Week 10 Administering Medications Flashcards
Name and explain the different drug names
Chemical: the exact description of the drug’s chemical composition and molecular structure
Generic: (nonproprietary) name that is listed in publications, such as the USP and national formulary
Official: also the generic name that is listed in publications, such as the USP and NF
Brand (trade or proprietary): what the drug is sold as in stores; the brand name is easily recognized because it begins with a capital letter and sometimes has a registration mark at the upper right of the name; different manufacturers of the same med may give it a different brand name
What is the most important key point to remember when discussing mechanisms to promote drug safety
- looking it up must become second nature
- when in doubt, look it up!
What are the two types of medications systems
Stock supply:
- bulk quantity: measure the dose each time a client needs it
Unit dose:
- prescribed amount of drug the client receives at a single time
Automated dispenser:
- computerized system
- locked cart contains all the meds
- meds are packaged in unit doses, but some bulk meds may also be there
Self Administration:
- clients may self administer meds (SAM) that the hospital does not carry; otherwise, all personal meds must be left at home to avoid double dosing
Explain pharmacokinetics
What the body does to the drug
four processes determine the intensity and duration of a drug’s actions
- absorption
- distribution
- metabolism
- excretion of a drug
Explain pharmacodynamics
What the drug does to the body
Primary and secondary effects of the drugs
What must occur for excretion to occur with pharmacokinetics
drug molecules must be removed from their sites of action and eliminated from the body
Common organs of excretion:
- kidneys, liver, GI tract, lungs, exocrine glands (sweat and salivary)
Explain the factors the affect absorption
Route of administration
Drug solubility:
- enteric coated drugs; cannot be decomposed by gastric secretions
- coating thus prevents the med from being diluted before it reaches the intestines
- decreases irritating effects of the med on the stomach
- Timed release meds: formulated to dissolve slowly, releasing small amounts for absorption over sever hours (DO NOT CRUSH)
Name and explain the factors affecting distribution
Local blood flow:
-rate of distribution depends on the adequacy of local blood flow in the target area and permeability of capillaries to the drug’s molecules
Membrane permeability
Protein-binding capacity
What are the factors affecting metabolism
Biotransformation: chemical conversions of a drug
Liver function:
- metabolism takes place mainly in the liver, but meds can be detoxified also in the kidney, blood plasma, intestinal mucosa and lungs
- if liver function is impaired, the drug will be eliminated more slowly and toxic levels may accumulate
Health/disease status: disease states also affect drug metabolism
First-pass effect:
- oral meds are absorbed from the GI tract and circulate through the liver before they reach the systemic circulation
- Many oral meds can be almost completely inactivated in this way
- this inactivation is known as first pass effect
- oral meds are formulated with higher concentration of the drug than are parenteral meds
What are the factors affecting excretion
- for excretion to occur, drug molecules must be removed from their sites of action and eliminated from the body
The following are common organs of excretion:
- Kidneys: primary site of excretion
- liver and GI tract: some drugs broken down by liver are excreted into GI tract and then eliminated in the feces
- Lungs: gases and volatile liquids administered by inhalation usually are removed through exhalation
- Exocrine glands: drug excretion through the exocrine glands is limited
Name and explain the concepts related to pharmacokinetics
Time until onset:
- time needs to reach a high enough blood level for effects to appear
Duration of drug action:
- length of time that particular drug is effective
Therapeutic range:
- at onset of action, serum drug level is minimal
- Peak level: highest concentration
- Trough level: lowest concentration; right before the next dose
- therapeutic level: concentration of a drug in the blood serum that produces the desired effect
Biological half-life:
- time it take for half of the drug to be eliminated
Concentration of active drug:
- concentration at the intended site
What are the factors affecting pharmacokinetics
- age
- body mass (weight)
- gender
- pregnancy
- environment
- route of administration
- timing of administration
- fluids
- pathological states
- genetic factors
- psychological factors
What are the primary effects of the drugs with pharmacodynamics
- Primary = effects that are predicted, intended, and desired (what we want to happen
Types of primary effects include:
- Palliative = relieve the signs and symptoms of a disease
- Supportive = support the integrity of body functions
- Substitutive = replace either body fluids or a chemical required by the body for improved functioning
- Chemotherapeutic = destroy disease producing microorganisms or body cells
- Restorative = return the body to or maintain the body at optimal levels of health
Explain the secondary effects of drugs when discussing pharmacodynamics
- Secondary effects = all effects other than the intended effect for which the drug was prescribed
- most common side effects are nausea, vomiting, diarrhea, dizziness, drowsiness, dry mouth, abdominal distention or distress, and/or constipation
Can be:
- predictable
- harmless
- harmful
Key point:
- nursing role includes teaching client what side effects to anticipate and how to manage them
When discussing pharmacodynamics, what are the types of secondary effects
Adverse reactions:
- harmful, unitended, usually unpredicted reactions
- require discontinuation of the drug
- FDA defines sever adverse reactions as those that are: life threatening, require intervention, lead to problems