Conventional video-electroencephalography (cEEG) is the reference standard for diagnosing and managing neonatal seizures. However, continuous bedside cEEG services are not available in most neonatal units. Hence, an alternative and relatively simple method called amplitude-integrated EEG (aEEG), which uses a limited number of scalp electrodes, has become popular. aEEG allows continuous bedside monitoring of the electrical activity of the brain in neonates. The primary objective of the review was to assess the accuracy of aEEG against the reference standard cEEG for the detection of 'neonates with seizures' and 'individual seizures'. Detection of 'neonates with seizures' refers to the ability of the test to correctly identify a 'neonate' as 'seizure positive' or 'seizure negative' based on the detection of at least one seizure episode in the entire aEEG recording. Detection of 'individual seizures' refers to the ability of the test to correctly identify 'individual' seizure episodes within the same neonate rather than just diagnosing the neonate as 'seizure positive' or 'seizure negative'. We searched CENTRAL, MEDLINE, Embase, clinical trials registries, and grey literature (Open Grey, Trove, and American Doctoral Dissertations) to 26 July 2022. We did not apply any language or publication status restrictions or any other filters. We included prospective and retrospective studies investigating the accuracy of aEEG (index test) against the reference standard cEEG for the detection of neonatal seizures. To be eligible for inclusion, the studies must have compared aEEG with simultaneously recorded cEEG. There was no restriction on the number of leads, use of raw EEG traces, or experience and training of an aEEG interpreter. cEEG should have been recorded using at least nine electrodes and interpreted by a qualified person experienced in the interpretation of neonatal cEEG. Working independently, two review authors collected data from the included studies in a prespecified form and assessed the quality of the included studies using the QUADAS-2 tool. For the outcome of 'neonates with seizures', we used a bivariate mixed-effects regression model to conduct a meta-analysis to derive pooled sensitivity, specificity, positive and negative likelihood ratios (LR), and their respective 95% confidence intervals (CI). We generated a summary receiver operating characteristic (SROC) curve to display the results of individual studies. We calculated post-test probabilities based on Bayes' theorem through Fagan nomograms. For the outcome of 'individual seizures', pooling of data was not possible because of the 'unit of analysis' issue. Instead, we performed a narrative synthesis. We assessed the certainty of the evidence using GRADE guidelines. We included 16 studies (562 infants) in the systematic review, of which only two studies interpreted the aEEGs prospectively at the bedside. Out of 16 studies, three studies (97 infants) described the accuracy of aEEG only for detecting 'infants with seizures', three studies (72 infants) described only 'individual seizures', while 10 studies (393 infants) described the accuracy of aEEG for detecting both. Ten of 16 studies were conducted in term and late preterm infants. Half of the included studies did not use raw EEG traces. Fourteen studies reported outcomes based only on retrospective interpretation. Ten of 16 studies used four electrodes (making this the most common approach amongst the included studies), and 10 studies' aEEG recordings exceeded six hours. Only two included studies used a seizure detection algorithm. In 14 studies, a neonatal or neurology consultant performed aEEG interpretation, and most (in 10 of 14 studies) had prior experience in aEEG interpretation. Accuracy of aEEG to diagnose 'neonates with seizures'. The only two prospective studies (53 participants) which interpreted aEEGs 'live' at the bedside, reported sensitivities of zero and 0.57 and specificities of 0.82 and 0.92, respectively. Meta-analysis of 13 studies (490 neonates) found that aEEG had a pooled sensitivity of 0.71 (95% CI 0.57 to 0.83), specificity of 0.84 (95% CI 0.59 to 0.95), positive LR of 4.50 (95% CI 1.55 to 13.04), and negative LR of 0.34 (95% CI 0.22 to 0.53) for the detection of 'neonates with seizures'. However, when we analysed only studies with low risk of bias (3 studies), sensitivity (0.56, 95% CI 0.02 to 0.99) and specificity (0.78, 95% CI 0.60 to 0.90) were even lower. There was significant statistical heterogeneity, which could not be explained based on threshold effect and exploratory analyses of forest plots. We graded the certainty of the evidence as low, in view of the high or unclear risk of bias in many studies, imprecision, and significant heterogeneity. Accuracy of aEEG to detect 'individual seizures' in neonates. The reported sensitivities of aEEG for the detection of 'individual seizures' ranged from 0 to 0.86 (13 studies, 465 neonates). We rated the certainty of the evidence as low. The common causes of missed seizures on aEEG (i.e. false negative) as reported by studies were short duration of seizures, localisation of seizures away from aEEG leads, low voltage, and inexperienced interpreter. The false-positive rates were high when interpreted live at the bedside and if the interpreters were inexperienced. Artefacts resulting from muscle movement, patting, hiccups, and insufficient electrode attachment were other common causes of false-positive results. Low-certainty evidence suggests that aEEG has only moderate sensitivity and specificity for detecting 'neonates with seizures', and its ability to detect 'individual seizures' varies widely. These findings suggest that aEEG may not be sufficiently accurate for diagnosing neonatal seizures as it can under-diagnose or over-diagnose seizures. Studies with low risk of bias are needed to address the issue definitively.
Rakshasbhuvankar et al. (Mon,) studied this question.