Clinical Effects and Toxicokinetic Evaluation Following Massive Topiramate Ingestion

Abstract

Background

Topiramate is used to treat a variety of neurologic and psychiatric diseases due to its benign safety profile. Data regarding the toxicity and toxicokinetics of topiramate in acute overdose are limited. A case of massive, acute ingestion resulting in the highest reported topiramate level is presented, including toxicokinetic evaluation.

Case Report

A 37 yo woman presented with coma unresponsive to naloxone following topiramate ingestion. She had normal vital signs without respiratory depression. She was intubated for airway protection, given 3.5mg lorazepam IV for facial and neck muscle twitching, and transferred to our facility. No additional sedation was required for 18 hours on the ventilator. Following mental status improvement, the patient was extubated. Confusion, dysarthria and imbalance resolved over the next 2 days. Nonanion gap metabolic acidosis persisted for 3 days. Peak serum topiramate level was 356.6mcg/ml(5–20).

Discussion

Massive topiramate ingestion led to prolonged coma with normal vital signs and nonanion gap metabolic acidosis. Coma of this severity has not been previously reported. Serum half-life which has not been studied after overdose was 15.79 hours. Despite the large ingestion and significant presenting symptoms, the patient recovered fully with supportive intensive care alone.

Conclusion

Massive acute topiramate ingestion may lead to nonanion gap metabolic acidosis and prolonged coma which resolves with intensive supportive care. Toxicokinetic data following large, suicidal ingestion of topiramate were similar to previously published pharmacokinetic information.

Background

Topiramate is a sulfamate-substituted monosaccharide anticonvulsant used in the treatment of various seizure disorders and as a mood stabilizer. Pharmacologic activities include reduction in voltage-gated sodium currents, increase in the frequency of GABA receptor binding, and antagonism of kainate binding at the kainate/AMPA site of the glutamate receptor.¹ Topiramate is also an inhibitor of the CA-II and CA-IV isoenzymes of carbonic anhydrase.¹ Pharmacokinetic studies have shown a plasma elimination half-life of 18–24 hours.² Less than 20% of the drug is metabolized, with the inactive metabolites 10-hydroxytopiramate, 2,3-O-desisopropylidene topiramate, 9-hydroxytopiramate and 4,5-O-desisopropylidene topiramate identified.³

In therapeutic doses, topiramate is generally well tolerated.⁴ However, the data regarding topiramate toxicity in humans continues to be limited to few case reports and one poison center review. The most commonly reported symptoms in a large poison center review included neurologic abnormalities such as tremor, sedation, ataxia, nystagmus, and slurred speech.⁵ Coma was only reported in 1/567 cases reported to poison centers.⁵ Metabolic acidosis related to its carbonic anhydrase activity is a well-known adverse effect of topiramate, but is not associated with significant morbidity.^6,7,8,9 Pediatric ingestions have yielded similar toxicity as well as hallucinations in young children.^8,10 There is one published report of a fatality attributed to topiramate ingestion. Postmortem central blood topiramate concentration was 170 mcg/mL with levels also measured in the liver, stomach, and vitreous fluid.¹¹ Case reports of survival following topiramate toxicity demonstrated levels of 9.4 mcg/ml and 10.5 mcg/ml.^8,10 The reference range for topiramate levels in the laboratory at our institution is 5–20 mcg/ml.

Experience with topiramate toxicity is limited, but would indicate that serious adverse effects may occur but fatalities are rare. Toxicokinetic data following massive overdose has not been reported. We report a case of the largest acute ingestion of topiramate based on a Medline search of topiramate toxicity in the English literature, including toxicokinetic analysis.

Case Report

A 37 year old woman with a history of bipolar disorder treated with topiramate and diazepam presented to an outlying emergency department via Emergency Medical Service when her husband was unable to wake her. In addition to her prescribed medications, the only medication she had access to was ibuprofen. He had last seen her awake and acting normally roughly 12 hours earlier. In the emergency department she was witnessed to have facial twitching and clonic movements of her head which were interpreted as seizure activity. These movements resolved with 3.5 mg of intravenous lorazepam. The patient remained unresponsive following naloxone administration and was intubated for airway protection without need for further sedation or paralytic administration. An arterial blood gas drawn at that time revealed a metabolic acidosis with pH 7.26, pCO₂ 41 mmHg, and pO₂ 320 mmHg. Serum chemistry evaluation included a bicarbonate of 21 mEq/L with an anion gap of 16. Urine pH was 8.0. Serum salicylate, acetaminophen, and ethanol levels were undetectable. The remainder of her laboratory evaluation was unremarkable. Computed tomography of the brain without contrast did not reveal acute pathology. As this was felt to be related to a toxic ingestion, the patient was transferred to a regional toxicology treatment center.

Examination revealed no evidence of distress on the ventilator without sedation or paralysis. Her vital signs were temperature 36.8°C, pulse 68 beats per minute, respirations 14–16 breaths per minute with the ventilator set to 14–16 breaths per minute, and blood pressure 110/58 mmHg. Intact brainstem reflexes and brisk extremity reflexes without clonus were evident on neurologic examination. Her pupils were 3mm and normally reactive bilaterally. The patient responded with localization to painful stimuli in bilateral upper and lower extremities. With the exception of chronic bilateral upper and lower extremity skin excoriations, the remainder of her physical examination was unremarkable.

Arterial blood gas results were pH 7.31, pCO₂ 36 mmHg, pO₂ 374 mmHg. Basic metabolic panel included the following: sodium 141 mEq/L, potassium 3.4 mEq/L, chloride 111 mEq/L, bicarbonate 16 mEq/L, BUN 10 mg/dl, creatinine 1.0 mg/dl, and an anion gap of 14. Her arterial lactate was 1.0 mmol/L. Liver function tests, complete blood count, and coagulation studies were all within normal limits. Urinalysis revealed a urine pH of 9.0 and was otherwise unremarkable. Urine comprehensive drug screen performed using gas chromatography and mass spectrometry (GC/MS)¹² showed large spikes corresponding to topiramate (retention time 19.9 minutes) and ibuprofen. A smaller peak (retention time 20.9 minutes) was identified by its fragmentation spectrum in the GC/MS library as 10-hydroxytopiramate. Medications the patient was known to take or have access to were detectable by GC/MS. Serum topiramate level was measured to be 356.6 mcg/ml (reference range 5–20 mcg/ml) using a specific immunoassay for topiramate (Polymedco Clinical Diagnostics, Cortland Manor, NY). Topiramate levels are available and routinely performed at our institution. The serum sample required dilution with drug-free serum in order to bring the concentration within the linear range for the immunoassay. The linear range of the topiramate assay in our lab extends to 75 mcg/mL. We assayed the sample using 5-, 10-, and 20-fold dilutions. These gave values of 366 mcg/mL (using 5-fold dilution), 354 mcg/mL (using 10-fold dilution) and 350 mcg/mL (using 20-fold dilution). The mean of these three values was 356.6 mcg/mL. The coefficient of variation for these values is 2.3% showing little variation introduced by the dilutions. A serum ibuprofen level measured by high-performance liquid chromatography¹³ from blood drawn concurrently with the topiramate level was 12.0 mcg/ml(5–50).

The patient slowly woke over the following 12 hours. She was extubated on hospital day two without evidence of acute pulmonary disease. Prior to extubation, 18 hours following admission, repeat arterial blood gas was pH 7.30, pCO₂ 30 mmHg, and pO₂ 179 mmHg. Serum chemistries at that time revealed a measured bicarbonate of 14 mEq/L with an anion gap of 10. Her speech continued to be slurred for the next 24 hours with ataxia, nystagmus, and mild persistent somnolence. This gradually improved by the third day of the hospitalization when she was ambulatory, conversant, and tolerating a normal diet. Her nonanion gap metabolic acidosis persisted. Serum chemistry evaluation on day three showed no significant change in nonanion gap metabolic acidosis with a measured bicarbonate of 13mEq/L and anion gap of 11.

Serial serum topiramate levels were obtained in order to determine elimination toxicokinetics. The initial level of 356.6 mcg/ml is far greater than previously reported levels, more than double a postmortem level associated with death.¹¹ We measured four levels. The first, at 1615 on hospital day one, was 356.6 mcg/ml. The next level performed at 0955 the following day was 173.6 mcg/ml. The next two levels were 61.2 mcg/ml and 44.0 mcg/ml on the third day of hospitalization at 0841 and 1555, respectively (See Figure 1). These levels, plotted on a semi-log graph versus time, demonstrate first order kinetics with a calculated serum half-life of 16 hours. The patient was unable to remember the time or dose of ingestion. She had been on topiramate for the previous year and was currently prescribed 100 mg by mouth twice a day. She had no previous drug levels available for review. The patient did report that she was not fully compliant with the dosing.

Figure 1.

Serum Topiramate Levels vs. Time. The time at which the topiramate level was drawn is time = zero hours as the exact time of ingestion was unkown. The linear distribution of topiramate levels on a semi-log plot indicate first-order elimination kinetics.

The patient was transferred to an inpatient psychiatric facility on the third day of admission due to the suicidal intent of her ingestion. At the time of transfer, her symptoms had significantly improved despite persistent acidosis and elevated topiramate levels.

Discussion

Topiramate is a commonly used anticonvulsant and mood stabilizer. Though its use at therapeutic levels has a benign safety profile, we have relatively little experience with this drug in the setting of intentional overdose. This case documents the clinical course and elimination kinetics in a patient following a massive ingestion of topiramate.

It is unclear whether this patient’s movements represented true seizure activity versus myoclonic jerks prior to our evaluation. She had no evidence of seizure activity during our observation. Previous reports of seizure-like activity following topiramate ingestion have included two patients providing a history of very large topiramate doses (>400 mg/kg) and one case of a patient naïve to the drug.^6,7 However, qualitative urine GC/MS evaluation and serum levels confirming topiramate exposure were not performed. Animal studies have proposed an early proconvulsant mechanism of topiramate followed by delayed anticonvulsant activity which may explain reported seizure activity.¹⁴

This patient also demonstrated coma. She tolerated endotracheal intubation and mechanical ventilation for approximately 18 hours following initial presentation without additional sedation after the 3.5 mg of intravenous lorazepam given at the outlying emergency department. Coma of this depth and duration has not been reported. Altered level of consciousness without coma as well as unusual behavior have most commonly been described.^5,8,10 One case series of six patients described stuporous encephalopathy in patients taking therapeutic doses of topiramate in combination with valproic acid or other anticonvulsants, but not with topiramate alone.¹⁵ Despite her comatose state, the patient did not exhibit significant respiratory depression or vital sign abnormalities. With supportive intensive care, the patient recovered quickly.

The patient also displayed nonanion gap metabolic acidosis with alkaline urine consistent with topiramate’s known carbonic anhydrase activity. Multiple case reports and case series have demonstrated nonanion gap metabolic acidosis without clinical significance.^6,7,8,9 Despite her significantly depressed serum bicarbonate concentrations, the patient never developed severe acidemia. Following transfer from the emergency department, her arterial blood pH was never below 7.3 and she did not require intravenous bicarbonate infusion.

Finally, toxicokinetic evaluation of topiramate’s elimination following the largest documented ingestion does not reveal significant alteration in the half-life. In this patient, the elimination half-life of 16 hours is slightly shorter than what has been previously reported following therapeutic dosing (18–25 hours), but not significantly so.^2,16 Further evaluation of absorption and distribution could not be performed as the original dose remained unknown.

Conclusion

We present this case of suicidal topiramate overdose in order to add to the limited existing data, particularly in patients with large, intentional ingestions. Due to its increasing use as a mood stabilizer in psychiatric patients, it is likely that we will continue to be confronted with these ingestions. Close observation and supportive care would be our recommendations based on this patient and review of the literature regarding this drug.