LE1 Flashcards
Baby Boy M was born full term. Labor was uneventful. He was given breast milk. He was apparently well when he was noted to have yellowish discoloration of the skin on the 30th hour of life. No associated symptoms noted. Total serum bilirubin level was 8 mg/dl. What is your impression?
A. pathologic jaundice
B. physiologic jaundice
C. neonatal sepsis
D. G6PD deficiency
B. physiologic jaundice
Rationale: According to Nelson’s Pediatrics, physiologic jaundice typically appears on the 2nd to 4th day of life and peaks around the 3rd to 5th day. A total serum bilirubin level of 8 mg/dl in the first 24-72 hours of life without other symptoms suggests physiologic jaundice, which is common in newborns due to increased bilirubin production and immature hepatic conjugation mechanisms.
A 1-month-old baby was brought to a pediatrician because of hypotonia and constipation. Birth history was uncomplicated. The mother also noted persistence of umbilical hernia and protrusion of the tongue. Which of the following metabolic disorders would you consider?
A. G6PD deficiency
B. Galactosemia
C. Congenital hypothyroidism
D. Hypoglycemia
C. Congenital hypothyroidism
Rationale: Nelson’s Pediatrics highlights that congenital hypothyroidism can present with symptoms such as hypotonia, constipation, prolonged jaundice, large fontanelles, umbilical hernia, and a large tongue. The persistence of an umbilical hernia and protrusion of the tongue are particularly characteristic.
The baby was delivered via C-section due to a non-reassuring fetal heart beat pattern. On PE, the baby was cyanotic, limp, in cardiorespiratory distress. You noted that the baby’s umbilical cord was stained with meconium. Few hours after birth, seizure was noted. Perinatal asphyxia was then considered. The following are the criteria for diagnosis of perinatal asphyxia EXCEPT:
A. Apgar < 3 beyond 5 minutes
B. CNS manifestations
C. Multiorgan failure
D. Blood pH 7.3
A. Apgar < 3 beyond 5 minutes
Rationale: Perinatal asphyxia is defined in Nelson’s Pediatrics as having at least one of the following: a 10-minute Apgar score of 5 or less, the need for resuscitation lasting more than 10 minutes, metabolic acidosis (pH ≤ 7.0) or base excess of -12 mmol/L in umbilical artery or within the first hour of life, and/or evidence of CNS involvement or multiorgan failure. An Apgar score of < 3 beyond 5 minutes indicates severe asphyxia, but for the diagnosis, the criteria are typically assessed within the first 10 minutes of life.
Polycythemia is a neonatal complication seen in:
A. Placenta previa
B. Abruptio placenta
C. Delayed clamping of the umbilical cord
D. Donor twin
C. Delayed clamping of the umbilical cord
Rationale: According to Nelson’s Pediatrics, delayed clamping of the umbilical cord can lead to an increased transfusion of blood from the placenta to the neonate, which can result in polycythemia (an abnormally high hematocrit).
Baby A was born full term via Cesarean section. He developed rapid respiration in the 3rd hour of his life. Chest x-ray showed widened intercostal spaces and fluid in interlobar fissures. The most likely diagnosis is:
A. Neonatal pneumonia
B. Transient tachypnea of the newborn
C. Hyaline membrane disease
D. Bronchopulmonary dysplasia
B. Transient tachypnea of the newborn
Rationale: Nelson’s Pediatrics describes transient tachypnea of the newborn (TTN) as a condition that commonly follows uneventful normal or cesarean deliveries. It presents with rapid breathing and characteristic x-ray findings, including prominent pulmonary vascular markings and fluid in the fissures. TTN usually resolves within 72 hours.
Term baby was delivered in respiratory distress with a note of drooling of saliva and difficulty in inserting orogastric tube during suctioning of secretions per orem. Chest x-ray showed coiling of the feeding tube in the upper esophagus. The infant is suspected to have:
A. Pyloric Stenosis
B. Intestinal Obstruction
C. Congenital diaphragmatic hernia
D. Tracheoesophageal fistula
D. Tracheoesophageal fistula
Rationale: The clinical presentation of drooling, respiratory distress, and inability to pass an orogastric tube, along with the x-ray finding of coiling in the upper esophagus, is characteristic of tracheoesophageal fistula, as described in Nelson’s Pediatrics.
A premature infant, 28 weeks by pediatric aging, developed abdominal distension on the 8th day of life with feeding intolerance and bloody stools. Which of the following is the most likely diagnosis?
A. Necrotizing Enterocolitis
B. Hypertrophic pyloric stenosis
C. Tracheoesophageal fistula
D. Congenital megacolon
A. Necrotizing Enterocolitis
Rationale: Nelson’s Pediatrics identifies necrotizing enterocolitis (NEC) as a serious gastrointestinal emergency in preterm infants. It presents with symptoms such as abdominal distension, feeding intolerance, and bloody stools, typically occurring around the first 2-3 weeks of life.
A radiographic finding that is pathognomonic of necrotizing enterocolitis (NEC) is:
A. Double bubble sign
B. Pneumatosis intestinalis
C. Absence of presacral gas
D. Thickened bowel loops
B. Pneumatosis intestinalis
Rationale: Nelson’s Pediatrics identifies pneumatosis intestinalis, which is the presence of gas within the wall of the intestines, as a pathognomonic radiographic finding for necrotizing enterocolitis (NEC). This finding confirms the clinical suspicion of NEC.
A preterm baby was born to an 18-year-old mother, birth weight is 900 g, and pediatric aging is equal to 30 weeks AOG. The baby started grunting and chest retractions in the 6th hour of life and was hooked up to a mechanical ventilator. What is the most likely diagnosis?
A. Hyaline membrane disease
B. Respiratory distress syndrome
C. Bronchopulmonary dysplasia
D. Transient tachypnea of the newborn
A. Hyaline Membrane disease
Rationale: Hyaline membrane disease, also known as respiratory distress syndrome (RDS), is common among preterm infants and is associated with surfactant deficiency. Nelson’s Pediatrics describes typical clinical features such as grunting, chest retractions, and the need for mechanical ventilation shortly after birth.
Radiographic findings of respiratory distress syndrome:
A. Fistuling of the lobes
B. Flattened diaphragm
C. Hyperinflated lung
D. Groundglass appearance
D. Groundglass appearance
Rationale: According to Nelson’s Pediatrics, the classic radiographic finding in respiratory distress syndrome (RDS) is a ground-glass appearance, which results from the diffuse atelectasis and decreased lung volumes due to surfactant deficiency.
A term baby weighing 4.3 kg is born without complications to a mother with gestational diabetes. At 12 hours of life, he appears mildly jaundiced. Vital signs are stable, he is feeding well and his blood type is the same as mother. Which of the following serum laboratory tests are most likely to help you evaluate this infant’s jaundice?
A. Total serum protein, serum albumin and liver transaminases
B. Total serum bilirubin and direct calcium level
C. Total serum bilirubin and glucose
D. Total serum bilirubin and hematocrit level
D. Total serum bilirubin and hematocrit level
Rationale: In Nelson’s Pediatrics, evaluating jaundice in newborns, especially those at risk for hemolytic disease, involves measuring total serum bilirubin to assess the severity of jaundice and hematocrit to check for signs of hemolysis or polycythemia.
In ABO blood group incompatibility:
A. Mother’s blood type A and baby’s blood type O
B. Mother’s blood type O and baby’s blood type A
C. Kernicterus is commonly seen
D. Jaundice occurs after 7 days of life
B. Mother’s blood type O and baby’s blood type A
Rationale: Nelson’s Pediatrics explains that ABO incompatibility occurs when a mother with blood type O has a baby with blood type A or B. This can lead to hemolytic disease of the newborn, which typically presents with jaundice within the first 24 hours of life, not after 7 days. Kernicterus is a severe complication but not commonly seen with ABO incompatibility due to early detection and treatment.
Baby Boy A, blood type B, Rh positive, was delivered full term with a good Apgar score. He developed jaundice in the 10th hour of life. His mother’s blood is Rh negative. What could have caused his jaundice?
A. Erythroblastosis fetalis
B. Vitamin K deficiency
C. Transplacental bleeding
D. Iron deficiency
A. Erythroblastosis fetalis
Rationale: Nelson’s Pediatrics explains that erythroblastosis fetalis occurs due to Rh incompatibility when an Rh-negative mother has an Rh-positive baby. This leads to hemolysis and jaundice within the first 24 hours of life.
Baby Boy A was born with a good Apgar score via uncomplicated repeat C-section. He was breastfed at the beginning of the 2nd hour of life. On the 5th hour, there was a note of vomiting of reddish mucus secretions. No associated symptoms noted. He passed a dark-colored stool on the 16th hour of life. Which of the following tests would tell that the baby’s condition is secondary to swallowed material?
A. CBC
B. Vitamin K assay
C. Kleihauer-Betke test
D. Apt test
D. Apt test
Rationale: According to Nelson’s Pediatrics, the Apt test differentiates fetal blood from maternal blood in the vomitus or stool. This test is used to determine if the bleeding is due to swallowed maternal blood.
Baby G was brought to the ER on the 2nd week of life because of yellowish discoloration of skin. He was lethargic with opisthotonus and spasticity. Total bilirubin was 30 mg/dl. The most likely diagnosis is:
A. Sepsis neonatorum
B. Perinatal asphyxia
C. Bilirubin encephalopathy
D. Persistent Pulmonary Hypertension
C. Bilirubin encephalopathy
Rationale: Nelson’s Pediatrics states that bilirubin encephalopathy (kernicterus) is caused by high levels of unconjugated bilirubin (>20 mg/dl), leading to central nervous system manifestations such as lethargy, opisthotonus, and spasticity.
A morbidity that is associated with monochorionic twinning involves the possibility of twin-to-twin transfusion syndrome (TTTS):
A. Growth retardation in the recipient twin
B. Growth retardation in the donor twin
C. Polycythemia in the donor twin
D. Anemia in the recipient twin
B. Growth retardation in the donor twin
Rationale: Nelson’s Pediatrics explains that in twin-to-twin transfusion syndrome (TTTS), the donor twin experiences growth retardation and anemia due to decreased blood flow, while the recipient twin may develop polycythemia and hypervolemia.
What is the most common cause of neonatal unconjugated hyperbilirubinemia?
A. Hemolytic disorders
B. Bacterial sepsis
C. Extrahepatic obstruction
D. Genetic disorder (e.g., Rotor-Dubin Johnson)
B. Bacterial sepsis
Neonatal jaundice is pathologic in all of the following conditions EXCEPT:
A. Clinical jaundice in the first 24 hours of life
B. If total serum bilirubin increased by 5 mg/dL/day
C. If direct serum bilirubin or B2 exceeds 1.5-2 mg/dL (> 10% of total serum bilirubin)
D. If clinical jaundice appears at 1 week or less in full term infant or 2 weeks or less in preterm infants
D. If clinical jaundice appears at 1 week or less in full term infant or 2 weeks or less in preterm infants
Rationale: Nelson’s Pediatrics indicates that jaundice appearing within the first week of life in full-term infants or within the first two weeks in preterm infants is generally physiologic. Pathologic jaundice presents earlier (within 24 hours) or persists longer than these time frames.
The neonate may acquire infection through the placenta. This organism is rarely transmitted through the placenta:
A. Toxoplasmosis
B. Herpes simplex
C. Cytomegalovirus
D. Rubella
Herpes simplex
Rationale: Nelson’s Pediatrics notes that herpes simplex virus is rarely transmitted through the placenta compared to other organisms like Toxoplasmosis and Rubella.
ABO incompatibility can be differentiated from Rh incompatibility in that the former is:
A. Milder, hydrops is not common
B. Mother is Rh positive, baby is Rh negative
C. Weakly positive on Coomb’s test
D. Occurs during the 2nd pregnancy
milder, hydrops not common
Rationale: Nelson’s Pediatrics describes ABO incompatibility as generally milder than Rh incompatibility, with less risk of severe outcomes such as hydrops fetalis.
Which of the following decreases the risk of neurologic damage in a jaundiced newborn?
A. Maternal ingestion of phenobarbital during pregnancy
B. Hypoalbuminemia
C. Acidosis
D. Sepsis
Maternal ingestion of phenobarbital during pregnancy
Rationale: According to Nelson’s Pediatrics, maternal ingestion of phenobarbital can induce hepatic glucuronyl transferase in the fetus, decreasing the risk of bilirubin-induced neurologic damage.
A baby was born small for gestational age (SGA) with opacities of both eyes and a grade 3/6 machinery-like murmur. The most likely diagnosis is:
A. Congenital toxoplasmosis
B. Congenital rubella syndrome
C. Congenital herpes infection
D. Congenital syphilis
Congenital rubella syndrome
Rationale: Nelson’s Pediatrics states that congenital rubella syndrome commonly presents with features such as cataracts, congenital heart disease, and microcephaly, which match the clinical description provided.
Which of the following statements regarding late-onset sepsis is NOT correct?
A. It is common after one week of life until 60 days
B. It is either community or hospital acquired infection
C. Meningitis and necrotizing enterocolitis are common complications
D. It is usually caused by E. coli infection
It is usually caused by E. coli infection
Rationale: Nelson’s Pediatrics indicates that late-onset sepsis in neonates is more commonly caused by organisms like Group B Streptococcus (GBS) rather than E. coli, which is more associated with early-onset sepsis.
The most common etiologic agent for early-onset sepsis is:
A. Staphylococcus aureus
B. Listeria monocytogenes
C. Group B Streptococcus (GBS)
D. Streptococcus pneumoniae
Group B Streptococcus (GBS)
Rationale: Nelson’s Pediatrics identifies Group B Streptococcus (GBS) as the most common etiologic agent for early-onset neonatal sepsis, usually presenting within the first week of life.