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A disadvantage of propofol is that it is painful on injection. Ketamine produces a different effect to other intravenous anaesthetics; analgesia, sensory loss, amnesia and muscle paralysis are produced without loss of consciousness, so-called dissociative anaesthesia, and with minimal respiratory depression. The site of action of ketamine is thought to be through inhibition at glutamate receptors. Ketamine is a phencyclidine derivative and as such has abuse potential. Phencyclidine was developed in the hallucinations and delirium.

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They should be used together with anticholinesterase drugs and once an improvement is seen the dose should be decreased. Long-term use of corticosteroids leads to serious side effects, including suppression of the pituitary-adrenal axis, immunosuppression, muscle wasting, osteoporosis and impaired wound healing. Immunosuppressants such as azathioprine are used when other forms of treatment fail to control the progression of myasthenia gravis.

A well-documented historical example of this is the competition between penicillin and probenecid. Penicillin is a drug that is approximately eliminated by a kidney transport system. This was a disadvantage in the days when penicillin was expensive and difficult to produce, because its action was prematurely terminated unless high doses were given.

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The aim is to use the lowest effective concentration of corticosteroid for the shortest period. However, it is preferable to use a high potency steroid for a short period rather than a low potency steroid for a longer period. This minimizes the damage to the skin structure and reduces the possibility of systemic adverse effects. Oral antihistamines that have a sedative effect may be useful at night to reduce nocturnal itching, which can cause skin damage and secondary infection. In very severe eczema, topical corticosteroids may not be sufficient to relieve the inflammation.

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