Pediatric Conditions Flashcards

1
Q

Differentials for non-bilious vomiting

A
  • Gastroenteritis
  • Acute viral illness
  • Food allergy
  • Pyloric stenosis
  • GERD
  • Meconium ileus
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2
Q

Differentials for bilious vomiting

A
  • Volvulus with rotation
  • Intussusception
  • Ileus (meconium, septic, etc)
  • Meconium plug syndrome
  • Bowel perforation
  • Hirschsprung
  • Intestinal atresia
  • Necrotising enterocolitis
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3
Q

Clinical features of Meckel’s diverticulum

A
  • Typically asymptomatic, incidental finding - most frequently symptomatic <2y
  • Commonly presenting with painless GI bleeding (hematochezia or melena)
  • Abdominal pain (usually RLQ)
  • Intestinal obstructive symptoms (if herniated or twisted)
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4
Q

Diagnosis and management of Meckel’s diverticulum

A
  • Diagnostic:
    • Meckel’s scan (Technetium-99 scan)
    • X-ray: limited but can be used for detecting obstruction or perforation
  • Management:
    • Asymptomatic:
      • Resection indicated for all children or young adults
    • Symptomatic: diverticulectomy or segmental resection
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5
Q

Clinical features of intussusception

A
  • Most commonly in children between 3m - 5y old
  • Initially non-bilious vomiting, bilious if becomes obstructive
  • Abdominal pain: acute, cyclical, colicky
  • Palpable abdominal mass - usually RUQ
  • Bloody stools: “currant jelly”
  • Lethargy, pallor, other sympoms of shock
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6
Q

Diagnostic and management of intussusception

A
  • Abdominal ultrasound: target sign
  • Air or barium enema
  • Management:
    • Initial steps: NG decompression and fluid resuscitation
    • Non-surgical: air enema
    • Surgical reduction
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7
Q

Clinical features of pyloric stenosis

A
  • Forceful projectile vomiting after feeds
  • Difficulty feeds and irritable
  • Palpable, non-tender, epigastric mass
  • Visible peristaltic waves
  • Dehydration symptoms:
  • Presenting around 2-7 weeks of life
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8
Q

Diagnostic and management of pyloric stenosis

A
  • Definitive imaging: abdominal ultrasound or barium studies
  • FBE: late signs include electrolyte derangements (hypochloremic metabolic alkalosis)
  • Management:
    • Correct any electrolyte derangment and fluid replacement
    • NPO
    • Surgical procedure: pyloromyotomy
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9
Q

Clinical features of Hirschsprung

A
  • Initial presentation
    • Meconium not passing in the first 48h of life
    • Abdominal bloating and tenderness
    • Bilious vomiting
  • Late presentation
    • Chronic presentation (in milder cases)
    • Failure to thrive/poor feeds

DRE exam findings: tight anal spinchter, squirt sign (explosive stool release after finger removal)

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10
Q

Diagnosis and management of Hirschsprung

A
  • Initial imaging: X-ray and barium enema
  • Diagnostic imaging: rectal biopsy
  • Management:
    • Initial:
      • correct fluid and electrolyte disturbance
      • NG decompression and colonic irrigation
      • screen for signs of enterocolitis
    • Surgical resection of aganglionic region
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11
Q

Differential diagnosis of delayed passage of meconium

A
  • Hirschsprung
  • Meconium ileus
  • IND
  • Congenital hypothyroidism
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12
Q

Types of acyanotic congenital heart disease

A

VSD, ASD, PDA, coarctation of aorta

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13
Q

Types of cyanotic congenital heart diseases

A
  • Tetralogy of Fallot
  • Transposition of the great vessels
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13
Q

Difference between acyanotic and cyanotic lesions

A
  • Acyanotic conditions (“pink babies”): Have left-to-right shunts in which oxygenated blood from the lungs is shunted back into the pulmonary circulation.
  • Cyanotic conditions (“blue babies”): Have right-to-left shunts in which deoxygenated blood is shunted into the systemic circulation
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14
Q

Describe Eisenmenger syndrome

A

Reversal of left-right shunt to right-left shunting due to increased pulmonary pressures (pulmonary hypertension), leading to cyanosis.

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15
Q

Clinical features and auscultation findings of VSD

A
  • Holosystolic murmur - best heard in the LLSE
    • Louder in small defects
    • Louder with maneuvers increasing afterload (e.g. handgrip)
  • Presenting with recurrent chest infections, dyspnea, CHF, failure to thrive
16
Q

Clinical features and auscultation findings of ASD

A
  • Systolic ejection murmur over ULSE - widely fixed split S2
  • Recurrent respiratory infection, easily fatigued, failure to thrive
17
Q

Management of ASD/VSD

A
  • Most septal defects close spontaneously
  • Follow-up echo based on size
  • If CHF developmnes: initial treatment includes diuretics + inotropes + ACEi
18
Q

Clinical features and auscultation findings of PDA

A
  • Typically asymptomatic; patients with large defects may present with FTT, recurrent lower respiratory tract infections, clubbing, and CHF.
  • Continuous “machinery murmur” at the second left intercostal space at the sternal border
19
Q

What do you give to close a PDA? When is this contraindicated?

A
  • Indomethacin (NSAID)
  • Contraindicated in cyanotic lesions that require PDA for survival (transposition of great vessels, tetralogy of Fallot, coarctation of aorta)
20
Q

Clinical features of coractation of aorta

A

Narrowing of aorta at the aortic isthmus - in the descending or abdominal aorta
* Features:
* Differential cyanosis - affecting lower extremities
* Asymptomatic hypertension, lower extrimity claudication,
* Continous murmur may be heard diffusely over the torso

21
Q

Management of coarctation of aorta

A
  • Prostaglandin - reopen PDA
  • Surgical repair or balloon dilatation
22
Q
A