- Among mood stabilizers, carbamazepine and VPA are associated with the highest incidence of hepatotoxicity.
- Although there are case reports of hepatotoxicity with oxcarbazepine, it may have a better liver safety profile than carbamazepine.
- Hepatotoxicity with lamotrigine is rare, although fatal cases have been reported
Antipsychotics
- When initiating an antipsychotic, a temporary, benign increase in liver enzymes can be expected, but typically discontinuation is unnecessary.
- Phenothiazines in particular can cause increases in liver enzymes in 20% of patients.
- Hepatotoxicity with benzodiazepines is infrequent, with a few cases of cholestatic injury reported with diazepam, chlordiazepoxide, and flurazepam
SSRI
- are relatively safe; incidents of hepatic injury are rare.
- Among SSRIs, paroxetine is most frequently associated with hepatotoxicity.
- Abnormal liver function tests have been observed with fluoxetine (0.5% of long-term recipients) and other SSRIs
Antidepressants
- Antidepressants with dual norepinephrine and serotonin reuptake inhibitor properties carry a higher risk of liver injury, especially duloxetine.
- Hepatocellular, cholestatic, and mixed types of hepatotoxicity are associated with duloxetine-induced hepatotoxicity
Monitoring recommendations
- Before prescribing potentially hepatotoxic medications, order baseline liver function tests.
- During therapy, periodic liver function monitoring is recommended. Elevated transaminase concentrations (>3 × the upper limit of normal), bilirubin (>2 × the upper limit of normal), and prolonged prothrombin times are indicators of hepatic injury.
- Caution should be taken to prevent polypharmacy with multiple hepatotoxic medications and over-the-counter use of hepatotoxic drugs and supplements.
- When choosing a psychotropic, take into account patient-specific factors, such as underlying liver disease and alcohol consumption.
- Patients on potentially hepatotoxic medications should be counseled to recognize and report symptoms of liver dysfunction, including nausea, vomiting, jaundice, and lower-extremity edema
References:
1. How to modify psychotropic therapy
for patients who have liver dysfunction, Current Psychiatry Vol. 13, No. 12
2. Antipsychotic Drugs –
Prescribing & Monitoring in Adults Information for Primary Care
3. MANAGEMENT OF MARKED LIVER ENZYME
INCREASE DURING OLANZAPINE TREATMENT:A CASE REPORT AND REVIEW OF THE LITERATURE. Psychiatria Danubina, 2011; Vol.
23, Suppl. 1, pp 15–17
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