introduction to winter 2013 1 1. 8/3/2015 winter 2013 2 instructor joan saalwaechter msn, rn...
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Winter 2013Winter 2013 11Winter 2013
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INSTRUCTORINSTRUCTORJOAN SAALWAECHTER MSN, RNJOAN SAALWAECHTER MSN, RN
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CONTACTING MECONTACTING ME
PHONE – 303-292-0015 X3629PHONE – 303-292-0015 X3629CELL – 303-726-0692CELL – 303-726-0692OFFICE – 2OFFICE – 2ndnd floor #210 floor #210 [email protected] GRADESJUPITER GRADESOFFICE HOURS – IN SYLLABUSOFFICE HOURS – IN SYLLABUS
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SUGGESTED MATERIALSSUGGESTED MATERIALS
EVERY BOOK YOU HAVE THAT EVERY BOOK YOU HAVE THAT RELATES TO HEALTH CARERELATES TO HEALTH CARE
PLUSPLUS
THE INTERNET !!THE INTERNET !!
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CLASSROOM RULESCLASSROOM RULES
BE NICEBE NICESHARESHARE
DON’T DISTURB YOUR DON’T DISTURB YOUR NEIGHBORNEIGHBOR
IF YOU ARE TALKING, YOU IF YOU ARE TALKING, YOU ARE NOT LISTENINGARE NOT LISTENING
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TIPS FOR STUDYINGDON’T READ THE BOOK LIKE A NOVEL – USE IT TO
INVESTIGATE THE DRUGS and CONCEPTS WE DISCUSS IN CLASS
WORK BOOK
TIPS OUTLINED IN TEXT
BOXES, DRUG PROFILES, TABLES, LIFESPAN CONSIDERATIONS,
HERBAL THERAPIES, CRITICAL THINKING ACTIVITIES, POINTS TO
REMEMBER, PATIENT TEACHING TIPS, NCLEX REVIEW
QUESTIONS, CASE STUDIES, VOCABULARY
EVOLVE STUDENT SITE HESI PRACTICE EXAM
NCLEX REVIEW BOOK04/19/23 6Winter 2013
IMPORTANT !!!
KNOW THE VOCABULARY
THIS IS A NEW LANGUAGE THAT YOU ARE LEARNING
LOOK UP THE WORDS THAT YOU DO NOT KNOW
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Resources Resources for Drug Drug informationinformation
LilleyLilleyDavis drug guideDavis drug guideOther texts and drug referencesOther texts and drug referencesInternetInternet
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Inside the World of a Drug BookInside the World of a Drug BookClassificationsClassificationsIV compatibility chartIV compatibility chartTall Man ListTall Man ListDrug picturesDrug picturesDrugs, generic names in alphabetical Drugs, generic names in alphabetical
orderorderPink boxesPink boxes
Trade namesTrade namesPregnancy categoriesPregnancy categoriesClassificationClassification
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Drug ClassificationsPINK BOXES IN DRUG BOOKPINK BOXES IN DRUG BOOK
Therapeutic Based on the therapeutic response
expected from the drugExample: Antidepressant
Pharmacologic A description of the chemical action of the
drug. Example: Selective Serotonin Reuptake
Inhibitor
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Drug ClassificationsDrug ClassificationsDrugs are grouped or categorized Drugs are grouped or categorized
according to their effect on the body, according to their effect on the body, the condition they are treating or their the condition they are treating or their chemical characteristicschemical characteristics CNS depressantsCNS depressants AntidepressantsAntidepressants AdrenergicsAdrenergics
Some drugs fit into more than one Some drugs fit into more than one categorycategory
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CNS DEPRESSANTS
OPIOIDS SEDATIVES HYPNOTICS MUSCLE RELAXANTS
DIRECT ACTING
CENTRAL ACTING
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Drug NamesChemical name
Describes the drug’s chemical composition and molecular structure
Generic name (nonproprietary name)
Name given by the United States Adopted Name Council
Trade name (proprietary name)
The drug has a registered trademark; use of the name is restricted by the drug’s patent owner (usually the manufacturer)
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Naming of DrugsNaming of DrugsChemical name
(+/-)-2-(p-isobutylphenyl) propionic acid
Generic nameIbuprofen
Trade nameMotrin, Advil
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Naming of drugs, cont.Naming of drugs, cont.
Chemical nameN-acetyl-para-aminophenol (APAP)
Generic name acetaminophen
Trade name (Proprietary name)Tylenol
LET’S TALK ABOUT LET’S TALK ABOUT DRUG CARDS AND DRUG CARDS AND WEEKLY QUIZZESWEEKLY QUIZZES
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Generic & Brand Name
Student namecefazolin sodium (Ancef; Kefzol)
Classification Antibiotic, cephalosporin class – First generation
Action Inhibits cell wall mucopeptide synthesis
IndicationsFirst 10
Infection of bone, joint, respiratory tract, skin and skin structure, urinary tract, genital tract, biliary tract; septicemia; prostatitis; endocarditis; epididymitis, surgical prophylaxis. Active against the following organisms in vitro and in clinical infections: S. Aureus (including Penicillinase-producing strains); S. epidermidis; Streptococcus pneumoniae, Escherichia col, Proteus mirabilis, Klebsiella sp. Enterobacter aerogenes, Haemophilus influenzae
Dosing RangeAdult only
Adults: Mild-severe infections: 500 mg – 1.5 grams IM/IV every 6-8 hrs. Maximum 12 grams/day. Renal dosing considerations required.Adult Prophylaxis: 1 gram IV or IM administered 0.5-1 h prior to the start of
surgery.
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Adverse Effects
MOST COMMON
Diarrhea, oral candidiasis (oral thrush), vomiting, nausea, stomach cramps, anorexia and pseudomembranous colitis. Onset of pseudomembranous colitis symptoms may occur during or after antibiotic treatment. Anaphylaxis, eosinophilia, itching, drug fever, skin rash, Stevens-Johnson syndrome. Neutropenia, leukopenia, thrombocytopenia, thrombocythemia. Genital and anal pruritus.
Contraindications/PrecautionsNo more than 10 +
life-threatening
Known allergy to cephalosporins; Caution if impaired renal function, may have cross-allergenicity to penicillins; history of antibiotic-associated colitis; seizure disorder; if also receiving nephrotoxic drugs. Transient rise in ALT, AST, and alkaline phosphatase levels has been observed. As with other cephalosporins, reports of hepatitis have been received. Pregnancy category B
Drug-Drug, Drug-Herbal Interactions
10 only
Probenecid may decrease renal tubular secretion of cephalosporins when used concurrently, resulting in increased and more prolonged cephalosporin blood levels.
DON’T FORGET TO CHECK HERBAL INTERACTIONS
Nursing Interventions/
Patient Teaching
Check allergies. Monitor BUN and creatinine. May be associated with a fall in prothrombin activity. Prothrombin time should be monitored in patients at risk and exogenous vitamin K administered as indicated. Drug should be taken exactly as directed. Skipping doses or not completing the full course of therapy may: (1) decrease the effectiveness of the immediate treatment, and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by cefazolin sodium or other antibacterial drugs in the future.
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CONCEPTS AND PRINCIPLES OF CONCEPTS AND PRINCIPLES OF PHARMACOLOGYPHARMACOLOGY
Chapter TwoChapter Two
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WHAT IS PHARMACOLOGY?WHAT IS PHARMACOLOGY?THE STUDY OF DRUGS THE STUDY OF DRUGS
(CHEMICALS) THAT ALTER THE (CHEMICALS) THAT ALTER THE FUNCTION OF LIVING FUNCTION OF LIVING ORGANISMSORGANISMS
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Drug PrototypesDrug PrototypesIndividual drugs that represent groups
of similar drugsSometimes the original drug in a class
Penicillin Aspirin Digoxin
Pharmacologic PrinciplesPharmaceutics
PharmacokineticsPharmacodynamicsPharmacotherapeuticsPharmacognosy
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PharmacokineticsThe study of what the body does to
the drugAbsorptionDistributionMetabolismExcretion
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PharmacodynamicsThe study of what the drug does to
the bodyThe mechanism of drug actions in
living tissues
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PharmacotherapeuticsThe use of drugs and the clinical
indications for drugs to prevent and treat diseasesEmpirical therapeuticsRational therapeutics
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Pharmacokinetics: Absorption
The rate at which a drug leaves its site of administration, and the extent to which absorption occursBioavailabilityBioequivalency
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Factors That Affect Absorption
Absorption characteristics vary according to the dosage form and route
Food or fluids administered with the drug Dosage formulation Status of the absorptive surface Rate of blood flow to the small intestine Acidity of the stomach Status of GI motility
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Routes A drug’s route of administration
affects the rate and extent of absorption of that drugEnteral (GI tract)ParenteralTopical
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PharmacokineticsAbsorption
Route of delivery effects bioavailability IV – Drug 100% available, fastest absorptionPO – Less than (<)100% because of passage
through liver (first pass effect) IM – 100% Available, quick absorptionSC – 100% Available, slower absorption ID – 100% Available, minimal absorptionTopical – (skin, mucus membranes, inhalation,
Intra-nasal) consistent absorption, longer duration of action
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First-Pass Effect The metabolism of a drug and its passage from
the liver into the circulation
A drug given via the oral route may be extensively metabolized by the liver before reaching the systemic circulation (high first-pass effect)
The same drug—given IV—bypasses the liver, preventing the first-pass effect from taking place, and more drug reaches the circulation
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Parenteral RouteIntravenous (fastest delivery into the blood
circulation)IntramuscularSubcutaneousIntradermalIntraarterialIntrathecalIntraarticular
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Topical RouteSkin (including transdermal patches)EyesEarsNoseLungs (inhalation)RectumVaginaTransdermal
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DistributionThe transport of a drug in the body by the bloodstream to its site of action
Protein-binding
Water soluble vs. fat soluble
Blood-brain barrier
Areas of rapid distribution: heart, liver, kidneys, brain
Areas of slow distribution: muscle, skin, fat
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Metabolism/BiotransformationThe biochemical transformation of a drug into an inactive metabolite, a more soluble compound, or a more potent metabolite
Liver (main organ) Skeletal muscle Kidneys Lungs Plasma Intestinal mucosa
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Metabolism/Biotransformation
Prodrugs Drugs that are inactive then become active after they are changed by metabolism
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Metabolism/Biotransformation (cont’d)
Delaying drug metabolism causes:
Accumulation of drugs
Prolonged action of the drugs drug toxicity
Stimulating drug metabolism causes:
Diminished pharmacologic effects
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ExcretionThe elimination of drugs from the bodyKidneys (main organ)LiverBowel
Biliary excretionEnterohepatic recirculation
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Half-lifeThe time it takes for one half of the
original amount of a drug to be removed from the body
A measure of the rate at which a drug is removed from the body
Most drugs considered to be effectively removed after about five half-lives
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Onset, Peak, and Duration of Action
OnsetThe time it takes for the drug to elicit a
therapeutic responsePeakThe time it takes for a drug to reach its
maximum therapeutic response DurationThe time a drug concentration is sufficient to
elicit a therapeutic response
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Therapeutic Drug Monitoring
Peak levelHighest blood level
Trough levelLowest blood level
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Serum Drug LevelsSerum Drug Levels
The amount of drug in the blood at a single point The amount of drug in the blood at a single point in timein timeReflects dosage, absorption, bioavailability, Reflects dosage, absorption, bioavailability,
half-life, and rates of metabolism and excretionhalf-life, and rates of metabolism and excretionMinimum effective concentration (MEC) must Minimum effective concentration (MEC) must
be present for the drug to be effectivebe present for the drug to be effective
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Ways Drugs Produce Therapeutic Effects
Once the drug is at the site of action, it can modify the rate (increase or decrease) at which the cells or tissues function
A drug cannot make a cell or tissue perform a function it was not designed to perform
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Pharmacodynamics:
Mechanisms of Action (what the drug does to the body)
Receptor interactionsEnzyme interactionsNonselective interactions
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Receptor Theory of Drug Receptor Theory of Drug ActionAction
Agonist – Substance (hormone, neurotransmitters) binds to a receptor site on a cell and causes a cellular function
Antagonist – Substance (hormone, neurotransmitter) binds to a receptor site on a cell and inhibits a cellular function
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Non-receptor Drug actionsNon-receptor Drug actionsAntacids (generally speaking)Osmotic diureticsSome anticancer drugsMetal chelating agents
Chemical inactivation of a substance (drug, metal) rendering it harmless
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Pharmacotherapeutics: Types of Therapies
Acute therapyMaintenance therapySupplemental/replacement
therapyPalliative therapySupportive therapyProphylactic therapyEmpiric therapy
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ContraindicationsAny characteristic of the patient, especially
a disease state, that makes the use of a given medication dangerous for the patient
It is important to assess for contraindications!
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MonitoringThe effectiveness of the drug therapy
must be evaluatedOne must be familiar with the drug’s:
Intended therapeutic action (beneficial)Unintended but potential adverse
effects (predictable, adverse reactions)
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Monitoring (cont’d)Therapeutic index
Ratio of a drug’s toxic level to the level that provides therapeutic benefits
ToleranceDecreasing response to repeated
drug dosesDependence
Physiologic or psychological need for a drug
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Monitoring (cont’d)
Interactions may occur with other drugs or food A drug interaction is the alteration of a drug’s action by:
Other prescribed drugs Over-the-counter medications Herbal therapies
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Monitoring (cont’d)
Drug interactionsAdditive effect
1+1=2Synergistic effect
1+1=3Antagonistic effect
1+1=0Incompatibility
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Monitoring (cont’d) Adverse drug events
Medication errors Adverse drug reactions
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Why Learn about Adverse Drug Why Learn about Adverse Drug Reactions (ADR)?Reactions (ADR)?
Over 2 MILLION serious ADRs are reported yearly
100,000 DEATHS yearlyADRs 4th leading cause of death ahead of
pulmonary disease, diabetes, AIDS, pneumonia, accidents, and automobile deaths
Nursing home patients ADR rate – 350,000 yearly
Institute of Medicine, National Academy Press, 2000
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Adverse EffectsCNS
Confusion, headache, agitation, seizures
GINausea, vomiting, diarrhea
Hematologic effectsCoagulation disorders
Hypersensitivity / allergic reactionItching, hives, bronchospasms
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Adverse ReactionsAdverse Reactions
Davis Drug GuideIn RED and CAPITAL letters indicates a life-
threatening reactionUnderlined indicates most common side
effectsPrentice Hall Nurse’s Drug Guide 2008
Underlined effects are life threateningCommon adverse effects are in Italics
AngioedemaAngioedema
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Monitoring (cont’d)Adverse drug reactions Pharmacologic reactions,
including adverse effects Hypersensitivity (allergic) reaction Idiosyncratic reaction Drug interaction
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Other Drug-Related Effects
TeratogenicMutagenicCarcinogenic
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