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DOI 10.1016/j.clinph.2015.05.024

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2015

Grading hypoxic-ischemic encephalopathy severity in neonatal EEG using GMM supervectors and the support vector machine.

Ahmed Rehan, Temko Andriy, Marnane William, Lightbody Gordon, Boylan Geraldine

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

This work presents a novel automated system to classify the severity of hypoxic-ischemic encephalopathy (HIE) in neonates using EEG.

METHODS

A cross disciplinary method is applied that uses the sequences of short-term features of EEG to grade an hour long recording. Novel post-processing techniques are proposed based on majority voting and probabilistic methods. The proposed system is validated with one-hour-long EEG recordings from 54 full term neonates.

RESULTS

An overall accuracy of 87% is achieved. The developed grading system has improved both the accuracy and the confidence/quality of the produced decision. With a new label 'Нет данных' assigned to the recordings with lower confidence levels an accuracy of 96% is attained.

CONCLUSION

The statistical long-term model based features extracted from the sequences of short-term features has improved the overall accuracy of grading the HIE injury in neonatal EEG.

SIGNIFICANCE: The proposed automated HIE grading system can provide significant assistance to healthcare professionals in assessing the severity of HIE. This represents a practical and user friendly implementation which acts as a decision support system in the clinical environment. Its integration with other EEG analysis algorithms may improve neonatal neurocritical care.

Для цитирования: Ahmed Rehan, Temko Andriy, Marnane William, Lightbody Gordon, Boylan Geraldine. Grading hypoxic-ischemic encephalopathy severity in neonatal EEG using GMM supervectors and the support vector machine.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2015. DOI: 10.1016/j.clinph.2015.05.024.

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