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Application of Tsallis Entropy to EEG: Quantifying the Presence of Burst Suppression After Asphyxial Cardiac Arrest in Rats

Burst suppression (BS) activity in EEG is clinically accepted as a marker of brain dysfunction or injury. Experimental studies in a rodent model of brain injury following asphyxial cardiac arrest (CA) show evidence of BS soon after resuscitation, appearing as a transitional recovery pattern between...

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Published in:IEEE transactions on biomedical engineering 2010-04, Vol.57 (4), p.867-874
Main Authors: Zhang, Dandan, Jia, Xiaofeng, Ding, Haiyan, Ye, Datian, Thakor, Nitish V.
Format: Article
Language:English
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Summary:Burst suppression (BS) activity in EEG is clinically accepted as a marker of brain dysfunction or injury. Experimental studies in a rodent model of brain injury following asphyxial cardiac arrest (CA) show evidence of BS soon after resuscitation, appearing as a transitional recovery pattern between isoelectricity and continuous EEG. The EEG trends in such experiments suggest varying levels of uncertainty or randomness in the signals. To quantify the EEG data, Shannon entropy and Tsallis entropy (TsEn) are examined. More specifically, an entropy-based measure named TsEn area (TsEnA) is proposed to reveal the presence and the extent of development of BS following brain injury. The methodology of TsEnA and the selection of its parameter are elucidated in detail. To test the validity of this measure, 15 rats were subjected to 7 or 9 min of asphyxial CA. EEG recordings immediately after resuscitation from CA were investigated and characterized by TsEnA. The results show that TsEnA correlates well with the outcome assessed by evaluating the rodents after the experiments using a well-established neurological deficit score (Pearson correlation = 0.86, p ¿ 0.01 ). This research shows that TsEnA reliably quantifies the complex dynamics in BS EEG, and may be useful as an experimental or clinical tool for objective estimation of the gravity of brain damage after CA.
ISSN:0018-9294
1558-2531
DOI:10.1109/TBME.2009.2029082