Study Guide 1 Flashcards

1
Q

scope of practice for APRN prescribing

A

2 components

  1. right to prescribe independently
  2. right to prescribe w/o limitation
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2
Q

med adherence

A

extent to which pts take their meds as prescribed by LIP and agreed to by pt

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3
Q

medication hx and factors to consider when prescribing

A
  1. cost
  2. disease guidelines
  3. interactions (drugs and polypharmacy)
  4. s/e
  5. allergies
  6. liver and renal fx
  7. need for monitoring
  8. special populations
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4
Q

teratogen

A

substance which will cause permanent abnormalitiy, growth retardation, or death if fetus exposed

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5
Q

renal function when prescribing

A

look at creatinine clearnace

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6
Q

e- prescribing

A

trend bc less likely to have errors

cannot e-prescribe scheduled meds or narcs

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7
Q

pharmacokinetics

A

study of drug movement throughout the body

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8
Q

first pass effect

A

o Refers to the rapid heaptic inactivation of certain PO drugs. when drugs are absorbed from the GI tract, they are carried direcly to the liver through the hepatic portal vein before they enter the systemic circulation. If the capacity of the liver to metabolize a drug is extremely high, that drug can be completely inacticated on its first pass through the liver. As a result, no therapeutic effects can occur. To circumvent the first pass effect, a drug that undergoes rapid hepatic metabolism is often administered parenterally.

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9
Q

steady level aka plateau

A

Administering repeated doses will cause a drug to build up in the body until a plateau (steady level) has been achieved.

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10
Q

time to plateau

A

approximately 4 half lives with constant dose

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11
Q

decline from plateau

A

 When drug administration id dc’ed, most (94%) of drug in the body will be eliminated over an interval equal to about 4 half lives.

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12
Q

excretion

A

removal of drugs from the body

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13
Q

most common organ for drug excretion

A

renal

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14
Q

absorption

A

movement of drug from site of admin into systemic circulation

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15
Q

factors affecting drug absorption

A
	Rate of dissolution
	Surface area
	Blood flow
	Lipid solubility
	Ph partitioning
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16
Q

half life

A

time required for the amount of drug in the body to decrease by 50%

17
Q

passage of drugs across membranes

A

ADME

18
Q

3 ways to cross cell membrane

A
  1. passage through channels or pores
  2. passage with aid of transport system
  3. direct penetration of membrane
19
Q

polar molecules

A

molecules that have no net charge and uneven distribution of electrical charge

20
Q

ions

A

molecules that have net electrical charge- positive or negative

unable to cross membranes

21
Q

ion trapping/og oartutuibubg

A

• Bc of ionization of drugs is Ph depdendent, when the ph of the fluid on 1 side of a membrane differs from the ph of the fluid on the other side, drug molecules tend to accumulate on the side where the ph most favors their ionization. Accordingly, bc acidic drugs tend to ionize in basic meida, and bc basic drugs tend to ionie in acidic media, when there is a ph gradient between 2 sides of a membrane, the following occurs
o Acidc drugs accumulate on the alkaline side
o Basic drugs accumulate on the acidic side
• The process whereby a drug accumulates on 1 side of a membrane where the ph most favors its ionization is referred to as ion trapping or ph partitioning

22
Q

metabolism

A

aka biotransformation

enzymatic alteration of drug structure

takes place in liver

23
Q

p450 system

A

o Metabolism that takes place in the liver is perfroemd by hepatic microsomal enzyme system, known as P450 system. The term P450 refers to cytochrome P450, a key component of this enzyme system.

24
Q

therapeutic consequences of drug metabolism

A
	Accelaterated renal excretion of drugs
	Drug inactivation
	Increased therapeutic action
	Activation of prodrugs
	Increased toxicity
	Decreased toxicity
25
Q

special considerations in drug metabolism

A
	Age
	Induction and inhibition of drug-metabolisng enzymes
	First-pass effect
	Nutrition status
	Competion between drugs
26
Q

protein binding

A

o Drugs can form reversible bonds with various proteins in the body. Of all the proteins with which drugs can bind, plasma albumin is the most important. Like other proteins, albumin is a large molecule. Bc of its size, albumin is too large to leave the bloodstream.

27
Q

pharmacodynamics

A

o Study of biochemical and physiologic effects of drugs on the body and the molecular mechanisms by which those effects are produced

28
Q

TI

A

o The measure of a drug’s safety

29
Q

AGNOIST

A

 Molecules that activate receptors
 Bc neurotransmitters, hormones, and other endogenous regulators activate the receptors to which they bind, all of these compounds are considered agonists. When drugs act as agonists, they simply bind to receptors and mimic the actions of the body’s own regulatory molecules.

30
Q

antagonist

A

 Produce their effects by preventing receptor activation by endogenous regulatory molecules and drugs. antagonists have virtually no effects on their own receptor function

31
Q

maximal efficacy

A

largest effect that a drug can produce

32
Q

potency

A

amount of drug we must give to elicit a response

33
Q

pediatrics BBB

A

o Not fully developed at birth
Drugs and other chemicals have relatively easy access to the central nervous system (CNS)
o Infants especially sensitive to drugs that affect CNS function
o Dosage should also be reduced for drugs used for actions outside the CNS if those drugs are capable of producing CNS toxicity as a side effect

34
Q

requirements when writing prescriptions

A

 Prescriber name, license #, contact info
 DEA # (if applicable, only when prescribing controlled substances)
 Patient name and DOB
 Name of medication
 Strength of medication
 Number of tablets/capsules to dispense
 Number of refills