Diamorphine hydrochloride

CLINICAL USE

Opiate analgesic:Control of severe pain Pain relief in myocardial infarction (MI) Acute pulmonary oedema

DOSE IN NORMAL RENAL FUNCTION

Severe pain: Oral/SC/IM: 5–10 mg 4 hourly, increasing dose as necessaryAcute MI, pulmonary oedema: IV: 2.5–5 mg. Elderly patients – reduce dose by half

PHARMACOKINETICS

  • Molecular weight                           :423.9
  • %Protein binding                           :35
  • %Excreted unchanged in urine     : 0.1
  • Volume of distribution (L/kg)       :40–50 litres
  • half-life – normal/ESRD (hrs)      :1.7–5.3 minutes/–

    DOSE IN RENAL IMPAIRMENT

    GFR (mL/MIN)

  • 20 to 50     : Dose as in normal renal function
  • 10 to 20     : Use small doses, e.g. 2.5 mg SC/IM approx 6 hourly and titrate to response
  • <10           : Use small doses, e.g. 2.5 mg SC/IM approx 8 hourly and titrate to response

    DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES

  • CAPD                :Not dialysed. 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 drugsAnti-arrhythmics: delayed absorption of mexiletineAntidepressants: possible CNS excitation or depression with MAOIs – avoid concomitant use and for 2 weeks after stopping MAOI; possible CNS excitation or depression with moclobemide; increased sedative effects with tricyclicsAntipsychotics: enhanced sedative and hypotensive effectSodium oxybate: enhanced effect of sodium oxybate – avoid concomitant use

    ADMINISTRATION

    Reconstition

    1 mL water for injection or sodium chloride 0.9% (less may be used, e.g. for SC injection use 0.1 mL for 10 mg)

    Route

    IV, IM, SC, oral

    Rate of Administration

    IV: 1 mg/minute

    Comments

    Monitor BP and respiratory rates

    OTHER INFORMATION

    Increased cerebral sensitivity in renal impairment which can result in excessive sedation and serious respiratory depression necessitating ventilationMore rapid onset and shorter duration of action than morphineExtreme caution with regular dosing – accumulation of active metabolites may occurNaloxone must be readily available for reversal if required

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