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PATIENT
Kenanga marwan s
Departemen anestesiologi & terapi intensif
FK Unlam-RSUD Ulin Banjarmasin
Having identified the high-risk patient, how do
we then set about improving outcome ?
Induction agents
1. Thiopentone (sulphur analogue of pentobarbitone):
Remains the most rapidly effective drug for the induction of
general anaesthesia. Rapid sequence induction for the
purposes of securing the airway is best performed with
Thiopentone. Thiopentone is the only induction agent that
reduces the brain’s metabolic requirement for oxygen and is
hence neuroprotective. It produces depression of myocardial
contractility together with vasodilation resulting in a fall of BP.
However, it is noteworthy that in the hypovolaemic or
shocked patient the sleep dose of Thiopentone is greatly
reduced as compared to the healthy patient
• Etomidate (carboxylated imidazole): The main
advantage is said to be cardiovascular stability
when compared to Thiopentone. It inhibits
17α, 11β hydroxylase enzymes in adrenal
steroid synthesis. Therefore, it is
contraindicated as an infusion due to the
above adrenal suppression resulting in
increased mortality in patients sedated with
this agent.
• Propofol (di-isopropyl phenol): Rapid onset
(although a little slower than Thiopentone)
and obtunds pharyngeal and glottal reflexes to
a greater extent than Thiopentone. Widely
used for total IV anaesthesia and ICU sedation.
The hypotension produced is chiefly
secondary to vasodilation rather than
myocardial depression.
• Ketamine (phencyclidine derivative):
Sympathomimetic effects main- tain BP but the
increases in heart rate (HR) and stroke volume
increase myocardial work. It is profoundly
analgesic and is an effective analgesic agent at
subanaesthetic doses. Despite sympathomimetic
effects, it may cause cardiac depression,
myocardial ischaemia and collapse in shocked
patients in whom catecholamine stores may be
exhausted.
• Opioids
• The key issue is the cautious use of short acting agents. The shortest available is
Remifentanil.
Advantages:
• very short acting (metabolised by plasma cholinesterase),
• no accumulation in hepatorenal failure,
• very potent,
• suitable as an adjunct to sedation,
• may reduce the need for muscle relaxants.
Disadvantages:
• must be reconstituted from powder,
• profound respiratory depression,
• must be infused,
• no postoperative analgesia,
• causes decrease in BP (decrease in SVR and myocardial contractility) – worsened in
hypovolaemia.
Other Opioids
• Fentanyl: minimal effect on the cardiovascular
system in the stable, calm patient undergoing
cardiac surgery. In shocked patients exhibiting
high sympathetic tone, abolition of this with
Fentanyl results in a fall in BP.
• Morphine should be used with great care in the
critically ill patient as it has pharmacologically
active metabolites and is reliant on the liver and
kidneys for its elimination.
Muscle relaxants
• There are four main factors governing the choice of muscle
relaxant for anaesthesia:
– Onset – All critically ill patients are assumed to have a full
stomach. Despite recent introduction of faster onset non-
depolarising drugs such as Rocuronium, Suxamethonium
remains the ‘gold standard’ for rap- idly securing the airway. If
cardiac instability is a major concern, Rocuronium may be a
better choice.
– Cardiovascular effects – Rocuronium has least cardiac effects of
the relax- ants followed by Vecuronium. However, the vagolytic
and sympatho- mimetic effects of Pancuronium may make it an
appropriate choice in shocked patients
• Termination of effect and excretion – Agents not
dependent on the kidney or liver for termination
of effect sound attractive in the shocked patient
but from a practical point of view few critically ill
patients are ‘reversed’ at the end of the
operation and, thus, length of action of the
muscle relaxants is not a big problem.
• Duration – In a similar manner, short or long
duration is not usually an issue.
• Inhalational agents
• 1. Enflurane – Greatest degree of myocardial
depression for equivalent MAC.
• 2. Sevoflurane – Less increase in cerebral blood
volume. Short acting.
• 3. Halothane – Rarely used nowadays. Long
acting with more active metabolites retained in
body than other volatile agents with potential for
liver toxicity. Sensitises the heart to endogenous
and exogenous catecholamines with the potential
for arrhythmias.
• 4. Isoflurane – Impressive safety profile in large numbers of
patients. Hypotension chiefly by vasodilation rather than
myocardial depression. Early concerns re-coronary steal are
unfounded in conventional usage.
• 5.Desflurane – Specialised delivery systems required. Short acting.
Some concerns re-coronary steal.
• 6. Nitrous oxide – In normal patients mild indirect sympathetic
stimula- tion reduces any myocardial depressant actions of N2O.
Following haemorrhage this protecting effect is lost and N2O has
the same depres- sant effects on the heart as Halothane. With the
additional concerns re-lesser inspired oxygen concentrations and
the potential for expansion of air spaces, for example,
pneumothoraces, it is difficult to see a major role for N2O in
critically ill patients.