34.1 - Medication Administration Flashcards
Canadian drug legislation
The Health Protection Branch of the federal government is responsible for the administration of the Food and Drug Act and the Controlled Drugs and Substances Act. New drugs need to apply to the Health Protection Branch for approval
Guidelines for Safe Narcotic Administration and Control
- Must be kept double locked
- Narcotics are counted and a record is kept separate from the patient administration record
- Narcotics are counted every time they are accessed and counted by 2 nurses at shift change – one coming on and one going off shift
- Use a special inventory record each time a narcotic is dispensed
- Report discrepancies in narcotic counts immediately
Pharmacokinetics 4 fundamental processes:
Absorption, distribution, metabolism and excretion
Factors that influence absorption:
- Route of administration (IV fast, topical slow)
- Ability of the medication to dissolve
- Blood flow to site of administration (increase temp = increased blood flow = increase rate of absorption)
- Surface area
- Lipid solubility of medication
Fastest absorption
1) IV bypasses absorption, it’s automatically in the blood
2) Inhalation
3) Injection into muscle
4) Subcutaneous is slower
5) Topical from skins surface is slowest
where are acid/base absorbed?
Basic meds are absorbed in small intestine (enteric coated)
Acidic meds are absorbed in stomach through gastric lining
buffered just means that the drug contains ions to decrease acidity and slow absorption of acidic drugs.
Do not crush or chew or open drugs that
1) extended release (high dose of medication intended to be released slowly over time) as the entire dose may be released at once,
2) enteric coated (have a hard waxy coating designed to be released in the small intestine, or medications with oral effects such as extremely bitter taste, stain teeth or irritate the mucosa
Distribution depends on
Circulation
Membrane permeability
Protein binding
drugs that can cross placenta
(alcohol, cocaine, caffeine, some prescription meds),
Protein binding
Most medications bind to proteins to some extent and the amount they bind affects the distribution. Medications bound to albumin cannot exert pharmacological activity. The unbound, or free, medication is the active form of the medication. People with a decrease in albumin, such as older people or people with decreased liver function, will have a higher amount of unbound medication. This means they may be at risk for an increase in medication activity or toxicity, or both.
Warfarin 99% bound, leaves 1% of the drug that is free or unbound
Gentamicin is 10% bound or 90% free
Ration of bound drug to unbound drug is constant. As the free drug exits the blood, an equal proportion becomes unbound to replace the free drug that exited the system. This can create a reservoir of unused drug because the drug is prevented from leaving the blood stream. It can slow the rate of disappearance from the plasma and it limits the rate of accumulation of drug in the tissue.
Medications are excreted via
Kidneys – primary location of excretion, as urine
Liver – broken down and secreted in bile
Bowel– excreted in feces
Lungs – most drugs excreted from lungs unmetabolised
Exocrine glands – salivia, sweat, breast milk
Mild Allergic Reactions
- Urticaria raised, irregularly shaped skin eruptions with varying sizes and shapes; eruptions have reddened margins and pale centre
- Rash Small, raised vesicles that are usually reddened; often distributed over entire body
- Pruritus Itching of skin; accompanies most rashes
- Rhinitis Inflammation of mucous membranes lining nose; causes swelling and clear, watery discharge
Factors that affect med Blood concentration
The drugs half life The size of the dose Frequency Pharmacokinetic processes Route
Factors that Influence Drug Action
Body weight and composition
Genetics
Physiological factors – hormones, age and disease
Environmental condition – cold causes vasoconstriction
Psychological
4 sites of injection:
1) Intradermal (ID): Injection into the dermis just under the epidermis into dermis of skin. More blood vessels than sc. Allergy testing, Mantoux. 0.1-0.2mls. Sites: upper back, scapula, high upper chest, inner forearm
> Subcutaneous and intradermal. Difference between these is depth.
2) Subcutaneous (subcu): Injection into tissues just below the dermis into fat tissue: insulin, heparin,
3) Intramuscular (IM): Injection into a muscle
4) Intravenous (IV): Injection into a vein