Pharm. Special patients groups Flashcards

(33 cards)

1
Q

Targeted special groups in pharm

A

Pregnancy

Lactation

Pediatrics

Geriatrics

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2
Q

Which two groups have a scarce amount of data about pharmacokinetics/pharmacodynamics and why?

A

Infant/child populations and pregnant women because nobody is willing to risk that patient population for research.

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3
Q

FDA preganancy medication categories

A
A
B
C
D
X
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4
Q

A class medication

A

Remote possibility of fetal harm

No risk of fetal harm demonstrated in controlled trials

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5
Q

B class medicaiton

A

Animal studies have not demonstrated fetal harm, but human studies have not been done.

Or Animal studies have demonstrated some fetal harm but human studies have been done with no evidence of harm

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6
Q

C class medication

A

Animal studies have demonstrated potential fetal harm, but there are no controlled trials to confirm the event in humans

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7
Q

D class medication

A

Evidence of fetal risk has been demonstrated in humans, but use may be justified in some cases based on benefit:risk

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8
Q

X class medication

A

Teratogens

Studies in animals or humans have demonstrated significant fetal harm or deformation.

Completely contraindicated in women who are pregnant

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9
Q

Pregnancy pharmacokinetic changes to oral medications

A

Decreased gastric motility and gastric secretions

Nausea and vomiting

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10
Q

Pregnancy pharmacokinetic changes to transdermal medications

A

increased blood flow (peripheral vasodilation)

Increased body water

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11
Q

Pregnancy pharmacokinetic changes to pulmonary sytem

A

Cardiac and tidal volumes are increased by approximately 50% = hyperventilations and increased pulmonary blood flow

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12
Q

Pregnancy pharmacokinetic changes to distribution

A

Increased blood volume (30-50%)

INcreased adipose deposition

Decreased albumin concentration

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13
Q

Pregnancy pharmacokinetic changes to metabolism

A

Induced and inhibited CYP enzyme activity related to estrogen and progesterone levels

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14
Q

Pregnancy pharmacokinetic changes to elimination

A

Increased renal blood flow

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15
Q

Pregnancy pharmacokinetic changes summary

A

Changes are rarely clinically significant as dosage adjustments are not typically warranted and difficult to predict

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16
Q

Epilepsy in pregnancy

A

Treatment options are limited as all the medications are harmful to the fetus.

Valproic acid is the only medication that is always stopped during pregnancy.

17
Q

Potential adverse effects noticed in the infant following passive exposure from lactation

A

Drowsiness/sedation (Analgesics, antihistamins, antidepressants, anti-epileptics)

Diarrhea (antibiotics)

Withdrawal symptoms (antidepressants, nicotine, drugs of abuse)

18
Q

Pharmacotherapy techniques in lactation

A

Minimizing exposure to the infant (breast feeding during a trough in the medication regimen)

Avoid unnecessary medications

Coordinate medications and feeding schedules (pump and dump schedule)

19
Q

What drugs inhibit prolactin which inhibit lactation?

A

Oral contraceptives, levadopa, repinirole

20
Q

Why can’t pediatric pharmacology be simplified to small adult principles?

A

Because children are not small adults! many physiological differences.

21
Q

Geriatric pharmacology population

A

Adults > 65 yo comprising 13% of the population

it is a growing population

22
Q

Geriatric pharmacokinetic elimination consideration

A

REduced muscle mass may exaggerate creatinine clearance calculations. (may not have any muscle mass)

23
Q

Beers criteria

A

Evidence based approach for medications used in elderly populations

24
Q

STOPP criteria

A

Screening tool of older persons with potentially inappropriate prescriptions

25
Polypharmacy
Complex drug regimens
26
Strategies to avoid polypharmacy
Education, reinforcement, education! Review medication profile routinely
27
Allergies as an adverse event
Immune-mediated response to certain chemical substances No way of predicting initial reaction
28
Side effects as an adverse event
Medications have side effects! Predictable May be caused via same or different mechanism as therapeutic use of drug
29
Adverse drug reaction
Unintended noxious response to a drug when used at normal doses for usual purposes Cannot be predicted
30
Pregnancy summary
Changing kinetics throughout pregnancy Exposure to fetus Non-pharmacologic strategies must be considered Minimal effective dose for the shortest duration Use medications with the best safety profile Risk:benefit
31
Lactation summary
Avoid unnecessary medications Non-pharmacologic strategies must be considered Coordinate medications with feeding schedule Minimal effeective dose for the shortest duration Risk:benefit Monitor the infant for effects
32
Pediatrics
Not small adults!! Diverse population Changing pharmacokinetics Consider age and weight for dosing Use multiple resourses
33
Geriatrics
Sensitive to side effects Beer's criteria STOPP criteria Polypharmacy is a problem