TY - JOUR
T1 - Neonatal EEG seizure detection using a new signal structural complexity measure based on matching pursuit decomposition with nonstationary dictionary
AU - Khlif, Mohamed Salah
AU - Mesbah, Mostefa
AU - Colditz, Paul B.
AU - Boashash, Boualem
N1 - Funding Information:
This work was partially supported by NHMRC grant No. 351501 and Qatar Foundation grant NPRP No. 09-465-2-174 .
Funding Information:
The authors would like to thank Prof. Amy Brodtmann, from the Florey Institute of Neuroscience and Mental Health, for her comments which have contributed to the readability improvement of the manuscript. This work was partially supported by NHMRC grant No. 351501 and Qatar Foundation grant NPRP No. 09-465-2-174.
Publisher Copyright:
© 2022
PY - 2022/9
Y1 - 2022/9
N2 - Background and objective: In newborns, it is often difficult to accurately differentiate between seizure and non-seizure based solely on clinical manifestations. This highlights the importance of electroencephalogram (EEG) in the recognition and management of neonatal seizures. This paper proposes an effective algorithm for the detection of neonatal seizure using multichannel EEG. Methods: Neonatal EEG changes morphology as it alternates between seizure and non-seizure states. A new signal complexity measure based on matching pursuit (MP) decomposition is proposed and used to detect transitions between these two states. The new measure, referred to as weighted structural complexity (WSC), was used for the detection of seizures in 30 newborn EEG records. Multiple IIR filters and an MP-based filter were designed and used to remove artifacts from the EEG data. Geometrical correlation between the EEG data channels was applied to reduce the number of false detections caused by remnant artifacts. The seizure detector's performance was assessed using several epoch-based (e.g., accuracy) and event-based (GDR = good detection rate and FD/h = false detections per hour) metrics. Results: Compared to the neurologist marking, the proposed detector was able to detect EEG seizures with 94% accuracy, 90.9% GDR, and 0.14 FD/h (95% CI: [0.06, 0.34]). Conclusions: The high performance of the MP-based detector may have significant implications for the accurate diagnosis of neonatal seizures and the appropriate use of anticonvulsants and ongoing clinical assessment and care of the newborn.
AB - Background and objective: In newborns, it is often difficult to accurately differentiate between seizure and non-seizure based solely on clinical manifestations. This highlights the importance of electroencephalogram (EEG) in the recognition and management of neonatal seizures. This paper proposes an effective algorithm for the detection of neonatal seizure using multichannel EEG. Methods: Neonatal EEG changes morphology as it alternates between seizure and non-seizure states. A new signal complexity measure based on matching pursuit (MP) decomposition is proposed and used to detect transitions between these two states. The new measure, referred to as weighted structural complexity (WSC), was used for the detection of seizures in 30 newborn EEG records. Multiple IIR filters and an MP-based filter were designed and used to remove artifacts from the EEG data. Geometrical correlation between the EEG data channels was applied to reduce the number of false detections caused by remnant artifacts. The seizure detector's performance was assessed using several epoch-based (e.g., accuracy) and event-based (GDR = good detection rate and FD/h = false detections per hour) metrics. Results: Compared to the neurologist marking, the proposed detector was able to detect EEG seizures with 94% accuracy, 90.9% GDR, and 0.14 FD/h (95% CI: [0.06, 0.34]). Conclusions: The high performance of the MP-based detector may have significant implications for the accurate diagnosis of neonatal seizures and the appropriate use of anticonvulsants and ongoing clinical assessment and care of the newborn.
KW - Artifact removal
KW - EEG
KW - Matching pursuit
KW - Newborn seizure
KW - Time-frequency analysis
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U2 - 10.1016/j.cmpb.2022.107014
DO - 10.1016/j.cmpb.2022.107014
M3 - Article
C2 - 35849896
AN - SCOPUS:85134181212
SN - 0169-2607
VL - 224
JO - Computer Methods and Programs in Biomedicine
JF - Computer Methods and Programs in Biomedicine
M1 - 107014
ER -