Lisinopril

CLINICAL USE

Angiotensin-converting enzyme inhibitor:Hypertension, heart failure, following myocardial infarction in haemodynamically stable patientsDiabetic nephropathy

DOSE IN NORMAL RENAL FUNCTION

2.5–80 mg dailyAfter a myocardial infarction: 2.5–10 mg daily

PHARMACOKINETICS

  • Molecular weight                           :441.5
  • %Protein binding                           :0
  • %Excreted unchanged in urine     : 80–90
  • Volume of distribution (L/kg)       :0.44–0.51
  • half-life – normal/ESRD (hrs)      :12/40–50

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

  • 20 to 50     : Initial dose 2.5 mg daily and titrate according to response
  • 10 to 20     : Initial dose 2.5 mg daily and titrate according to response
  • <10           : Initial dose 2.5 mg daily and titrate 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

    Close monitoring of renal function during therapy is necessary in those with renal insufficiencyRenal failure has been reported in association with ACE inhibitors and has been mainly in patients with severe congestive heart failure, renal artery stenosis, and post renal transplantHigh 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 avoidedHyperkalaemia and other side effects are more common in patients with impaired renal function.

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