Halothane |
CNS: fast smooth induction with an absence of stadium 2. Increase in cerebral blood flow and an increase in intracranial pressure. Cardiovascular: Decrease in blood pressure. Sensitized myocardium for arythmogenic effects of catecholamines. Hepatic: hepatotoxicity can occur (rare, and unpredictable) Uterus: decrease in muscle contractions that can lead to external twisting of a baby. Respiratory: no saliva, bronchial excretions or cough. Autonomic: bradycardia |
Enflurane |
CNS: fast, smooth induction. Convulsions can sometimes occur, thus it shouldn’t be used in epileptics. Cardiovascular: no sensitization of the myocardium. There is less suppression on the CVS than with Halothane. Respiratory: more suppression than with Halothane. |
Isoflurane |
CNS: faster induction and recovery than with Halothane. Cardiovascular: less suppression than with Halothane or Enflurane. There is also no sensitization of the myocardium. Respiratory: potent suppressor. This is because of the potent skeletal muscle relaxing effects. |
Desflurane |
CNS: even faster induction and recovery than Isoflurane. Increase in cerebral blood flow and intracranial pressure. Cardiovascular: less suppression than with Halothane and Enflurane. Respiratory: strong smell that can irritate the airways if it is used as an induction drug. This can cause coughing, shortness of breath and even laryngospasm. |
Sevoflurane |
The effects are similar to that of Desflurane. But in the respiratory system it is less irritating on the airways. |
Nitrous oxide |
CNS: weak anaesthetic, potent analgesic and can cause amnesia. CVS: there is no effect on the cardiovascular system. Respiratory: pure N2O can cause hypoxia. That is why it should always be mixed with pure O2 or air. During the recovery phase, N2O has a fast diffusion from the blood to the alveoli. Thus there will be a decrease in O2 pressure which would cause hypoxia. |