1st line management for seizures, status epilepticus, alcohol withdrawl rxns
Common choice sedation interventional procedures (if gen anaesthetic unsuitable)
ST tx = anxiety, insomnia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q
BENZODIAZEPINES: MOA
A
Target is y-aminobutyric acid type A (GABA-A)
GABA-A receptor is a chloride channel that opens in response to binding with GABA
Opening the channel allows chloride to flow into the cell, cell more resistant to depolarisation
BENZOD’s facilitate and enhance binding of GABA to the GABA-A receptor
Widespread depressant effect on synaptic transmission
Clinical manifestations = Reduced anxiety, sleepiness, sedation and anticonvulsive effects
Ethanol also acts on the GABA receptor and in chronic excessive use the patient becomes tolerant to its presence
Abrupt cessation = provokes the excitatory state of alcohol withdrawl
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q
BENZODIAZEPINES: ADVERSE EFFECTS
A
Dose dependent drowsiness, sedation and coma
Loss of AW reflexes can lead to AWO + Death
Use for more than a few weeks = state of dependence can develop
Abrupt cessation = a withdrawl rxn similar to alcohol withdrawl
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q
BENZODIAZEPINES: WARNINGS
A
Elderly more susceptible to its effects
Avoid in respiratory impairment patients or NMDx (myasthenia gravis)
Avoid in Liver Failure = may precipitate HEPATIC ENCEPHALOPATHY
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q
BENZODIAZEPINES: INTERACTIONS
A
The effects of benzodiazepines are additive to those of other sedating drugs, including alcohol and opioids
Most depend on cytochrome P450 enzymes for elimination, so concurrent use with cytochrome P450 inhibitors (e.g. amiodarone, diltiazem, macrolides, fluconazole, protease inhibitors) may increase their effects.