Flumazenil, the first benzodiazepine antagonist, is currently used wid
ely as an emergency drug: and has also been utilized in planned proced
ures, to time arousal intra- or post-operatively. It is known that flu
mazenil, used at the end of a procedure, causes instant recovery by re
versing the residual effects of, for example, midazolam. An agonist-an
tagonist concept, midazolam-flumazenil, where benzodiazepine sedation
or anaesthesia is terminated at will, is, therefore, finding increasin
g application. In neuroanaesthesia, for example, it facilitates immedi
ate recovery cardiovascular stabilization and the use of midazolam as
an alternative to thiopentone and inhalational agents, and in ear, nos
e and throat endoscopies, it permits more rapid turnover of patients a
nd is a good choice for haemodynamic stability in patients with a high
cardiovascular risk factor. There continues to be debate over the ter
m used to describe the level of sedation remaining after the effects o
f the antagonist have worn off 'Resedation' is often used incorrectly
to describe what is in reality residual sedation. Given the correct us
e of midazolam or the exploitation of synergism using opioids, flumaze
nil will cause arousal, while maintaining the benefit of opioid analge
sia. Such a technique may eliminate the need for formal recovery facil
ities in many ambulatory patients, thereby reducing dependence on trol
leys: beds and nurses. This has major implications for health economic
s, particularly in relation to endoscopy clinics and when co-induction
of anaesthesia is employed.