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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- Congresul consacrat aniversării a 75-a de la fondarea Universității de Stat de Medicină și Farmacie „Nicolae Testemițanu” din Republica Moldova
- Culegere de postere
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/13005
Title: | Local anesthetic solutions in dentistry: a comparative study |
Authors: | Vetrila, Cătălina Levco, Simion |
Keywords: | local anesthetic;articaine;lidocaine;dentistry |
Issue Date: | Oct-2020 |
Publisher: | Universitatea de Stat de Medicină şi Farmacie "Nicolae Testemiţanu" |
Abstract: | Introduction.
Pain control requires the study of local anesthesia. Local anesthetics have been
available in dentistry since 1884 and today lidocaine and articaine are most
often used. The main question is which one is more suitable and presents more
advantages. Material and methods.
In order to carry out the study, there were studied a large number of dental books –
14 and foreign clinical studies from PubMed – 7, researchgate – 4, emedicine – 5
and US Library – 6. Purpose: Analysis of specialty literature to determine if articaine or
lidocaine is more effective. Results.
The chemical and pharmacologic properties of a local anesthetic can give valuable
information about the clinical effects . The most important ones for both articaine
and lidocaine are listed in Table 1.
The dissociation constant (pKa) affects the onset of action. Lower pKa, means that
more molecules are present to diffuse through the nerve, thus the onset time is
decreased. Lipid solubility affects the anesthetic potency. Increased lipid solubility enhances
diffusion through the nerve, which itself is 90 % lipid (Malamed 2013), more easily.
Articaine differs from lidocaine,because it contains both ester and amide linkages.
As a result, it is more lipid soluble (Isen 2000).
Protein binding affects the duration. Increased protein binding allows anesthetic
cations to be more firmly attached to proteins located at receptor sites. Thus the
duration of action is increased.
Approximately 70 % of lidocaine undergoes liver biotransformation . Patients with
poor liver function are unable to biotransform it at a normal rate. This leads to
increased toxicity. The extra ester linkage in articaine alows it to be 90-95 %
metabolized with the help of the cholinesterase enzyme in blood, and only 5-10 % in
the liver. This feature is clearly demonstrated when the half-life between articaine
and lidocaine is compared, 27 min versus 90 min.
Malamed & al conducted a study to compare the safety between articaine 4 % with
adrenaline 1:100 000, and lidocaine 2 % with adrenaline 1:100 000. A total of 1325
subjects participated in these study, 882 in the articaine group, and 443 in the
lidocaine. These are the most common adverse effects: Conclusion.
Lidocaine is considered to be more safe, being administrated to children under 4,
pregnant woman and allergic pacients, but articaine has a 1,5 times bigger potency,
it diffuses faster, binds better with the plasmatic proteins and also is better for
pacients with liver problems.
Paraesthesia is the most common side effect of articaine (Jacques A. Baart), but
lidocaine also can cause adverse events, which must be taken in consideration.
If we have a standard patient, then articaine will be more suitable to use. |
URI: | https://stiinta.usmf.md/ro/manifestari-stiintifice/zilele-universitatii http://repository.usmf.md/handle/20.500.12710/13005 |
Appears in Collections: | Culegere de postere
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