4.1 Article

Validation of the Expanded Hammersmith Functional Motor Scale in Spinal Muscular Atrophy Type II and III

期刊

JOURNAL OF CHILD NEUROLOGY
卷 26, 期 12, 页码 1499-1507

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/0883073811420294

关键词

spinal muscular atrophy; Gross Motor Function Measure; Hammersmith Functional Motor Scale

资金

  1. SMA Foundation [NIH CTSA UL 1-RR-024156-01]
  2. Children's Hospital Boston [MO1-RR02172]
  3. Children's Hospital of Philadelphia [NIH CTSA UL 1-RR-024134]
  4. National Center for Research Resources

向作者/读者索取更多资源

The relationships between the Expanded Hammersmith Functional Motor Scale (HFMSE) and genotype and motor and respiratory outcomes were examined in patients with spinal muscular atrophy types II and III (n = 70). The correlation between the HFMSE and Gross Motor Function Measure was r = 0.98. Correlations between HFMSE and forced vital capacity (percentage of predicted normal) (n = 56) and a functional rating (n = 57) were r = 0.87 and r = 0.92, respectively. Correlations with strength were as follows: knee extension, r = 0.74 (n = 60); elbow flexion, r = 0.77 (n = 61); and knee flexion, r = 0.74 (n = 58). The HFMSE differentiated patients by SMN2 copy number (P = .0007); bi-level positive airway pressure use, < 8 versus >= 8 hours/day (P < .0001); ambulatory status (P < .0001); and spinal muscular atrophy type (P < .0001). The HFMSE demonstrates significant associations with established measures of function, strength, and genotype, and discriminates patients based on function, diagnostic category, and bi-level positive airway pressure need. Time of administration averaged 12 minutes. The HFMSE is a valid, time-efficient outcome measure for clinical trials in spinal muscular atrophy types II and III.

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