eMedicine Specialties > Emergency Medicine > Toxicology
Toxicity, Valproate: Follow-up
Updated: Jan 26, 2009
Follow-up
Further Inpatient Care
- Depending on level of toxicity, patients with valproic acid overdose usually require admission to the intensive care unit (ICU) for continuous monitoring.
- Their condition may progressively deteriorate as valproic acid is absorbed and moves from the intravascular compartment to the CNS compartment.
- Intestinal absorption after overdose may be delayed several hours.
- Patients with overdose must be evaluated from a psychiatric point of view for plan of suicide or grave disability.
Further Outpatient Care
- After the patient's condition is stabilized and he or she is discharged, an ongoing relationship between the patient and a mental health professional is recommended if the overdose was intentional.
Transfer
- After patients are medically cleared, they may be transferred to a psychiatric facility. However, this disposition highly depends on the patient's symptoms and the amount of ingestion.
- In one multicenter case series of 134 patients with valproic acid ingestions (80 with toxic VPA levels at admission), the mean hospital stay for all patients was 44.7 hours (standard deviation, 28 h).4
Complications
- Valproic acid is used in the treatment of mood disorders in addition to its use as an antiseizure medication. Emergency personnel must consider the possibility of multidrug overdoses and availability of other antiseizure medications, including sedative-hypnotics, lithium, and other medications used to treat mood disorders.
- Patients must be monitored for signs and symptoms of other toxic syndromes.
- Obtain acetaminophen levels to rule out ingestion of this substance (see Laboratory Studies).
Prognosis
- The prognosis depends on the amount ingested, the decontamination and elimination strategies administered (if indicated), and the supportive care given.
- Severe ingestions may resolve without sequelae after aggressive decontamination, elimination, and adequate supportive care.
- L-carnitine is reportedly helpful in valproic acid overdose associated with hyperammonemia, hepatotoxicity, and coma. However, its role remains to be confirmed. Some authors recommend its empiric use in overdoses when levels are greater than 450 mg/L.
- The optimum dose, frequency, and route of administration (oral or intravenous) remain to be determined.
Patient Education
- For excellent patient education resources, visit eMedicine's Drug Overdose Center and Poisoning - First Aid and Emergency Center. Also, see eMedicine's patient education articles Poisoning, Drug Overdose, Activated Charcoal, and Poison Proofing Your Home.
Miscellaneous
Medicolegal Pitfalls
- Failure to diagnose a concomitant ingestion or underlying medical condition that results in serious morbidity
- Failure to obtain serial serum valproic acid levels, especially after ingestion of extended-release formulations
- Failure to aggressively decontaminate GI tract with whole-bowel irrigation after exposure to the extended-release formulation
The staff, faculty, and fellows of the San Francisco Bay Area Regional Poison Control Center contributed insight, review, and encouragement for this review.
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Further Reading
Keywords
valproic acid, toxicity valproate, valproate overdose, valproate poisoning, VPA, valproic acid overdose, anticonvulsant, antiseizure, seizure treatment, valproate, divalproate, sodium valproate toxicity, dipropylacetic acid toxicity, divalproex sodium toxicity, valproate semisodium toxicity, 2-propylpentanoic acid toxicity, 2-propylvaleric acid toxicity, Depacon, Depakene, Depakote, Depakote ER, Epilim, Ergenyl, Leptilan, Valkote, Sprinkles
Follow-up: Toxicity, Valproate