Pharmacology Flashcards

Covers: Neonatal Considerations; Neonatal Therapeutics

1
Q

Neonates have slower or faster absorption when compared to adults.

A

(Slower)

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2
Q

Neonates have higher or lower absorption when compared to adults.

A

(Higher)

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3
Q

Neonates have higher or lower bioavailability when compared to adults.

A

(Higher)

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4
Q

Which of the following does not lead to increased bioavailability associated with neonates when compared to adults?

A - Decreased efflux pumps
B - Decreased metabolizing enzymes
C - Being on a milk diet
D - Increased intestinal permeability
E - Incomplete GI flora

A

(C) - Being on a milk diet

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5
Q

Which of the following neonatal characteristics leads to decreased activation of prodrugs?

A - Decreased efflux pumps
B - Decreased metabolizing enzymes
C - Being on a milk diet
D - Increased intestinal permeability
E - Incomplete GI flora

A

(B) - Decreased metabolizing enzymes

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6
Q

How does the larger extracellular fluid compartment of neonates impact water soluble drugs?

A

(Effects the dose needed to be administered to get the same effect, you will need a HIGHER dose in neonates to get the same plasma concentration as you would in adults on a normal dose)

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7
Q

How does the larger extracellular fluid compartment of neonates impact lipid soluble drugs?

A

(It doesn’t, there is a smaller intracellular fluid compartment but the difference in concentrations reached is much smaller for lipid soluble drugs and dose adjustments are not often needed)

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8
Q

What results from leaky vessels, lack of p-glycoprotein efflux pumps, and lack of metabolizing enzymes in neonates?

A

(Incomplete diffusion barriers such as the BBB)

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9
Q

Why is there no significant difference in renal elimination between neonates and adults in horses, cattle, and sheep?

A

(Bc the neonatal kidneys have a similar GFR and RBF to adults by the first few days of life in those species)

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10
Q

Are weak acids excreted slower or faster in neonates?

A

(Slower, neonates have acidic urine when compared to adults so the weak acids will not be ionized in urine so they can be reabsorbed easier)

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11
Q

Are weak bases excreted slower or faster in neonates?

A

(Faster, neonates have acidic urine when compared to adults so the weak bases will be more readily ionized in the urine and will get trapped and excreted)

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12
Q

What is the preferred route of medication administration in a septic neonate?

A

(IV; PO and SC are crappy, IM ain’t great; IO is a possibility)

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13
Q

What drug category can be used to improve the hemodynamic status of neonates and may improve absorption of other drugs?

A

(Pressors i.e. dobutamine, norepinephrine, vasopressin, etc.)

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14
Q

Why do increased portions of drugs reach the brain and heart in a neonate with sepsis?

A

(Blood is being shunted away from the less important organs such as the kidneys, spleen, and gut and instead shunted to the brain and heart)

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15
Q

What is the ‘third spacing’ phenomenon?

A

(Interstitial edema results from increased capillary permeability in patients with endothelial damage, water soluble drugs can distribute to that edema and cause a need for higher drug doses to get an adequate plasma concentration)

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16
Q

Which of the following parasiticides are not suggested in neonates and young animals (<6 weeks in puppies and <4 months in horses)? Multiple correct answers.

A - Pyrantel pamoate
B - Ivermectin/moxidectin
C - Fenbendazole
D - Metronidazole
E - Sulfadimethoxine

A

(B, D → CNS toxicity)

17
Q

Why does ketamine have less of an analgesic effect in neonates?

A

(Bc their NMDA receptors are immature, this has been found in human neonates)

18
Q

What is the anesthetic of choice for neonates?

A

(Propofol)

19
Q

What class of sedatives should be used with caution at very low doses and avoided entirely if there is already respiratory or circulatory compromise in your neonatal patient?

A

(Alpha-2 agonists)