Iran Specialty Board - Pediatrics flashcards
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- Apgar score
- A 0–2 score for heart rate, respiratory effort, muscle tone, reflex irritability, and color at 1 and 5 minutes; it guides resuscitation but does not diagnose asphyxia.
- Surfactant therapy
- Endotracheal administration of natural surfactant (poractant alfa or beractant) for respiratory distress syndrome; early rescue within 2 hours reduces pneumothorax and mortality.
- Physiologic jaundice
- Unconjugated hyperbilirubinemia appearing after the first 24 hours of life from immature hepatic conjugation; jaundice within the first 24 hours is always pathologic.
- Mid-parental height
- Boys: (father + mother + 13 cm)/2; girls: (father + mother − 13 cm)/2. The target range is ±8.5 cm around this value.
- Autism screening
- M-CHAT-R/F is administered at 18 and 24 months. Diagnosis requires deficits in social communication plus restricted or repetitive behaviors across multiple settings.
- Failure to thrive
- Weight below the 3rd percentile or crossing two major percentile lines; evaluation addresses caloric intake, malabsorption, and endocrine or renal causes.
- Phenylketonuria
- Phenylalanine hydroxylase deficiency detected by newborn screening; a low-phenylalanine diet and sapropterin for responsive patients prevent intellectual disability.
- Galactosemia
- Classic form presents with jaundice, hepatomegaly, cataracts, and E. coli sepsis in the neonate; treatment is strict avoidance of galactose and lactose.
- MCAD deficiency
- Medium-chain acyl-CoA dehydrogenase deficiency causing hypoketotic hypoglycemia triggered by fasting or illness; avoid prolonged fasting and give IV dextrose during illness.
- Hepatitis B birth dose
- All infants receive the vaccine within 24 hours of birth; infants of HBsAg-positive mothers also receive HBIG within 12 hours.
- Kawasaki disease
- Fever for at least 5 days plus 4 of conjunctivitis, oral changes, rash, extremity changes, and cervical lymphadenopathy; treat with IVIG 2 g/kg and aspirin.
- Anaphylaxis treatment
- Epinephrine 0.01 mg/kg IM (max 0.5 mg) into the anterolateral thigh, repeated every 5–15 minutes; adjuncts include fluids, oxygen, and antihistamines.
- Cow milk protein allergy
- Extensively hydrolyzed formula is first line; amino acid formula for severe or refractory cases; soy formula is not recommended before 6 months of age.
- SCID
- Severe combined immunodeficiency presents with failure to thrive, chronic diarrhea, and opportunistic infections; live vaccines are contraindicated and HSCT is curative.
- Prostaglandin E1
- Maintains ductal patency in ductal-dependent congenital heart lesions such as transposition, pulmonary atresia, and critical coarctation until surgical or catheter intervention.
- Infective endocarditis prophylaxis
- Amoxicillin 50 mg/kg (max 2 g) 30–60 minutes before dental procedures, only for high-risk lesions such as prosthetic valves or prior endocarditis.
- Cystic fibrosis diagnosis
- Autosomal recessive CFTR mutation; newborn screening uses immunoreactive trypsinogen; a sweat chloride of 60 mmol/L or greater is diagnostic.
- Croup treatment
- Dexamethasone 0.15–0.6 mg/kg as a single dose; nebulized epinephrine is added for moderate-to-severe inspiratory stridor and retractions.
- Celiac disease
- Tissue transglutaminase IgA plus total IgA; duodenal biopsy showing villous atrophy confirms; lifelong gluten-free diet is the treatment.
- Pyloric stenosis
- Nonbilious projectile vomiting at 3–6 weeks; ultrasound shows pyloric thickness over 3 mm and length over 15 mm; correct hypochloremic alkalosis before surgery.
- Nephrotic syndrome
- Edema, proteinuria with urine protein/creatinine ratio above 2, hypoalbuminemia, and hyperlipidemia; minimal change disease is the most common childhood cause.
- Hemolytic uremic syndrome
- Microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury, usually after Shiga toxin-producing E. coli; avoid antibiotics and antimotility agents.
- Diabetic ketoacidosis
- pH below 7.3, bicarbonate below 15 mEq/L, and ketonemia; fluid resuscitation over 48 hours and insulin infusion 0.05–0.1 U/kg/h; watch for cerebral edema.
- Congenital hypothyroidism
- Elevated TSH on newborn screening; levothyroxine 10–15 mcg/kg/day started within 2 weeks prevents intellectual disability and supports normal growth.
- Congenital adrenal hyperplasia
- 21-hydroxylase deficiency causes virilization in girls and salt wasting; elevated 17-hydroxyprogesterone; treat with hydrocortisone and fludrocortisone.
- Sickle cell disease
- Hydroxyurea reduces vaso-occlusive crises; penicillin prophylaxis until age 5; acute chest syndrome is treated with oxygen, antibiotics, and transfusion.
- Immune thrombocytopenia
- Isolated thrombocytopenia with petechiae and bruising; IVIG or corticosteroids for significant bleeding; avoid platelet transfusion unless bleeding is life-threatening.
- Status epilepticus
- A seizure lasting more than 5 minutes; first-line treatment is a benzodiazepine, then fosphenytoin 20 mg/kg IV or levetiracetam 60 mg/kg IV.
- Duchenne muscular dystrophy
- X-linked dystrophin deficiency with Gowers sign, calf pseudohypertrophy, and elevated CK; treat with corticosteroids and exon-skipping agents.
- PALS epinephrine dose
- Epinephrine 0.01 mg/kg IV/IO (0.1 mL/kg of 1:10,000) every 3–5 minutes; defibrillate at 2 J/kg, then 4 J/kg for shockable rhythms.
- Activated charcoal
- Given at 1 g/kg within 1 hour of ingestion when the airway is protected; it binds many toxins but is ineffective for iron, lithium, and alcohols.
- DKA cerebral edema
- Suspect with headache, bradycardia, hypertension, and altered mental status during treatment; give hypertonic saline or mannitol and slow the fluid rate.