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Severe but reversible encephalopathy associated with cefepime.
P Jallon1, L Fankhauser, R Du Pasquier
1Epilepsy and EEG Unit, Geneva Cantonal Hospital, 1211 Geneva 14, Switzerland.
Neurophysiologie Clinique = Clinical Neurophysiology
|February 24, 2001
Summary
Severe encephalopathy was observed in 19 patients with renal impairment treated with cefepime. Symptoms resolved after drug discontinuation, indicating a need for dosage reduction in renally impaired patients.
Area of Science:
- Pharmacology
- Nephrology
- Neurology
Background:
- Cefepime is a broad-spectrum parenteral cephalosporin antibiotic.
- Renal impairment can affect drug clearance and increase the risk of adverse events.
- Encephalopathy is a serious neurological complication that can occur in various clinical settings.
Purpose of the Study:
- To report and analyze cases of severe encephalopathy associated with cefepime use in patients with renal impairment.
- To investigate the relationship between cefepime administration and the development of encephalopathy.
- To provide recommendations for cefepime dosage adjustments in renally impaired individuals.
Main Methods:
- Retrospective analysis of 19 patients with renal impairment who developed severe encephalopathy.
- Patients received cefepime for various infections over a three-year period.
- Clinical presentation, electroencephalogram (EEG) findings, and response to cefepime discontinuation were documented.
Main Results:
- All 19 patients (aged 57-91 years) exhibited a prolonged confusional state.
- EEG revealed diffuse rhythmic non-reactive triphasic sharp waves.
- Electroclinical symptoms resolved within 24-48 hours after discontinuing cefepime, establishing a clear drug-related link.
Conclusions:
- Cefepime administration can precipitate severe encephalopathy in patients with compromised renal function.
- The observed encephalopathy is directly related to cefepime intake and is reversible upon drug withdrawal.
- It is crucial to reduce cefepime dosage in patients with renal impairment to mitigate the risk of neurological toxicity.