Assessment every 6 months
- 
clinical assessment of functional status 
- 
Fluid staus - 
body weight 
- 
JVP 
- 
peripheral oedema 
- 
postural hypotension 
 
- 
- 
Cardiac exam - 
rhythm - ecg
 
- 
heart sounds 
- 
chest crepitations 
 
- 
- 
cognitive and nutritional status 
Testing
- 
electrolytes and cr assess before initiation then at one week if HF or 4-6wk if for HTN 
- 
every 3-6 months in lower risk 
Spironolactone
- 
hyperkalaemia - 
elderly - >60
 
- 
DM 
- 
impaired renal function - stage 3 or above
 
- 
concurrent: - 
NSDAID 
- 
ACEi 
- 
Cyclosporin 
 
- 
 
- 
Thiazide or loop
- 
hyponatramia and hypokalaemia 
- 
mild hypercalcaemia 
In hyperterthension
- 
electolytes - 
within 4-6 weeks of starting 
- 
every 6-12 months 
- 
clinical condition changes or potentially interacting drug added 
 
- 
- 
if hypokalameia - 
review therapy 
- 
increase intake of K 
- 
consider elevated aldosterone 
 
- 
- 
if serum cr increase >20% or egfr falls >15% - 
remeasure 2weeks 
- 
if continues to worsen consider specialist advice 
 
- 
In heart failure
- 
renal function - 
at baseline then @ 1wk then 
- 
1-2 weeks after each dose increase in low risk 
- 
5-7d after increase in high risk 
- 
during illness 
- 
3-6mo in stable higher risk 
- 
annually in stable lower risk 
 
- 
- 
if hypokalaemia - 
review 
- 
increase K 
 
- 
- 
if serum cr ises >20% or eGFR falls >15% - 
remeasure 2 weeks 
- 
consider referral 
 
- 
Potassium sparing
in hypertension
- 
electrolytes - 
baseline (shouldn’t be started in K >5) 
- 
after 5-7 days with dose titration 
- 
every 5-7d until K stable 
- 
6-12mo low risk 
- 
high risk (older, renal/cardiac dysfunction) every 4-8wk 
 
- 
in heart failure
- 
renal function - 
at baseline 
- 
q5-7d with titration 
- 
every 5-7d until K stable 
- 
6-12mo for low risk 
- 
high risk every 4-8 wk 
 
- 
- 
if K 5.5-5.9 or cr rises significantly above baseline but \<2000 - 
reduce to 25mg on alternate days 
- 
monitor renal function 
 
- 
- 
K >6 or Cr >200 - 
stop 
- 
seek specialist advice 
 
- 
Interactions
- 
NSAID - 
Thiazide/loops - 
fluid retention - antagonise effects of diuretics
 
- 
if combined iwth ACEi increased effects 
 
- 
- 
Spironolactone - 
increase risk of hyperkalaemia and renal fialure 
- 
avoid with ACEi 
 
- 
 
- 
- 
Digoxin - 
Thiaizde/loops - 
cause hypokalaemia - predispose to digoxin toxicity
 
 
- 
- 
Spironolactone - 
increase plasma concentration of digoxin 
- 
spiro and its metabolite may interfere with digoxin assay = difficult to evaulate 
- 
monitor closely 
 
- 
 
- 
- 
ACEi/ARB - 
Thiazide/loop - 
first dose hypotension may occur - especially if high dose diuretic
 
- 
potetiate ACEi induced AKI - ++ if NSAID
 
 
- 
- 
Spironolactone - 
increase risk of severe hyperkalaemia 
- 
keep below 25mg od 
 
- 
 
- 
- 
Lithium - 
thiazide/loop - 
increase lithium levels - 
lethargy 
- 
muscle weakness 
- 
lack of coordination 
 
- 
 
- 
- 
Spironolactone - clearance may be reduced
 
 
- 
- 
Cyclosporin - 
Thiazide/loop - 
nephrotoxicity reported 
- 
increase risk of gout 
 
- 
- 
Spironolactone - may result in hyperkalaemia
 
 
-