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Clinical Trials |

Substitution Monotherapy With Levetiracetam vs Older Antiepileptic Drugs:  A Randomized Comparative Trial

Tahir Hakami, MBBS; Marian Todaro, PhD; Slave Petrovski, MSc; Lachlan MacGregor, MBBS; Dennis Velakoulis, MBBS; Meng Tan, MBBS; Zelko Matkovic, MBBS; Alexandra Gorelik, MSc; Danny Liew, PhD; Raju Yerra, MBBS; Terence J. O’Brien, MD, PhD
Arch Neurol. 2012;69(12):1563-1571. doi:10.1001/archneurol.2012.2203.
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Objective  To determine whether patients who fail their first antiepileptic drug (AED) have better neuropsychiatric and quality-of-life (QOL) outcomes if substituted to levetiracetam monotherapy compared with a second older AED.

Design  Randomized comparative trial. Participants with partial epilepsy who had failed monotherapy with phenytoin sodium, carbamazepine, or valproate sodium were randomized to substitution monotherapy with levetiracetam or a different older AED. Assessments were performed at baseline, 3 months, and 12 months using questionnaires measuring neuropsychiatric, QOL, seizure control, AED adverse effects, and neurocognitive outcomes.

Setting  Epilepsy service of a teaching hospital.

Patients  Fifty-one patients were randomized to levetiracetam and 48 were randomized to a second older AED (25 to valproate and 23 to carbamazepine).

Main Outcome Measures  Proportions showing improvements in depression (on the Hospital Anxiety and Depression Scale) and QOL scores (on the 89-item Quality of Life in Epilepsy Inventory) at 3 months.

Results  There were no differences between the groups in depression scores at 3 months (improvement in 17 of 43 patients [39.5%] in the levetiracetam group and 15 of 44 patients [34.1%] in the older AED group; P = .60), but a greater proportion of the older AED group improved on the 89-item Quality of Life in Epilepsy Inventory compared with the levetiracetam group (27 of 38 patients [71.1%] vs 21 of 43 patients [48.8%], respectively; P = .04). The QOL, anxiety, and AED adverse effects scores were improved in both groups at 3 and 12 months after randomization.

Conclusions  Substitution monotherapy in a patient experiencing ongoing seizures or tolerability issues is associated with sustained improvements in measures of QOL, psychiatric, and adverse events outcomes. Patients switched to levetiracetam do not have better outcomes than those switched to a second older AED.

Trial Registration  anzctr.org.au Identifier: ACTRN12606000102572

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Figure 1. Allocation of participants to the treatment groups receiving substitution monotherapy with the newer antiepilepsy drug (AED) levetiracetam or with older AEDs (carbamazepine or valproate sodium) (A) and outline of the visit schedule and assessments performed (B).

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Figure 2. Flow diagram of patient enrollment, treatment allocation, and follow-up for the KONQUEST (Keppra vs Older AEDs evaluating Neuropsychiatric, Neurocognitive and QUality of life outcomes in treatment of Epilepsy as Substitution monoTherapy) study. SUDEP indicates sudden unexplained death in epilepsy.

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Figure 3. Hospital Anxiety and Depression Scale (HADS) depression scores (A) and HADS anxiety scores (B) for levetiracetam and older antiepileptic drugs (AEDs) (carbamazepine or valproate sodium) at baseline, 3 months, and 12 months.

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Figure 4. Mean 89-item Quality of Life in Epilepsy Inventory overall scores at baseline, 3 months, and 12 months for treatment groups (levetiracetam and older antiepileptic drugs [AEDs]) (error bars indicate SEM) (A), and mean 89-item Quality of Life in Epilepsy Inventory score changes over the first 3 months (B) and 12 months (C) for treatment groups.

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Figure 5. Mean global Liverpool Adverse Events Profile scores at baseline, 3 months, and 12 months for treatment groups (levetiracetam and older antiepileptic drugs [AEDs]) (error bars indicate SEM) (A), and comparison of changes over the first 3 months (B) and 12 months (C) in the proportion of patient reports for each Liverpool Adverse Events Profile symptom according to treatment groups.

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Figure 6. Mean IntegNeuro score changes over 3 months for treatment groups (levetiracetam and older antiepileptic drugs [AEDs]). The overall score did not differ between baseline and 3 months for either group (P = .52 and P = .72, respectively), nor did it differ between the groups (P = .71).

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Figure 7. Proportion of patients who remained on the drug to which they were randomized at 12 months (A), proportion of patients who remained seizure free after 12 months (B), and proportion of patients who failed treatment with the drug to which they were randomized (C). AEDs indicates antiepilepsy drugs.

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