Pediatrics Flashcards

1
Q

What are the usual doses of common pain medications in children?

A

acetaminophen: 12.5 mg/kg
ketorolac: 0.5 mg/kg
fentanyl: 1-2 mcg/kg
morphine: 0.05 mg/kg

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2
Q

What are the usual doses of common induction agents in children?

A

midazolam: 0.1 mg/kg IV, 1 mg/kg PO
propofol: 2-4 mg/kg
ketamine: 2 mg/kg IV, 4 mg/kg IM
succinylcholine: 1-2 mg/kg IV, 2-4 mg/kg IM

atropine (pre-med): 0.01-0.02 mg/kg IV/IM

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3
Q

What are the usual doses of common ACLS medications in children?

A

epinephrine: 0.01 mg/kg
atropine: 0.02 mg/kg

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4
Q

What is the most common type of EA/TEF?

A

a blind esophageal pouch and a fistula linking the distal esophagus to the trachea

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5
Q

What syndrome is associated with EA/TEF?

A

VACTERL

vertebral anomalies

anal canal defects

cardiac abnormalities

TEF

renal dysplasia

limb defects

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6
Q

What is the risk of placing a gastrostomy in a patient with EA/TEF?

A

inhaled gas can bypass the lungs and exit through the trachea (especially if lung compliance is poor)

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7
Q

If an infant with EA/TEF cannot be ventilated, what are the salvage options?

A

emergency ligation through an abdominal or thoracic approach

placement of a ballon catheter through a gastrostmy and inflated to occlude the fistula

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8
Q

What are the options for ETT position during EA/TEF repair?

A

below the fistula but above the carina

if fistula is small, above the fistula with low ventilation pressures

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9
Q

Where are most congenital diaphragmatic hernias?

A

85% on the left, through the foramen of Bochdalek

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10
Q

Why are babies with CDH hypoxemic?

A

less ventilation (low lung compliance)

less surface area for gas exchange (fewer alveoli)

R-to-L shunting through the PDA (pulmonary HTN)

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11
Q

How should a baby with CDH be managed immediately after birth?

A

NO MASK VENTILATION

intubation

OG tube for stomach decompression

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12
Q

Is CDH a surgical emergency?

A

no

hemodynamics, respiratory support, and acid/base status should be optimized first

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13
Q

What are the likely causes of abrupt hypotension, hypoxia, and bradycardia after CDH repair?

A

tension pneumothorax (usually contralateral to the repair)

IVC compression (undersized peritoneal cavity)

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14
Q

Discuss pediatric fluid management.

A

maintenance fluids: 5% dextrose in 1/2 NS at 4 mL/kg/hr

insensible losses: LR or NS 6-8 mL/kg/hr

blood loss: 3 mL LR or 1 mL albumin/1 mL EBL

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15
Q

What are the components of Tetralogy of Fallot?

A

RV outflow obstruction

RV hypertrophy

large VSD

overriding aorta

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16
Q

What is the QP:QS ratio for maximal oxygen delivery?

A

1:1

17
Q

What are the principles of treating a “Tet spell?”

A

give 100% O2

increase SVR to reduce the R-to-L shunt (squat, treat metabolic acidosis, give phenylephrine)

increase preload (fluids, beta blockers)

18
Q

When is full correction of TOF done? What does it entail?

A

between 2-10 months

relieving RV outflow obstruction, VSD closure, shunt ligation

19
Q

How can a patent ductus arteriosus be maintained? Closed?

A

maintained: prostaglandin E1
closed: indomethacin

20
Q

What are the most common connection between the pulmonary and systemic circulation in transposition of the great arteries?

A

PDA and PFO

21
Q

What are the metabolic derangements associated with pyloric stenosis?

A

early: hypokalemic, hypochloremic metabolic alkalosis

late: metabolic acidosis due to hypovolemic shock

22
Q

What are usual ETT sizes?

A

newborn: 3.0

6 months: 3.5

12 months: 4.0

older: 4 + age/4

23
Q

What are the components of treating post-extubation croup?

A

humidified supplemental oxygen

racemic epinephrine

steroids (delayed action)

24
Q

How does stridor correlate with the location of obstruction?

A

inspiratory: supraglottic or laryngeal
expiratory: intrathoracic
biphasic: laryngeal and subglottic

25
Q

How would you induce anesthesia in a child with epiglottitis?

A

AVOID AGITATION AND CRYING

inhalational induction

careful laryngoscopy

muscle relaxant only after successful mask ventilation

26
Q

What abnormalities are associated with DiGeorge syndrome?

A

CATCH-22

cardiac defects

abnormal facies

thymic aplasia

cleft palate

hypocalcemia