Myth: Cerebral palsy cannot be predicted by neonatal brain imaging

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Summary

There is controversy in the literature about the value of brain imaging in neonates regarding the prediction of cerebral palsy (CP). The aim of this review was to unravel the myth that CP cannot be predicted by neuroimaging in neonates. Major intracranial lesions in the preterm infant should be recognized with sequential cranial ultrasound and will predict those with non-ambulatory CP. Magnetic resonance imaging (MRI) at term-equivalent age will refine the prediction by assessment of myelination of the posterior limb of the internal capsule. Prediction of motor outcome in preterm infants with subtle white matter injury remains difficult, even with conventional MRI. MRI is a better tool to predict outcome in the term infant with hypoxic-ischaemic encephalopathy or neonatal stroke. The use of diffusion-weighted imaging as an additional sequence adds to the predictive value for motor outcome. Sequential and dedicated neuroimaging should enable us to predict motor outcome in high risk newborns infants.

Introduction

The aim of this review is to refute the myth that cerebral palsy (CP) cannot be predicted by neonatal brain imaging in neonates when combining sequential cranial ultrasonography (cUS) for a sufficient length of time with conventional magnetic resonance imaging (MRI) at term-equivalent age (TEA) in the preterm infant and when using first week MRI including diffusion-weighted imaging (DWI) in the term infant.

Section snippets

The preterm infant

Preterm birth is still increasing. The rate of neurodevelopmental impairment in survivors remains high and recent data have failed to show an improvement in neurodevelopmental outcome in infants with a gestational age (GA) of ≤25 weeks.1, 2 Others have reported a significant decrease in the rates of CP, severe cognitive impairments, and overall neurodevelopmental impairment, but these studies include infants with a GA >25 weeks and are hospital- rather than population-based studies.3, 4, 5

The term infant

Newer techniques, such as evoked potentials, amplitude-integrated electroencephalography (aEEG), and neuroimaging have been used to predict outcome, in particular the development of CP, in term neonates with hypoxic-ischaemic encephalopathy. These techniques were used to assess the severity of the hypoxic-ischaemic insult, to evaluate the effects of neonatal intensive care, and to identify patients who might benefit from interventions such as physical therapy.53, 54

Although electrophysiology

Acknowledgements

The authors would like to thank Frances Cowan for her helpful comments when reading the manuscript and the enthusiasm and patience of magnetic resonance technicians.

References (83)

  • F. Groenendaal et al.

    Selection of babies for intervention after birth asphyxia

    Semin Neonatol

    (2000)
  • F. Cowan et al.

    Origin and timing of brain lesions in term infants with neonatal encephalopathy

    Lancet

    (2003)
  • M. Martinez-Biarge et al.

    Outcomes after central grey matter injury in term perinatal hypoxic–ischaemic encephalopathy

    Early Hum Dev

    (2010)
  • J.D. Winter et al.

    Apparent diffusion coefficient pseudonormalization time in neonatal hypoxic–ischemic encephalopathy

    Pediatr Neurol

    (2007)
  • M. Rutherford et al.

    Assessment of brain tissue injury after moderate hypothermia in neonates with hypoxic–ischaemic encephalopathy: a nested substudy of a randomised controlled trial

    Lancet Neurol

    (2010)
  • B.E. Hamilton et al.

    Annual summary of vital statistics

    Pediatrics

    (2007)
  • S.R. Hintz et al.

    Early-childhood neurodevelopmental outcomes are not improving for infants born at <25 weeks’ gestational age

    Pediatrics

    (2011)
  • B.R. Vohr et al.

    Center differences and outcomes of extremely low birth weight infants

    Pediatrics

    (2004)
  • D. Wilson-Costello et al.

    Improved neurodevelopmental outcomes for extremely low birth weight infants in 2000–2002

    Pediatrics

    (2007)
  • van Haastert IC, Groenendaal F, Uiterwaal CSPM, et al. Decreasing incidence and severity of cerebral palsy in...
  • M. Hack et al.

    Trends in the rates of cerebral palsy associated with neonatal intensive care of preterm children

    Clin Obstet Gynecol

    (2008)
  • T.M. O’Shea et al.

    Prenatal events and the risk of cerebral palsy in very low birth weight infants

    Am J Epidemiol

    (1998)
  • M. Wheater et al.

    Perinatal infection is an important risk factor for cerebral palsy in very low birthweight infants

    Dev Med Child Neurol

    (2000)
  • A.J. Spittle et al.

    Preventive care at home for very preterm infants improves infant and caregiver outcomes at 2 years

    Pediatrics

    (2010)
  • A.P. Neubauer et al.

    Erythropoietin improves neurodevelopmental outcome of extremely preterm infants

    Ann Neurol

    (2010)
  • F. Correa et al.

    A. Posterior fontanelle sonography: an acoustic window into the neonatal brain

    Am J Neuroradiol

    (2004)
  • L.S. Miall et al.

    Posterior fossa abnormalities seen on magnetic resonance brain imaging in a cohort of newborn infants

    J Perinatol

    (2003)
  • C. Limperopoulos et al.

    Cerebellar hemorrhage in the preterm infant: ultrasonographic findings and risk factors

    Pediatrics

    (2005)
  • S.J. Steggerda et al.

    Cerebellar injury in preterm infants: incidence and findings on US and MR images

    Radiology

    (2009)
  • V. Pierrat et al.

    Ultrasound diagnosis and neurodevelopmental outcome of localised and extensive cystic periventricular leucomalacia

    Arch Dis Child Fetal Neonatal Ed

    (2001)
  • L.R. Ment et al.

    Practice parameter: neuroimaging of the neonate: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society

    Neurology

    (2002)
  • D.K. Shah et al.

    Adverse neurodevelopment in preterm infants with postnatal sepsis or necrotizing enterocolitis is mediated by white matter abnormalities on magnetic resonance imaging at term

    J Pediatr

    (2008)
  • M.A. Verboon-Maciolek et al.

    White matter damage in neonatal enterovirus meningoencephalitis

    Neurology

    (2006)
  • M.A. Verboon-Maciolek et al.

    Human parechovirus causes encephalitis with white matter injury in neonates

    Ann Neurol

    (2008)
  • S.R. Hintz et al.

    Interobserver reliability and accuracy of cranial ultrasound scanning interpretation in premature infants

    J Pediatr

    (2007)
  • D.L. Harris et al.

    Variable interpretation of ultrasonograms may contribute to variation in the reported incidence of white matter damage between newborn intensive care units in New Zealand

    Arch Dis Child Fetal Neonatal Ed

    (2006)
  • A.L. Stewart et al.

    Ultrasound appearance of the brain in very preterm infants and neurodevelopmental outcome at 18 months of age

    Arch Dis Child

    (1983)
  • B. Vollmer et al.

    Predictors of long-term outcome in very preterm infants: gestational age versus neonatal cranial ultrasound

    Pediatrics

    (2003)
  • P.Y. Ancel et al.

    Cerebral palsy among very preterm children in relation to gestational age and neonatal ultrasound abnormalities: the EPIPAGE cohort study

    Pediatrics

    (2006)
  • K.J. Rademaker et al.

    Unilateral haemorrhagic parenchymal lesions in the preterm infant: shape, site and prognosis

    Acta Paediatr

    (1994)
  • H. Bassan et al.

    Neurodevelopmental outcome in survivors of periventricular hemorrhagic infarction

    Pediatrics

    (2007)
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