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Meconium aspiration syndrome

Abstract

Meconium is the first stool of the neonate. It is composed of substances that are swallowed by the fetus during „in utero“ period: epithelial cells, fetal hair, mucus, bile and water. Meconium aspiration syndrome (MAS) is defined as respiratory distress that develops soon after birth, with radiologically confirmed aspiration pneumonitis and presence of meconium stained amniotic fluid (MSAF). Prenatal asphyxia is the main cause of MAS. The exact mechanism of intrauterine meconium evacuation remains unknown, but it is thought that fetal distress and vagal stimulation are two possible causes. MSAF occurs in 5-22% of all pregnancies, and 1-12% of infants born from MSAF develop MAS. If the child is vigorous after birth, there is no need for specific therapeutic measures. However, if the neonate is depressed, it should be intubated and aspirated immediately. MAS is a condition that can present only with mild respiratory symptoms but also, lethal outcomes can be seen despite all treatment measures (mechanical ventilation + iNO + high frequency mechanical ventilation + ECMO). We present a case of male neonate, born at our institution ( 39+6/7 weeks of gestation) and admitted to our neonatal unit (level 2) with clinical signs of the MAS. The clinical picture was moderate and the radiologic findings were impressive. He was given surfactant and respiratory support with nasal Continuous Positive Airway Pressure (nCPAP) was started. We acchieved adequate oxygenation and ventilation, and the clinical picture improved in the next few days. Using non-invasive respiratory support, we minimized the possibility for the development of air leak syndromes and lung injury and preventing long term sequelae like cronic lung disease and bronchopulmonary dysplasia

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