Abstract
To obtain insight into the severity of lesions and for better prognostication, it is recommended that a scoring system be applied for GMH-IVH, PVE and PVL. These scoring systems are presented in Appendices 6.1–6.3, respectively.
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References
De Vries LS et al (1992) The spectrum of leukomalacia using cranial ultrasound. Behav Brain Res 49:1–6
Van Wezel-Meijler G et al (1998) Magnetic resonance imaging of the brain in premature infants during the neonatal period. Normal phenomena and reflection of mild ultrasound abnormalities. Neuropediatrics 29:89–96
Volpe JJ (1989) Intraventricular hemorrhage in the premature infant – current concepts. II. Ann Neurol 25:109–116
Further Reading
Groenendaal F et al (2010) Complications affecting preterm neonates from 1991 to 2006: what have we gained? Acta Paediatr 99:354–358
Leijser LM et al (2009) Brain imaging findings in very preterm infants throughout the neonatal period: Part I. Incidences and evolution of lesions, comparison between ultrasound and MRI. Early Hum Dev 85:101–109
Leijser LM et al (2010) Is sequential cranial ultrasound reliable for detection of white matter injury in very preterm infants? Neuroradiology 52:397–406
Miller SP et al (2003) Comparing the diagnosis of white matter injury in premature newborns with serial MR imaging and transfontanel ultrasonography findings. AJNR Am J Neuroradiol 24(8):1661–1669
Van Wezel-Meijler G et al (2011) Ultrasound detection of white matter injury in very preterm neonates: practical implications. Dev Med Child Neurol 53 (suppl4):29–34
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Appendices
Appendix 6.1: Classification of Germinal Matrix – Intraventricular Haemorrhage
Adapted from Volpe (1989):
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Grade 1: GMH with no or minimal IVH (Fig. 6.1)
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Grade 2: IVH (10–50% of the ventricular area on parasagittal view) (Fig. 6.2, see also Fig. 4.7b)
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Grade 3: IVH (>50% of the ventricular area on parasagittal view, usually distends the lateral ventricle) (Fig. 6.3)
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Separate notation: PHVD (Fig. 6.4, see also Figs. 4.7c and 4.8)
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Separate notation: concomitant periventricular echodensity (including location and extent), referred to as “IPE” (intraparenchymal echodensity), representing PVHI (Fig. 6.5)
Appendix 6.2: Classification of Periventricular White Matter Echodensity (PVE)
Adapted from van Wezel-Meijler et al. (1998):
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Grade 0 PVE: normal echogenicity of the periventricular white matter (the echogenicity of the periventricular white matter being less than that of the choroid plexus) (Fig. 6.6, see also Figs. 3.3, 3.5, 4.2, 4.6a, b, 4.7a)
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Grade 1 PVE: moderately increased echogenicity of the periventricular white matter, the affected region (or smaller areas within the affected region) being (almost) as bright as the choroid plexus (Figs. 6.7 and 6.8 see also Figs. 3.6, 4.5c, 5.1f)
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Grade 2 PVE: seriously increased echogenicity, the affected region (or smaller areas within the affected region) being brighter than the choroid plexus (Fig. 6.9, also see Figs. 4.5d, e, 5.1b, 5.2b)
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Separate notation: homogeneous, inhomogeneous (For inhomogeneous PVE see Figs. 4.5d, e, 5.1b, f, 5.2b, 5.3a, 6.9)
Appendix 6.3: Classification of Periventricular Leukomalacia
According to de Vries et al. (1992):
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Grade 1: transient PVE persisting for ≥7 days
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Grade 2: transient PVE evolving into small, localised fronto-parietal cysts (Fig. 6.10)
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Grade 3: PVE evolving into extensive periventricular cystic lesions (Fig. 6.11)
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Grade 4: densities extending into the deep white matter evolving into extensive cystic lesions (Fig. 6.12)
It should be noted that the incidence of “classic” PVL where this classification refers to has importantly declined over the last decade and that there has been a shift towards a more subtle, diffuse form of white matter injury (so-called diffuse white matter injury). For the detection of diffuse white matter injury, MRI is needed as it is not reliably depicted by cUS (see also Chapter 5).
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Meijler, G. (2012). Scoring Systems. In: Neonatal Cranial Ultrasonography. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-21320-5_6
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