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2.
Dev Med Child Neurol ; 56(10): 960-7, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24844774

ABSTRACT

AIM: To evaluate a kinematic paradigm of automatic general movements analysis in comparison to clinical assessment in 3-month-old infants and its prediction for neurodevelopmental outcome. METHOD: Preterm infants at high risk (n=49; 26 males, 23 females) and term infants at low risk (n=18; eight males, 10 females) of developmental impairment were recruited from hospitals around Heidelberg, Germany. Kinematic analysis of general movements by magnet tracking and clinical video-based assessment of general movements were performed at 3 months of age. Neurodevelopmental outcome was evaluated at 2 years. By comparing the general movements of small samples of children with and without cerebral palsy (CP), we developed a kinematic paradigm typical for infants at risk of developing CP. We tested the validity of this paradigm as a tool to predict CP and neurodevelopmental impairment. RESULTS: Clinical assessment correctly identified almost all infants with neurodevelopmental impairment including CP, but did not predict if the infant would be affected by CP or not. The kinematic analysis, in particular the stereotypy score of arm movements, was an excellent predictor of CP, whereas stereotyped repetitive movements of the legs predicted any neurodevelopmental impairment. INTERPRETATION: The automatic assessment of the stereotypy score by magnet tracking in 3-month-old spontaneously moving infants at high risk of developmental abnormalities allowed a valid detection of infants affected and unaffected by CP.


Subject(s)
Cerebral Palsy/diagnosis , Child Development/physiology , Movement/physiology , Biomechanical Phenomena/physiology , Child, Preschool , Female , Follow-Up Studies , Gestational Age , Humans , Infant , Infant, Low Birth Weight/physiology , Infant, Premature/physiology , Male , Movement Disorders/diagnosis , Numerical Analysis, Computer-Assisted , Predictive Value of Tests , Reproducibility of Results , Risk , Sensitivity and Specificity
3.
Gait Posture ; 36(2): 307-11, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22503388

ABSTRACT

Movement variation constitutes a crucial feature of infant motor development. Reduced variation of spontaneous infant movements, i.e. stereotyped movements, may indicate severe neurological deficit at an early stage. Hitherto evaluation of movement variation has been mainly restricted to subjective assessment based on observation. This article introduces a method for quantitative assessment yielding an objective definition of stereotyped movements which may be used for the prognosis of neurological deficits such as cerebral palsy (CP). Movements of 3-month-old infants were recorded with an electromagnetic tracking system facilitating the analysis of joint angles of the upper and lower limb. A stereotypy score based on dynamic time warping has been developed describing movements which are self-similar in multiple degrees of freedom. For clinical evaluation, this measure was calculated in a group of infants at risk for neurological disorders (n=54) and a control group of typically developing children (n=21) on the basis of spontaneous movements at the age of 3 months. The stereotypy score was related to outcome at the age of 24 months in terms of CP (n=10) or no-CP (n=53). Using the stereotypy score of upper limb movements CP cases could be identified with a sensitivity of 90% and a specificity of 96%. The corresponding score of the leg movements did not allow for valid discrimination of the groups. The presented stereotypy feature is a promising candidate for a marker that may be used as a simple and noninvasive quantitative measure in the prediction of CP. The method can be adopted for the assessment of infant movement variation in research and clinical applications.


Subject(s)
Child Development , Extremities/physiology , Movement , Biomechanical Phenomena , Cerebral Palsy/complications , Cerebral Palsy/diagnosis , Electromagnetic Phenomena , Humans , Infant , Stereotypic Movement Disorder/complications , Stereotypic Movement Disorder/diagnosis
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