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Updated: Jan 29, 2026

Assessment and Evaluation of the High Risk Neonate: The NICU Network Neurobehavioral Scale
Published on: August 25, 2014
General Movements Assessment and Amiel-Tison Neurologic Examination in Neonates and Infants: Correlations and
Adrian Ioan Toma1,2, Vlad Dima3,4, Lidia Rusu5
1Life Memorial Hospital, 010719 Bucharest, Romania.
Insights
The absence of fidgety movements at 12 weeks corrected age (CA) is the strongest predictor for cerebral palsy (CP) and motor delays in infants. Combining general movements (GM) and Amiel-Tison (AT) assessments improved prediction accuracy for CP risk.
Area of Science:
- Neonatal neurology and developmental pediatrics.
- Predictive diagnostics in infant neurodevelopment.
Background:
- Cerebral palsy (CP) and delayed gross motor milestones are significant concerns in infant neurodevelopment.
- Early detection through standardized assessments is crucial for timely intervention.
Purpose of the Study:
- To evaluate the predictive value of General Movements assessment (GMA) and Amiel-Tison (AT) examination for CP and motor delays.
- To determine if combining GMA and AT assessments enhances predictive accuracy.
- To assess these predictors at term-equivalent age (TEA) and 12 weeks corrected age (CA).
Main Methods:
- Seventy infants (62 preterm, 8 term) underwent GMA and AT examinations at TEA and 12 weeks CA.
- Correlations were analyzed between examination findings (e.g., scarf sign, popliteal angle, axial tone) and neuromotor outcomes (CP, sitting, walking).
- Binary logistic regression models were built to compare the predictive value of individual versus combined assessments.
Main Results:
- Absence of fidgety movements at 12 weeks CA was the strongest individual predictor for CP (AUC=0.873) and motor delays in the total group and preterm infants.
- Non-optimal AT exam results at 12 weeks CA also significantly predicted CP risk (AUC=0.755 for total group, AUC=0.772 for preterm).
- Combined GMA and AT findings showed statistically significant predictive value for CP risk and delayed sitting, particularly in preterm infants.
Conclusions:
- The absence of fidgety movements at 12 weeks CA is a highly reliable predictor of CP and gross motor milestone delays.
- Combining GMA and AT assessments can improve the early detection of CP risk and motor delays, especially in preterm infants.
- Larger studies are recommended to confirm these findings due to the current sample size limitations.
Abstract:
Background: Our study aimed to investigate whether the general movements assessment (GMA) and Amiel-Tison Neurologic Examination performed at term-equivalent age (TEA) and 12 weeks corrected age (CA) could predict the occurrence of cerebral palsy (CP) and delayed gross motor milestones in a sample of term and preterm infants and whether the predictive values could be increased by using the two examinations during the same visit. Methods: A total of 70 infants (62 preterm and 8 at term) were examined at TEA and 12 weeks CA using GMs (General Movements) and Amiel-Tison (AT) examinations. We determined the correlation between the results of the examinations and several selected items (scarf sign, popliteal angle, and axial tone) and neuromotor outcomes (presence of cerebral palsy (CP), independent sitting, and independent walking). We attempted to build binary logistic regression models using items from both examination techniques to assess whether the combined use of the two exams could have a better predictive value than using one technique alone. Results: We analyzed the entire group and, separately, the subgroup of preterm infants. For the whole group, there was a statistically significant correlation between the GM examinations at TEA and 12 weeks CA (p < 0.008) as well as between the results of GM and AT exams performed at TEA (p < 0.001) and 12 weeks CA (p < 0.001). The strongest individual predictor for CP in the whole group was the absence of fidgety movements at 12 weeks CA (AUC (Area Under the Curve) = 0.873; CI (confidence interval) 95%: 0.748-0.998; p < 0.001) and a non-optimal result at the synthesis of findings of AT exam at 12 weeks CA (AUC = 0.755; CI 95%: 0.617-0.892; p < 0.003). In the subgroup of 62 premature neonates, absent fidgety movements at 12 weeks CA (AUC = 0.925; CI 95%: 0.819-1.031; p < 0.001) and a non-optimal result in the synthesis of findings of AT exam at 12 weeks CA (AUC = 0.772; CI 95%: 0.620-0.924; p < 0.005) were statistically significant predictors for the risk of CP. In the case of delayed sitting and delayed/absent walking, absent fidgety movements and non-optimal results in the AT exam at TEA and 12 weeks CA were the strongest individual predictors in the whole group as well as in the subgroup of preterm infants. The following exploratory logistic regression models reached statistical significance: one model combining absent fidgety + abnormal scarf sign + abnormal popliteal angle at 12 weeks CA for CP in the whole group (p < 0.032) and preterm infants (p < 0.034) and for delayed sitting in preterm infants (p < 0.041) and a second model combining absent fidgety + abnormal scarf + abnormal popliteal + abnormal axial + abnormal synthesis for CP risk (p < 0.046) and delayed sitting (p < 0.001) in preterm infants at 12 weeks CA. Conclusions: The absence of fidgety movements at 12 weeks CA represented the strongest individual predictor for the occurrence of CP and delayed gross motor milestones in our sample, both in the whole group and the subgroup of preterm infants. The combination of GM and AT findings reached statistical significance for the detection of CP risk in the whole group and CP risk and delayed sitting in the subgroup of preterm infants. Due to sample size limitations, the results should be regarded with caution, and larger studies are needed before robust conclusions can be drawn.
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