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Published on: August 25, 2022
Deep cerebral venous abnormalities in premature babies with GMH-IVH: a single-centre retrospective study
Thomas Kent1, Vikash Sinha2, Elvan Ceyhan3
1University of Florida College of Medicine, Gainesville, Florida, USA thomaskent@ufl.edu.
Insights
Deep venous abnormalities are linked to germinal matrix haemorrhage/intraventricular haemorrhage (GMH-IVH) in preterm infants. These abnormalities worsen with increasing GMH-IVH grade, suggesting a significant association.
Area of Science:
- Neuroimaging
- Pediatric Radiology
- Cerebral Venous Anatomy
Background:
- Germinal matrix haemorrhage/intraventricular haemorrhage (GMH-IVH) is a complex injury in preterm neonates.
- Previous research has identified normal variants in deep cerebral venous anatomy associated with GMH-IVH using MRI susceptibility weighted imaging (SWI).
Purpose of the Study:
- To compare deep venous systems in preterm neonates with GMH-IVH to controls using SWI.
- To identify novel retrospective SWI imaging findings related to GMH-IVH.
Main Methods:
- Retrospective evaluation of 3T MRI SWI and phase imaging in 56 preterm neonates with GMH-IVH and 27 controls.
- Scoring of venous irregularities (patency, susceptibility, collaterals) at eight specific venous locations.
- Statistical analysis of variables and inter-rater reliability assessment.
Main Results:
- Deep venous abnormalities were significantly more prevalent in neonates with GMH-IVH.
- A significant increase in decreased venous patency, increased lumen susceptibility, and collateral formation was observed with higher GMH-IVH grades.
- Venous abnormalities positively correlated with GMH-IVH grade (I-IV).
Conclusions:
- Deep venous abnormalities are significantly correlated with GMH-IVH and its severity.
- Further research is required to establish a causal relationship between venous abnormalities and GMH-IVH.
Purpose:
Germinal matrix haemorrhage/intraventricular haemorrhage (GMH-IVH) is a multifactorial injury with both anatomic and haemodynamic involvement. Normal variants in preterm deep cerebral venous anatomy associated with GMH-IVH have been previously described using MRI susceptibility weighted imaging (SWI). The aims of this study were to use SWI to compare the deep venous systems of a cohort of preterm neonates with various grades of GMH-IVH to a group of age-matched controls without GMH-IVH and to present novel retrospective SWI imaging findings.
Methods:
A neuroradiologist retrospectively evaluated 3T MRI SWI and phase imaging of 56 preterm neonates with GMH-IVH (14 of each grade) and 27 controls without GMH-IVH, scoring the venous irregularities according to three variables: decreased venous patency, increased lumen susceptibility and the presence of collaterals. Eight different venous locations, including indicated bilateral components, were evaluated: straight sinus, vein of galen, internal cerebral, direct lateral, thalamostriate, atrial and the anterior septal veins. Variables were analysed for statistical significance. Inter-rater reliability was determined via subset evaluation by a second paediatric radiologist.
Results:
Deep venous abnormalities were significantly more common in patients with GMH-IVH, with Wilcoxon Rank Sum Test demonstrating significant increase with GMH-IVH for total decreased venous patency (W=0, p<0.0001), increased lumen susceptibility and collateral formation. Venous abnormalities were also positively correlated with an increase in GMH-IVH grade from I to IV (patency, ρ=0.782, p<0.01) (increased lumen susceptibility, ρ=0.739, p<0.01) (collaterals, ρ=0.649, p<0.01), not just GMH-IVH alone.
Conclusion:
Deep venous abnormalities are significantly correlated with GMH-IVH alone and an increase in GMH-IVH grade. Further study is needed to determine cause and effect.
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