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89 Cards in this Set

  • Front
  • Back
Nurses responsibilites
1. administer drugs
2. asses drug effects
3. interventions to make drug regimen more tolerable/effective
4. client/ family teaching
5. policies, procedures, laws
Framework of Drug Information requires knowledge of...
1. anatomy, physiology & pathophysiology
2. drug standards/guidelines
3. major drug categories
4. client as unique human being with consideration for holistic nature
Plant/ Herbal products
1. codeine and morphine (poppy seed plant)
2. digitalis products (foxglove)
3. alfalfa: arthritis pain- topical or oral
4. aloe: burns & wounds- topical
5. ginger: nausea/ motion sickness
6. ginkgo: cognitive functioning- vasodilator: increase blood flow to brain, not used with aspirin
Animal sources
1. insulin: pancreas of cows & pigs
2. thyroid drugs: thyroid & hypothalamus tissue
3. growth hormones
Inorganic compounds
1. aluminum: antacid- gastric acidity
2. flouride: dental cavities & osteoporosis
3. iron: anemias
4. gold: rheumatoid arthritis
Synthetic sources
1. patterned after drugs made from plants/animals
2. production of chemicals that are therapeutic
3. enhance effectiveness
example: Marional (comes from marijuana for cancer patients, nausea and appitite)
Preclinical Trials
- tested on lab animals
- determine if presumed effects exist
- evaluate adverse effects
Reasons for drugs being discarded- Preclinical trials
1. lack therapeutic activity
2. too toxic
3. highly teratogenic
4. small safety margins
Phase 1 Studies
- healthy human volunteers
- emphasis on safety
- tightly controlled
-special concerns women, minorities, and children
Reasons drugs are discarded- Phase 1 studies
1. lack therapeutic effects
2. adverse effects unaccept.
3. highly teratogenic
4. too toxic
Phase 2 Studies
- drugs tried in patients who have the disease the drug is meant to treat
- informed benefits & risks
- emphasis on effectiveness
Reason for drug discard- Phase 2 studies
1. less effective than anticipated
2. too toxic
3. unaccept. adverse effects
4. low benefit to risk ratio
5. no more effective than similar drugs
Phase 3 Studies
- used in vast clinical market
- 5 to 6 years or longer
- info collected and provided to drug comp. and FDA
-widely used, unexpected adverse effects may occur
Phase 4 Ongoing Evaluation
-prescribers expect to report unexpected effects to FDA
Nurse's role in drug approval
1. informed concent (literacy level, glasses, hearing)
2. administering drugs in clinical phases
3. client/family teaching
4. can work for FDA
5. research
6. help clients find trials
Generic name
original destination drug was given when the company applied for approval process
(acetaminophen)
Brand (trade) name
approved drug given a name by pharmaceutical company who developed it
(Tylenol)
Chemical name
name that reflect the chemical structure of the drug
(n-acetyl-para-aminophenol)
Federal Food, Drug, and Cosmetic Act
mandates tests for drug toxicity, means for drug recall, gave FDA enforcement power
Durham-Humphrey Amendment
tightened control of certain drugs, certain drugs needed to be labeled & need prescription to be distributed
Kafauver-Harris Act
tightened control over quality of drugs
Controlled Substance Act
defined drug abuse, classified with potenital risk for abuse
Orphan Drug Act
drugs that have been discovered but not finanically viable b/c they have limited market or narrow margin. provided company w/ incentives
OTC drugs
- previously a prescription
- drugs used so long w/o adverse effects
- OTC can:
1. mask signs and symptoms
2. drug interactions: interfere w/ drug therapy
3. serious overdoses
Pharmacodynamics
how drugs affect the body
Pharmacokinetics
how body acts to the drug
Drug Actions of pharmacodynamics
-replace or substitute missing chemicals (insulin)
-increase or stimulate: certain cellular activities
-depress or slow: cellular activities, discharges in central nervous system
-interfere w/ fuction of foreign cells: invading microorganisms
Agonist
drugs that interact directly w/ receptor sites to cause same activity that natural chemicals would at this site, stimulate receptor
Antagonist
acts to prevent breakdown of natural chemicals stimulating receptor sites, bind to receptor & prevent response from occuring
Selective Toxicity
-ability of drug to attack
- attack systems only found in foreign cells (penicillin-bacteria)
-anti-neoplasms (cancer cells-bone marrow, hair, gi cells)
Passive transport- pharmacokinetics
-diffusion
-major way drugs absorb in body
-high concentration to low
-no cellular energy required
Active transport
-process uses energy to move molecule across cell membrane
Filtration
-movement through pores in cell membrane
- down concentration gradient
- result of pulling of plasma proteins
Factors to consider
1. route of administration
2. timing
3. critical concentration: amount of drug needed for therapeutic effects
4. half-life: time it takes for amt. of drug to decrease 1/2 of peak level
Absorption- Oral administration
-most frequent used route
-non-invasive
-less expensive
-safest
-barriers: acid, food, pathology (previous illness effect absorption of meds)
Factors affecting absorption
1. perfusion: of blood to area
2. fat content: subcut. tissue
3. temp: of muscle/tissue (vasoconstriction= warm; vasodilation= cold)
4. first-pass effect: breakdown of drug in liver immediately after absorption
Factors affecting distribution
1. lipid solubility: many drugs bound w/ protein & lipid soluble
2. perfusion of area: decreased blood flow to effected areas
3. cardiac output
4. binding to plasma proteins
Factors influencing body's response to a drug
-weight
-age
-gender
-physiological
-pathological: different diseases, g.i., BP
-genetic: lack enzymes for metabolizing
-immunological: allergies
-psychological:attitude
Factors influencing body's response to a drug cont.
-environment: light, temp, noise
-tolerance
-cumulation: excessive doses, accumulation, toxicity
-drug to drug: 2 drugs adverse effects on each other
-drug to food
-drug to lab tests: some drugs alter lab results
Nurse's role on toxic effects of drugs
-anticipate
-prevent
-assess: sign/symptoms
-document: baseline vitals for any changes
Primary adverse effects
-an extension of drug's desired effect
-most common
-result of simple overdose
-diuretic=electrolyte imbalance
Secondary adverse effects
-wide variety of effects in addition to what is desired
-antihistamine aids in breating, can cause drowsniness, can't drive on it
Hypersensitivity adverse effects
-excessive response to primary & secondary effects
-allergic reactions
-toxic effects if can't secrete
Anaphylactic reaction
-antibody reacts w/ site
-histamine released
-swelling, bronchospasms, repiratory stress
Stomatitis
inflammation of mucous membranes, swollen gums and tongue
Superinfections
several kinds of drugs that disturb normal flora of body, usually controlled by organisms (fever, diarrhea, black hairy tongue)
Blood dyscrasia
bone marrow supression by drug effects, cell death occurs (fever, sore throat, low BCC)
Drug Induced Tissue and Organ Damage
1. alterations in glucose metabolism- hypo/hyperglycemia
2. electrolyte imbalance: low potassium levels
increase= slow HR, cramps
decrease= low BP & urine output
3. neurological effects
4. g.i. disturbances
5. teratogenicity
Antibiotics
bacterial infections
(penicillin, sulfonamides)
Antivirals
prevent & treat influenza, herpes, HIV, and AIDS
Antifungals
range from athlete's foot to life-threatening mycosil (fungus) infections
Antoprotozols
include anti-maleria drugs
Anthelmintics
treat local and systemic infections (helminthes=worms)
Aminoglycosides
(major classes of antibiotics)
powerful antibiotics used to treat serious infections (gentamycin, streptomycin)
Fluroquinolones
(cipro) relatively new, broad spectrum, made synthetically, mild adverse drug affects
Marcolides
penicillin allergies
Penicillins
first antibiotic used for clinical use
Sulfonamides & Tetracylcines
not commonly used, widespread resistance
Hypersensitivity reactions
past reactions (rash, hives, couldn't breathe)
Superinfections
destruction of normal flora that invades tissue
Nephrotoxicity
kidney damage, frequently w/drugs metabolized in renals
GI Toxicity
nausea, vomitting, diarrhea, upset stomach
Neurotoxicity
damage to nerve tissue, 8th cranial nerve- most common damage, dizziness, loss of hearing
Corticosteroids
(anti-inflammatory agents)
block inflammatory & immune systems, used topically to produce a local anti-inflammatory effect w/o adverse effects
Antihistamines
block release of histamine in initiation of inflammatory response
Salicylates
-blocks inflammatory response
-fever & pain reducer
-inhibits synthesis of prostaglandins
-acts on hypothalamus
-inhibits platelet aggrevation
-produces analegesic effect (mild-moderate pain)
Salicylates
pharmacokinetics & cautions
-readily absorbed in stomach
-crosses placenta/ breastmilk
-bleeding abnorm.= platelet (prevent strokes, MI's)
-upcoming surgeries (bleeding)
-pregnancy
-impaired renal function
Salicylates
adverse effects
1. G.I. (nausea, heartburn..)
2. bleeding
3. cultural (blacks have decreased sensitivity to pain, increased doses)
4. salicylism: dizziness, ringing in ears, confusion
5. hypernea: labored rapid breathing, tachypnea
Non-steriodal anti-inflammatory drugs
-most common (ibuprofin)
- doesn't prevent strokes, MI
-readily available in G.I.
-metabolized in liver
-excreted in urine
-in breastmilk
Non-steriodal anti-inflammatory drugs
cautions
1.allergy to salicyates
2. cardiovascular, hypertension, peptic ulcers
3. g.i. bleeds
4. pregnancy
5. renal function
Acetaminophen
-pain and fever
-readily absorbed in g.i tract
-metabolized in liver
-excreted in urine
-crosses placenta/breastmilk
Acetaminophen cautions
-allergy to acetaminophen
-pregnancy
-chronic alcoholism
-hepatic dysfunction
Cardiovascular disease
-includes all conditions affecting heart & blood vessels
- #1 cause of death in US
-peripheral vascular disease, coronary artery disease, etc.
Hyptertension
-high BP, more than 2 readings
-most common cardiovascular
-blacks highest rate
-#1 killer of women
Prehypertension
120-139 /
80-89
Stage 1 hypertension
140-159 /
90-99
Stage 2 hypertension
160 or above /
100 or above
Blood pressure control
1. heart rate
2. stroke volume (amount of blood pumped out of ventricle w/ each heart beat)
3. total peripheral resistance: resistance to muscular arteries to blood being pumped through
Step 1: Lifestyle modifications
-weight reduction
-smoking cessation
-moderate alcohol intake
-reduction of salt in diet
-increase physical activity
Step 2: Inadequate response
-continue lifestyle modifications
-medication initiated:
1. diuretic or beta blocker: decrase sodium, HR
2. ACE inhibitor, calcium channel blocker
Step 3: Inadequate response
-increase drug dose
-substitute another drug
-add 2nd drug from another class
Step 4: Inadequate response
-add 2nd or 3rd agent or diuretic
Calcium channel blockers
-prevent calcium into cardiac and smooth muscle cells
-interferes with cell's ability to contracts leading to loss of smooth muscle
-vasodilation
-decreased peripheral resistance (decrease BP, cardiac workload, mycardial oxygen consumption)
ACE inhibitors
-block conversion of angiotension I to angiotension II
-decreased BP, aldosterone secretion, serum sodium & flud
-increases serum potassium
Vasodilators
-emergency, life-threatening hypertension
-relaxation of vascular smooth muscle
- decreased BP, peripheral resistance
-oral renin inhibitors
Calcium channel blockers adverse effects
-headache
-anxiety
-g.i. disturbances
-bradycardia: slow HR
ACE inhibitors adverse effects
-nausea/ vomitting
-change in taste perception
-dry persistant cough
Vasodilators adverse effects
-hypotension
-orthostatic hypotension
-dizziness
-fatigue
Thromboembolic disorders
-decreased blood flow or total occlusion of the blood vessel
-predispose to the formation of clots
-example: CAD (narrowing of coronary arteries caused by damage to the epithelial lining in these vessels)