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Prognostic Utility of Magnetic Resonance Imaging in Neonatal Hypoxic-Ischemic Encephalopathy:  Substudy of a Randomized Trial

Jeanie L. Y. Cheong, MD; Lee Coleman, FRANZCR; Rod W. Hunt, PhD; Katherine J. Lee, PhD; Lex W. Doyle, MD; Terrie E. Inder, MD; Susan E. Jacobs, MD; for the Infant Cooling Evaluation Collaboration
Arch Pediatr Adolesc Med. 2012;166(7):634-640. doi:10.1001/archpediatrics.2012.284.
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Objective  To investigate the effects of hypothermia treatment on magnetic resonance imaging (MRI) patterns of brain injury in newborns with hypoxic-ischemic encephalopathy compared with normothermia, including the prognostic utility of MRI for death and/or disability at a postnatal age of 2 years.

Design  Substudy of a randomized controlled trial.

Setting  Participating centers in the Infant Cooling Evaluation trial.

Participants  Trial participants (gestational age ≥35 weeks with moderate to severe hypoxic-ischemic encephalopathy, randomized to whole-body hypothermia or normothermia) with available MRIs.

Main Exposure  We performed qualitative evaluation of T1- and T2-weighted and diffusion MRIs. The posterior limb of the internal capsule was classified as normal or abnormal, whereas the basal ganglia and thalami, white matter, and cortical gray matter were classified as normal or mildly abnormal or moderately/severely abnormal.

Main Outcome Measures  Death or major disability at 2 years.

Results  We evaluated 127 MRIs (66 patients treated with hypothermia and 61 with normothermia; mean age at scan, 6 postnatal days). The odds of having moderate/severe white matter or cortical gray matter abnormalities on T1- and T2-weighted MRI were reduced by hypothermia (white matter odds ratio, 0.28 [95% CI, 0.09-0.82]; gray matter odds ratio, 0.41 [0.17-1.00]). Abnormal MRI findings predicted adverse outcomes, with T1- and T2-weighted and diffusion MRI abnormalities in the posterior limb of the internal capsule and basal ganglia and thalami demonstrating the greatest predictive value. There was little evidence that prognostic value of the MRI was modified by therapeutic hypothermia (all interactions, P > .05).

Conclusions  Brain injury on T1- and T2-weighted MRI is reduced in hypothermia-treated newborns. Abnormal MRI findings are prognostic of long-term outcome in moderate to severe hypoxic-ischemic encephalopathy regardless of treatment with hypothermia.

Trial Registration  anzctr.org.au Identifier: ACTRN12606000036516

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Figures

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Grahic Jump Location

Figure 1. Appearance of hypoxic-ischemic encephalopathy on T2-weighted axial magnetic resonance imaging. A, A normal brain in a term newborn with myelination in the posterior limb of the internal capsule (PLIC). B, Severely abnormal basal ganglia and thalamus (BGT) lesions, absent myelination of the PLIC, and abnormal signal in the white matter, especially in the frontal lobes. C, Moderately abnormal BGT involving the putamen and thalamus, with myelination of the PLIC present. D, Abnormal signal in the Rolandic cortex.

Place holder to copy figure label and caption
Grahic Jump Location

Figure 2. Appearance of hypoxic-ischemic encephalopathy on T1-weighted axial magnetic resonance imaging. A, A normal brain in a term newborn. B, Severely abnormal basal ganglia and thalami (BGT), absent myelination in the posterior limb of the internal capsule (PLIC), and widespread abnormal cortical gray matter. C, Moderately abnormal BGT signal involving the putamen and thalamus, with myelination of the PLIC present.

Place holder to copy figure label and caption
Grahic Jump Location

Figure 3. Appearance of hypoxic-ischemic encephalopathy on axial diffusion-weighted magnetic resonance imaging. A, A normal brain in a term newborn with no areas of restricted diffusion. B, Severely restricted diffusion in the basal ganglia and thalami, posterior limb of the internal capsule, and white matter. C, Focal restricted diffusion in the putamen and optic radiations.

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