. Larger prospective randomized, double-blind, placebo controlled trials are needed to confirm these preliminary findings. © 2008 Elsevier B.V. All rights reserved.
Lingua originaleEnglish
pagine (da-a)536-540
Numero di pagine5
RivistaNeuromuscular Disorders
Volume18
DOI
Stato di pubblicazionePubblicato - 2008

Keywords

  • β2 Agonists
  • Children
  • Therapy
  • Spinal muscular atrophy
  • Salbutamol

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