| Normal/Mild | Moderate | Severe |
---|---|---|---|
Preterm injury | Â | Â | Â |
• Cranial ultrasound scan (cUSS) | • Normal | • Grade III IVH | • Grade IV IVH |
• Grade I/II Intraventricular haemorrhage (IVH) | • Non-cystic Periventricular leucomalacia (PVL) | • Periventricular haemorrhage infarction (PVHI) | |
• Ventricular index (VI) < 13 mm Term equivalent age (TEA) OR | • VI 13-15 mm TEA OR | • Cystic PVL | |
• VI < 97th percentile for corrected gestational age (CGA) | • VI >97th percentile but < 4 mm above 97th percentile for CGA | • Subcortical leucomalacia | |
• VI at TEA >15 mm OR | |||
• VI >4 mm above 97th percentile for CGA | |||
• Basal ganglia (BG) lesions | |||
• Focal infarction | |||
Term hypoxic ischaemic encephalopathy | Â | Â | Â |
• Magnetic resonance imaging (MRI) | • Focal subtle abnormalities of BG with normal appearance of the posterior limb of the internal capsule (PLIC) | • Multi-focal lesions in BG with equivocal or abnormal signal intensity within PLIC | • Widespread abnormalities involving all Basal ganglia-Thalamus (BGT) structures and PLIC |
• cUSS where MRI unavailable | • Periventricular white matter changes difficult to differentiate from normal appearances and therefore not classified as abnormal | • Small focal lesions of without loss of grey matter (GM)/WM differentiation. | • Larger areas of abnormality with loss of GM/WM differentiation, consistent with infarction |
• Changes confined to cerebral cortex and subcortical white matter (WM) |  | • Central grey matter hyperechogenicity +/− more extensive cortical and subcortical hyperechogenicity | |
Term infarction | Â | Â | Â |
• MRI (cUSS where MRI unavailable) |  | • Focal, non-territorial infarct | • Territorial infarct |