PowerPoint 1 Flashcards

1
Q

Nurses Role in Drug Therapy

A

Nurses use core drug knowledge and core patient variables:

To maximize the therapeutic effects of a drug
To minimize the adverse effects of a drug
To provide patient and family education

Enteral: through mouth/goes through GI
Parenteral: IV, intramuscular, through the blood, intra-arterial, etc. (Injections)

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2
Q

Managing Drug Therapy Through the Nursing Process: Assessment

A

Assessment of core drug knowledge
Assessment of core patient variables: initial gatherings from assessing the patient (health history)

Why is heart disease important for drug therapy? It won’t circulate well enough throughout the body

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3
Q

Drugs

A

Any chemical that affects the process of a living organism can broadly be defined as a drug

Drugs are chemicals that are introduced into the body that cause some sort of change

When drugs are administered, the body begins a sequence of processes designed to handle the new chemicals; which involves breaking down and eliminating the drugs.

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4
Q

Components of core drug knowledge are:

A

Pharmacotherapeutics
Therapeutic effect

Pharmacokinetics: ADME (Absorption, Distribution, Metabolism and Excretion)
Changes occur to drug in body

Pharmacodynamics
Effects on body

Contraindications and precautions: exclusions to why the patient shouldn’t take the med.
Adverse effects: side effects
Drug interactions

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5
Q

Sources of Drugs

A

Plants, foods, salts
Animal products
Inorganic compounds (i.e. aluminum, fluoride, iron, gold)
Synthetic sources

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6
Q

Drug Evaluation

A

After drugs are developed and identified, they must evaluate their actual therapeutic and toxic effects. This process in the US is tightly controlled and regulated by the FDA
Several (4) “phases” of clinical trials are performed

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7
Q

Purpose of Drug Therapy

A

Treat diseases
Prevent diseases
Diagnose diseases

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8
Q

Approaches to drug classification

A

Clinical indications

Body systems approach

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9
Q

9 Categories of Drugs

A
Nervous System Agents
Cardiovascular System Agents
Renal System Agents
Respiratory System Agents
Musculoskeletal System Agents
Endocrine System Agents
GI System Agents
Immune System Agents
Chemotherapeutic Agents
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10
Q

Common Drug Grouping: Family Group

A

Penicillin

Beta Blockers

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11
Q

Common Drug Grouping: Therapeutic Group

A

Antihypertensive
Analgesics
Anti-anxiety

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12
Q

Medication Preparations:

Local and Systemic

A

Local: effects confined to one area of body
0.1% topical hydrocortisone for a rash pr 1% lidocaine injected to anesthetize a wound.
Some topical drugs are absorbed through skin and have a systemic effect.

Systemic: absorbed into vascular system and delivered into cells, tissues, and organs.

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13
Q

Pharmacology

A

Is the study or science of drugs and the biological effects of chemicals

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14
Q

Pharmacotherapeutics

A

A branch of pharmacology
Incorporates the principles of drug actions
The use of drugs and the clinical indications for drugs to prevent and/or treat diseases
The desired outcome
Addresses two key concerns: drug’s effects on the body and the body’s response to the drug

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15
Q

Pharmacodynamics

A

Relates to how the drug affects the body; drug action

Turn on, turn off, promote, or block a response.

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16
Q

Pharmacokinetics

A

Relates to how the body acts on the drug
Involves the study of absorption, distribution, metabolism (biotransformation), and excretion of drugs (A D M E principle)
In clinical practice, it includes: onset of drug action, drug half-life, timing of the peak effect, duration of action, metabolism of the drug, and the site of excretion

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17
Q

Critical Concentration

A

In order for a drug to have a therapeutic effect in the reactive tissues, it must maintain a sufficiently high concentration in the body

The amount of a drug that is needed to cause a therapeutic effect is called the critical concentration

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18
Q

Loading Dose

A

Some drugs take a long time to reach a critical concentration level, so if their effects are needed quickly, a loading dose is recommended
Therefore, in order to reach therapeutic effects, the INITIAL dose is usually a higher dose and the critical concentration is maintained by recommended dosing schedule

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19
Q

Absorption

A

Absorption refers to what happens to a drug from the time it is introduced to the body until it reaches the circulating fluids and tissues.

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20
Q

Factors Influencing Absorption

A

Rate of absorption depends on route of administration.
Greater rate of absorption w/ increased blood flow because more blood to carry drug molecules into circulation.
Lipid soluble drugs absorbed faster because they can readily cross lipid cell membrane.
food or other drugs in stomach; Acidity of the stomach
gastric/intestinal motility
injection site heat or cold (cold-vasoconstriction, decreases absorption; hot- vasodilation, increases absorption)

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21
Q

Bioavailability

A

A term used to quantify the extent of drug absorption

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22
Q

Administration Routes

A

Oral (PO): Oral route is the most common, not invasive and less expensive. It is also the safest way to deliver drugs.

Rectal (PR): Administered via the rectum, usually given this route when patient is unable to take PO (ex. Tylenol/ASA suppositories)

Intravenously (IV): These drugs are injected directly into the vein, they reach their full strength at the time of injection, avoiding initial breakdown (ex. Gtts)

Intramuscular (IM): Drugs injected IM route are absorbed directly into the capillaries in the muscle and sent into circulation (ex. Vitamin B-12)

Subcutaneous Injections (Sub Q): Deposits the drug just under the skin, where it is slowly absorbed into circulation. Timing of absorption varies, depending on the fat content of the injection site and the state of local circulation (ex. Insulin, heparin)

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23
Q

Administration Routes Cont.d

A

Mucous Membranes (Sublingual, buccal): Usually given for fast absorption, i.e. SubLingual NiTroGlycerin

Topical (skin): Long acting, absorbed slowly. Fevers may increase absorption (temperatures causes the membrane to disintegrate, releasing more drug), i.e. Narcotic patches, birth control

Inhalation: Inhaled through the mouth or nose. Usually to treat respiratory condition, i.e. Albuterol, Spiriva.

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24
Q

Distribution

A

Process by which the drug is delivered to tissues

Distribution of an absorbed drug depends on: 
Blood flow
Protein binding
Free, unbound drug = active drug
Solubility
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25
Q

Protein-Bound Drugs

A

When the drug is bound to protein, it is unable to pass through the capillary walls.
The bonds will dissolve in time, and the drug molecules will become free and active.
When the patient has a lower-than-expected protein level, the distribution of the drug is altered.

26
Q

Factors that affect distribution of drugs:

A
Perfusion of the reactive tissue
Scar tissue- avascular
Adipose tissue – poor blood supply 
Abscesses 
Solid tumors
Protein binding
Drug’s lipid solubility
27
Q

Metabolism (Biotransformation)

A

Chemical reactions the body uses to convert drugs and other chemicals into non toxic substances. It is the process by which drugs are changed into new, less active chemicals

The liver is the single most important site of drug metabolism

28
Q

Products of drug metabolism:

Metabolites

A

Inactive or active

Active metabolites
Therapeutic or adverse

29
Q

First Pass Effect

A

This phenomenon occurs when an orally administered drug, after being absorbed, travels through the circulatory system into the liver where the drug is metabolized and loses much of its effectiveness.

For this reason, oral doses are usually much higher, taking into consideration the first pass effect.

30
Q

First Pass Route

A

Oral Route

Everything else is non-first route

31
Q

Cytochrome P-450 System

A

Primary oxidative enzyme responsible for biotransformation of many drugs.
Some drugs can induce or inhibit this system, altering metabolism of other drugs.
Some drugs can compete with each other for the enzyme
Underdeveloped in children, & decreased in elderly and patients with liver disease.

32
Q

Excretion

A

Excretion is the removal of a drug from the body.

Sources of Excretion:
Kidneys: play the most important role 
Skin
Saliva
Lungs
Bile
Feces
33
Q

Processes Involved in Renal Excretion

A

Glomerular filtration.
Most drug particles pass easily through the spaces of the capillary walls into the urine in the proximal tubule.

Passive tubular reabsorption.
The drug particles will try to move from the area of greater concentration to that of lesser concentration.

Active tubular secretion.
Active transport systems in the renal tubule work to move some drugs from the blood and into the urine.

34
Q

Factors That Affect

Renal Excretion

A

Drug excretion can be increased if the pH of the urine encourages the drug to become an ion.
Overuse of the active transport system also affects excretion.
As the transport system becomes overloaded, some of the drug particles will remain in the blood until they can be moved by the transport system.
Two drugs can be given together to deliberately slow the rate of excretion of one or both of the drugs.

35
Q

Half-Life

A

The time it takes for the amount of drug in the body to decrease to one-half of the peak level it previously achieved.

Example: If a patient takes 20mg of a drug with a half-life of 2 hours, 10mg of the drug will remain 2 hours after administration; 2 hours later, 5mg will be left and in 2 more hours 2.5mg will remain.

It helps the nurse determine the appropriate timing for a drug dose or determining the duration of a drug’s effect on the body

36
Q

Clearance

A

The rate at which drug molecules disappear from the circulatory system is effected by several factors.
This rate is called clearance or clearance rate of a drug.
Renal excretion and hepatic metabolism are the major modes of clearance.
The gender of the patient can also alter the clearance of some drugs.

37
Q

Pharmacodynamics

A

The biologic, chemical, and physiologic actions of a particular drug within the body.
The pharmacodynamics of a drug are responsible for its therapeutic effects and sometimes its adverse effects.
Drugs cannot create new responses in the body; they can only turn on, turn off, promote, or block a response that the body is inherently capable of producing.

38
Q

Drug–Receptor Interactions

A

Most drugs create their effects in the body by attaching to special sites, called receptors.
At the receptor site, the drug is able to stimulate the cell to act in a way that the cell is designed to act.
An agonist causes the cell to act.
An antagonist or blocker prevents something else from attaching to the cell blocking and action.

39
Q

Variables That Influence the Dose of a Drug

A

Potency (amount needed) and efficacy (how well did response occur)
The level of the drug needed in the body to produce an effect

Maintenance and loading doses
Maintenance dose—daily dose
Loading dose—larger than usual dose to reach an therapeutic effect quicker

Therapeutic index
The difference between an effective dose and a toxic dose

40
Q

Peaks & Troughs

A

Onset: time it takes for the drug to elicit a therapeutic response
Peak: time it takes for a drug to reach its maximum effect
Duration: time that drugs concentration is sufficient to elicit a response

Peak & Trough levels may be ordered by a physician to determine the levels of a drug and adjust the dose and time as needed. Peak level is drawn 1 hour AFTER administration and trough is drawn 30 minutes PRIOR to next dose

Peak = adjust dose (Vancomycin 500mg or 1 gram)
Trough = adjust time or frequency (Q12 hours, Q24 hours)
41
Q

Adverse Effects

A

An adverse effect of drug therapy is a usually undesirable effect other than the intended therapeutic effect.
Too much of a therapeutic effect.
Other pharmacodynamic effects of the drug.

42
Q

Allergic and Idiosyncratic Response

A

The most serious allergic response is called anaphylaxis.
Bronchospasms, vasodilation, increased vascular permeability (edema of the airways, angioedema: difficulty breathing, swallowing, etc.)
Idiosyncratic responses- unusual; the opposite of what is anticipated (aka.. paradoxical effect)

43
Q

Toxicities

A

Neurotoxicity (central nervous system)
Signs and symptoms: drowsiness, auditory and visual disturbances, and seizures.

Hepatotoxicity (liver)
If liver damage occurs, the drug will not be metabolized as efficiently. Hepatitis, jaundice, elevated liver enzymes, fatty liver.

Nephrotoxicity (kidneys)
Signs and symptoms: decreased urinary output, elevated blood urea nitrogen, increased serum creatinine, altered acid-base balance, and electrolyte imbalances.

Ototoxicity (eighth cranial nerve)
Signs and symptoms: tinnitus, hearing loss, light-headedness, vertigo, and nausea.

Cardiotoxicity (heart)
Signs and symptoms: irregularities in conduction, heart failure, and damage to the myocardium.

Immunotoxicity (immune system)
Signs and symptoms: immunosuppression.

44
Q

Drug Interactions

A

A drug interaction occurs when two drugs or a drug and another element have an effect on each other.

This interaction may:
Increase or decrease the therapeutic effect of the drugs.
Create a new effect.
Increase the incidence of an adverse effect.

Negative effects from drug interactions are those that decrease the therapeutic effect &/or increase the adverse effects.
Drug interactions may take place in any phase of pharmacokinetics.
Drug interactions can also change the pharmacodynamics of a drug.
They may be beneficial!

45
Q

Drug Interactions Affecting Absorption

A

Drug absorption is often decreased because of drug interactions.
If a drug binds with another substance in the GI tract, less of the drug is available to be absorbed.
This binding of a drug is termed chelation.
Drug absorption may also be increased as a result of a drug interaction or the presence of food in the GI tract.

46
Q

Two Types of Distribution

A

Competitive protein binding.
i.e. NSAIDS can displace protein-bound warfarin from its binding sites.

Drug alteration of the extracellular pH.
Drugs move into the higher pH EC environment to be ionized. Once ionized, trapped on that side of the membrane.

47
Q

Drug Interactions Affecting Metabolism

A

Probably the most important and common drug interaction is one that alters the metabolism of a drug.

If two drugs that affect the cytochrome P-450 system must be administered to a patient together, the dose of one of the drugs may have to be adjusted.
Consider: grapefruit juice, certain herbs (i.e. St. John’s wort), alcohol, age.

48
Q

Drug Interactions Affecting Excretion

A

Glomerular filtration is dependent on blood flow to the kidney.
Drugs that decrease cardiac output decrease the amount of circulating blood that is sent to the kidneys.
Renal reabsorption of a drug is dependent on whether a drug is ionized.

49
Q

Drug Interactions Affecting Pharmacodynamics

A

The drug that has the weaker affinity for the receptor will not be able to exert its therapeutic effect.

50
Q

Additive Effect

A

An additive effect occurs when two or more “like” drugs are combined.
An additive effect may be intentional or may unintentionally cause harm.
1+1=2

51
Q

Synergistic Effect

A

When two or more “unlike” drugs are used together to produce a combined effect
1+1 = 3

52
Q

Potentiated Effect

A

When one drug enhances another.

In other words, a drug that has a mild effect enhances the effect of a second drug.

53
Q

Antagonistic Effect

A

The opposite of a synergistic effect.
Results in a therapeutic effect that is less than the effect of either drug alone because the second drug either diminishes or cancels the effects of the first drug.
Two drugs bind and “cancel” each other out
1+1 = 0

54
Q

Chemical incompatibilities

A

Chemical incompatibilities between drugs change both the drug’s structure and its pharmacologic properties… beneficial or harmful.

55
Q

Physical incompatibilities

A

Physical incompatibilities occur when two drugs are mixed together.
The mixture results in the formation of a precipitate.

56
Q

Assessment of Core Patient Variables: Health Status

A

Concurrent medical conditions may increase the risk of adverse effects from drug therapy.
A patient’s chronic health condition may also necessitate drug therapy that may interact with other drugs.

57
Q

Assessment of Core Patient Variables: Life Span and Gender

A

A patient’s age can greatly increase the risk of adverse effects from drug therapy.
Consider the old and the very young.
In addition, older adults are more likely to be receiving polypharmacy for multiple chronic illnesses.

58
Q

Assessment of Core Patient Variables: Lifestyle, diet, and habits

A

The patient’s lifestyle, diet and other health habits can have an impact on drug interactions.

59
Q

Assessment of Core Patient Variables: Environment

A

The patient’s environment may increase the likelihood that a certain adverse effect will occur.
For instance, some antibiotics can cause the adverse effect of photosensitivity.
The environment in which drug therapy is administered can also play a role in the early detection of adverse effects.

60
Q

Assessment of Core Patient Variables: Culture and Inherited Traits

A

Researchers are beginning to study responses to drug therapy that are genetically determined in various ethnic and racial populations.
These responses may place the patient at greater risk than the rest of the global population for adverse effects or drug interactions.

61
Q

Pharmacology and

the Nursing Process

A
Assess the problem
Assess the options
Select the therapy
Nursing actions
Re-assessment
62
Q

6 Rights of Medication Administration

A
Right Drug
Right Route
Right Time
Right Dose
Right Client
Right Documentation