| Literature DB >> 33709264 |
Shaurya Taran1, Wael Ahmed2, Ruxandra Pinto2, Esther Bui3, Lara Prisco4,5, Cecil D Hahn6, Marina Englesakis7, Victoria A McCredie8,2,9,10.
Abstract
PURPOSE: We systematically reviewed existing critical care electroencephalography (EEG) educational programs for non-neurologists, with the primary goal of reporting the content covered, methods of instruction, overall duration, and participant experience. Our secondary goals were to assess the impact of EEG programs on participants' core knowledge, and the agreement between non-experts and experts for seizure identification. SOURCE: Major databases were searched from inception to 30 August 2020. Randomized controlled trials, cohort studies, and descriptive studies were all considered if they reported an EEG curriculum for non-neurologists in a critical care setting. Data were presented thematically for the qualitative primary outcome and a meta-analysis using a random effects model was performed for the quantitative secondary outcomes. PRINCIPALEntities:
Keywords: brain injuries; critical care; electroencephalography; medical education; neurophysiology; seizures
Mesh:
Year: 2021 PMID: 33709264 PMCID: PMC7952081 DOI: 10.1007/s12630-021-01962-y
Source DB: PubMed Journal: Can J Anaesth ISSN: 0832-610X Impact factor: 6.713
Figure 1Simplified schematic of EEG forms. EEG = electroencephalogram
Figure 2Study selection
Characteristics of included studies
| Author (year) | Number of centres | Study setting | Participant background | Number of participants | EEG program characteristics | |||||
|---|---|---|---|---|---|---|---|---|---|---|
| Recording | Data used for EEG teaching | Primary goal of training | Teaching methods | Assessment method | Length of program | |||||
| RCT | ||||||||||
| Chari | 3 | ED | ED physicians | 30 | Intermittent EEG | Raw waveform | Seizure identification | Didactic lectures, PowerPoint | Written quiz | N/A |
| Cohort studies | ||||||||||
| Amorim | 2 | Adult Neuro-ICU | ICU nurses | 33 | Continuous EEG | Processed—CDSA | Seizure identification | Small group discussion | Written quiz | <3 hours |
| Chau | 1 | Adult Neuro-ICU | ICU fellows | 9 | Continuous EEG | Raw waveform | EEG theory and waveform interpretation | Bedside/interactive, didactic lectures, one-on-one review | Written quiz | 3–6 hrs |
| Citerio | 2 | Adult Neuro-ICU | ICU physicians | 86 | Continuous EEG | Both raw (cEEG) and processed (CDSA, aEEG) | Recognition of seizures, artefacts, sedation, and symmetry | Case-based learning, didactic lectures | N/A | N/A |
| Dericioglu | 1 | Adult Neuro-ICU | ICU nurses, neurology residents | 4 | Continuous EEG with video | Processed—CDSA and aEEG | Seizure identification | One-on-one review, small group discussion | Off-line review of processed EEG | 3–6 hrs |
| Fahy | 1 | Adult Neuro-ICU and intraoperative | Anesthesiology residents | 33 | Intermittent and real- time EEG | Raw waveform | EEG theory and waveform interpretation | Bedside/interactive, didactic lectures, one-on-one review | Written quiz | >1 day |
| Fahy | 1 | Adult Neuro-ICU and intraoperative | Anesthesiology residents | 8 | Intermittent and real-time EEG | Raw waveform | EEG theory and waveform interpretation | Bedside/interactive, one-on-one review | Written quiz | >1 day |
| Fahy | 1 | Adult Neuro-ICU and intraoperative | Anesthesiology residents | 81 | Intermittent EEG | Raw waveform | EEG theory | Didactic lectures | Written quiz | >1 day |
| Fahy | 1 | Adult Neuro-ICU | ICU fellows | 9 | Intermittent EEG | Raw waveform | EEG theory and waveform interpretation | Self-study, small group discussion | Written quiz | N/A |
| Seiler | 1 | Adult Neuro-ICU | ICU nurses | 47 | Continuous EEG | Raw waveform | EEG theory | PowerPoint, small group discussion | Written quiz | N/A |
| Kang | 1 | Adult Neuro-ICU | ICU nurses | 20 | Continuous EEG | Processed—aEEG and rhythmicity spectrogram (similar to CDSA) | Seizure identification | Bedside/interactive, PowerPoint | Real- time/bedside interpretation | <3 hr |
| Herta | 2 | Adult ICU | ICU nurses, other | 18 | Continuous EEG with video | Processed—data displayed as aEEG on Neurotrend monitor | Seizure identification | Didactic lectures | Written quiz | <3 hr |
| Kyriakopoulos | 1 | Adult ICU | Neurology residents | 16 | Intermittent EEG | Raw waveform | Seizure identification | Self-study, bedside/interactive, small group | Real- time/bedside interpretation | N/A |
| Legriel | 6 | Adult ICU | Attending physicians, fellows, residents, medical students, nurses | 250 | Continuous EEG | Raw waveform | EEG theory and waveform interpretation | Didactic lectures, self-study | Written quiz | <3 hr |
| Leira | 1 | Adult ICU | ICU fellows, ICU nurses, neurosurgery residents, neurology residents, other | 50 | Intermittent EEG | Raw waveform | EEG theory and waveform interpretation | Didactic lectures, PowerPoint | Written quiz | N/A |
| Lybeck | 1 | Adult ICU | ICU physicians | 5 | Continuous EEG | Both raw (cEEG) and processed (aEEG) | EEG waveform interpretation | Bedside/interactive, didactic lectures, case-based learning | Real- time/bedside interpretation | 7 hr–1 day |
| Nitzschke | 1 | Adult ICU | ICU physicians | 4 | Continuous EEG | Processed—aEEG displayed on Neuroscreen monitor | Seizure identification | Bedside/interactive, didactic lectures, one-on-one review, question and answer | Real- time/bedside interpretation | <3 hr |
| Swisher | 1 | Adult ICU | ICU nurses, other | 17 | Continuous EEG | Both raw (cEEG) and processed (CDSA, aEEG) displayed on Persyst | Seizure identification | Didactic lectures, PowerPoint | Real- time/bedside interpretation | <3 hr |
| Topjian | 1 | Adult ICU | ICU physicians, ICU fellows, ICU nurses | 39 | Continuous EEG | Processed—CDSA using Persyst | Seizure identification | Didactic lectures, PowerPoint, question and answer | Real- time/bedside interpretation | N/A |
| Bourgoin | 1 | Pediatric ICU | ICU nurses | 51 | Continuous EEG | Processed—aEEG | Recognition of pathologic pattern (severely altered background or seizures) | Online modules, small group discussion | Real-time/bedside interpretation | 3–6 hr |
| Du Pont-Thibodeau | 1 | Pediatric ICU | ICU physicians, ICU fellows, nurses | 23 | Continuous EEG | Processed—aEEG and CDSA | Seizure identification | Didactic lectures, PowerPoint | Written quiz | <3 hr |
| Lalgudi Ganesan | 1 | Pediatric ICU | ICU fellows, ICU nurses, other | 12 | Continuous EEG | Processed—aEEG and CDSA | Seizure identification | Bedside/interactive, one-on-one review | Written quiz | <3 hr |
| Goswami | 2 | Neonatal ICU | ICU nurses | 230 | Continuous EEG with video | Both raw (cEEG) and processed (aEEG) displayed using Persyst | EEG lead application and monitor setup | Bedside/interactive | N/A | N/A |
| Griesmaier | 2 | Neonatal ICU | ICU physicians, ICU nurses, other residents | 60 | Continuous EEG | Processed—aEEG | Seizure identification | Didactic lectures | Written quiz | 3–6 hr |
| Guan | 1 | Pediatric ICU | ICU physicians, ICU nurses, other | 6 | Continuous EEG with video | Processed—aEEG | Seizure identification | Didactic lectures, textbook readings | Real- time/bedside interpretation | >1 day |
| Poon | 1 | Neonatal ICU | ICU physicians, ICU nurses | 37 | Continuous EEG | Processed—aEEG | EEG theory and waveform interpretation | Didactic lectures, online modules, PowerPoint, small group discussion | Written quiz | 3–6 hr |
| Rennie | 1 | Neonatal ICU | ICU physicians | 4 | Continuous EEG with video | Processed—cerebral function monitor (aEEG) | Seizure identification | Bedside/interactive, one-on-one review, question and answer | Real- time/bedside interpretation | 3–6 hr |
| Descriptive studies | ||||||||||
| Sacco | 1 | Neonatal ICU | ICU nurses | N/A | Continuous EEG | Processed—aEEG | Seizure identification | Didactic lectures, question and answer, simulation | Written quiz | 7 hr–1 day |
| Whitelaw | 1 | Neonatal ICU | ICU physicians | N/A | Continuous EEG | Raw EEG | EEG theory and waveform interpretation | Bedside/interactive, case-based learning, didactic lectures, question and answer, simulation | Written quiz | 7 hr–1 day |
aEEG = amplitude-integrated electroencephalogram; CDSA = colour density spectral array; cEEG = continuous electroencephalogram; EEG = electroencephalogram; ICU = intensive care unit; N/A = not applicable; NR = not reported; RCT = randomized controlled trial
Figure 3Forest plot assessing performance change after undergoing a training program. CI confidence interval, NIH National Institute of Health, RE random effects
Figure 4Forest plot for agreement for seizure identification between non-experts and experts. CI confidence interval, NIH National Institute of Health, RE random effects
NIH quality assessment of non-descriptive observational studies
N/A = not applicable; NIH = National Institute of Health
For observational cohort studies
1. Was the research question or objective in this paper clearly stated?
2. Was the study population clearly specified and defined?
3. Was the participation rate of eligible persons at least 50%?
4. Were all the subjects selected or recruited from the same or similar populations (including the same time period)? Were inclusion and exclusion criteria for being in the study pre-specified and applied uniformly to all participants?
5. Was a sample size justification, power description, or variance and effect estimates provided?
6. For the analyses in this paper, were the exposure(s) of interest measured prior to the outcome(s) being measured?
7. Was the timeframe sufficient so that one could reasonably expect to see an association between exposure and outcome if it existed?
8. For exposures that can vary in amount or level, did the study examine different levels of the exposure as related to the outcome (e.g., categories of exposure, or exposure measured as continuous variable)?
9. Were the exposure measures (independent variables) clearly defined, valid, reliable, and implemented consistently across all study participants?
10. Was the exposure(s) assessed more than once over time?
11. Were the outcome measures (dependent variables) clearly defined, valid, reliable, and implemented consistently across all study participants?
12. Were the outcome assessors blinded to the exposure status of participants?
13. Was loss to follow-up after baseline 20% or less?
14. Were key potential confounding variables measured and adjusted statistically for their impact on the relationship between exposure(s) and outcome(s)?
For pre-post studies
1. Was the study question or objective clearly stated?
2. Were eligibility/selection criteria for the study population pre-specified and clearly described?
3. Were the participants in the study representative of those who would be eligible for the test/service/intervention in the general or clinical population of interest?
4. Were all eligible participants that met the pre-specified entry criteria enrolled?
5. Was the sample size sufficiently large to provide confidence in the findings?
6. Was the test/service/intervention clearly described and delivered consistently across the study population?
7. Were the outcome measures pre-specified, clearly defined, valid, reliable, and assessed consistently across all study participants?
8. Were the people assessing the outcomes blinded to the participants’ exposures/interventions?
9. Was the loss to follow-up after baseline 20% or less? Were those lost to follow-up accounted for in the analysis?
10. Did the statistical methods examine changes in outcome measures from before to after the intervention? Were statistical tests done that provided p values for the pre-to-post changes?
11. Were outcome measures of interest taken multiple times before the intervention and multiple times after the intervention (i.e., did they use an interrupted time-series design)?
12. If the intervention was conducted at a group level (e.g., a whole hospital, a community, etc.) did the statistical analysis take into account the use of individual-level data to determine effects at the group level?
Cohort studies were assigned a score of “good” if they met all of questions 4, 9, and 11; fair if they met one or two of questions 4, 9, and 11; and poor if they met none of questions 4, 9, and 11
Pre-post studies were assigned a score of “good” if they met all of questions 6, 10, and 11; fair if they met one or two of questions 6, 10, and 11; and poor if they met none of questions 6, 7, and 11