OMSB Pediatrics (OEPEDS) flashcards
OMSB Pediatrics (OEPEDS) · Build recall with a focused review session.
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- APGAR score components
- Appearance, Pulse, Grimace, Activity, and Respiration, each scored 0-2 at 1 and 5 minutes; a score of 7-10 is generally reassuring and 4-6 indicates moderate depression.
- Surfactant deficiency signs
- Respiratory distress syndrome in preterm infants presents with grunting, retractions, and ground-glass opacities with air bronchograms; antenatal corticosteroids reduce severity, and exogenous surfactant is given early.
- Kernicterus risk factors
- Severe neonatal hyperbilirubinemia causes bilirubin encephalopathy; risk rises with hemolysis, prematurity, sepsis, acidosis, and total bilirubin above 25 mg/dL; acute signs include lethargy and hypertonia.
- Necrotizing enterocolitis features
- Preterm infants develop feeding intolerance, abdominal distension, and bloody stools; radiographs show pneumatosis intestinalis; treatment is bowel rest, decompression, and antibiotics, with surgery for perforation.
- Tetralogy of Fallot components
- The four features are ventricular septal defect, overriding aorta, pulmonary stenosis, and right ventricular hypertrophy; the physiology causes cyanosis with decreased pulmonary blood flow and hypercyanotic spells.
- Kawasaki disease criteria
- Fever for at least five days plus four of conjunctivitis, oral mucosal changes, cervical lymphadenopathy, rash, and extremity changes; treat with IVIG and aspirin to prevent coronary artery aneurysms.
- Prostaglandin E1 indication
- Used to maintain ductal patency in duct-dependent congenital heart lesions such as transposition of the great arteries, critical pulmonary stenosis, interrupted aortic arch, and severe coarctation.
- Hypercyanotic spell management
- Knee-chest position, oxygen, morphine, and fluid bolus increase systemic vascular resistance and pulmonary blood flow; refractory cases receive phenylephrine or a beta-blocker; avoid dehydration and crying.
- Asthma reversibility criterion
- In children aged six years or older, asthma is supported by an increase in FEV1 of at least 12% after a bronchodilator, together with compatible symptoms and variable expiratory airflow limitation.
- Cystic fibrosis diagnosis
- Diagnosis requires a sweat chloride of at least 60 mmol/L on two occasions or two disease-causing CFTR mutations; newborn screening uses immunoreactive trypsinogen and is confirmed by sweat testing.
- Croup treatment
- A single dose of dexamethasone 0.15-0.6 mg/kg is given for barking cough and inspiratory stridor; nebulized epinephrine is added for moderate to severe stridor while the airway is monitored.
- Epiglottitis airway caution
- Sudden high fever, drooling, muffled voice, and tripod positioning suggest epiglottitis; do not inspect the throat or agitate the child, and secure the airway with anesthesia present.
- Pyloric stenosis findings
- First-born males at three to six weeks present with non-bilious projectile vomiting and an olive-shaped mass; ultrasound shows pyloric thickness of at least 3 mm; correct hypochloremic alkalosis before surgery.
- Intussusception presentation
- Children aged six to 36 months have colicky pain, drawing up of the legs, a sausage-shaped mass, and red currant jelly stool; ultrasound shows a target sign; air enema reduces it if no perforation.
- Celiac disease testing
- Tissue transglutaminase IgA with a total IgA level screens for celiac disease; duodenal biopsy shows villous atrophy and crypt hyperplasia; lifelong gluten-free diet is the treatment.
- Biliary atresia timing
- Neonatal cholestasis with conjugated bilirubin above 1 mg/dL requires urgent evaluation; biliary atresia is treated with Kasai portoenterostomy, ideally before 60 days of age to improve bile drainage.
- Simple febrile seizure
- A generalized seizure lasting under 15 minutes in a child aged six months to five years with fever and no CNS infection; it occurs once in 24 hours and does not require long-term anticonvulsants.
- Status epilepticus sequence
- A seizure lasting over five minutes is treated first with a benzodiazepine, then a second benzodiazepine, then a second-line agent such as levetiracetam, fosphenytoin, or valproate.
- Bacterial meningitis empiric therapy
- Infants receive ampicillin plus cefotaxime or ceftriaxone plus vancomycin; dexamethasone is given before or with the first antibiotic dose when pneumococcal meningitis is suspected.
- Guillain-Barré syndrome features
- Ascending symmetric weakness with areflexia, albuminocytologic dissociation in cerebrospinal fluid, and nerve conduction slowing; monitor vital capacity and treat with IVIG or plasma exchange.
- Diabetic ketoacidosis criteria
- Glucose above 200 mg/dL with venous pH below 7.3 or bicarbonate below 15 mmol/L and ketonemia; treatment uses isotonic fluid, insulin infusion after the initial bolus, and electrolyte monitoring.
- Congenital hypothyroidism treatment
- Newborn screening detects elevated TSH; levothyroxine 10-15 µg/kg/day is started within two weeks of life to prevent intellectual disability, and thyroid function is reassessed after three years.
- Congenital adrenal hyperplasia
- 21-hydroxylase deficiency causes virilization in girls and salt wasting with hyponatremia and hyperkalemia in severe forms; treatment is hydrocortisone and fludrocortisone replacement.
- Precocious puberty definition
- Breast or pubic hair development before age eight in girls or nine in boys; a GnRH stimulation test distinguishes central from peripheral causes, and central precocious puberty is treated with a GnRH agonist.
- Infant fever evaluation
- Infants younger than three months with fever without a source need blood, urine, and cerebrospinal fluid cultures and empiric ampicillin plus gentamicin or cefotaxime; those under 28 days are admitted.
- Measles clinical features
- Koplik spots, coryza, cough, conjunctivitis, and a descending maculopapular rash; use airborne precautions and give vitamin A, which reduces morbidity and mortality in children with measles.
- Hand foot mouth disease
- Coxsackievirus A16 and enterovirus A71 cause vesicles on the palms, soles, and oral mucosa; enterovirus A71 can cause brainstem encephalitis and cardiopulmonary failure.
- Severe malaria treatment
- Children with fever, anemia, and hepatosplenomegaly after travel to endemic areas are tested with smears or rapid diagnostic tests; severe malaria is treated with intravenous artesunate.
- Pediatric assessment triangle
- Appearance, work of breathing, and circulation to skin are assessed from the doorway; an abnormal finding prompts an immediate primary survey and resuscitation without delaying treatment.
- Pediatric defibrillation energy
- For ventricular fibrillation or pulseless ventricular tachycardia, deliver 2 J/kg for the first shock, then 4 J/kg for subsequent shocks, with compressions at 100-120 per minute.
- Anaphylaxis epinephrine dose
- Give intramuscular epinephrine 0.01 mg/kg of the 1 mg/mL concentration, maximum 0.5 mg, into the anterolateral thigh; repeat every 5-15 minutes, because epinephrine is first-line therapy.
- Pediatric fluid bolus
- Give 20 mL/kg of isotonic crystalloid for shock and reassess after each bolus; use 10 mL/kg in cardiogenic shock and diabetic ketoacidosis, and watch for signs of fluid overload.
- Growth chart red flag
- A child crossing two or more major percentile lines on weight-for-age, length-for-age, or weight-for-length charts warrants evaluation for failure to thrive, including CBC, celiac serology, and urinalysis.
- Iron deficiency anemia treatment
- Microcytic hypochromic anemia with low ferritin is treated with oral elemental iron 3 mg/kg/day for three months after hemoglobin normalizes; universal screening occurs at 12 months.