Module 2 Pharm Flashcards

1
Q

Which system does not change with pregnancy?

a) endocrine
b) kidney
c) liver
d) GI

A

a)endocrine

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2
Q

How much does renal blood flow increase in pregnancy (and thus GFR)?

A

Twice (doubles)

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3
Q

What can be a consequence of increased GFR?

a) accelerated drug clearance
b) decreased drug clearance
c) decreased metabolism
d) toxicity

A

a)accelerated drug clearance

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4
Q

What percentage of congenital anomalies are due to genetic factors?

a) 10%
b) 15%
c) 20%
d) 25%

A

d)25%

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5
Q

When are teratogens most dangerous?

a) preimplantation/presomite
b) embryonic
c) fetal
d) more than one of the above

A

a)preimplantation/presomite

The period from conception to week 2. Teratogens act in ALL or NOTHING fashion.

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6
Q

Teratogen exposure in embryonic period causes what?

a) death of conceptus
b) gross malformations
c) function issues
d) none

A

b)gross malformations can occur if teratogen exposure occurs in embryonic period (1st trimester)

Teratogen exposure in fetal period (2nd and 3rd trimester) can result in brain/behavior/functional issues

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7
Q

True or false: proof of teratogenicity means a drug will cause a congenital anomaly at every exposure?

A

False.

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8
Q

True of false: lack of proof of teratogenicity does not mean a drug is safe?

A

True

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9
Q

What causes neonates and infants to be at risk for drug reactions?

a) immature liver
b) immature kidney
c) immature immune system
d) one or more of the above
e) none of the above

A

d) one or more of the above

rationale: infant organ systems are immature which places them at risk for drug sensitivity

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10
Q

In infants and children, there is a risk for drug effects which are ______ and ______.

a) mild and short
b) intense and prolonged
c) intense and short
d) none

A

b) intense and prolonged

Because drugs remain above MEC longer than in adults

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11
Q

True or false: dosing infants on body size alone is safe.

A

False. This is not safe as the issue with drug sensitivity relates to immature organ systems and immature pharmacokinetic processes.

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12
Q

An infants’ GI may affect drugs via:

a) delayed gastric emptying
b) increased gastric emptying
c) low (acidic) gastric pH
d) high (basic) gastric pH
e) one or more of the above

A

Answer:

a & c

Infant gut has delayed and erratic emptying so drugs may be more absorbed. Additionally, gastric acidity is low so acid-labile (loving) drugs have an increased absorption

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13
Q

IM administration of drugs in infants is _____ than in adults.

a) faster
b) slower
c) the same

A

b) slower

Low blood flow through muscles slows the absorption rate of IM drugs

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14
Q

Transdermal administration in infants is ____ than in adults.

a) faster
b) slower
c) the same

A

a) faster

Skin is thin and blood flow greater to the skin so there is a risk for toxicity associated with topical drugs.

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15
Q

Drug protein is limited in the infant due to:

a) low albumin
b) competition from endogenous compounds
c) low perfusion
d) increased hepatic metabolism
e) one or more of above

A

answer:

a &b

Drug binding to protein is limited due to low albumin (less places to bind) and competition with endogenous compounds (less places to bind). This causes free drug levels to be higher.

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16
Q

True or false: the blood brain barrier is fully mature at birth.

A

False. It is not well developed and thus drugs have easy access to CNS.

17
Q

At what age (roughly) do pharmacokinetic systems reach adult-ish maturity?

A

Age 1

Hepatic and renal metabolism and excretion are low until age 1.

18
Q

True or false: children older than age 1 metabolize drugs faster than adults?

A

True. This lasts until about age 2.

19
Q

How are pediatric dosages determined?

a) pediatric dosages are established based on data/research for all drugs
b) they are extrapolated from adult dosages
c) they are calculated with adult dosage and body surface area
d) one or more of the above
e) none

A

answer: b&c

o Dosages extrapolated from adult doses
o Child’s BSA x adult dosage / (1.73 m²)=pediatric dosage

20
Q

True or false: geriatric patient alterations in GI absorption are not a major factor?

A

True. The percentage of dosage absorbed does not usually change with age, but the RATE OF ABSORPTION may be slowed.

21
Q

What are complications of liver metabolism decreases in geriatric patients?

a) half-lives decreased
b) enzyme activity decreased
c) first-pass metabolism increased
d) one or more of above

A

answer: d
o Decreased liver blood flow, mass, enzyme activity
 Half-lives can be increased
 First-pass metabolism can be increased because fewer drugs are inactivated before entering systemic circulation

22
Q

True or false: Drug accumulation due to reduced renal excretion is most important cause of ADRs in older adults?

A

True.

23
Q

Which lab value should we measure to assess kidney function?

a) creatinine clearance
b) serum creatinine

A

a)creatinine clearance

In older patients, serum creatinine (lean muscle mass) decreases along with kidney function. Thus creatinine level may look normal even though renal function is decreased.

24
Q

___ percentage of nonadherance in older adults is INTENTIONAL.

A

75%