Watt-Smith, Stephen R.; (1994) Assessment Of The Effectiveness of Phentolamine In Reducing The Duration Of Dental Local Anaesthesia. Doctoral thesis (M.D), UCL (University College London).

Text Assessment of the effectiveness of phentolamine in reducing the duration of dental local anaesthesia.pdf Download (18MB)

Abstract

Effective local anaesthesia is required to ensure pain-free dental procedures, but existing anaesthetics produce persistent soft tissue anaesthesia well beyond the average time for the painful treatment. This may result in lip and tongue biting in young children and the handicapped. The study reports the clinical attempts to usefully reduce this level of unwanted soft tissue anaesthesia by injecting into the anaesthetised tissues a potent vasodilating agent, phentolamine. Lignocaine and adrenaline is the standard dental local anaesthetic combination, with the adrenaline included to prolong the duration and depth of anaesthesia in the highly vascular perioral tissues. The added catecholamine prevents the anaesthetic from being rapidly absorbed from the injection site by producing intense vasoconstriction. An alternative dental local anaesthetic is the combination of prilocaine and felypressin. This also produces excessively long periods of soft tissue anaesthesia despite the vasoconstriction not being mediated through ?-adrenoceptors. Investigation of the clinical effects of reversing residual soft tissue anaesthesia produced by prilocaine and felypressin were thought worthwhile to enable the clinical safety of a potentially inappropriate drug combination to be assessed. It also produced comparative data for interpreting the catecholamine reponses to the routine lignocaine and adrenaline anaesthetics. Phentolamine is a short-acting and potent a-adrenoceptor blocking agent. The investigations confirm that a 2mg/ml phentolamine reversal solution, when injected after a 30 minute delay into the perioral tissues in the vicinity of the local anaesthetic solution, quickly reverses the vasoconstrictor effects of adrenaline in vivo. Maxillary infiltration soft tissue anaesthesia was reduced from 138.1 to 16.9 minutes (95% CI) and pulp anaesthesia from 40.3 to 4.8 minutes (95% CI). Inferior dental nerve block reversals were reduced from 160.3 to 17.3 minutes (95% CI) and pulp anaesthesia from 59.5 to 11.1 minutes (95% CI). Multiple injections of 6ml 2% lignocaine + 1:80,000 adrenaline were reversed with 3ml 2mg/ml phentolamine, and venous plasma local anaesthetic concentrations assayed using High Performance Liquid Chromatography (HPLC). No statistically significant increase in plasma lignocaine concentration (95% CI) was observed. Venous plasma lignocaine and catecholamine concentrations were measured after multiple perioral injections of 5.4ml 2% lignocaine with three differing adrenaline concentrations; 1:50,000, 1:80,000 and 1:100,000. No statistically significant difference in plasma lignocaine concentrations was noted between the groups. Plasma adrenaline concentrations were statistically raised in the 1:50,000 group (95% CI), but the noradrenaline concentrations showed no significant variation. The perioral injection of 3 ml 2mg/ml phentolamine reversal agent after the 30 minute delay produced increases in plasma lignocaine concentrations, with the weakest 1:100,000 adrenaline anaesthetic the most statistically significant (95% CI). The intense local vasodilatation was demonstrated to be effective against the nonadrenaline alternative anaesthetic prilocaine and felypressin, with a statistically significant rise in the venous plasma prilocaine concentration (95% CI). Plasma local anaesthetic concentrations failed to reach accepted levels of toxicity, and no adverse cardiovascular events were recorded. Venous plasma adrenaline concentrations were measured before and after dental surgical extractions under lignocaine and adrenaline or prilocaine and felypressin local anaesthesia. Venous plasma adrenaline concentrations were significantly raised in only half the cases, but the prilocaine and felypressin group showed a marked reduction in data scatter. Additional experiments attempting to reverse the soft tissue anaesthesia following injection of another dental local anaesthetic combination, mepivacaine and adrenaline, are presented as appendices. Plasma mepivacaine concentrations were not statistically raised compared with placebo. Venous plasma catecholamine concentrations were measured following perioral injection of 6ml 2% mepivacaine + 1:100,000 adrenaline, and after a 30 minute delay, with 3ml 2mg/ml phentolamine or placebo. No statistical difference was noted between the groups for adrenaline or noradrenaline concentrations, but a trend for the noradrenaline concentration to rise over the 2 hour test period was observed. No adverse local reactions or systemic cardiovascular changes were observed in any of the studies, implying that the prolonged soft tissue effects of dental local anaesthesia may be safely and rapidly reversed by injection of small increments of phentolamine into the adjacent perioral tissues. Such a facility will be useful in clinical dental practice where needlessly prolonged anaesthesia may have significant consequences to patients, such as lip biting in the handicapped.

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