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however, it is hypertonia rather than muscle twitching that occurs.Glavinia and Robertshaw described a case of myoclonic spasm in a 59-year-old woman who received a bolus of 3 mg of intrathecal morphine for intractable pain [2] while Jayawardena and Hill described a case of myoclonus in a 65-year-old woman 24 h after discontinuing a diamorphine infusion into the epidural space [3].In both the previously reported cases of myoclonic spasms following the administration of morphine and diamorphine, the drugs had been infused spinally in much smaller doses.The 100-fold difference in dose before the development of myoclonus is probably related to the concentration gradient between the intravenous and cerebrospinal compartments, this being a function of a lipid solubility of diamorphine.Terminally ill patients at the Hospice commonly receive comparable doses of diamorphine and morphine to that initially given to this patient without developing myoclonic spasms, but ureteric obstruction leading to chronic renal insufficiency may have accelerated central neuronal toxicity in this patient as it would impair excretion of unconjugated active morphine.
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Hamza et al. (1992) studied this question.
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