Pediatrics Flashcards

1
Q

What is the number one cause of death in children?

A

trauma

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2
Q

What is the best indicator of shock in pediatric patients?

A

tachycardia

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3
Q

What is considered tachycardia for the following age groups:

  • neonates
  • 1-6 years old
  • 6-12 years old
  • 13 years or older
A
  • neonates: > 150 bpm
  • 1-6 years old: > 120 bpm
  • 6-12 years old: > 110 bpm
  • 13 years or older: > 90
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4
Q

What is the appropriate volume for boluses in children of crystalloid and blood?

A
  • crystalloid: 20cc/kg

- blood: 10cc/kg

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5
Q

When should blood be transfused in pediatric trauma patients?

A

if still hypotensive after two crystalloid boluses

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6
Q

What is considered adequate urine output in neonates, infants, and toddlers?

A
  • neonates: 2-3 mL/kg/hr
  • infants: 2-3 mL/kg/hr
  • toddlers: 1 mL/kg/hr
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7
Q

What is the appropriate size and type of ETT in children less than 10 years old?

A
  • they always get an uncuffed tube

- use a tube with same diameter as patient’s pinkie or use Breslow tape to decide

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8
Q

Describe the presentation, diagnosis, and treatment of pyloric stenosis.

A
  • presents with projective, non-bilious emesis and an olive-like mass palpable in the epigastrium
  • labs reveal hypochloremic, hypokalemic, metabolic alkalosis
  • US shows a pylorus > 3mm thick and > 14mm long
  • treat with resuscitation (NS) then dextrose-containing mIVF and take to the OR for pyloromyotomy
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9
Q

What is the most common type of tracheoesophageal fistula?

A

a blind ending of the esophagus with distal TE fistula

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10
Q

What are the VACTERL syndrome components?

A
  • Vertebral anomalies
  • Anorectal (imperforate anus)
  • Cardiac
  • TE fistula
  • Renal
  • Limb anomalies
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11
Q

In addition to the workup and treatment of a TE fistula, what other diagnostic studies are required to work up the VACTERL syndrome?

A
  • vertebral anomalies: sacral US
  • anorectal: digital exam for imperforate anus
  • cardiac: TTE
  • TE fistula: AXR
  • renal: ultasound
  • limb anomalies: exam
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12
Q

How is TE fistula treated?

A

primary repair through a right extra pleural thoracotomy plus a G-tube

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13
Q

What are the five types of TE fistula?

A
  • A: isolated esophageal atresia
  • B: esophageal atresia with proximal fistula
  • C: esophageal atresia with distal fistula
  • D: esophageal atresia with double fistula
  • E: isolated fistula
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14
Q

What are the most common etiologies for intussusception in children?

A

1) inflamed peers patches after viral illness
2) lymphoma
3) Meckel’s diverticulum

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15
Q

How is ileocolonic intussusception managed in children? Adults?

A
  • begin with air-contrast enema
  • repeat enema if it recurs
  • operate if unable to reduce with enema, they are peritonitis, or they are obstructed
  • always operate for adults since malignant lead point is much more common
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16
Q

What is the etiology for malrotation with midgut volvulus?

A
  • malrotation secondary to failure of normal 270-degree rotation during intestinal development
  • volvulus secondary to Ladd’s bands (adhesions to right retroperitoneum)
17
Q

Describe the presentation, etiology, diagnosis, associations, and treatment of malrotation with mid-gut volvulus.

A
  • presents with bilious emesis, typically before one year of age
  • malrotation (asymptomatic) is due to failure of 270-degree rotation while volvulus (symptomatic) is due to Ladd’s bands (adhesions to right RP)
  • diagnosed with an upper GI series, which will show that the duodenum does not cross the midline
  • associated with congenital diaphragmatic hernia and omphalocele
  • treat with resection of Ladd’s bands, counterclockwise detorsion to place the small intestine on the right and large intestine on the left, and appendectomy
18
Q

What is the treatment for malrotation with volvulus?

A
  • resection of Ladd’s bands
  • counterclockwise detorsion, placing the small bowel on the right and large bowel on the left (think “turn back time” for counterclockwise)
  • appendectomy to prevent later diagnostic confusion
19
Q

Malrotation with midgut volvulus is associated with what two other anomalies?

A
  • congenital diaphragmatic hernia

- omphalocele

20
Q

How is duodenal atresia diagnosed?

A
  • AXR showing double bubble sign is usually first

- follow with an upper GI series

21
Q

What causes small bowel atresia?

A
  • duodenal atresia is failure of re-canalization

- other intestinal atresias are due to intrauterine vascular accidents (usually jejunum)

22
Q

Give the etiology, diagnostic workup, and treatment for duodenal atresia.

A
  • due to failure of re-canalization
  • diagnosed with AXR and UGI series
  • treated with primary reconnection
23
Q

Describe the presentation, associations, diagnosis, and treatment of meconium ileum.

A
  • presents with failure to pass meconium in the first 24hrs of life
  • diagnosed with AXR showing dilated small bowel without air fluid level and a positive sweat chloride test given the high association with cystic fibrosis
  • treated with gastrhogafin enema or N-acetylcysteine enema
  • operate for perforation or ostomy creation for anterograde NAC enemas
24
Q

What is the most common cause of colonic obstruction in neonates?

A

Hirschsprung’s disease

25
Q

How is Hirschsprung’s disease diagnosed?

A

with suction rectal biopsy showing an absence of ganglion cells in the myenteric plexus

26
Q

What is the treatment for Hirschsprung’s disease?

A

resection of affected rectum and colon with delayed anastomosis

27
Q

What is the treatment for Hirschsprung’s colitis?

A

rectal irrigations, may require emergent colectomy