Term newborns: How imaging contributes to the understanding of the development of brain injury after birth asphyxia
Pia Wintermark1

1McGill University

Synopsis

Term newborns are at risk to develop brain injury. Magnetic resonance imaging has permitted to better understand how brain injury develops despite standard available treatments. The use of magnetic resonance imaging has also given clues of which newborns would benefit from additional treatments, and indications for possible alternative treatments. However, magnetic resonance imaging in these newborns remains challenging, and must imperatively be improved to allow further detection and treatment. This education session will cover the advantages and limitations of magnetic resonance imaging in term newborns.

Target audience

Scientists and clinicians interested in learning what can be learnt from imaging in term newborns and how those methods can be applied in their daily practice for research and clinical applications

Objectives

Upon completion of this lecture, the participants should be able to:

- Have an overview of the specifics of the term neonatal brain

- Improve the understanding of what imaging brings to the understanding of the development of brain injury in term newborns

- Learn how imaging in these newborns may permit to develop new treatments

Purpose

Term newborns can be critically ill and are thus at risk to develop brain injury. At that age, the brain is still maturating and injury will still impact the normal brain development. Brain injury most often develops in these newborns following birth asphyxia. Hypothermia treatment has been introduced now as standard of care for these newborns. However, some asphyxiated newborns treated with hypothermia still develop brain injury.

Methods

The different imaging techniques available in term newborns will be reviewed, as well as the results obtained so far in asphyxiated newborns treated with hypothermia. More specifically, diffusion-weighted imaging, diffusion-tensor imaging, spectroscopy and arterial spin labeling results will be outlined. Their potential use and their limitations will be discussed in more details.

Discussion

Magnetic resonance imaging in term newborns has permitted to understand why asphyxiated newborns develop brain injury despite hypothermia treatment, has started to give clues how treatments may need to be adjusted to prevent or repair these brain injuries, and has allowed to identify which newborns should be targeted with these new treatments.

Conclusions

This education session will cover the challenges of imaging term newborns, but also the possibilities of these imaging techniques to better detect brain injury and to help in developing improved treatments for these newborns.

Acknowledgements

Pia Wintermark receives research grant funding from the FRSQ Clinical Research Scholar Career Award Junior 1, and the New Investigator Research Grant from the SickKids Foundation and the CIHR Institute of Human Development, Child and Youth Health (IHDCYH).

References

1. Wintermark P, Lechpammer M, Kosaras B, Jensen FE, Warfield SK. Brain perfusion is increased at term in the white matter of very preterm newborns and newborns with congenital heart disease: May this reflect activated angiogenesis? Neuropediatrics. 2015;46(5):344-351.

2. Kwan S, Boudes E, Benseler A, Gilbert G, Saint-Martin C, Shevell M, Wintermark P. Evolution of apparent diffusion coefficient and fractional anisotropy in the cerebrum of asphyxiated newborns treated with hypothermia over the first month of life. Neural Plast. 2015;653727.

3. Kwan S, Boudes E, Gilbert G, Saint-Martin C, Albrecht S, Shevell M, Wintermark P. Injury to the cerebellum in term asphyxiated newborns treated with hypothermia. AJNR Am J Neuroradiol. 2015;36(8):1542-1549. Impact factor 3.59.

4. Shaikh H, Lechpammer M, Jensen FE, Warfield SK, Hansen AH, Kosaras B, Shevell M, Wintermark P. Increased brain perfusion persists over the first month of life in term asphyxiated newborns treated with hypothermia: Does it reflect activated angiogenesis? Transl Stroke Res. 2015;6(3):224-233.

5. Boudes E, Tan X, Saint-Martin C, Shevell M, Wintermark P. Magnetic resonance imaging obtained during versus after hypothermia in asphyxiated newborns. Arch Dis Child Fetal Neonatal Ed. 2015;100(3):F238-242.

6. Boudes E, Gilbert G, Leppert IR, Tan X, Pike GB, Saint-Martin C, Wintermark P. Measurement of brain perfusion in newborns: pulsed arterial spin labeling (PASL) versus pseudo-continuous arterial spin labeling (pCASL). Neuroimage Clin. 2014;6:126-133.

7. Wintermark P, Hansen A, Warfield SK, Dukhovny D, Soul J. Near-infrared spectroscopy versus magnetic resonance imaging to study brain perfusion in newborns with hypoxic-ischemic encephalopathy treated with hypothermia. NeuroImage. 2014;85 Pt 1:287-293.

8. Wintermark P, Hansen A, Gregas MC, Soul J, Labrecque M, Robertson RL, Warfield SK. Brain perfusion in asphyxiated newborns treated with therapeutic hypothermia. AJNR Am J Neuroradiol. 2011; 32(11):2023-2029.

9. Wintermark P, Hansen A, Soul J, Labrecque M, Robertson RL, Warfield SK. Early versus late MRI in asphyxiated newborns treated with hypothermia. Arch Dis Child Fetal Neonatal Ed. 2011;96(1):F36-44.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
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