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Defining the nature of the cerebral abnormalities in the premature infant: a qualitative magnetic resonance imaging study - 29/08/11

Doi : 10.1067/S0022-3476(03)00357-3 
Terrie E Inder, MD, PhD , Scott J Wells, MD, Nina B Mogridge, Carole Spencer, Joseph J Volpe, MD
From Murdoch Children's Research Institute, University of Melbourne, Royal Women's Hospital, and Howard Florey Institute, University of Melbourne, Australia; and the Department of Pediatrics and Neonatal Intensive Care Unit, and Department of Radiology, Christchurch Hospital, and Canterbury Radiology Group, Christchurch Hospital, Christchurch, New Zealand; and the Department of Neurology, Children's Hospital, Harvard Medical School, Boston, Massachusetts, United Kingdom 

Reprint requests: Terrie E. Inder, MD, Department of Neurology, Royal Children's Hospital, 2nd Floor, Flemington Rd, Parkville VIC 3052, Australia.

Abstract

Objectives The aim of this study was to define qualitatively the nature and extent of white and gray matter abnormalities in a longitudinal population-based study of infants with very low birth weight. Perinatal factors were then related to the presence and severity of magnetic resonance imaging (MRI) abnormalities.

Methods From November 1998 to December 2000, 100 consecutive premature infants admitted to the neonatal intensive care unit at Christchurch Women's Hospital were recruited (98% eligible) after informed parental consent to undergo an MRI scan at term equivalent. The scans were analyzed by a single neuroradiologist experienced in pediatric MRI, with a second independent scoring of the MRI using a combination of criteria for white matter (cysts, signal abnormality, loss of volume, ventriculomegaly, corpus callosal thinning, myelination) and gray matter (gray matter signal abnormality, gyration, subarachnoid space). Results were analyzed against individual item scores as well as the presence of moderate-severe white matter score, total gray matter score, and total brain score.

Results The mean gestational age was 27.9±2.4 weeks (range, 23-32 weeks), and mean birth weight was 1063±292 g. The greatest univariate predictors for moderate-severe white matter abnormality were lower gestational age (odds ratio [OR], 1.3; 95% confidence interval [CI], 1.1-1.7; P<.01), maternal fever (OR, 2.2; 95% CI, 1.1-4.6; P<.04), proven sepsis in the infant at delivery (OR, 1.8; 95% CI, 1.1-3.6; P=0.03), inotropic support (OR, 2.7; 95% CI, 1.5-4.5; P<.001), patent ductus arteriosus (OR, 2.2; 95% CI, 1.2-3.8; P=.01), grade III/IV intraventricular hemorrhage (P=.015), and the occurrence of a pneumothorax (P=.05). There was a significant protective effect of intrauterine growth restriction (OR, 0.51; 95% CI, 0.23-0.99; P=.04). Gray matter abnormality was highly related to the presence and severity of white matter abnormality. A unique pattern of cerebral abnormality consisting of significant diffuse white matter atrophy, ventriculomegaly, immature gyral development, and enlarged subarachnoid space was found in 10 of 11 infants with birth gestation <26 weeks. Given the later outcome of these infants, this pattern may have very high risk for later global neurodevelopmental disability.

Conclusions This MRI study confirms a high incidence of cerebral white matter abnormality at term in an unselected population of premature infants, which is predominantly a result of noncystic injury in the extremely immature infant. We confirm that the major perinatal risk factors for white matter abnormality are related to perinatal infection, particularly maternal fever and infant sepsis, and hypotension with inotrope use. We have defined a distinct pattern of diffuse white and gray matter abnormality in the extremely immature infant.

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Keywords : MRI, OR, US, VLBW, WM


Plan


 Supported by the Neurological Foundation of New Zealand, Lottery Health New Zealand, and the Health Research Council of New Zealand.


© 2003  Mosby, Inc. Tous droits réservés.
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Vol 143 - N° 2

P. 171-179 - août 2003 Retour au numéro
Article précédent Article précédent
  • Postnatal growth in VLBW infants: significant association with neurodevelopmental outcome
  • Beatrice Latal-Hajnal, Kurt von Siebenthal, Helen Kovari, Hans U. Bucher, Remo H. Largo
| Article suivant Article suivant
  • Daily metabolic rate in healthy infants
  • Russell Rising, Debora Duro, Maribel Cedillo, Sandra Valois, Fima Lifshitz

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