Pharmacology for peds (Kinder) Flashcards

1
Q

Chlorampehenicol

A

gray baby syndrome

o Abdominal distention, vomiting, diarrhea, gray color, resp distress, hypotension, progressive shock

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2
Q

thalidomide

A

phocomelia

congenital abnormalities
polyneuritis, nerve damage, mental retardation

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3
Q

sulfonamide

A

kernicterus

bilirubin deposits in the brain

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4
Q

benzyl alcohol

A

gasping baby syndrome

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5
Q

gastric pH in babies (full term vs. preterm)

A

full term infant –> 6-8 at birth

drops 1-3 within 24 hours

premature infants –> immature acid secretion so their pH tends to remain elevated

once the babies begin to be fed, gastric acid production begins leading to gastric pH ‘s approaching adult levels

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6
Q

gastric empyting in neonatal period

A

irregular and unpredictable

most orally absorbed drugs are absorbed in the intestine and this can be affected in the baby!

slow/prolonged gastric emptying in premature infants –> prolonged contact time

inverse relationship b/w gestational age and gastric retention

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7
Q

IM injections in babies

A

inconsistent absorption in ped’s patients -

  • relative muscle mass (low in neonate)
  • poor perfusion -(low CO or resp distress which means poor blood flow at the site of injection)
  • peripheral vasomotor instability
  • insufficient muscle contractions

IM is reserved for emergencies when IV access cannot be obtained

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8
Q

skin absorption in babies

A

related to skin hydration and relative absorption area

substantially increased percutaneous absorption- underdeveloped epidermal barrier

compromised skin integrity
increased skin hydration

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9
Q

rectal absorption in babies?

A

indicated if there is nausea, vomiting, seizures, or being prepared for surgeries

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10
Q

total body water in fetus

A

94%

premature infants 85%

full term 78%

adults 60%

must use higher doses per kg of body weight to achieve comparable plasma and tissue concentrations

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11
Q

protein binding in neonate

A

decreased due to decreased plasma protein concentration b/c albumin don’t reach higher levels until 10-12 months of age
alpha-acid glycoprotein levels decreased (basic drugs)

lower binding capacity of proteins in baby

decreased affinity for drug binding

competition for certain binding sites by endogenous compounds

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12
Q

sulfation pathway in babies

A

well developed

acetaminophen can be used in young children b/c of this

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13
Q

gucuronidation pathway is underdeveloped

A

morphine–> need higher serum concentrations

however, clearance quadruples

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14
Q

Glomerular filatruation
tubular secretion
tubular absorption

A

don’t develop fully until later and can affect drug metabolism

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15
Q

Neonatla sepsis common bacterial pathogens

what antimicrobial agents do you use?

A

group b strep
e coli
listeria monocytogenes

use:
ampicillin
gentamicin
third generation cephalosporin
acyclovir (not routinely used)
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16
Q

ampicillin

MOA

A

MOA: inhibits bacterial cell wall synthesis. leads to cell wall lysis

dosing by birth weight

17
Q

meningitis treatment?

A

cover for at least 14 days

18
Q

gentamicin

A

MOA - covers gram negative
inhibits bacterial protein synthesis
results in defective cell membrane

age (gestational age) and weight based dosing

19
Q

Cefotaxime

A

inhibits bacterial cell wall synthesis. Inhibits PBP–> leads to bacteral cell wall lysis

dosing on birth weight

20
Q

acyclovir

A

inhibits viral DNA synthesis and viral replication

dosing 20 mg/kg/dose IV every 8 hours

21
Q

viral myocarditis

phases?

A

acute phase–> inflammatory cell invasion of myocardium and mycoardial necrosis and apoptosis

T-cell invasion–> most destructive 7-14 days after inoculation

Healing phase–> myocardial fibrosis, continued inflammation and persistent viremia may lead to LV dysfunction and dilation

may need transplant….

22
Q

treatment in the acute phase of viral myocarditis

A

inotropes

afterload reduction
mechanical ventilation
ECMO
immune therapy –> IVIG, immunosuppressive agents

23
Q

Intravenous immunoglobulin

A

sterile solution of human immune globulin

primarily IgG with trace IgA and IgM

protects against infection, suppress inflammatory processes

replace primary and secondary immunodeficiencies

dosing–> 2 g/Kg IV as a single dose over 24 hrs

provide immediate antibody levels and can last 3-4 weeks

SENSE OF DOOM

24
Q

ECMO

A

prolonged cardiopulmonary bypass (3-10 days)

neonatal indications:

  • pulmonary HTN
  • meconium aspiration syndrome
  • resp distress syndrome
  • group B strep

complications!!
-drug binding interactions with the circuit

25
Q

gentamicin dose adjustment in ECMO

A

2.5 mg/kg/dose every 18-24 hrs

26
Q

vancomycin dose adjustment in ECMO ?

A

15-20 mg/kg/dose every 18-24 hrs

27
Q

Vasopressors adjustment in ECMO?

A

no change in dosing in ECMO