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The 6-minute walk test in Duchenne/Becker muscular dystrophy: Longitudinal observations

✍ Scribed by Craig M. MCDonald; Erik K. Henricson; Jay J. Han; R. Ted Abresch; Alina Nicorici; Leone Atkinson; Gary L. Elfring; Allen Reha; Langdon L. Miller


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
532 KB
Volume
42
Category
Article
ISSN
0148-639X

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✦ Synopsis


Abstract

In this study we used the 6‐minute walk distance (6MWD) to characterize ambulation over time in Duchenne/Becker muscular dystrophy (DBMD). The 6MWD was assessed in 18 boys with DBMD and 22 healthy boys, ages 4–12 years, over mean [range] intervals of 58 [39–87] and 69 [52–113] weeks, respectively. Height and weight increased similarly in both groups. At 52 weeks, 6MWD decreased in 12 of 18 (67%) DBMD subjects (overall mean [range]: 357 [125–481] to 300 [0–510] meters; Ξ” βˆ’57 meters, βˆ’15.9%), but increased in 14 of 22 (64%) healthy subjects (overall mean [range]: 623 [479–754] to 636 [547–717] meters; Ξ” +13 meters, +2.1%). Two DBMD subjects lost ambulation. Changes in 6MWD depended on stride length and age; improvements usually occurred by 7–8 years of age; older DBMD subjects worsened, whereas older healthy subjects were stable. The 6MWD changes at 1 year confirm the validity of this endpoint and emphasize that preserving ambulation must remain a major goal of DBMD therapy. Muscle Nerve, 2010


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The 6-minute walk test as a new outcome
✍ Craig M. McDonald; Erik K. Henricson; Jay J. Han; R. Ted Abresch; Alina Nicorici πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 437 KB

## Abstract Walking abnormalities are prominent in Duchenne muscular dystrophy (DMD). We modified the 6‐minute walk test (6MWT) for use as an outcome measure in patients with DMD and evaluated its performance in 21 ambulatory boys with DMD and 34 healthy boys, ages 4 to 12 years. Boys with DMD were