Trandolapril
Trandolapril.JPG

CLINICAL USE

Angiotensin converting enzyme inhibitor: Hypertension Heat failure After myocardial infarction

DOSE IN NORMAL RENAL FUNCTION

0.5–4 mg once daily

PHARMACOKINETICS

  • Molecular weight                           : 430.5
  • %Protein binding                           : >80 (as trandolaprilat)
  • %Excreted unchanged in urine     : 10–15
  • Volume of distribution (L/kg)       : 18 litres
  • half-life – normal/ESRD (hrs)      : 16–24/– (as trandolaprilat)

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

  • 20 to 50     : Dose as in normal renal function
  • 10 to 20     : Dose as in normal renal function
  • <10           : Initial dose 500 mcg once daily, and increase according to response

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                : Unknown dialysability. Dose as in GFR <10 mL/min
  • HD                     : Dialysed. Dose as in GFR <10 mL/min
  • HDF/high flux   : Dialysed. Dose as in GFR <10 mL/min
  • CAV/VVHD      : Unknown dialysability. Dose as in GFR 10 to 20 mL/min

    IMPORTANT DRUG INTERACTIONS

    Potentially hazardous interactions with other drugs
  • Anaesthetics: enhanced hypotensive effect
  • Analgesics: antagonism of hypotensive effect and increased risk of renal impairment with NSAIDs; hyperkalaemia with ketorolac and other NSAIDs
  • Ciclosporin: increased risk of hyperkalaemia and nephrotoxicity
  • Diuretics: enhanced hypotensive effect; hyperkalaemia with potassium-sparing diuretics
  • Epoetin: increased risk of hyperkalaemia; antagonism of hypotensive effect
  • Lithium: reduced excretion (possibility of enhanced lithium toxicity)
  • Potassium salts: increased risk of hyperkalaemia
  • Tacrolimus: increased risk of hyperkalaemia and nephrotoxicity

    ADMINISTRATION

    Reconstition

    Route

    Oral

    Rate of Administration

    Comments

    OTHER INFORMATION

    Hyperkalaemia and other side effects are more common in patients with impaired renal function Close monitoring of renal function required during therapy in patients with renal insufficiency Renal failure has been reported in association with ACE inhibitors in patients with renal artery stenosis, post renal transplant, and those with congestive heart failure High incidence of anaphylactoid reactions has been reported in patients dialysed with high-flux polyacrylonitrile membranes and treated concomitantly with an ACE inhibitor – this combination should therefore be avoided Normal doses can be used in CKD 5 .



    See how to identify renal failure stages according to GFR calculation

    See how to diagnose irreversible renal disease

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