(Redirected from Local anaesthetic)A 'local anesthetic' is a
drug that reversibly inhibits the propagation of signals along
nerves. When it is used on specific nerve pathways, effects such as
analgesia (loss of
pain sensation) and
paralysis (loss of
muscle power) can be achieved.
Clinical local anesthetics belong to one of two classes: aminoamide and aminoester local anesthetics. ''synthetic local anesthetics'' are structurally related to
cocaine. They differ from cocaine mainly in that they have no abuse potential and do not act on the
sympathoadrenergic system, i.e. they do not produce
hypertension or local
vasoconstriction.
Local anesthetics vary in their
pharmacological properties and they are used in various techniques of
local anesthesia such as:
★
Topical anesthesia (surface)
★ Infiltration
★ Plexus block
★ Epidural (extradural) block
★ Spinal anesthesia
The local anesthetic
lidocaine is also used as a Class Ib
antiarrhythmic drug.
Mechanism of action
Local anesthetic drugs act mainly by inhibiting
sodium influx through sodium-specific
ion channels in the
neuronal
cell membrane, in particular the so-called voltage-gated sodium channels. When the influx of sodium is interrupted, an
action potential cannot arise and signal conduction is inhibited. The receptor site is thought to be located at the cytoplasmic (inner) portion of the sodium channel. Local anesthetic drugs bind more readily to "open" sodium channels, thus onset of neuronal blockade is faster in neurons that are rapidly firing. This is referred to as state dependent blockade.
Local anesthetics are weak
bases and are usually formulated as the hydrochloride salt to render them water-soluble. At physiologic
pH the protonated (ionised) and unprotonated (unionised) forms of the molecule exist in an equilibrium but only the unprotonated molecule diffuses readily across cell membranes. Once inside the cell, the lower pH results in the molecule being protonated, thus inhibiting its passage back out of the cell. This is referred to as "ion-trapping". In the protonated form, the molecule binds to the local anaesthetic binding site on the inside of the ion channel near the cytoplasmic end.
Acidosis such as caused by inflammation at a wound partly reduces the action of local anesthetics. This is partly because most of the anaesthetic is ionised and therefore unable to cross the cell membrane to reach its cytoplasmic-facing site of action on the sodium channel.
Undesired effects
The conduction of electric impulses follows a similar mechanism in peripheral nerves, the
central nervous system, and the
heart. The effects of local anesthetics are therefore not specific for the signal conduction in peripheral nerves. Side effects on the central nervous system and the heart may be severe and potentially fatal. However, toxicity usually occurs only at
nuclear plasma levels which are rarely reached if proper anesthetic techniques are adhered to.
Central nervous system
Depending on local tissue concentrations of local anesthetics, there may be excitatory or depressant effects on the central nervous system. At lower concentrations, a relatively selective depression of inhibitory neurons results in cerebral excitation, which may lead to generalized
convulsions. A profound depression of brain functions occurs at higher concentrations which may lead to
coma,
respiratory arrest and death. Such tissue concentrations may be due to very high plasma levels after intravenous injection of a large dose. Another possibility is direct exposure of the central nervous system through the CSF, i.e. overdose in
spinal anesthesia or accidental injection into the
subarachnoid space in
epidural anesthesia.
Cardiovascular system
The conductive system of the heart is quite sensitive to the action of local anesthetics. Lidocaine is often used as an antiarrhythmic drug and has been studied extensively, but the effects of other local anesthetics are probably similar to those of Lidocaine. Lidocaine acts by blocking sodium channels, leading to slowed conduction of impulses. This may obviously result in
bradycardia, but
tachyarrhythmia can also occur. With high plasma levels of lidocaine there may be higher-degree atrioventricular block and severe bradycardia, leading to coma and possibly death.
Treatment of overdose: "
Lipid rescue"
There is evidence that
Intralipid, a commonly available intravenous lipid emulsion, can be effective in treating severe cardiotoxicity secondary to local anaesthetic overdose, including human case reports of successful use in this way ('
lipid rescue').
[1]
[2][3][4][5]
Hypersensitivity/Allergy
Adverse reactions to local anesthetics (especially the Esters) are not uncommon, but true
allergy is very rare. Allergic reactions to the Esters does not result in cross-allergy to Amides. Therefore, Amides can be used as alternatives in those patients. Non-allergic reactions may resemble allergy in their manifestations. In some cases, skin tests and provocative challenge may be necessary to establish a diagnosis of allergy. There are also cases of allergy to paraben derivatives, which are often added as preservatives to local anesthetic solutions.
★ ''Main Article:''
Allergic reactions during anaesthesia
Methemoglobinemia
The systemic toxicity of
prilocaine is comparatively low, however its metabolite, o-toluidine, is known to cause
methemoglobinemia. As methemoglobinemia reduces the amount of
hemoglobin that is available for oxygen transport, this side effect is potentially life-threatening. Therefore dose limits for prilocaine should be strictly observed. Prilocaine is not recommended for use in infants.
Local anesthetics in clinical use
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Amino esters
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Benzocaine
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Chloroprocaine
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Cocaine
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Procaine
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Tetracaine
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Amino amides
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★
Bupivacaine
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★
Levobupivacaine
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Lidocaine
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★
Mepivacaine
★
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Prilocaine
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Ropivacaine
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Articaine
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★
Trimecaine
Esters are prone to producing allergic reactions, which may necessitate the use of an Amide. The names of Amides contain an "i" somewhere before the -aine. Esters do not.
★ Combinations
★
★
Lidocaine/prilocaine (EMLA)
References
1. Weinberg GL, VadeBoncouer T, Ramaraju GA, Garcia-Amaro MF, Cwik MJ. Pretreatment or resuscitation with a lipid infusion shifts the dose-response to bupivacaine-induced asystole in rats. Anesthesiology 1998; 88: 1071-5.
2. Weinberg G, Ripper R, Feinstein DL, Hoffman W. Lipid emulsion infusion rescues dogs from bupivacaine-induced cardiac toxicity. Regional Anesthesia and Pain Medicine 2003; 28: 198-202..
3. Picard J, Meek T. Lipid emulsion to treat overdose of local anaesthetic: the gift of the glob. Anaesthesia 2006;61:107-9. PMID 16430560
4. Rosenblatt MA, Abel M, Fischer GW, Itzkovich CJ, Eisenkraft JB. Successful Use of a 20% lipid emulsion to resuscitate a patient after a presumed bupivacaine-related cardiac arrest. Anesthesiology 2006;105:217-8. PMID 16810015
5. Litz, RJ, Popp M, Stehr S N, Koch T. Successful resuscitation of a patient with ropivacaine-induced asystole after axillary plexus block using lipid infusion. Anaesthesia 2006;61:800-1.
External links
★
More on lipid rescue
See also
★
Anesthetic
★
General anaesthetic