2015
DOI: 10.4103/0970-4388.165646
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Phentolamine mesylate: It′s role as a reversal agent for unwarranted prolonged local analgesia

Abstract: Administration of local anesthesia is an integral procedure prior to dental treatments to minimize the associated pain. It is learned that its effect stays more than the time required for the dental procedure to be completed. This prolonged soft tissue anesthesia (STA) can be detrimental, inconvenient, and unnecessary. Phentolamine mesylate, a Food and Drug Administration-approved drug essentially serves the purpose of faster recovery from numbness at the site of local anesthesia. This article reviews the deve… Show more

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Cited by 8 publications
(3 citation statements)
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“…The present preliminary clinical trial study was designed to evaluate the efficacy of photobiomodulation in reversal of soft-tissue local anesthesia. In a previous study, this was achieved by injection of phentolamine mesylate, and novel LLLT therapy might be considered as a non-invasive treatment adjunct to local anesthesia [ 39 , 40 ].…”
Section: Discussionmentioning
confidence: 99%
“…The present preliminary clinical trial study was designed to evaluate the efficacy of photobiomodulation in reversal of soft-tissue local anesthesia. In a previous study, this was achieved by injection of phentolamine mesylate, and novel LLLT therapy might be considered as a non-invasive treatment adjunct to local anesthesia [ 39 , 40 ].…”
Section: Discussionmentioning
confidence: 99%
“…PM is a non-specific α-adrenergic inhibitor whose effect is vasodilation of the vascular system [7,8,11,17]. It inhibits the ability of sympathomimetic amines, such as norepinephrine and epinephrine, to stimulate vascular contraction [19,20]. Given that it is an α-adrenergic inhibitor, special attention should be paid to any cardiovascular changes that may occur, such as hypotension and/or tachycardia following the injection [9].…”
Section: Introductionmentioning
confidence: 99%
“…PM is a non-specific α-adrenergic inhibitor whose effect is vasodilation of the vascular system [7,8,11,17]. It acts by inhibiting the ability of sympathomimetic amines, such as norepinephrine and epinephrine, to stimulate vascular contraction [19,20]. Because it is an α-adrenergic inhibitor, special attention should be paid to any cardiovascular changes that may occur, such as hypotension and/or tachycardia after injection [9].…”
Section: Introductionmentioning
confidence: 99%