Electroencephalographic markers of brain development during sevoflurane anaesthesia in children up to 3 years old.
Electroencephalographic markers of brain development during sevoflurane anaesthesia in children up to 3 years old.
复制标题
DOI:
10.1016/j.bja.2018.01.037
复制
发表时间:
2018-06
影响因子:
9.8
通讯作者:
Berde CB
中科院分区:
文献类型:
--
作者:
Cornelissen L;Kim SE;Lee JM;Brown EN;Purdon PL;Berde CB
General anaesthetics generate spatially defined brain oscillations in the EEG that relate fundamentally to neural-circuit architecture. Few studies detailing the neural-circuit activity of general anaesthesia in children have been described. The study aim was to identify age-related changes in EEG characteristics that mirror different stages of early human brain development during sevoflurane anaesthesia. Multichannel EEG recordings were performed in 91 children aged 0–3 yr undergoing elective surgery. We mapped spatial power and coherence over the frontal, parietal, temporal, and occipital cortices during maintenance anaesthesia. During sevoflurane exposure: (i) slow–delta (0.1–4 Hz) oscillations were present in all ages, (ii) theta (4–8 Hz) and alpha (8–12 Hz) oscillations emerge by ∼4 months, (iii) alpha oscillations increased in power from 4 to 10 months, (iv) frontal alpha-oscillation predominance emerged at ∼6 months, (v) frontal slow oscillations were coherent from birth until 6 months, and (vi) frontal alpha oscillations became coherent ∼10 months and persisted in older ages. Key developmental milestones in the maturation of the thalamo-cortical circuitry likely generate changes in EEG patterns in infants undergoing sevoflurane general anaesthesia. Characterisation of anaesthesia-induced EEG oscillations in children demonstrates the importance of developing age-dependent strategies to monitor properly the brain states of children receiving general anaesthesia. These data have the potential to guide future studies investigating neurodevelopmental pathologies involving altered excitatory–inhibitory balance, such as epilepsy or Rett syndrome.
登录
查看更多内容
影响因子:
8.8
作者:
Blain-Moraes S;Tarnal V;Vanini G;Alexander A;Rosen D;Shortal B;Janke E;Mashour GA
通讯作者:
Mashour GA
影响因子:
3
作者:
Hight, Darren;Voss, Logan J.;Sleigh, Jamie
通讯作者:
Sleigh, Jamie
影响因子:
7.7
作者:
Cornelissen L;Kim SE;Purdon PL;Brown EN;Berde CB
通讯作者:
Berde CB
DOI:
10.1073/pnas.1017069108
发表时间:
2010-12-28
影响因子:
11.1
作者:
Ching, ShiNung;Cimenser, Aylin;Kopell, Nancy J.
通讯作者:
Kopell, Nancy J.
影响因子:
9.8
作者:
Gaskell, A. L.;Hight, D. F.;Sanders, R. D.
通讯作者:
Sanders, R. D.