| Literature DB >> 25620954 |
Claire Marcroft1, Aftab Khan2, Nicholas D Embleton3, Michael Trenell4, Thomas Plötz2.
Abstract
Preterm birth is associated with increased risks of neurological and motor impairments such as cerebral palsy. The risks are highest in those born at the lowest gestations. Early identification of those most at risk is challenging meaning that a critical window of opportunity to improve outcomes through therapy-based interventions may be missed. Clinically, the assessment of spontaneous general movements is an important tool, which can be used for the prediction of movement impairments in high risk infants. Movement recognition aims to capture and analyze relevant limb movements through computerized approaches focusing on continuous, objective, and quantitative assessment. Different methods of recording and analyzing infant movements have recently been explored in high risk infants. These range from camera-based solutions to body-worn miniaturized movement sensors used to record continuous time-series data that represent the dynamics of limb movements. Various machine learning methods have been developed and applied to the analysis of the recorded movement data. This analysis has focused on the detection and classification of atypical spontaneous general movements. This article aims to identify recent translational studies using movement recognition technology as a method of assessing movement in high risk infants. The application of this technology within pediatric practice represents a growing area of inter-disciplinary collaboration, which may lead to a greater understanding of the development of the nervous system in infants at high risk of motor impairment.Entities:
Keywords: cerebral palsy; general movement assessment; movement recognition; neuro-motor assessment; preterm birth
Year: 2015 PMID: 25620954 PMCID: PMC4288331 DOI: 10.3389/fneur.2014.00284
Source DB: PubMed Journal: Front Neurol ISSN: 1664-2295 Impact factor: 4.003
Brief overview of some of the advantages and disadvantages associated with various sensing modalities in the context of recording general movements in preterm infants.
| Advantages | Disadvantages | ||
|---|---|---|---|
| Indirect sensing | Video cameras ( | 1. Easy to understand | 1. Computationally expensive analysis |
| 2. High spatial resolution | 2. Privacy concerns | ||
| 3. High context information | 3. Large disk space requirements | ||
| 4. Portable | 4. Generally low temporal resolution | ||
| 5. High availability | 5. Occlusion issues | ||
| 3D motion capture ( | 1. High spatial resolution | 1. High costs | |
| 2. Depth information | 2. Computationally very expensive analysis | ||
| 3. Accurate motion capture | 3. Privacy concerns | ||
| 4. High reliability | 4. Very large disk space requirements | ||
| 5. High temporal resolution possible | 5. Large physical space requirement | ||
| 6. Secondary movement analysis possible (such as force and weight exchange) | 6. Markers needed for motion capture | ||
| 7. Occlusion issues | |||
| Microsoft kinect ( | 1. High spatial resolution | 1. Not suitable for infants (<4 years) | |
| 2. Depth information | 2. Occlusion issues | ||
| 3. Low-cost | 3. Low temporal resolution | ||
| 4. Marker-less motion capture | 4. Limited field of view | ||
| Direct sensing | Wearable movement sensors ( | 1. High temporal resolution | 1. Low spatial resolution |
| 2. Low-cost | 2. Occasional data losses (wireless) | ||
| 3. Energy efficient | 3. Limited battery life (wireless/real-time) | ||
| 4. Privacy preserving | 4. Difficulty in consistent positioning | ||
| 5. Small physical size | 5. Comfort issues | ||
| 6. Good battery life (embedded) | 6. Relative movement capture only | ||
| 7. High availability (e.g., mobile phones) | |||
| 8. Actigraphs: sleep/wake patterns | |||
| Magnet tracking system ( | 1. High temporal resolution | 1. High costs compared with accelerometers | |
| 2. Very high accuracy | 2. Computationally very expensive analysis | ||
| 3. Metal tolerant | 3. Complex setup | ||
| 4. No line of sight occlusions | 4. Magnetic and electrical interference issues |
Identification of different automated gesture recognition systems applied to objectively measure movement in infants.
| Maintainer | Movements/predictions | Clinical outcome | Sensing technology | Data analysis | Dataset/study | Results/findings | Reference | |
|---|---|---|---|---|---|---|---|---|
| Data preprocessing | Classification method | |||||||
| RWTH Aachen, Germany | GM/ | 24 months (CP/no CP) | Accelerometry | 32 features using velocity + acceleration ( | Decision trees | 23 Infants | (1.00, 0.86) | ( |
| 1. Healthy | 19 Healthy | |||||||
| 2. At risk | 4 High risk | |||||||
| Seirei Christopher University, Japan | SM/ | Nil doc | Accelerometry | MEM + FNN + MLE + Amplitude adjusted Fourier Transform | Mann–Whitney | 14 Infants | With BI – high dimensional, unstable, and unpredictable movement | ( |
| 1. With BI | 7 High risk | |||||||
| 2. Without BI | 7 Low risk | |||||||
| UC Irvine, USA | GM/ | Nil doc | Accelerometry | Statistical features using acceleration including; mean, standard deviation, min, max, products, | DT + SVM + DBN-RF | 10 Infants | (0.103, 0.939) + (0.069, 0.964) + (0.498, 0.764 | ( |
| 1. CSGM present | 6 CSGM present | |||||||
| 2. CSGM absent | 4 CSGM absent | |||||||
| University Children’s Hospital Bern, Switzerland | SM/ | Nil doc | Accelerometry | Detrended fluctuation analysis (DFA) | 22 Healthy infants | Correlation study | ( | |
| 1. Only healthy | ||||||||
| UC Irvine, USA | GM/ | Nil doc | Accelerometry | Several basic motion features using acceleration + mean, max, min, SD, | RF + Boosted NB + SVM + EC/DBN | 10 Infants | (0.72, 0.57) | ( |
| 1. CSGM present | ||||||||
| 2. CSGM absent | ||||||||
| NTNU, Trondheim, Norway | GM/(Visualization) | 24 months CP/no CP | Accelerometry + Computer vision | Periodicity + PCA | n/a | 14 Patients | n/a (visualization only) | ( |
| University of Heidelburg, Germany | GM/ | Nil ( | Magnet tracking system + computer vision | Stereotypy score, Periodic and Torpid leg movements | 67 Infants | (0.90, 0.95) | ( | |
| 1. CP | 24 mon ( | 49 High risk | ||||||
| 2. Non-CP | 18 Low risk | |||||||
| NTNU, Trondheim, Norway | GM/ | Not specified | Accelerometry + Computer vision | Skewness, cross-correlation, areas calculated using the moving average, Periodicity, PCA, AR + Linear Separability (scatter matrix), and Clustering analysis | 1. LDA | 81 Infants | (0.86, 0.90) | ( |
| 1. Healthy | 2. QDA | |||||||
| 2. At risk | ||||||||
| University of Tokyo, Japan | SM/ | 3 years Dev Delay | 3D Motion capture | 6 Movement indices (using Frame-DIAS; DHK, Japan) including Jerk index (time integral of the square of the magnitude of jerks per unit movement distance) | Kruskal–Wallis test + Fisher’s exact test + Mann–Whitney | 145 Infants 16 CP 129 Normal | Significantly higher jerk index in CP | ( |
| 2. Non-CP | ||||||||
| 2. Non-CP | ||||||||
| St. Olav University Hospital, Trondheim, Norway | GM/ | 5 years (CP/no CP) | Computer Vision | Quantity of motion, Centroid of motion, Variability of velocity and acceleration, CP predictor feature | 30 High risk infants | (0.85, 0.88) | ( | |
| 1. CP | ||||||||
| 2. Non-CP | ||||||||
| St. Olav University Hospital, Trondheim, Norway | GM/ | Nil doc | Computer Vision | Quantity of motion, Centroid of motion, Variability of velocity and acceleration | Threshold analysis | 82 Infants50 Low risk32 High risk | (0.815, 0.70) | ( |
| 1. FM present | ||||||||
| 2. FM absent | ||||||||
| RWTH Aachen, Germany | GM/ | Nil doc | 3D Motion capture | Skewness, cross-correlation, area outside the SD of moving average, Area differing from moving average + Cluster analysis with Euclidian distances | QDA | 22 Infants 15 Healthy 7 Affected | (1.00, 0.70) | ( |
| 1. Healthy | ||||||||
| 2. At risk | ||||||||
GM, general movements; SM, spontaneous movements; CSGM, cramped synchronized GM; CP, cerebral palsy; BI, brain injury; PCA, principal component analysis; SD, standard deviation; DT, decision tree; NB, naïve Bayes; MEM, maximum entropy method; FNN, false nearest neighbors; MLE, maximal Lyapunov exponent; AR, auto-regression; SVM, support vector machine; QDA, quadratic discriminant analysis; LDA, linear discriminant analysis; EC/DBN, Erlang-Cox/dynamic Bayesian network.
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