Perinatal asphyxia of full-term newborns: from pathophysiology to long-term outcomes
نویسندگان
چکیده
The fetal environment and circulatory patterns are very different from that of extrauterine life. fetus evolved to thrive grow in a relative hypoxemic adapted several mechanisms response changes oxygen concentration the blood ensure optimal delivery brain heart. However according estimates World Health Organization world 4 9 million newborns born annually state perinatal asphyxia. In economically underdeveloped countries, this indicator is higher than developed but general, frequency asphyxia remains at rather high level modern world. Perinatal or hypoxic-ischemic encephalopathy, can cause multiple organ dysfunction neonatal period, severe diseases future, lead disability infant mortality. characterized by violation gas exchange, which varying degrees hypoxia, hypercapnia acidosis, depending on duration degree interruption air flow, however, obstructed exchange does not have precise biochemical criteria. addition, exact pathophysiology been fully studied, as result “gold standard” treatment an active area research. publication reflects views main stages pathogenesis asphyxia, shows circulation during presents current data emerging disorders newborn’s body against background hypoxic ischemic encephalopathy.
منابع مشابه
The value of ultrasonography and Doppler sonography in prognosticating long-term outcomes among full-term newborns with perinatal asphyxia.
BACKGROUND AND OBJECTIVE The aim of the study was to determine the correlation of hypoxic-ischemic (HI) brain injury in full-term neonates detected via ultrasonography (USG) and blood flow parameters evaluated via Doppler sonography (DS) with long-term outcomes of mental and neuromotor development at the age of 1-year. MATERIALS AND METHODS In total, 125 full-term neonates (78 subjects of cas...
متن کاملSeizure-associated brain injury in term newborns with perinatal asphyxia.
BACKGROUND There is controversy over whether seizures, the most common manifestation of neonatal brain injury, may themselves damage the developing brain. OBJECTIVE To determine if neonatal seizures are independently associated with brain injury in newborns with perinatal asphyxia. METHODS Ninety term neonates were studied with MRI and single-voxel (1)H-MRS on median day of life 6 (range 1 ...
متن کاملBeta-2-microglobulin in the assessment of renal function in full term newborns following perinatal asphyxia.
In order to evaluate the clinical usefulness of serum and urinary beta 2 microglobulin (beta 2-m) determination as a marker of renal damage following perinatal asphyxia, twenty asphyxiated and twenty healthy full term newborns were studied. Renal function was monitored on the first and third day after birth by traditional tests such as creatinine (Cr), endogenous creatinine clearance (Ccr), and...
متن کاملShort and long term prognosis in perinatal asphyxia: An update.
Interruption of blood flow and gas exchange to the fetus in the perinatal period, known as perinatal asphyxia, can, if significant, trigger a cascade of neuronal injury, leading on to neonatal encephalopathy (NE) and resultant long-term damage. While the majority of infants who are exposed to perinatal hypoxia-ischaemia will recover quickly and go on to have a completely normal survival, a prop...
متن کاملPerinatal Factors Leading to Birth Asphyxia among Term Newborns in a Tertiary Care Hospital
OBJECTIVE To determine various perinatal factors leading to birth asphyxia among term newborns in a tertiary care hospital. METHODS In a cross sectional study, a total of 196 asphyxiated cases were selected through consecutive non-probability sampling technique from neonatal intensive care unit (NICU) of a tertiary care Military Hospital in Pakistan from 1st December 2012 to 1st December 2013...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Nevrologi?eskij žurnal imeni L.O. Badalâna
سال: 2023
ISSN: ['2686-8997', '2712-794X']
DOI: https://doi.org/10.46563/2686-8997-2023-4-2-88-96