course work Flashcards
What is phlebitis and what are the three types of phlebitis?
inflammation of a vein
mechanical - movement of cannula within vein causes friction
chemical - caused by the drug or fluid being infused (for example, antibiotics are reported to increase the
incidence of chemical phlebitis due to
their low pH)
infective - caused by the introduction of bacteria into the vein
How much fluid may be injected into the deltoid?
1 ml or less of clear, non-irritating solutions
Whaat does ISBAR stand for?
Identify, Situation, Background, Assessment, Recommendation
When do you assess the patency of an IV cannula?
each time it is accessed for use
at least once every shift
any time a patient is transferred between wards or departments
Aside from patency, what other assessments are involved when caring for a patient with an IV
cannula? (6)
erythema tenderness pain swelling dressing integrity PIVC position
How long does an IV cannula remain insitu?
no more than 72 hours, unless there is no sign of infection and either replacement is likely to be difficult or it’s likely to be needed for no more than 24 hours more
what are the four essential elements of valid consent?
it must be voluntary, specific, informed, and the person must have legal capacity
what is measured in a FBC or CBC and diff?
RBC count haemoglobin haematocrit (PCV) blood smear platelet count mean platelet volume red blood cell indices WBC count
what are the two different classifications of WBCs?
granulocytes - neutrophils, basophils and eosinophils
non-granulocytes
resp rate: normal range
12 - 20
(adult)
pulse rate: normal range
60 - 100 (adult)
body temp (tympanic): normal range
35.5 - 37.5 (adult)
define affinity
the extent of binding of a drug to a receptor
how well the drug fits into the receptor
define specificity and selectivity
The specificity of a drug describes the number of effects the drug produces, while selectivity describes the number of molecular targets the drug interacts with.
An ideal drug would interact with a single molecular target, at a single site, and cause only one effect. Such a drug would be described as having complete specificity; unfortunately, no drugs can lay claim to that title. Most drugs show some degree of selectivity – that is, a preference for a molecular target – but may lack specificity either because they act on more than one molecular target or because they act on a molecular target that is located in multiple organs or tissues throughout the body.
define efficacy
the ability of a drug to produce an effect once it is bound to the molecular target.
The maximal efficacy of a drug is the maximum response a drug can produce.
The clinical effectiveness of a drug depends on its efficacy, not on its potency.
important: only an agonist has efficacy - an antagonist has affinity but not efficacy
define potency
the relative amount of a drug that has to be present to produce a desired effect
the more potent the drug, the lower the dose required to acheive effect (ie fentanyl is much more potent than oxycodone)
important - efficacy and potency are not the same thing
what are the four aspects of pharmacokinetics?
absorption, distribution, metabolism, excretion
what factors influence the absorption of drugs?
- surface area of absorbing site
- blood circulation to site of administration
- drug solubility - (lipids and lipid soluble absorbs faster)
- ionisation, which is determined by pH of the environment (acid drugs absorb well in acid environment; basic drugs in basic)
- size of the molecule of the drug (smaller is faster)
- formulation eg, SR, enteric coating
how are most drugs absorbed in the body?
simple diffusion
how do almost all drugs work, with the exception of many chemotherapy drugs?
by binding to proteins, which are known as molecular targets or sites of action
many chemo drugs are the exception because the bind to DNA, which is not a protein
what are the four main types of molecular drug targets?
transporters eg SSRIs
ion channels eg calcium channel blockers
enzymes eg ACE inhibitors
receptors - largest and most diverse type of molecular drug target eg morphine and other opiates work on opioid receptors
what factors influence the magnitude of a pharmacological effect of a drug?
the nature of the interaction with the target
the affinity of the drug for the target
the concentration of a drug at the site of action
what factors influence the concentration of a drug at the site of action?
the absorption, distribution, metabolism and excretion of the drug (ie pharmacokinetics)
what is the interaction of a drug with a enzyme called?
inhibition (the drugs are ‘enzyme inhibitors’)