Clinical Trial Details
— Status: Not yet recruiting
Administrative data
NCT number |
NCT06145256 |
Other study ID # |
Radiological Evaluation of HIE |
Secondary ID |
|
Status |
Not yet recruiting |
Phase |
|
First received |
|
Last updated |
|
Start date |
December 10, 2023 |
Est. completion date |
March 31, 2025 |
Study information
Verified date |
December 2023 |
Source |
Assiut University |
Contact |
Esraa Azab Abdelatty, Master |
Phone |
01100328593 |
Email |
esraaazab700[@]gmail.com |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
To compare between Transcranial Ultrasound , MRI and CT in patients with Hypoxic Ischemic
Encephalopathyas regards diagnostic accuracy and prognostic value .
Description:
- Hypoxic Ischemic Encephalopathy (HIE) is an injury to the brain, occurring in the
neonatal period (under 28 days old) in which there is deprivation of oxygen supply to
brain. It is a common cause of neonate mortality and developmental psychomotor disorders
in the pediatric population worldwide.This is one of the major causes of cerebral
palsy."
- Hypoxic ischemic encephalopathy (HIE) is one of the most serious birth complications
affecting full term infants. It occurs in 1.5 to 2.5 per 1000 live births in developed
countries and 2.3-26.5 per 1000 live births in developing countries . The incidence of
HIE has not declined even with advances in obstetric care (i.e. fetal monitoring) aimed
at preventing the hypoxicischemic event; thus much of the current neonatal research
about HIE focuses on minimizing the extent of subsequent brain injury.
- HIE is a disorder in which clinical manifestations indicate brain dysfunction.While the
exact cause is not always identified, antecedents include cord prolapse, uterine
rupture, abruptio placenta, placenta previa, maternal hypotension, breech presentation,
or shoulder dystonia. The manifestations of perinatal HIE in early postnatal life
include abnormal fetal heart rate tracings, poor umbilical cord gases (pH < 0.7 or base
deficit ≥ 12 mmol/L),low Apgar scores, presence of meconium stained fluid,or the need
for respiratory support within the first several minutes of postnatal life.
- The infant usually develops seizure within first 24 h of life. Children with
periventricular leukomalacia (PVL) may develop spastic CP in the form of diplegia,
quadriplegia, or hemiplegia.Involvement of subcortical white matter produces severe
mental retardation and impaired vision.Basal ganglia (BG) and thalamic involvement
result in extrapyramidal symptoms. Multicystic encephalopathy is associated with
quadriplegia, bulbar and choreoathetoid symptoms, microcephaly and mental retardation.
Abnormal electroencephalographic (EEG) findings may predict adverse clinical outcome
such as long-term neurologic sequelae or impending death.
- Multiple neuroimaging techniques are available to visualize brain injury in the neonatal
period. Cranial ultrasonography is a helpful noninvasive tool to detect antenatal onset
of injury and abnormalities that may mimic HIE. Abnormalities related to HIE can be
recognized with ultrasonography as well, but it will take 48-72 h to see these changes
develop in the white matter or deep gray nuclei . Magnetic resonance imaging (MRI) which
includes diffusion-weighted imaging (DWI) is the preferred imaging modality during the
first week after birth to determine the extent of brain injury and predict
neurodevelopmental outcome in infants with symptoms of HIE, without its prognostic
utility being altered by therapeutic hypothermia .
- CT image could be used as important diagnostic indication in the assessment of HIE
neonate CT could identify subarachnoid hemorrhage. It is valuable in clinical
application