front 1 What is a therapeutic index? | back 1 Drugs desired therapeutic effects and it's adverse effects |
front 2 What is the difference between a narrow and wide therapeutic index? | back 2 A narrow index is more difficult to manage
-
may require close monitoring for toxicity or adverse
effects
-
EX. seizure meds
A
wider therapeutic index is safer and
requires less monitoring
- EX is antibiotics and propranolol
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front 3 Type of Drug Responses:
Graded | back 3 biological effects that can be measured continually up to the maximum
responding capacity of the biological system
- BLOOD PRESSURE
- HEART RATE
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front 4 Type of Drug Responses:
Quantal | back 4 biological effects are present or not present
effects of a response that may or may not happen
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front 5 What is Pharmacodynamics?
What are some factors of Pdyamics? | back 5 What the drug does to the body
- Ease of titration
- Therapeutic index
-
A narrow
therapeutic index is more difficult to manage.
- A wider therapeutic index
is safer and requires less monitoring.
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front 6 What is pharmacokinetics?
What are factors of Pkinetics? | back 6 The movement of the drug to the bodies circulation
- Distribution
- Ability to cross blood–brain
barrier
- Cytochrome P450 (CYP450) metabolism
- Renal elimination
- Dose–concentration curve
- Half-life
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front 7
Pharmacokinetics: Absorption
What is Absorption? | back 7 The movement of the drug to the body's circulation |
front 8
Pharmacokinetics: Absorption
What are things to consider with Absorption of a drug?
**think how you administer it & how body absorbs it | back 8 Things to consider:
-
Route of Administration
- IV, IM, oral,
sublingual, intranasal
- ***IV fastest
method of drug absorption
-
Site of Administration
- Topical-
targets the site
- Inhaler- goes straight to
lungs
- Ophthalmic- goes to the eyes
-
Bioavailability
- % of the drug that is
truly absorbed/administered
- IV- 100% vs Oral
10-90%
- "availability of drug that is truly
absorbed"
-
Peak blood levels
- highest level of drug in
the body
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front 9
Pharmacokinetics: Distribution
What is Distribution?
What is required for adequate distribution of a drug? | back 9 The movement of the drug to the target organ/tissues
- Good blood supply
- Drug distributed to areas of high
blood flow first then to low blood flow areas
- EX:
Kidneys, liver first then adipose tissue
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front 10
Pharmacokinetics: Distribution
What are things to consider with Distribution ?
**think size, environment, and how it gets around | back 10
Size of molecule
-
smaller molecules are better able to diffuse than larger
molecules in passive diffusion
Acid & Base Environments
Protein binding
-
Plasma proteins in blood
-
Albumin is a major protein in the blood
-
Consider pts with renal/ liver disease because proteins are
produced less or excreted
Transporters
-
influenced by transporters, membrane proteins that
facilitate the movement of molecules across the cell
membranes
Volume of Distribution |
front 11
Pharmacokinetics: Distribution
What are things to consider when crossing the blood brain barrier
& placental barrier? | back 11 Blood-Brain Barrier
- very protected- impenetrable
- only lipid soluble
drugs can pass
Placental Barrier
- Many drugs can pass barrier
- Low molecular weight
drugs pass easier
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front 12
Pharmacokinetics: Distribution
Things to consider with protein binding? | back 12 Drugs exists in bound or unbound status
Travel when bound and cross membranes when unbound
-
Drug action occurs when drug is unbound
Highly protein bound drug means that less of the drug is available
Low plasma protein (low albumin d/t decrease liver, renal fnx,
malnourished, cancer pts-cells feed off body) will result in more free drug |
front 13
Pharmacokinetics: Metabolism
What is metabolism? | back 13 Chemical alteration of drug to metabolites
Metabolism increase or decreases onset, duration, and toxicity of
the drug
The breakdown of the drug in the liver |
front 14
Pharmacokinetics: Metabolism
What does first pass mean and half-life? | back 14
First pass IS FOR ORAL DRUGS
- Concentration of the medication function that is reduced
before it reaches circulation
- Occurs in the liver or
gut
-
first pass may break down most function of drug so may need to
consider another route of administration
Half life
- Time it takes for 50 % of the drug to be eliminated
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front 15
Pharmacokinetics: Metabolism
What is CYP450 and things to consider? | back 15 It is a major drug metabolizing enzyme
Organized into numbered families
Enzymes can slow or increase drug metabolism
Concurrent administration w/ inhibitor or inducer can alter
metabolism of medication
Pro-drugs-- need to go through metabolism to become an active form
of drug |
front 16
Pharmacokinetics: Metabolism
Factors that affect metabolism?
***person, environment | back 16 - Age
- Genetics
- Pregnancy
- Diet
- ETOH
- Liver disease
- Environment
- Timing
- Drug Interactions
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front 17
Pharmacokinetics: Excretion
What is excretion?
What organs eliminate drugs? | back 17 Removal of drug from body to organs of elimination
***The drug moving to the potty
-
Kidney
- GI
- Lungs- ETOH, Ketosis
- Skin- Sweat
- Saliva
- Mammary Glands- via breast milk
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front 18
Pharmacokinetics: Excretion
Factors that affect renal excretion? | back 18
Kidney function
Age
-
Infants/Older adults @ risk for ADR bc renal function (immature
or decreased)
Hydration
Cardiac Output |
front 19
Pharmacodynamics
What is a dose curve response? | back 19
Read graph from left to right to represent increase dose
concentration
-
Dose- response
curve shows the relationship between drug dose and magnitude on
effect
- Dose below the curve do not produce a
pharmacological response
- Dose above the curve do not
produce additional pharmacological response
- May have
unwanted side effects = toxicity
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front 20
Expressing a drug response
What is potency?
What is efficacy?
What is intrinsic activity? | back 20 Potency: the amount of the drug needed to produce a biological effect
Efficacy: The maximum effect a drug can produce
Intrinsic activity: ability to produce a response once the drug is
attached to the receptors |
front 21 Drug Selectivity
What is drug selectivity?
What is minimum effective concentration?
What is minimum toxic concentration?
What is therapeutic index? | back 21 Ratio of the dose producing undesired effects
Minimum effective concentration (MEC): level below
therapeutic effects will not occur
Min toxic concentration (MTC): level above which
toxic effects occur
Therapeutic Index: ratio of MTC to MEC |
front 22 What are the components to rational drug selection?
***think Problem, Plan, Educate | back 22 Define the patient problem
Specify the therapeutic objective
Collaborate with the patient
Choose the treatment
Educate the patient
Monitor effectiveness |
front 23
Define the patient problem
What are the ANP actions to define the problem? | back 23 Assess the patient
Develop differential diagnosis
Use diagnostic test to confirm |
front 24
Specify the therapeutic objective
What is your goal of treatment? | back 24 Cure the disease?
Help relieve S/S
Long term prevention
Replace what is needed- Insulin, Vitamin D
make the patient comfortable with palliative therapy |
front 25
Collaborate with the patient
What does the World Health Organization recommend? | back 25 The World Health Organization recommends including the patient in
developing the therapeutic objectives of drug therapy. |
front 26
Choose the treatment
What are things to consider before choosing the drug therapy? | back 26 -
first determine
what the appropriate therapy would be using evidence-based
guidelines
- second, individualize the drug
choice for the specific patient
- consider pharmacokinetics
& -dyamics
- Determine the cost of the drug
- When writing a prescription, discuss whether patient has
ability to pay for prescription.
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front 27
Educate the patient
What should you educate the patient about?
What does poor adherence to meds result in?
**think about what i educate about insulin | back 27 - Patient education should be at the 5th or 6th grade
level.
-
Include in
education:
- Purpose of
medication
- Instructions for
administration
- Adverse drug
reactions (ADRs)
- Poor adherence
contributes to worsening disease, hospital admissions, and
death.
***purpose of insulin is to control BG, how to administer insulin,
SE of hypoglycemia. IF do not take medication- can contribute to
worsen diabetes, hospital readmission, death |
front 28
DRUG FACTORS INFLUENCING DRUG SELECTION: Monitor the
effectiveness of the drug
What is passive & active monitoring? | back 28 - Passive monitoring: Passive monitoring includes educating the
patient on the expected outcome of the drug therapy and instructing
the patient to contact the provider if the treatment is not
effective or if adverse drug effects occur
- Active monitoring: Follow-up laboratory tests
or monitoring to measure therapeutic effectiveness.
- EX
seizure medications, anticoags
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front 29
DRUG FACTORS INFLUENCING DRUG SELECTION: Therapeutics Factors
What are sources to find evidence of therapeutic factors of a medication? | back 29 -
therapeutic impact of a drug is reviewed in the literature and
observed in
the individual patient
- Evidence for therapeutic impact
- Clinical
trials
- Clinical practice guidelines
- Systematic
reviews
- Randomized controlled trials
- Extrapolate with caution because tend to use
healthy individuals when in reality, patients are complex
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front 30
DRUG FACTORS INFLUENCING DRUG SELECTION: Safety
What are safety platforms and considerations for patients | back 30 - The safety profile of a drug is taken into consideration
and weighed against
other factors when
prescribing. -
Safety is initially determined in clinical trials and is
outlined in the precautions and contraindications in the drug
monograph. - Safety may vary with the
population.
- Tetragons
- Liver or renal disease
- Drug allergies
-
The U.S. Food and
Drug Administration (FDA) collects information on
and monitors the
safety of drugs via postmarketing surveillance by the
MedWatch
program -
The FDA issues a
“Public Health Advisory” when there is drug safety information
that needs to be conveyed to patients or caregivers.
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front 31
DRUG FACTORS INFLUENCING DRUG SELECTION: Cost
What are things to consider with drug cost? | back 31 - Cost to patient
- High drug cost = patient may
decrease adherence
- Ask about prescription drug
coverage
- Consider $4 retail pharmacy lists
- Cost to society
- Thoughtful prescribing considers
cost to healthcare system
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front 32 DRUG FACTORS INFLUENCING DRUG SELECTION: Patient factors | back 32 Previous experience w/ ADRs
- ADRs can be a significant factor in nonadherence
- Renal pts more at risk for ADRs
Health Beliefs
Current Drug Therapy
- Drug interactions
- If a patient is on a complex
medication regimen, consultation with a pharmacist or PharmD who has
access to drug interaction software is warranted for patient
safety.
Age
- either the very young or the very old
Pregnant |
front 33 DRUG FACTORS INFLUENCING DRUG SELECTION: Provider factors | back 33 - Ease of prescribing or monitoring
- Formularies
- Nurse practitioners need to be familiar with the
formularies they are allowed to prescribe.
- Personal
formulary: Each provider develops a small list of drugs they are
comfortable prescribing.
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front 34 INFLUENCES ON RATIONAL PRESCRIBING | back 34 - Pharmaceutical promotion
- May influence
prescribing
- Changes in prescribing
recommendations
- When guidelines change, providers may
need to be coached or reeducated regarding appropriate
prescribing.
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front 35 What is pharmacogenetics? | back 35 - Pharmacogenomics is the branch of pharmacology that deals with
the influence of genetic variations on drug response in
patients by correlating gene expression with a drug’s efficacy or
toxicity.
- In other words, drugs and drug combinations are optimized for
each individual’s unique genetic makeup.
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front 36 What is Heterogeneity?
What system mostly metabolizes drugs? | back 36 Genetic makeup contribute to many variations in pharmacokinetics
Most drugs are metabolized through cytochrome P450 enzyme system
various factors contribute to specific observable pharmacodynamics differences |
front 37 What are basic concepts of CYP450? | back 37 - CYP450 enzymes are involved in about 75% of drug metabolism and
bioactivation in the liver
- Some CYPs metabolize only one
(or a very few) drug(s), whereas others may metabolize multiple
drugs
-
The CYP3A
subfamily is responsible for over 50% of drug
metabolism
- Race, gender, environmental
factors, and drugs may alter the gene expression of individual
CYP450 families and subfamilies
-
40% of Asians
display drug polymorphism
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front 38 What are Inhibitors and Inducers of CYP450? | back 38 - What are the clinical implications when substrates inhibit
CYP450 enzymes?
- An inhibitor may decrease the
metabolism of substrates and generally lead to increased
drug effect.
- What are the clinical implications
when substrates induce CYP450 enzymes
- An inducer may
increase the metabolism of substrates and generally lead to
decreased drug effect.
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front 39 What are the different types of Metabolizers? | back 39 - Poor metabolizers
- break down meds slowly
- experience side effects at the standard dose
- Intermediate metabolizers
- may have too much medication
on board at a standard dose, causing side effects
- Extensive metabolizers
- normal rate of
metabolism
-
Ultra-rapid
metabolizers
-
meds are
rapidly broken down
-
meds may be
removed from the system before providing any symptom
relief
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front 40 What is Pharmacoeconomics? | back 40 - Pharmacoeconomics defined
- Provides a framework
for evaluating drug treatments in terms of comparing one treatment
with another
- Pharmacoeconomics studies
- Generic drugs
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front 41 Generic Drugs
General concepts | back 41 - Generic drugs may or may not be less expensive.
- Pharmacy coverage may determine whether a generic drug is
used.
- Tiered benefit
-
Many benefit plans have a two- or three-tiered benefit, in
which the patient pays a greater co-payment for brand-name
drugs than for generic equivalent prescriptions
- Lower co-pay for generic drugs
- Retail
prescription drug programs.
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front 42 Generic substituition
What are prescribers influenced by? | back 42 - 69% of prescriptions filled with generic drugs
- Prescriber influenced by:
- Innovator company
- Payer
- Patient
- Innovator companies
support for health care
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| back 43 - FDA regulates and sets standards for bioequivalence
-
Be bioequivalent (an equal rate and extent of drug absorbed
in the bloodstream)
- FDA Orange Book: Approved Drug Products with Therapeutic
Equivalence Evaluations is:
- Available
online
- Searched by active ingredient
- Searched by
proprietary name
- Updated daily
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front 44 What are concepts of pharmacoeconomics to consider in practice | back 44 - Prescribing generic vs brand-name drugs
- Pharmacist may
substitute a less expensive drug that is therapeutic equivalent
- “Dispense as written”
- Patients may switch due to
costs and prescription benefit.
- Retail drug
programs
- Walmart, Target, Kroger, Sam’s Club
- $4
for a 30-day supply of common generic drugs for Metoformin vs 70%
brand name
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