Table 3.
Current non-invasive clinical technologies for neurologic monitoring in patients on ECMO.
Monitoring technique | Description |
---|---|
Neurological pupil index (NPi) | • Automatedly assesses pupil size • Neurological deterioration is always associated with a sudden drop in NPi value below 2.8–3.0 • Influenced by ambient light and high concentrations of opioids |
Cerebral near-infrared spectroscopy | • Monitors of regional oxygen saturation (rSO2) • Decreases from baseline (>25% drop) and a large right-left rSO2 difference (>10%) may predict acute neurologic injury • Affected by ambient light and skin color |
Electroencephalography (EEG) | • Assess neurologic status • Continuous EEG can detect non-convulsive seizures or status epilepticus • Occurrence of suppressed EEG background is associated with poor neurological outcome and mortality • Early Standard EEG can be used for prognostication • As the results of EEG depend on technician's experience and expertise, quantitative EEG can be applied in the future studies |
Transcranial doppler (TCD) ultrasound | • Measures the pattern of cerebral blood flow, hemodynamic reserve, and microembolic signals • Effectiveness of TCD is uncertain with continuous, non-pulsatile, arterial flow in some patients on venoarterial ECMO • Detects intracranial artery microembolic signals, which may eventually lead to acute ischemic stroke |
Biomarkers | • Serum protein biomarkers of cerebral injury, such as NSE, and S100B • Serial measurement can increase diagnostic accuracy • Serum half-life of NSE is long, and can be affected by hemolysis or cancer • S100B can be released from not only brain but also heart, bone and adipose tissue |
Neuroimaging | • Cranial CT is the main technology for revealing and excluding acute cerebral injury • MRI is limited due to hardware incompatibility |
ECMO, extracorporeal membrane oxygenation; NSE, neuron-specific enolase; CT, computerized tomography; MRI, magnetic resonance imaging.