Professional Documents
Culture Documents
Anes 1
Anes 1
The clinically used aminoamides include lidocaine, mepivacaine, prilocaine, bupivacaine (racemic and its levo-
enantiomer), ropivacaine, and etidocaine. The ester and amide local anesthetics differ in their chemical stability,
locus of biotransformation, and allergic potential.
Amides are extremely stable, whereas esters are relatively unstable in solution. Aminoesters are hydrolyzed in plasma by
cholinesterase enzymes, but the amides undergo enzymatic degradation in the liver.
p-Aminobenzoic acid is one of the metabolites of estertype compounds that can induce allergic-type reactions in a small
percentage of patients. The aminoamides are not metabolized to p-aminobenzoic acid, and reports of allergic reactions to
these agents are extremely rare
Anesthetic Potency
Onset of Action
Duration of Action
Protein binding, Lipid solubitily
epinephrine produces mild intensification of blockade, but only most modest prolongation of epidural or peripheral blocks
with bupivacaine. α2-Adrenergic receptors in the spinal cord are known to activate endogenous analgesic mechanisms,
and the increased depth of analgesic action produced by epinephrine and the α2-agonist clonidine
upper airway: oral cavity, nasal cavity, pharyng, laryng, oral cav
Models that use several risk factors, such as the Wilson risk sum score (weight, head and neck
movement, jaw movement, receding mandible, and buck teeth)
the El-Ganzouri risk index (mouth opening, thyromental distance, Mallampati class, neck
movement, prognathism, weight, and history of difficult intubation)
preoksigenasi
Preoxygenation is typically performed via a facemask
attached to either the anesthesia machine or a Mapleson
circuit. To ensure adequate preoxygenation, 100% oxygen
must be provided at a flow rate high enough to prevent
rebreathing (10 to 12 L/min), and no leaks around
the facemask must be present. An end-tidal concentration
of oxygen greater than 90% is considered to maximize
apnea time. Two primary methods are used to accomplish
preoxygenation. The first method uses tidal volume
ventilation through the facemask for 3 minutes, which
allows the exchange of 95% of the gas in the lungs.46
The second method uses vital capacity breaths to achieve
adequate preoxygenation more rapidly. Four breaths over
30 seconds is not as effective as the tidal volume method
but may be acceptable in certain clinical situations; eight
breaths over 60 seconds has been shown to be more effective.
46 Head-up positioning has been shown to improve
the quality of preoxygenation in both obese48 and nonobese
patients.49 The use of noninvasive positive-pressure
ventilation (PPV) for preoxygenation also prolongs apnea
time
Laringospasm
Bronkospasm