PowerPoint 1 Flashcards
Nurses Role in Drug Therapy
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)
Managing Drug Therapy Through the Nursing Process: Assessment
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
Drugs
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.
Components of core drug knowledge are:
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
Sources of Drugs
Plants, foods, salts
Animal products
Inorganic compounds (i.e. aluminum, fluoride, iron, gold)
Synthetic sources
Drug Evaluation
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
Purpose of Drug Therapy
Treat diseases
Prevent diseases
Diagnose diseases
Approaches to drug classification
Clinical indications
Body systems approach
9 Categories of Drugs
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
Common Drug Grouping: Family Group
Penicillin
Beta Blockers
Common Drug Grouping: Therapeutic Group
Antihypertensive
Analgesics
Anti-anxiety
Medication Preparations:
Local and Systemic
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.
Pharmacology
Is the study or science of drugs and the biological effects of chemicals
Pharmacotherapeutics
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
Pharmacodynamics
Relates to how the drug affects the body; drug action
Turn on, turn off, promote, or block a response.
Pharmacokinetics
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
Critical Concentration
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
Loading Dose
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
Absorption
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.
Factors Influencing Absorption
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)
Bioavailability
A term used to quantify the extent of drug absorption
Administration Routes
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)
Administration Routes Cont.d
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.
Distribution
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