PSA: monitoring drug therapy Flashcards
(26 cards)
Baseline tests methotrexate
Baseline tests should include FBC, U&E, LFT, ESR and CRP.
Selected patients may require
pulmonary function testing and CXR.
Drug monitoring methotrexate
FBC, U&E and LFT should be checked every 1-2 weeks until patient is stabilised and
then every 2-3 months thereafter (monthly in rheumatology).
ESR and CRP
should be re-checked every 3 months.
what should you ask about at every appt regarding methotrexate SE
Also ask about oral ulceration/sore throat, unexplained rash or unusual bruising at every
consultation.
what should you monitor hydroxycloriquine
bull’s eye retinopathy - may result in severe and permanent visual loss
Monitoring
baseline ophthalmological examination and annual screening is generally recommened
the BNF advises: ‘Ask patient about visual symptoms and monitor visual acuity annually using the standard reading chart’
After a change in dose, how often should lithium levels be checked
after a change in dose, lithium levels should be taken a week later and weekly until the levels are stable.
how many hours after a dose should lithium levels be checked
12 hours post dose
Therapeutic range lithium
0.4-1.0 mmol/L
When should thyroid and renal be checked when patients taking lithium
Every 6 months
when lithium levels are stable, how often are they checked
Once stable, blood test 12 hours post-dose every 3 months
baseline measurements therpaeutic monitoring lithium
renal: U&E, eGFR,
thyroid: free T4, TSH,
weight and height (plus FBC
and ECG if indicated).
what should be checked every 3 months lithium
serum lithium level (normal therapeutic range 0.4-1.0mmol/l, set target
for each patient)
what should be checked every 6 months lithium
thyroid and renal and BMI:
– fT4, TSH, U&E and eGFR
what should be checked every 12 months lithium
check height and weight (BMI)
how often do you monitor FBC in pts on clozapine
checking the FBC every week for the first 18 weeks, every second week up to 1 year, and then at monthly intervals.
when should theophylline plasma concentration be measured after treatment is commenced
5 days after therapy is commenced
how many hours after last dose should a theophylline plasma conc be taken
4-6 hours after the dose
theophylline plasma conc req for therapeutic effect
10-20mg/litre
drug monitoring amiodarone
Liver function tests required before treatment and then every 6 months.
Serum potassium concentration should be measured before treatment.
Chest x-ray required before treatment
Thyroid function tests should be performed before treatment, then at 6-monthly intervals, and for several months after stopping treatment (particularly in the elderly).
drug monitoring sodium valproate
Monitor liver function before therapy and during first 6 months especially in patients most at risk.
Measure full blood count and ensure no undue potential for bleeding before starting and before surgery.
what electrolyte disturbance increases risk of digoxin toxicity
hypokalameia
what should you monitor digoxin
serum conc if iv?
U&Es (renal function poor can increase risk of toxicity. hypokalameia increases risk of arrythmia)
drug monitoring statins
before treatment:
LIVER FUNCTION full lipid profile (non-fasting) and triglyceride concentrations, thyroid-stimulating hormone, and renal function should also be assessed.
During:
Liver function repeated within 3 months and at 12 months of starting treatment, unless indicated at other times by signs or symptoms suggestive of hepatotoxicity.
should you check CK before initiating statins?
in patients who have had persistent, generalised, unexplained muscle pain (whether associated or not with previous lipid-regulating drugs);
if the baseline concentration is more than 5 times the upper limit of normal (ULN), a repeat measurement should be taken after 7 days.
If the repeat concentration remains above 5 times the ULN, statin treatment should not be started;
if concentrations are still raised but less than 5 times the ULN, the statin should be started at a lower dose.
if want to initiate methotrexate but LFTs abnormal, what do you do?
dont initiate
risk of cirrhosis