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HIE - Imaging

Kenneth Williams discusses imaging patterns of hypoxic-ischemic injury in neonates. He notes that the appearance depends on brain maturity and insult severity/duration. Four basic patterns are described. MRI is generally the best exam but US and CT also have roles. Specific vulnerable structures and injury patterns are discussed for both term and preterm infants depending on insult severity. Proper history is important for accurate interpretation.
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0% found this document useful (0 votes)
81 views73 pages

HIE - Imaging

Kenneth Williams discusses imaging patterns of hypoxic-ischemic injury in neonates. He notes that the appearance depends on brain maturity and insult severity/duration. Four basic patterns are described. MRI is generally the best exam but US and CT also have roles. Specific vulnerable structures and injury patterns are discussed for both term and preterm infants depending on insult severity. Proper history is important for accurate interpretation.
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© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Imaging Evaluation of Neonatal

Hypoxic-Ischemic
Encephalopathy
(HI Injury)

Kenneth D. Williams, MD
Disclosures
• Financial Disclosures – None

• Off-Label Applications – None

• Acknowledge
– Dr. Krista L. Birkemeier
– Dr. Matthew B. Crisp
Key Points
• Hypoxic-Ischemic Injury findings depend on:
– Brain Maturity at the time of the event
– Severity and Duration of Hypoperfusion
• 4 Basic Patterns
• Appearance evolves over time. “ITITL”
• Modalities available:
– US – Easiest to obtain
– CT – Limited Role for Hemorrhage / Mass
– MRI – Best examination overall
Key Points
• HII is a metabolic insult and therefore it is
generally bilaterally symmetric in
appearance, i.e. can be tough to detect.

• We talk of patterns but, neonates can’t


read the medical literature.
– Mixture of various patterns
– Wild and crazy appearances
Proper History is Vital
Hypoxic-Ischemic Injury
• Combination of :
Hypoxia (Reduced Blood Oxygenation) &
Ischemia (Reduced Blood Flow).
• Vulnerable areas depend on brain maturity and
whether blood flow can be redistributed to
preserve the areas of greatest metabolic
demand.
• Severe insult – CBF cannot redistribute.
– Areas of highest metabolic activity are injured.
• Mild to Moderate insult – CBF can redistribute
– Vascular border zones are injured.
Brain Maturation
• Term Infant - 37 Weeks EGA or greater

• Preterm - < 37 Weeks EGA


– Late Preterm - 34 – 36 Weeks EGA
– Moderately Preterm - 32 – 33 Weeks EGA
– Severely Preterm - 28 – 31 Weeks EGA
– Extremely Preterm - < 28 Weeks EGA
Birth Weight
• Low Birth Weight < 2,500 g (35 wks)
– 11% of all births – 90% of neonatal deaths

• Very Low Birth Weight < 1,500 g (30 wks)


– 500 – 1,500 gm - 1% of all births – 60% deaths

• Extremely Low Birth Weight < 1,000 g (27wks)

500 g (22 wks)


Vulnerable Structures
• Areas at highest risk:
– Most myelinated
– Highest perfusion
– Most mature metabolism
– Greatest glucose uptake
• Cellular vulnerabilities
– Preoligodendrocytes
– Subplate neurons
– Germinal matrix capillary endothelium
Vascular Border Zones
Now cellular vulnerability

Premature Infant Term Infant

Periventricular WM Parasagittal

Ventriculopedal Ventriculofugal

Transition at 34 to 36 weeks gestation


Chao Radiographics 2006;26:S159-S172
Event Severity & Duration
• Mild to Moderate Hypoperfusion (Partial)
– 30 Minutes to several hours (Prolonged)
– CBF can redistribute

• Severe Hypoperfusion (Profound)


– Complete / Near complete cessation of blood flow
– > 10 - 15 minutes (Acute)
– Inadequate CBF redistribution
4 Major Patterns of Injury
Term Preterm

Mild/Mod Parasagittal BZ GMH


WMIP

Severe Lat Th/Post Put/GP Thal/BS


Hippo/Peri Rol/BS Cbll
Modalities
• Ultrasound – GMH > 5mm
Hydrocephalus
Cavitary WMIP

• CT – Evaluation of Large Hemorrhages

• MRI – Most sensitive test for Ischemic Injury


Non-cavitary WMIP
US – When ?
• Symptomatic neonate – Immediately
– Hemorrhage / Mass / Anomaly / Hydrocephalus
– Edema of early HII +/-
• GMH screening – Asymptomatic
– <1,500 gm and / or < 32 weeks EGA
– Initial at Day 7 (Range 4 – 14)
– Negative – FU Day 30, 42, 60, 36 w EGA, D/C
• Periventricular leukomalacia / Hydrocephalus
– Positive GMH - IVH – 1 week FU R/O PVD
• Progressive Posthemorrhagic Ventricular Dilatation
Ct – When ?
• Large Hemorrhages

• Large Masses

• Pre-surgical

• Ionizing Radiation

• Insensitive
MRI
www.mrineonatalbrain.com
MRI
• Coordination to insure a safe study
• STABLE patient / Monitor ABC’s
• Minimize delays in transit and scanning
• Dedicated neonatal head or knee coil
• Feed and Swaddle / Rare Chloral Hydrate
• Ear protection
• Real time image evaluation
MRI
• Prioritize sequences – more useful 1st
– Diffusion weighted imaging b 800 / 1,000
• Trace diffusion & ADC maps
– T1 weighted images - Inc TR 800+ msec
– T2 weighted images - Inc TR 9,000+ msec
– T2* weighted images (Hemorrhage)
• GRE / SWI
– Magnetic resonance spectroscopy
• Early scan < 48 hours or metabolic disorder ?
– High resolution 3D images / MRA or MRV
Diffusion Weighted Imaging
• Based on random molecular motion
– Infarction – cellular swelling constricts the
extracellular space leading to restricted
(reduced) free diffusion.
• Two main types of images
– Trace Diffusion Images - T2 & Diffusion
– ADC Maps - Diffusion only
• Restricted diffusion is always opposite the
signal of CSF which freely diffuses.
Arterial Ischemic Stroke

• Light bulb bright


restricted diffusion on
Trace images. Trace DWI

• ADC reduction
confirms it is not
T2 shine through
ADC Map
• Very rapid onset –
minutes.
DWI in HII
• More subtle abnormalities may be seen.
– Not a light bulb.
• More gradual onset.
– Can underestimate disease 24 – 48 hrs.
• Will return to normal – pseudonormalize –
at 5 – 7 days.
• Best at Day 3 to 5.
MRI – When ?
• Early < 24 – 48 hours
– MR Spectroscopy will be needed
– DWI and Standard images may underestimate extent
of injury
– Follow-up in 4 – 10 days may be needed
• Short term delay 3 to 5 days
– DWI reliable & not pseudonormalized
– T1 and T2 changes likely present
– Normal probably needs no later FU
• Second week imaging may best predict outcome.
• Longer term follow-up 3 to 6 months.
NICHD Cooling Protocol
• Meet Inclusion Criteria
– Term or Late Preterm Infant EGA => 36 w
– < 6 hours old
• Cooled for 72 hours to 34o C
– Whole-body Cooling
– Head Cooling Cap
• Rewarmed over 6 hours
Cooling for infants < 36 weeks EGA is unproven.
MR Spectroscopy
• Most important for:
– Early MRI < 24 – 48 hours
– Other metabolic disorders that emulate HII
• Lactate is a key finding
– Not present in a term neonate but is normal in a
premature infant and in the CSF.
• Elevated glutamate / glutamine
• Reduced NAA (normally lower in neonates)
• Sample Basal Ganglia & Parasagittal
Lactate @ 1.33 ppm

Chao Radiographics 2006;26:S150-S172.


Term Normal MRI

T1 T2
Term Normal MRI

Trace DWI ADC Map


30 Week EGA Normal MRI
Term – Mild / Moderate
• Parasagittal Borderzone injury
– Cortex and underlying white matter
– Between ACA, MCA, PCA territories

• MRI best modality


Term 3,860g Ap 8/9 Sz 10 hr

MRI Day 3
Term 3,670g Abruption Sz 5hr

MRI Day 8
Term 3,670g Abruption Sz 5hr

MRI 7 Months
Term - Severe
• Lateral Thalamus / Posterior Putamen
• Globus Pallidus
• Hippocampi
• Brainstem (dorsal)
• Sensorimotor cortex and corticospinal tracts

• Modalities – MRI best by far


US in very skilled hands
Vulnerable Areas
Term Apneic Episode Day 3 Sz

CT 24 Hours
Term Apneic Episode Day 3 Sz

MRI 4 days after Sz


Term Apneic Episode Day 3 Sz

5 Weeks Later
Term 3,700g Ap 0/3/4

Cooled US Day 4
Term 3,700g Ap 0/3/4

MRI Day 12
Preterm - Severe
• Thalamus

• Brainstem

• Cerebellum – Anterior vermis

• Modalities – MRI best by far


US in very skilled hands
36 W EGA 1,900 g Ap 1/4/4

MRI Day 10
31 w EGA 1,260 g

MRI Day 16
Total Cortical Injury Pattern
“White Cerebrum”
• Uncommon diffuse brain injury pattern.
– Barkovich 2 % of patients at UCSF.

• Cortex and subcortical injury.

• Cerebellum relatively spared.


Late Term Birth Anoxia Sz

MRI Day 2
Late Term Birth Anoxia Sz

23 Months Later
Preterm – Mild / Moderate
• Most often < 32 weeks EGA
• Germinal Matrix Hemorrhage (GMH)
– 4 Grades
• White Matter Injury of Prematurity (WMIP)
– Periventricular Leukomalacia (PVL)
• Cellular vulnerability > Border zone
• Modalities – US / MRI in some cases
Germinal Matrix
• Vascular area of neuron and glia
generation along ependymal surface.
– Most active weeks 8 to 28.
• Involutes in the third trimester.
• Ganglionic eminence at the caudothalamic
groove is the last to involute.
• GM Hemorrhage generally < 32 wk EGA
and < 1,000 gm
– Rare after 34 weeks / 90 % by Day 4 of life
GMH Grades – Papile 1978
• Grade 1 – Intraparenchymal at Gang Em
No intraventricular extension
• Grade 2 – Intraparenchymal with extension
Into the ventricle – NO dilatation
• Grade 3 – Intraparenchymal with ventricle
Extension and ventricular dilatation
• Grade 4 – Periventricular Hemorrhagic
Infarction (PVHI)
PVHI
• New term for Grade 4
GMH recognizing
etiology
• Terminal vein
compression by small
bleed leads to vein
occlusion and larger
venous infarction with
hemorrhage in the
medullary vein
territory
Germinal Matrix – Intraventricular Hemorrhage

Periventricular Venous Congestion

Periventricular Ischemia

Periventricular Hemorrhagic Infarction


Grade 1 Hemorrhage
Grade 2
Grade 2
Grade 3
Grade 3
Grade 4
Cerebellum
• 10 to 25 % of preterm
neonates have GMH
in the posterior fossa.
• External granular cell
layer of the
cerebellum is GM
• Supplemental
Posterior or Mastoid
Fontanelle views are
recommended
Cerebellar GMH US

MEDPIX from http://rad.usuhs.mil/medpix


27.5 w EGA 1,140 g Twin

GRE MRI at 2 Months


White Matter Injury
of Prematurity
• Older term – Periventricular Leukomalacia
– Not just from HII
• Infections, metabolic disease, hydrocephalus can
injure the periventricular white matter.
– It’s not just the periventricular white matter.
• Cavitary and Noncavitary
– US can detect cavitary disease but is
insensitive to noncavitary. (5 – 10 % neonates)
– Autopsy & MRI WMIP prevalence is 50 %
27.5 w EGA Asymptomatic

Day 18 Day 30

Cavitary WMIP
27.5 w EGA Asymptomatic

Day 60

Cavitary WMIP
Noncavitary WMIP MRI
• Punctate short T1 within larger areas of
long T2 seen at Day 3 to 4.
• Mild T2 shortening appears at Day 6 to 7.
– Areas of reactive astrogliosis
– Not hemorrhage (Lower T2 and GRE/SWI+)
• May be seen on DWI early on as well
34 w EGA 1,520 g Apgars 2/4/6

MRI Day 6
34 w EGA 1,520 g Apgars 2/4/6

MRI Day 6
34 w 3 d EGA Ap 2/6/8 Sz

MRI Day 4
Poor Prognosis
• Brainstem Injury – Death
• Total Cortical Injury pattern (Global)
• Abnormal PLIC –Ability to Walk
– Only for >36 weeks EGA
• Abnormal thalamus & basal ganglia - Motor
• Grade 3 and 4 GMH - Neurodevelopmental
• Abnormal MRS – Poor Outcome
ADC and Prognosis
• Hunt Pediatrics 2004
– PLIC < 0.74 um2/ms Survives – Bad Outcome
– Mean ADC PLIC
• Nonsurvivor 0.75 +/- 0.17
• Survivor 0.89 +/-0.17
• Wolf Radiology 2001
– > 1.0 um2/ms PLIC Controls
• Rutherford Pediatrics 2004
– WM infarctions <1 .1x10-3 mm2/s
– Thalamic infarctions < 0.8x10-3 mm2/s
• Vermuelen Radiology 2008
– PLIC < 85x10-5 mm2/s Poor Outcome
Radiology November 2008
Differential Diagnosis
• Neonatal Hypoglycemia
• Kernicterus
• Infection
– Type II Herpes encephalopathy
– Human parechovirus
• Metabolic disorders
– Maple syrup urine disease
– Non-ketotic hyperglycinemia
– Urea cycle disorders
– Leigh syndrome – Pyruvate dehydrogenase
• Nonaccidental trauma

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