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Lucie Hertz-Pannier

Publications and source records attributed to Lucie Hertz-Pannier.

3 recordsLinked to original sources

Investigating cerebral anomalies in preterm infants and associated risk factors with magnetic resonance imaging at term-equivalent age

Background: Being born very or extreme preterm is a major source of cerebral anomalies and neurodevelopmental disorders, whose occurrence depends on many perinatal factors. A better understanding of these factors could be provided by cerebral Magnetic Resonance Imaging (MRI) at term-equivalent age (TEA). Objective: To investigate, through cerebral TEA-MRIs, the relationship between the main perinatal factors, the occurrence of cerebral anomalies, and cerebral volumetry. Methods: We assembled a cohort of preterm babies born before 32 weeks of gestation who underwent a cerebral TEA-MRI. We assessed cerebral anomalies using a radiological scoring system -- the Kidokoro scoring -- and performed cerebral volumetry. We investigated the relationships between 9 clinical factors (birth characteristics, resuscitation treatments{\ldots}), Kidokoro scores, and brain volumes. Results: Among 110 preterms who underwent a cerebral MRI at TEA, only 6% suffered moderate-to-severe brain anomalies. We identified mechanical ventilation as a risk factor for cerebral anomalies (adjusted Odds-Ratio aOR = 4.6, 95% Confidence Interval CI [1.7-12.8]) and prolonged parenteral nutrition as a protective factor for white matter anomalies (aOR = 0.2, 95%CI [0.1-0.8]). Mechanical ventilation (p = 0.01) and being born small for gestational age (p < 0.001) were risk factors for the reduction of cerebral volumes. An increase in brain lesion severity was associated with decreased cerebral volumes (p = 0.016). Conclusion: Our study highlights the importance of treatment-related perinatal factors on the occurrence of cerebral anomalies in very and extreme preterms, and the interest in using both qualitative (Kidokoro scoring) and quantitative (volumetry) MRI-tools.

q-bio.NC↗

Neuro-imagerie néonatale : quelle valeur prédictive ?

Premature birth and various pre- and peri-natal stresses can lead to a variety of brain lesions and have clearly been identified as major risk factors for neurodevelopmental disorders, with variable but multiple consequences that can significantly alter the functional outcome of children in the short, medium and long term. The main aim of the various diagnostic and prognostic markers available, based in particular on clinical and neuroimaging data, is to facilitate early detection of the various disorders and to optimise the follow-up and management of these babies at risk of deficiencies.

q-bio.NC↗

Robust imaging of hippocampal inner structure at 7T: in vivo acquisition protocol and methodological choices

OBJECTIVE:Motion-robust multi-slab imaging of hippocampal inner structure in vivo at 7T.MATERIALS AND METHODS:Motion is a crucial issue for ultra-high resolution imaging, such as can be achieved with 7T MRI. An acquisition protocol was designed for imaging hippocampal inner structure at 7T. It relies on a compromise between anatomical details visibility and robustness to motion. In order to reduce acquisition time and motion artifacts, the full slab covering the hippocampus was split into separate slabs with lower acquisition time. A robust registration approach was implemented to combine the acquired slabs within a final 3D-consistent high-resolution slab covering the whole hippocampus. Evaluation was performed on 50 subjects overall, made of three groups of subjects acquired using three acquisition settings; it focused on three issues: visibility of hippocampal inner structure, robustness to motion artifacts and registration procedure performance.RESULTS:Overall, T2-weighted acquisitions with interleaved slabs proved robust. Multi-slab registration yielded high quality datasets in 96 % of the subjects, thus compatible with further analyses of hippocampal inner structure.CONCLUSION:Multi-slab acquisition and registration setting is efficient for reducing acquisition time and consequently motion artifacts for ultra-high resolution imaging of the inner structure of the hippocampus.

cs.CV↗