2012
DOI: 10.4172/2161-0495.1000126
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Unique Case with Seizures after Prolonged Use of Camphor Crème in Elderly Patient

Abstract: Camphor is a pleasant smelling cyclic ketone of the hydro aromatic terpene group. The mechanism by which camphor produces toxicity is unknown. Within a period of 5 to 15 minutes, patients commonly complain of mucus membrane irritation, nausea, vomiting, and abdominal pain. Generalized tonic-clonic convulsions are often the first sign of significant toxicity and can occur soon after ingestion. Central nervous system depression is commonly seen, such as headache, dizziness, confusion, agitation, anxiety, halluci… Show more

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Cited by 3 publications
(4 citation statements)
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“…The hyperpolarizing effect of TRPC1-BKCa coupling could serve to reduce agonist-induced membrane depolarization, thereby preventing excessive contraction of VS.MCs to contractile agonists. Interestingly, Orai1 was also shown to interact with BKCa [76]. In the latter work, the authors showed that Orai1 physically associates with BKCa to form a signaling complex in the rat mesenteric artery smooth muscle.…”
Section: Chelating Intracellular Camentioning
confidence: 80%
“…The hyperpolarizing effect of TRPC1-BKCa coupling could serve to reduce agonist-induced membrane depolarization, thereby preventing excessive contraction of VS.MCs to contractile agonists. Interestingly, Orai1 was also shown to interact with BKCa [76]. In the latter work, the authors showed that Orai1 physically associates with BKCa to form a signaling complex in the rat mesenteric artery smooth muscle.…”
Section: Chelating Intracellular Camentioning
confidence: 80%
“…Camphor oil preparations have been used both internally and externally in many countries, for a variety of ailments, ranging from respiratory problems to rheumatic pain. Camphor oil is applied to the skin as a rubefacient to promote circulation [ 8 - 9 ]. The mechanism by which camphor produces toxicity is unknown.…”
Section: Discussionmentioning
confidence: 99%
“…Within five to 15 minutes, patients commonly complain of mucus membrane irritation, nausea, vomiting, and abdominal pain. Chronic oral camphor has been reported to cause seizures and death as a form of NSSI [ 3 , 8 ].…”
Section: Discussionmentioning
confidence: 99%
“…The 3% to 11% concentration of camphor has been approved by the FDA for topical use as a pain reliever and anaesthetic [ 26 ]. The pharmaceutical industry produces medicines with a concentration of camphor in the range from 0.5% to 10.8%, although in some cases, higher concentrations are used [ 27 , 28 ]. The most common camphor drugs are camphor alcohol (10%), oil solutions (10%, 20%), liniment “Camphocin” (15%), camphor ointment (10%), and gel “Camphotrol ® ” (PureTek Corporation, Panorama City, CA, USA) with a combination of 4% camphor and 10% menthol [ 18 ].…”
Section: Introductionmentioning
confidence: 99%