Iraqi Board Pediatrics study materials
Iraqi Board Pediatrics study resources

Iraqi Board Pediatrics flashcards

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32 cards. Read the term and the definition here. The deck at the top of this page is optional.

Apgar score timing
Assigned at 1 and 5 minutes after birth; it never guides resuscitation decisions, which are made before delivery based on the clinical situation.
Physiologic jaundice timing
Jaundice that appears after 24 hours of life; jaundice within the first 24 hours is always pathologic and requires urgent bilirubin and Coombs testing.
Necrotizing enterocolitis hallmark
Feeding intolerance, abdominal distension, and bloody stools in a preterm infant; abdominal x-ray shows pneumatosis intestinalis. Treatment is bowel rest, decompression, and antibiotics.
Kawasaki disease criteria
Fever for at least 5 days plus 4 of 5 features: conjunctivitis, mucosal changes, rash, extremity changes, and cervical lymphadenopathy. Treat with IVIG and aspirin.
Febrile infant under 28 days
Any fever in an infant younger than 28 days warrants a full sepsis evaluation, admission, and empiric intravenous antibiotics regardless of appearance.
Primary immunodeficiency red flags
Two or more pneumonias, four or more ear infections per year, failure to thrive, family history, or need for intravenous antibiotics suggest immunodeficiency.
Tetralogy of Fallot spell
Hypercyanotic episode treated with knee-chest position, oxygen, morphine, intravenous fluids, and phenylephrine; avoid isoproterenol, which worsens obstruction.
Ductal-dependent lesions
Transposition of the great arteries, critical coarctation, and interrupted aortic arch depend on the ductus arteriosus; maintain patency with prostaglandin E1 infusion.
Innocent murmur features
Systolic, grade 2/6 or less, no thrill, normal S2, varies with position, no radiation, and an asymptomatic child.
Croup treatment
A single dose of dexamethasone 0.15-0.6 mg/kg; add nebulized epinephrine for moderate to severe stridor. Symptoms are barking cough and inspiratory stridor.
Bronchiolitis management
Supportive care with oxygen and hydration; respiratory syncytial virus is the most common cause; bronchodilators and corticosteroids are not routinely recommended.
Anaphylaxis epinephrine dose
Intramuscular epinephrine 0.01 mg/kg of 1:1000 concentration, maximum 0.5 mg, into the anterolateral thigh; repeat every 5-15 minutes as needed.
Pyloric stenosis findings
Nonbilious projectile vomiting at 3-6 weeks, visible peristalsis, olive-shaped mass, and hypochloremic hypokalemic metabolic alkalosis; treat with pyloromyotomy.
Bilious vomiting in neonate
A surgical emergency until malrotation with volvulus is excluded by an upper GI contrast study; do not delay surgical consultation.
Celiac disease diagnosis
Anti-tissue transglutaminase IgA with total IgA level; confirm with duodenal biopsy showing villous atrophy and crypt hyperplasia.
Simple febrile seizure
Generalized seizure lasting less than 15 minutes, occurring once in 24 hours, in a child 6 months to 5 years; no routine EEG or neuroimaging is indicated.
Status epilepticus first-line
A benzodiazepine such as lorazepam 0.1 mg/kg intravenously or midazolam 0.2 mg/kg intramuscularly; second-line is fosphenytoin or levetiracetam.
Duchenne muscular dystrophy signs
X-linked disorder with Gowers sign, calf pseudohypertrophy, and elevated creatine kinase; confirm with genetic testing; corticosteroids slow progression.
Diabetic ketoacidosis management
Isotonic fluid resuscitation, insulin infusion 0.05-0.1 units/kg/hour, and monitoring for cerebral edema; avoid rapid osmotic shifts in children.
Congenital hypothyroidism treatment
Levothyroxine 10-15 mcg/kg/day started within 2 weeks of life to prevent intellectual disability; newborn screening uses TSH.
Congenital adrenal hyperplasia
21-hydroxylase deficiency causes salt wasting, ambiguous genitalia in girls, and hyperkalemia with hyponatremia; treat with hydrocortisone and fludrocortisone.
Nephrotic syndrome treatment
Prednisone 60 mg/m²/day for 4-6 weeks then alternate-day therapy; findings are heavy proteinuria, hypoalbuminemia, edema, and hyperlipidemia.
Hemolytic uremic syndrome triad
Microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury, often after bloody diarrhea; management is supportive with dialysis as needed.
Hypospadias management
Do not circumcise; refer for surgical repair at 6-18 months of age because the foreskin may be needed for reconstruction.
Iron deficiency anemia treatment
Elemental iron 3-6 mg/kg/day for 3 months after hemoglobin normalizes; findings are microcytic hypochromic anemia with low ferritin and high TIBC.
Sickle cell prophylaxis
Penicillin prophylaxis from 2 months to 5 years, hydroxyurea for frequent crises, and pneumococcal vaccination.
Tumor lysis syndrome
Hyperkalemia, hyperphosphatemia, hyperuricemia, and hypocalcemia; prevent with hydration and allopurinol or rasburicase.
Acetaminophen toxicity antidote
N-acetylcysteine, most effective within 8 hours of ingestion; use the Rumack-Matthew nomogram at 4 hours post-ingestion to guide therapy.
Organophosphate poisoning
SLUDGE syndrome with salivation, lacrimation, urination, diarrhea, GI upset, and emesis; treat with atropine and pralidoxime.
Systemic JIA features
Quotidian fever, evanescent rash, arthritis, hepatosplenomegaly, and serositis; risk of macrophage activation syndrome.
IgA vasculitis features
Palpable purpura on the lower extremities, arthritis, abdominal pain, and nephritis; management is supportive with urine monitoring.
Autism screening
Use the M-CHAT at 18 and 24 months; refer for behavioral therapy and audiology; no single diagnostic test exists.