2.07 CME

नवजात शिशु की सर्जिकल आपात स्थितियों का प्रबंधन

वक्ता: Dr Kiran Kumar G

ओडी पीडियाट्रिक्स, कॉन्टिनेंटल हॉस्पिटल, हैदराबाद

लॉगिन करें प्रारंभ करें

विवरण

Management of neonatal surgical emergencies requires prompt diagnosis, stabilization, and surgical intervention. Common emergencies include necrotizing enterocolitis, intestinal atresia, malrotation with volvulus, congenital diaphragmatic hernia, and gastroschisis. Initial management focuses on airway stabilization, fluid resuscitation, temperature regulation, and infection control. Radiographic imaging aids in diagnosis, while surgical intervention is tailored to the condition. Multidisciplinary collaboration involving neonatologists, pediatric surgeons, and anesthesiologists is crucial. Postoperative care includes ventilatory support, pain management, and nutritional optimization. Early recognition and timely intervention significantly improve outcomes, reducing morbidity and mortality in neonates with life-threatening surgical conditions.

सारांश

  • Neonatal jaundice is a common medical condition requiring intervention, distinguished from hyperbilirubinemia which is a biochemical term. While neonatal jaundice is a clinical assessment of yellowish skin and sclera, hyperbilirubinemia refers to elevated blood bilirubin levels above a population cutoff. Universally, newborns will have jaundice to some degree.
  • Bilirubin, the end product of hematabolism, primarily originates from hemoglobin. Hemoxysinase converts hem to bilirubin, a rate-limiting step that varies among ethnicities and families. Bilirubin reductase then forms conjugated bilirubin, which travels to the liver for further processing and excretion. One gram of hemoglobin yields roughly 35 milligrams of bilirubin, with carbon monoxide produced as a byproduct during hem conversion.
  • Bilirubin binds to albumin for safe transport to the liver, protecting cells from damage. Low albumin levels result in free bilirubin, toxic to a newborn's developing brain. Newborns have more RBCs with shorter lifespans and immature UDP conjugating enzymes for bilirubin processing, contributing to neonatal jaundice.
  • Several factors influence the incidence of neonatal jaundice, including ethnicity (Asian babies are at higher risk), geography (high altitude), season (summer), family history, and genetic conditions like G6PD deficiency. Maternal conditions such as diabetes and obesity, medications like oxytocin, and blood group discrepancies (Rh incompatibility) also play a role. Premature, low birth weight, and male babies are more susceptible.
  • Physiological jaundice, typically appearing after 24-48 hours, is common in healthy newborns. It peaks in the first few days and diminishes within 7-10 days. In premature infants, it appears later and lasts longer. Asian babies tend to have higher bilirubin levels, peaking around day 4, with physiological jaundice reaching up to 10-12 mg/dL, rarely exceeding 17 mg/dL. Levels above 17mg/dL are considered exaggerated physiological jaundice.
  • Excessive bilirubin can cause bilirubin-induced neurological dysfunction. Levels above 17 mg/dL are significant, over 20 mg/dL are severe, and exceeding 25-30 mg/dL are extremely hazardous. Unconjugated bilirubin, converting to bilirubin acid in an acidic environment, inhibits respiration and mitochondrial function within cells, triggering apoptosis and harming immature neuronal cells.
  • Bilirubin encephalopathy is a severe consequence, facilitated by insufficient albumin and a compromised blood-brain barrier. The leptomeninges, lacking a fully developed blood-brain barrier, are particularly vulnerable. Conditions like birth asphyxia also compromise the barrier.
  • Acute bilirubin encephalopathy, if untreated, can progress to kernicterus, characterized by athetosis, dystonia, deafness, gaze palsies, and dental hypoplasia. Early intervention is critical, especially when infants exhibit hypotonia and poor suckling.
  • Preventing primary hyperbilirubinemia involves identifying risk factors, conducting blood grouping and ICT tests in pregnant women, and monitoring infants of Rh-negative mothers. Breastfeeding support and predischarge screening are vital to identifying babies that may develop significant hyperbilirubinemia once they leave the hospital environment.
  • Assessing jaundice involves clinical, non-invasive, and laboratory methods. The Kramer's rule estimates bilirubin levels based on cephalocaudal progression of jaundice. Transcutaneous bilirubinometry provides a non-invasive measurement correlating with blood tests, but it's less reliable above 15 mg/dL. Laboratory assessments include DCT and peripheral smear studies to identify underlying causes.
  • Managing jaundice includes phototherapy and, in severe cases, exchange transfusion. Phototherapy uses blue light to isomerize bilirubin, making it water-soluble for excretion. Intravenous immunoglobulin (IVIG) is used in RHISO immunization to block maternal antibodies and prevent hemolysis.
  • BiliTool.org is a resource to assess bilirubin risk. Based on clinical history and BiliTool output, proper follow-up is critical to ensure that bilirubin levels don't rebound and cause further complications. Future assessment may include mobile phone-based analysis of skin color to determine risk.

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