prescribing in special circumstances Flashcards
3 categories or risks when prescibing
- Risks particular to the drug, which we discuss in the adverse drug reactions session
- Risks associated with the prescriber and the context in which they are working, which we will discuss in the risk and error in prescribing session
- Risks generated by the individual characteristics of the person, including their comorbidity (co-existing illnesses), co-existing treatment (discussed in the Drug interactions session) and special circumstances (a broader term that extends to non-pathological states that may influence prescribing)
what is an allergy
In the context of drug therapy, allergy is a term that is generally taken to refer to immunologically-mediated adverse reactions
2 main risks associated with allergy to a drug
- The risk of immunological toxicity if a drug is prescribed which the person is allergic to
- The risk of inadequate treatment if a person is unable to receive the best available treatment, because they are allergic to it, or because they are inappropriately labelled as allergic
what is drug intolerance
Drug intolerance is a broader term that includes immunologically-mediated adverse reactions (‘allergies’) and non-immunological reactions
drugs that will have increased toxicity in renal impairment
o Kidneys are the main route of clearance for water soluble drug- minority of drugs used
o e.g. acyclovir, gentamicin, digoxin, gabapentin- kidneys important for clearance. Half-life will increase and so will concentrations in body tissues= increased risk of toxicity esp in drugs with a narrow therapeutic index.
o Not water-soluble drugs: hepatic metabolism, but may rely on kidneys for clearance of water-soluble metabolites e.g. morphine- metabolised in liver to various substances, including morphine 6 glucuronide- more potent opioid agonist than morphine hence greater effect in renal impairment
how do NSAIDs cause nephrotoxicty
renal impairment has less tolerance to further insult. Typical examples include NSAIDs via effects on regulation on glomerular perfusion. PGs maintain the size of the afferent arteriole, NSAIDs block PG synthesis which reduces the signal to the afferent arteriole to dilate, so afferent arteriole becomes more constricted, less flow and pressure in glomerulus= less glomerular filtration.
how does gentamicin cause kidney damage
o Gentamicin (aminoglycoside) in nephrotoxicity- some is taken into cells lining renal tubule. Tubular cells exposed to higher conc than in blood= damage- acute tubular necrosis.
how does allopurinol cause renal damage
o Allopurinol- incite inflammatory process in interstitium- acute interstitial nephritis.
how do acyclovir and methotrexate cause renal damage
in high doses e.g. viral encephalitis, can precipitate in renal filtrate- crystalluria, crystals block tubules and block renal function
what drugs might become less effective in renal impairment
o Nitrofurantoin- remains largely unchanged in the urine, if kidneys aren’t working, not exceted in urine so not in high enough conc in urine to fight infection. Also get higher levels in the blood cinreasing the risk of adverse effects
o Thiazide diuretics: need to be secreted into the tubular fluid to access the target (Nal/Cl transporter in luminal surface of DCT), if less is secreted into the tubule then the effect is lower
markers for renal function
creatinine conc
eGFR
Cr clearance
3 ways liver disease can affect prescribing
- Altered pharmacokinetics: reduced protein binding, reduced hepatic metabolism and excretion (particularly for drugs subject to significant first-pass metabolism)
- Altered pharmacodynamics: increased sensitivity to the effects of drugs, particularly those that can cause bleeding, renal impairment, sedation, constipation and hypokalaemia)
- Risk of hepatotoxicity: although the drugs may not be ‘more hepatoxic’ in a person with hepatic impairment, they may have ‘more to lose’ from any hepatotoxic effects that occur
describe 1st pass metabolism and how it can be affected in liver disease
o First pass metabolism: venous blood flow from GI tract passes through the liver before joining the systemic circulation- filtering before it goes round the circulation around the body- applies to many orally given drugs- may be metabolised at first pass through the liver- IV dose will be lower than oral dose to get the same clinical effect and in severe liver disease giving the same dose may result in a greater amount of the drug entering the systemic circulation so need to reduce the oral dose more than the equivalent IV dose.
o High first pass metabolism: most beta blockers, benzo, morphine, pethidine
what drugs should be avoided in liver failure
anticoagulants, NSAIDs, nephrotoxic drugs, drugs that cause sedation, constipation and hypokalaemia
drugs inappropriate in hepatotoxicity
include atorvastatin, azithromycin and methotrexate.