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Three Patients Needing High Doses of Valproic Acid to Get Therapeutic Concentrations
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Valproic acid (VPA) can autoinduce its own metabolism. Cases requiring VPA doses >4000 mg/day to obtain therapeutic plasma concentrations, such as these 3 cases, have never been published. Case 1 received VPA for seizures and schizophrenia and had >50 VPA concentrations in 4 years. A high dose of 5,250 mg/day of VPA concentrate was prescribed for years but this dose led to an intoxication when switched to the enterocoated divalproex sodium formulation, requiring a normal dose of 2000 mg/day. VPA metabolic capacity was significantly higher (t=-9.6; df = 6.3,p<0.001) during the VPA concentrate therapy, possibly due to autoinduction in that formulation. Case 2 had VPA for schizoaffective psychosis with 10 VPA concentrations during an 8-week admission. To maintain a VPA level≥50 μg/mL, VPA doses increased from 1500 to 4000 mg/day. Case 3 had tuberous sclerosis and epilepsy and was followed up for >4 years with 137 VPA concentrations. To maintain VPA concentrations≥50 μg/mL, VPA doses increased from 3,375 to 10,500 mg/day. In Cases 2 and 3, the duration of admission and the VPA dose were strongly correlated (raround 0.90;p<0.001) with almost no change after controlling for VPA concentrations, indicating progressive autoinduction that increased with time.
Title: Three Patients Needing High Doses of Valproic Acid to Get Therapeutic Concentrations
Description:
Valproic acid (VPA) can autoinduce its own metabolism.
Cases requiring VPA doses >4000 mg/day to obtain therapeutic plasma concentrations, such as these 3 cases, have never been published.
Case 1 received VPA for seizures and schizophrenia and had >50 VPA concentrations in 4 years.
A high dose of 5,250 mg/day of VPA concentrate was prescribed for years but this dose led to an intoxication when switched to the enterocoated divalproex sodium formulation, requiring a normal dose of 2000 mg/day.
VPA metabolic capacity was significantly higher (t=-9.
6; df = 6.
3,p<0.
001) during the VPA concentrate therapy, possibly due to autoinduction in that formulation.
Case 2 had VPA for schizoaffective psychosis with 10 VPA concentrations during an 8-week admission.
To maintain a VPA level≥50 μg/mL, VPA doses increased from 1500 to 4000 mg/day.
Case 3 had tuberous sclerosis and epilepsy and was followed up for >4 years with 137 VPA concentrations.
To maintain VPA concentrations≥50 μg/mL, VPA doses increased from 3,375 to 10,500 mg/day.
In Cases 2 and 3, the duration of admission and the VPA dose were strongly correlated (raround 0.
90;p<0.
001) with almost no change after controlling for VPA concentrations, indicating progressive autoinduction that increased with time.
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