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
-