2020
DOI: 10.1007/s12028-019-00894-2
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Cefepime-Induced Encephalopathy: A Possible Additional Mechanism of Neurotoxicity

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Cited by 2 publications
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“…Hypocarnitinemiaassociated encephalopathy has been reported with cefditoren, another cephalosporin, and carnitine deficiency may also be responsible for CIN through the inhibition of an organic cation/carnitine transporter gene (OCTN2) which could lead to an increased urinary loss of carnitine. [10][11][12][13] The neurotoxic effects may manifest as altered mental status, reduced consciousness, confusion, myoclonus, aphasia, agitation, seizures, and non-convulsive status epilepticus. 5 Unfortunately, critically ill patients may have similar neurological manifestations from infection, postoperative state, electrolyte disturbances, hypoglycemia, shock, alcohol withdrawal, pain, hypercapnia, and hypoxemia making it challenging to determine the true etiology of encephalopathy.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Hypocarnitinemiaassociated encephalopathy has been reported with cefditoren, another cephalosporin, and carnitine deficiency may also be responsible for CIN through the inhibition of an organic cation/carnitine transporter gene (OCTN2) which could lead to an increased urinary loss of carnitine. [10][11][12][13] The neurotoxic effects may manifest as altered mental status, reduced consciousness, confusion, myoclonus, aphasia, agitation, seizures, and non-convulsive status epilepticus. 5 Unfortunately, critically ill patients may have similar neurological manifestations from infection, postoperative state, electrolyte disturbances, hypoglycemia, shock, alcohol withdrawal, pain, hypercapnia, and hypoxemia making it challenging to determine the true etiology of encephalopathy.…”
Section: Introductionmentioning
confidence: 99%
“…Hypocarnitinemia-associated encephalopathy has been reported with cefditoren, another cephalosporin, and carnitine deficiency may also be responsible for CIN through the inhibition of an organic cation/carnitine transporter gene (OCTN2) which could lead to an increased urinary loss of carnitine. 10-13…”
Section: Introductionmentioning
confidence: 99%