Egyptian Board Pediatrics flashcards
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- Mid-parental height
- Boys: (father's height + mother's height + 13 cm)/2. Girls: (father's height + mother's height − 13 cm)/2. Target range is ±8.5 cm; a height outside this range suggests pathologic short stature.
- Language milestone red flags
- No babbling by 9 months, no single words by 16 months, no two-word phrases by 24 months, or loss of skills at any age warrants audiology testing and developmental evaluation.
- Apgar score components
- Scored at 1 and 5 minutes on Appearance, Pulse, Grimace, Activity, and Respiration, each 0–2. It guides resuscitation and response but does not define asphyxia or predict long-term outcome alone.
- Neonatal resuscitation compression ratio
- For newborns, chest compressions are delivered at a 3:1 compression-to-ventilation ratio when heart rate stays below 60/min despite effective positive pressure ventilation with supplemental oxygen.
- Kawasaki disease treatment
- Fever for at least 5 days plus four of five clinical features. Give intravenous immunoglobulin 2 g/kg as a single infusion with aspirin, and assess coronary arteries by echocardiography.
- Pertussis classic features
- Paroxysmal cough with inspiratory whoop and post-tussive vomiting, often with lymphocytosis. Azithromycin treats the infection and erases transmission; acellular vaccine immunity wanes over time.
- Croup management
- Barking cough, hoarseness, and inspiratory stridor in a young child. Give a single dose of dexamethasone; add nebulized epinephrine for moderate to severe stridor or retractions.
- Anaphylaxis first-line drug
- Epinephrine 0.01 mg/kg intramuscularly, maximum 0.5 mg, into the anterolateral thigh; repeat every 5–15 minutes. Antihistamines and steroids are adjuncts and never replace epinephrine.
- Tetralogy of Fallot spell
- Hypercyanotic spell with decreased pulmonary blood flow. Place knee-chest, give oxygen, morphine, intravenous fluids, and a beta-blocker; prostaglandin may be needed in duct-dependent neonates.
- Ventricular septal defect murmur
- A holosystolic murmur at the left lower sternal border. Small defects may close spontaneously; large defects cause failure to thrive, tachypnea, and pulmonary hypertension requiring closure.
- Oral rehydration solution
- Low-osmolarity solution (245 mOsm/L) given 50 mL/kg over 4 hours for mild dehydration and 100 mL/kg over 4 hours for moderate dehydration, with continued breastfeeding.
- Pyloric stenosis findings
- Nonbilious projectile vomiting at 3–6 weeks with hypochloremic hypokalemic metabolic alkalosis. Ultrasound shows pyloric thickness of at least 3 mm and length of at least 15 mm.
- Nephrotic syndrome criteria
- Edema with heavy proteinuria (urine protein/creatinine ratio above 2), albumin below 2.5 g/dL, and hyperlipidemia. Minimal change disease is commonest; treat with prednisolone.
- Hemolytic uremic syndrome
- Microangiopathic anemia, thrombocytopenia, and acute kidney injury after Shiga toxin-producing E. coli diarrhea. Avoid antibiotics and antimotility drugs; treatment is supportive, often with dialysis.
- Congenital hypothyroidism treatment
- Newborn screening shows elevated thyroid-stimulating hormone and low free T4. Start levothyroxine 10–15 mcg/kg/day within 2 weeks of life to prevent irreversible intellectual disability.
- Diabetic ketoacidosis potassium rule
- Total body potassium is depleted despite normal serum values. Insulin shifts potassium into cells, so replace potassium once serum level is at least 3.5 mEq/L to avoid arrhythmia.
- Iron deficiency anemia treatment
- Give oral ferrous sulfate 3–6 mg/kg/day of elemental iron. Reticulocytosis appears within 1–2 weeks; continue iron for 3 months after hemoglobin normalizes to replenish stores.
- Acute chest syndrome
- Fever, chest pain, hypoxia, and a new pulmonary infiltrate in sickle cell disease. Treat with oxygen, antibiotics, incentive spirometry, and transfusion for severe cases; it is a leading cause of death.
- Simple febrile seizure
- Age 6 months to 5 years, generalized, lasting under 15 minutes, occurring once in 24 hours, without central nervous system infection. Routine EEG and imaging are not indicated.
- Infantile spasms treatment
- Clusters of flexor or extensor spasms with hypsarrhythmia on EEG. Treat with adrenocorticotropic hormone or vigabatrin, especially when associated with tuberous sclerosis.
- Pediatric compression-to-ventilation ratio
- For children, use 30:2 with one rescuer and 15:2 with two rescuers, at a rate of 100–120/min and a depth of one-third of the chest diameter.
- Paracetamol overdose antidote
- N-acetylcysteine. Assess with the Rumack-Matthew nomogram at 4 hours after ingestion; treat when the level is above the treatment line or liver injury is present.
- Lead chelation threshold
- Blood lead level of 45 mcg/dL or higher needs chelation. Levels of 5 mcg/dL or higher need source removal, follow-up testing, and an iron-sufficient diet.
- Adolescent confidentiality limits
- Contraception and sexually transmitted infection care may be confidential under local law, but confidentiality yields when there is risk of harm, abuse, or a reportable condition.
- Vitamin K deficiency bleeding
- Late-onset bleeding occurs at 2–12 weeks in exclusively breastfed infants without prophylaxis. Prevent with intramuscular vitamin K 1 mg at birth for all newborns.
- Failure to thrive definition
- Weight below the 5th percentile or crossing two or more major percentile lines. Evaluate intake, absorption, and losses; hospitalize for severe malnutrition or suspected abuse.
- Congenital adrenal hyperplasia
- 21-hydroxylase deficiency causes virilization in females and salt-wasting crisis with hyponatremia and hyperkalemia. Treat with hydrocortisone and fludrocortisone; monitor 17-hydroxyprogesterone.
- Turner syndrome features
- Short stature, webbed neck, coarctation of the aorta, and streak ovaries. Karyotype is diagnostic; treat with growth hormone and estrogen replacement, and monitor thyroid and cardiac status.
- Immune thrombocytopenia management
- Isolated thrombocytopenia with petechiae in a well child. Treat only for significant bleeding; intravenous immunoglobulin or steroids for severe cases; intracranial hemorrhage is rare.
- Guillain-Barré syndrome
- Ascending symmetric weakness with areflexia and albuminocytologic dissociation in cerebrospinal fluid. Treat with intravenous immunoglobulin or plasma exchange; monitor respiratory function.
- Organophosphate poisoning
- Cholinergic crisis with salivation, lacrimation, urination, diarrhea, bradycardia, bronchorrhea, and miosis. Treat with atropine and pralidoxime after decontamination.
- Newborn screening timing
- Heel-prick blood spot at 24–72 hours of life, repeated after transfusion. It covers congenital hypothyroidism, phenylketonuria, cystic fibrosis, hemoglobinopathies, and hearing screening.