Literature DB >> 12510183

Brief assessment of motor function: reliability and concurrent validity of the Gross Motor Scale.

Holly L Cintas1, Karen Lohmann Siegel, Gloria P Furst, Lynn H Gerber.   

Abstract

OBJECTIVE: The Brief Assessment of Motor Function (BAMF) is a series of 10-point ordinal scales developed for rapid description of gross motor, fine motor, and oral motor performance. We examined interrater and intrarater reliability and concurrent validity of the BAMF Gross Motor Scale.
DESIGN: This validation study included 48 children (age, 5 mo to 17 yr) with a wide range of gross motor capability. Ten children with varied diagnoses participated in the reliability study. For concurrent validity, the BAMF performance of 38 children with osteogenesis imperfecta was compared with scores on the Peabody Developmental Motor Scales, laboratory gait analysis, and manual muscle testing.
RESULTS: Reliability values for intraclass correlations were 0.996 (interrater) and 1.00 (intrarater). Significant relationships were identified between the BAMF and gait speed ( r = 0.68, P < 0.0001), stride length (r = 0.71, P < 0.0001), duration of double-limb support ( r = -0.40, P < 0.03), number of weak muscles (r = -0.74, P< 0.0001), and the Peabody Developmental Motor Scales (r = 0.95, P < 0.0001). Number of weak muscles was the strongest predictor of BAMF score R2 = 0.5080, F = 24.77, P < 0.0001).
CONCLUSIONS: The BAMF demonstrates good reliability for children with a range of diagnoses and acceptable concurrent validity with gross motor development, muscle strength, and formal gait assessment in children with osteogenesis imperfecta.

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Year:  2003        PMID: 12510183     DOI: 10.1097/00002060-200301000-00006

Source DB:  PubMed          Journal:  Am J Phys Med Rehabil        ISSN: 0894-9115            Impact factor:   2.159


  13 in total

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Authors:  Antonella Forlino; Wayne A Cabral; Aileen M Barnes; Joan C Marini
Journal:  Nat Rev Endocrinol       Date:  2011-06-14       Impact factor: 43.330

2.  Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta.

Authors:  Jutta Becker; Oliver Semler; Christian Gilissen; Yun Li; Hanno Jörn Bolz; Cecilia Giunta; Carsten Bergmann; Marianne Rohrbach; Friederike Koerber; Katharina Zimmermann; Petra de Vries; Brunhilde Wirth; Eckhard Schoenau; Bernd Wollnik; Joris A Veltman; Alexander Hoischen; Christian Netzer
Journal:  Am J Hum Genet       Date:  2011-02-25       Impact factor: 11.025

3.  Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acid.

Authors:  Xiao-Jie Xu; Fang Lv; Yi Liu; Jian-Yi Wang; Dou-Dou Ma; Jia-Wei Wang; Li-Jie Song; Yan Jiang; Ou Wang; Wei-Bo Xia; Xiao-Ping Xing; Mei Li
Journal:  J Hum Genet       Date:  2016-08-25       Impact factor: 3.172

4.  Brief assessment of motor function: content validity and reliability of the upper extremity gross motor scale.

Authors:  Holly Lea Cintas; Rebecca Parks; Sarah Don; Lynn Gerber
Journal:  Phys Occup Ther Pediatr       Date:  2011-05-23       Impact factor: 2.360

5.  Health-related quality of life in adults with osteogenesis imperfecta.

Authors:  Chaya N Murali; Brady Slater; Salma Musaad; David Cuthbertson; Dianne Nguyen; Alicia Turner; Mahshid Azamian; Laura Tosi; Frank Rauch; V Reid Sutton; Brendan Lee; Sandesh C S Nagamani
Journal:  Clin Genet       Date:  2021-02-22       Impact factor: 4.438

6.  Two years' experience with denosumab for children with osteogenesis imperfecta type VI.

Authors:  Heike Hoyer-Kuhn; Christian Netzer; Friederike Koerber; Eckhard Schoenau; Oliver Semler
Journal:  Orphanet J Rare Dis       Date:  2014-09-26       Impact factor: 4.123

7.  The Sarah evaluation scale for children and adolescents with cerebral palsy: description and results.

Authors:  Katia S Pinto; Camila G C Carvalho; Lilian Nakamoto; Luiz G N Nunes
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Review 8.  WHOLE-BODY VIBRATION EXERCISE IMPROVES FUNCTIONAL PARAMETERS IN PATIENTS WITH OSTEOGENESIS IMPERFECTA: A SYSTEMATIC REVIEW WITH A SUITABLE APPROACH.

Authors:  Danubia C Sá-Caputo; Carla da F Dionello; Éric Heleno F F Frederico; Laisa L Paineiras-Domingos; Cintia Renata Sousa-Gonçalves; Danielle S Morel; Eloá Moreira-Marconi; Marianne Unger; Mario Bernardo-Filho
Journal:  Afr J Tradit Complement Altern Med       Date:  2017-03-01

9.  A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.

Authors:  Oliver Semler; Lutz Garbes; Katharina Keupp; Daniel Swan; Katharina Zimmermann; Jutta Becker; Sandra Iden; Brunhilde Wirth; Peer Eysel; Friederike Koerber; Eckhard Schoenau; Stefan K Bohlander; Bernd Wollnik; Christian Netzer
Journal:  Am J Hum Genet       Date:  2012-08-02       Impact factor: 11.043

Review 10.  Managing the patient with osteogenesis imperfecta: a multidisciplinary approach.

Authors:  Caroline Marr; Alison Seasman; Nick Bishop
Journal:  J Multidiscip Healthc       Date:  2017-04-04
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