Clinical Pharmacokinetics Flashcards

1
Q

Clinical considerations with tube feeds

A

Jejunal tubes are not great for enteral absorption

Not all tablets can be crushed or opened (sustained-/controlled-release drugs)

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2
Q

Blood-brain barrier - variation in permeability

A

Non-inflamed: tight web with minimal penetration
Inflamed: increased spaces, possibly better penetration
Less protein binding: more crossing the BBB

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3
Q

First and second phase of hepatic metabolism

A

Phase I: reduction-oxidation, hydrolysis

Phase II: conjugation

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4
Q

Must drugs are eliminated through the __

A

Kidneys

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5
Q

Actual serum creatinine instead of creatinine clearance could do what to the estimate of true renal function?

A

Overestimate it

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6
Q

Compare acute vs chronic renal insufficiency in regards to pharmacologic considerations.

A

With acute renal failure, you must readjust to more normal dosage after kidney injury is reduced. CKD will continue on that altered dosing regimen.

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7
Q

What can happen with hemodialysis?

A

Some of the drug can be filtered out, especially if they’re hydrophilic and small

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8
Q

What is another consideration with renal disease?

A

The dose will generally not need adjustment if the drug is primarily excreted through means other than the kidneys

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9
Q

Interpatient variabilites

A

Renal function, hydration status

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10
Q

Intrapatient variability

A

Clinical status

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11
Q

Skin of neonates

A

Increased hydration leads to increased absorption of topical products

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12
Q

Vd in neonates

A

Higher Vd of water soluble drugs due to increased extracellular fluid

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13
Q

What processes are immature at birth?

A

Phase II metabolism, tubular secretion, reabsorption

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14
Q

Skin of elderly patients

A

Thin; increased absorption

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15
Q

Vd in elderly patients

A

Increased Vd of fat soluble drugs due to increased adipose tissue
Decreased Vd of water soluble drugs due to decreased ECF

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16
Q

Renal function in elderly patients

A

Decreased

17
Q

Steady state is dependent only on what?

A

Half-life

18
Q

Examples of drugs that need TDM

A

Some antibiotics, antiepileptic agents, and anticoagulants

19
Q

Types of drug interactions

A

Drug-drug
Drug-nutrient
Drug-disease state
Level of drug action

20
Q

Examples of pharmacokinetic incompatibility: absorption

A

Chelation and changes in stomach pH

21
Q

Examples of pharmacokinetic incompatibility: distribution

A

Competition for binding sites
Changes in protein binding due to disease
Changes in extracellular fluid or adipose

22
Q

Examples of pharmacokinetic incompatibility: metabolism

A

Inducers/inhibitors of CYP450

23
Q

Examples of pharmacokinetic incompatibility: elimination

A

Competition for elimination pathways (renal is most common)

Decreased or increased elimination