Τόμος 1 (1983) – Τεύχος 1 – Άρθρο 3 – Επιθεώρηση Κλινικής Φαρμακολογίας και Φαρμακοκινητικής-Ελληνική Έκδοση – Volume 1 (1983) – Issue 1– Article 3 – Epitheorese Klinikes Farmakologias και Farmakokinetikes-Greek Edition

Τίτλος – Title Τοπικά Αναισθητικά στην Οδοντιατρική

Local anaesthetics in dentistry

Συγγραφέας – Author Γκυ Μπρις

Guy Briche

Παραπομπή – Citation Μπρις, Γ.: Τοπικά Αναισθητικά στην Οδοντιατρική, Επιθεώρηση Κλιν. Φαρμακολ. Φαρμακοκινητ. 1: 28-41 (1983)

Briche, G.: Local anaesthetics in dentistry, Epitheorese Klin. Farmakol. Farmakokinet. 1: 28-41 (1983)

 

Ημερομηνία Δημοσιευσης – Publication Date Απρίλιος – 1983 – April 1983
Γλώσσα Πλήρους Κειμένου –
Full Text Language
Ελληνικά – Greek
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Λέξεις κλειδιά – Keywords Οδοντιατρική,  τοπική αναισθησία, αντίδραση

 

Dentistry, local anaesthesia, reaction

Λοιποί Όροι – Other Terms Άρθρο
Article
Περίληψη – Summary Pain is one of the most commonly symptoms in dentistry. This sensory information travels to brain along nerves by a local flow of sodium ions into, and potassium out, of the axon. Local anaesthetic drugs injected into the tissues can cause a temporary, localised and reversible block to conduction by reducing the permeability of the neural membrane to sodium ions. The practicing dendist should have to choose between a wide variety of local anaesthetics the most convenient one for the particular patient and his needs. But the clinical use of these drugs depends upon Knowledge of their clinical pharmacological and pharmacokinetic properties and the physiological basis of neural blockade. Local anaesthetic drugs are weak bases with pka’s between 7.5 and 8.9. Changes in the pit of infected areas may interfere by changing the ratio of ionised to unionised lipid soluble drug. This fact in correlation to lipid solubility of the drug and the characteristics of the nerve (type and size) can influece the penetration of the drugs into the nerve before conduction is interrupted and local anaesthesia develops. The ester type local anaesthetics are at least partially metabolised by plasma cholinesterase and the amide type agents are extensively metabolised in the liver. But for all type agents the hepatic metabolism is important for their elimination. Other factors — properties to be considered: rapid onset and sufficient duration (equal to the time of intervention), allergies, concentration of the vasoconstrictor (greatly affecting the duration of the anaesthesia) and the absolute and relative toxicity depending of the absolute potency. It should be kept in mind that local anaesthetics are eventually absorbed into the general circulation and can have toxic manifestations.
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