Levetiracetam as second-line treatment of status epilepticus – which dose should be applied?

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Levetiracetam as second-line treatment of status epilepticus – which dose should be applied?

Johannes Rösche * / Bernd Schade

Keywords : levetiracetam, weight-based dosage, second-line treatment, efficacy rate

Citation Information : Journal of Epileptology. Volume 29, Pages 7-12, DOI: https://doi.org/10.21307/jepil-2021-001

License : (CC-BY-NC-ND 4.0)

Received Date : 21-May-2021 / Accepted: 15-July-2021 / Published Online: 27-July-2021

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ABSTRACT

Introduction.

Since 2004 many treatment episodes in different stages of status epilepticus (SE) have been reported. Nowadays the use of levetiracetam (LEV) is recommended as a second-line treatment of SE, when the use of a benzodiazepine was not successful.

Aim.

The evidence based on randomized controlled trials for the application of a particular weight-based dose of LEV as a second-line treatment in benzodiazepine refractory SE is investigated.

Methods.

Pubmedsearches were undertaken using the terms “Levetiracetam-status-epilepticus-trials” and “Levetiracetam-status-randomized” on May 8th 2021. We identified 17 studies reporting treatment with LEV as second line treatment and reporting dosages in mg/kg body weight. We grouped the studies according to the reported dosages (i.e. 20–25 mg/kg; 30 mg/kg; 40 mg/kg, 60 mg/kg). For each group we calculated the mean efficacy rate and the standard deviation of the efficacy rate weighted for the number of cases in the different studies. Twelve studies compared LEV with 20 mg/kg phenytoin (PHT). In these studies, we analysed the relative efficacy rate in comparison to PHT with the same procedure.

Results.

Seven studies used LEV 20–25 mg/kg, two studies 30 mg/kg, six studies 40 mg/kg and one study 60 mg/kg. Efficacy rate was highest in the group given 30 mg/kg (95% CI 87.5–90.1%). The relative efficacy rate with this weight-based dose was 1.12. This is just above the upper range of the 95% CI of the relative efficacy rate in studies using 40 mg/kg LEV (i.e. 1.11). The relative efficacy rates in the two other groups were considerably lower.

Conclusion.

According to the randomized controlled trials published so far a weight-based dose of 30–40 mg/kg LEV may be appropriate for the treatment of benzodiazepine-refractory SE.

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INTRODUCTION

Since 2004 (Arrigo et al., 2004) many reports on the treatment of status epilepticus (SE) with levetiracetam (LEV) have been published. Based on a Pub-Med search on December 12th, 2011, 37 case series with 727 treatment episodes were analysed in 2013 (Rösche et al., 2013) and the efficacy rate of LEV in terminating SE was estimated to be in a range between 53.7 and 58.1%. Dosages ranged from 500 mg to 9000 mg/day and were rarely reported in mg/kg. LEV had been used in all stages of SE. In an up-date in 2019 (Rösche et al., 2019) based on a new Pub-Med search on July 6th, 2018, additionally 13 case series or prospective studies with 412 treatment episodes were analysed and the efficacy rate of LEV was assessed as 55.0–59.4%. Eleven of the papers reported dosages in mg/kg and it was suspected that a loading dose of 30 mg/kg would be reasonable.

Nowadays the use of LEV is recommended as second-line treatment of SE, when the use of a benzodiazepine was not successful (Rosenow et al., 2020). Based on the interim analysis of the study by Chamberlain et al. (2020) presented by Kapur et al. (2019) a weight-based dose of 60 mg/kg was recommended.

AIM

The evidence based on randomized controlled trials for the application of a particular weight-based dose of LEV as a second-line treatment in benzodiazepine refractory SE is investigated.

METHOD

Pub-Med Searches with the terms “Levetiracetam-status-epilepticus-trials” and “Levetiracetam-status-randomized” on May 8th, 2021, revealed 137 plus 118 results. After excluding studies not reporting treatment with LEV as second line treatment and those not reporting dosages in mg/kg body weight, 17 studies remained. We grouped the studies according to the reported dosages (i.e. 20–25 mg/kg; 30 mg/kg; 40 mg/kg, 60 mg/kg). For each group we calculated the mean efficacy rate and the standard deviation of the efficacy rate weighted for the number of cases in the different studies. By this we calculated the 95% CI for the mean efficacy rates across the studies in each dosage group. Twelve studies compared LEV with 20 mg/kg phenytoin (PHT). In these studies, we analysed the relative efficacy rate in comparison to PHT. This was done by dividing the efficacy rate of LEV by the efficacy rate of PHT in each study. Then we calculated for each group the mean relative efficacy rate and the standard deviation of the relative efficacy rate weighted for the number of cases in the different studies. By this we calculated the 95% CI for the mean relative efficacy rates across the studies in each dosage group.

RESULTS

Nine studies were conducted in paediatric patients only. The mean age of patients in these studies ranged from 2.5 years (Nalisetty et al., 2020) to 4.9 years (Nazir et al., 2020). Just eight studies included adults or elderly people. In two of them, the mean age of patients was between 61.5 and 68.5 years (Wongjirattikarn et al., 2019; Nene et al., 2019). In 5 other studies the mean age ranged from 34.8 years (Mundlamuri et al., 2015) to 39.2 years (Misra et al., 2012). In the study by Chamberlain et al. (2020) the mean age of children was 6.1 years of adults 42.6 years and of older adults 73.8 years. Kapur et al. (2019) reported an interim analysis of Chamberlain et al. (2020). Therefore, this study was excluded from the statistical analysis. Six studies reported the treatment of generalized convulsive SE exclusively. Only two studies (Dalziel et al., 2019, Chamberlain et al., 2020) were not in the 20–25 mg/group.

No study included patients with absence status epilepticus. Seven studies applied LEV 20–25 mg/kg (table 1), two studies 30 mg/kg (table 2), six studies 40 mg/kg (table 3) and one study 60 mg/kg (table 4). From the study of Misra et al. (2012) only the subgroup of patients, who were treated because of ongoing seizure activity 10 minutes after the administration of LZP, was included. As can be seen in figure 1 efficacy rate was highest in the group given 30 mg/kg (95% CI 87.5– 90.1%). Only one study compared 22 patients given LEV 30 mg/kg with 30 patients given PHT 20 kg/kg. The relative efficacy rate was 1.12 (figure 2). This is just above the upper range of the 95% CI of the relative efficacy rate in the six studies comparing the use of 40 mg/kg LEV with 20 mg/kg PHT (i.e. 1.11). The relative efficacy rates in the two other groups were considerably lower.

Table 1.

Studies with administration of 20–25 mg/kg Levetiracetam

10.21307_jepil-2021-001-tbl1.jpg
Table 2.

Studies with administration of 30 mg/kg Levetiracetam

10.21307_jepil-2021-001-tbl2.jpg
Table 3.

Studies with administration of 40 mg/kg Levetiracetam

10.21307_jepil-2021-001-tbl3.jpg
Table 4.

Studies with administration of 60 mg/kg Levetiracetam

10.21307_jepil-2021-001-tbl4.jpg
Figure 1.

Efficacy rates of different Levetiracetam loading doses.

10.21307_jepil-2021-001-f001.jpg
Figure 2.

Relative efficacy rates in comparison to 20 mg/kg Phenytoin of different Levetiracetam loading doses.

10.21307_jepil-2021-001-f002.jpg

DISCUSSION

Although it seems reasonable to compare efficacy rates of randomized controlled trials in a defined clinical setting, several limitations of our study must be highlighted.

First of all, the study populations are not comparable. Chamberlain et al. (2020) reported a higher efficacy rate in children than in adults and elderly people. All studies applying 40 mg/kg were performed in a paediatric setting. Therefore, the high efficacy rates in this group may lead to an overestimation of the efficacy rates in adults and elderly. However, the relative efficacy rate in the subgroup of children given 60 mg/kg was 1.06, this was still lower than the lower limit of the 95% CI in the 40 mg/kg group (i.e. 1.09). One reason for the higher efficacy rates in paediatric patients may be the inclusion of episodes with febrile SE. On the other hand, apart from the older adults in the study by Chamberlain et al. (2020) the eldest patients were in the 20–25 mg/kg group (Wongjirattikarn et al., 2019; Nene et al., 2019). But out of the three other studies of adult patients in this group (Misra et al., 2012; Mundlamuri et al., 2015; Chakravarthi et al., 2015) only Mundlamuri et al. (2015) reported a higher efficacy rate. Therefor the low efficacy rate in the 20–25 mg/kg group cannot be explained by the inclusion of elderly patients.

It has to be emphasised that the efficacy rates were lower in studies of treatment of generalized convulsive SE only. A subgroup analysis of the four studies of generalized SE only in the 20–25 mg/kg group (Mundlamuri et al., 2015; Chakravarthi et al., 2015; Nene et al., 2019; Nazir et al., 2020) reveals a mean efficacy rate of 74.43% (SD 5.99%). The only study focussing on generalized convulsive SE in the 40 mg/kg group (Dalziel et al., 2019) had an efficacy rate of 50%. This is not much above the efficacy rate in the group of children reported by Chamberlain et al. (2020). But it is questionable whether the difference in types of SE is crucial for the different results because in a retrospective study comparing four intravenously applied antiseizure medications (ASMs) according to four different efficacy criteria, no criterion revealed a significant difference of efficacy rate of a specific ASMs in different types of SE (Redecker et al., 2017). The low efficacy rate in the study by Dalziel et al. (2019) may be a result of the efficacy criterion as well (see below).

Another problem may be that the published doses were not applied to all patients because the weight-based dosing was capped at a certain body weight. In the ESETT trial (Chamberlain et al., 2020) this was the case at a body weight of 75 kg. Since in this trial 48.2% of adults and 0.9% of children only had a higher body weight the really applied weight-based dose was obviously lower in adults than in children (Sathe et al., 2020). But at least in the adults the efficacy rate of LEV was not significantly lower in patients with a body weight higher than 75 kg than in the others. From this it may be suspected that lower weight-based doses than 60 mg/kg may be at least equally effective. Another problem may be consequent to the different outcome criteria. From preclinical data it is reasonable to assume that after intravenously application of LEV 1500 mg peak concentrations in the brain occur as late as after one hour (Nicolas et al., 2016). This may be an explanation for the results of Navarro et al. (2016), who found no superiority of 2500 mg LEV given immediately after 1 mg clonazepam over placebo when evaluated 9 minutes after the end of the infusion. As can be seen in table 3 one of the studies applying 40 mg/kg LEV evaluated the treatment effect five minutes after completion of the infusion (Dalziel et al., 2019) and had by far the lowest efficacy rate in this group (i.e. 50%). But even this was slightly higher than the efficacy rate in adults or elderly one hour after start of infusion of 60 mg/kg (Chamberlain et al., 2020). Therefore, the different outcome criteria may not explain the differences of efficacy rates between the groups of studies with different weight-based doses.

CONCLUSION

According to the randomized controlled trials published so far, a weight-based dose of 30–40 mg/kg LEV may be appropriate for the treatment of benzodiazepine-refractory SE. It may be more efficacious than PHT in these doses. This is in line with a review published in 2014 (Yasiry and Shorvon, 2014).

CONFLICTS OF INTEREST

J. Rösche reports speaker honoraria from Eisai unrelated to this work. B. Schade reports speaker honoraria from Novartis unrelated to this work and support for consulting hours for patients with multiple sclerosis from Bayer and Novartis unrelated to this work.

References


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  6. Gujjar A.R., Nandhagopal R., Jacob P.C., Al-Hashim A., Al-Amrani K., Ganguly S.S. et al. Intravenous levetiracetam vs phenytoin for status epilepticus and cluster seizures: A prospective, randomized study. Seizure: European Journal of Epileptology, 2017, 2017, 8–12. doi: 10.1016/j.seizure.2017.05.001
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  11. Mundlamuri R.C., Sinha S., Subbakrishna D.K., Prathyusha P.V., Nagappa M., Bindu P.S. et al. Management of generalised convulsive status epilepticus (SE): A prospective randomized controlled study of combined treatment with intravenous lorazepam with either phenytoin, sodium valproate or levetiracetam – Pilot study. Epilepsy Research, 2015, 2015, 52–58. doi: 10.1016/j.eplepsyres.2015.04.013
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FIGURES & TABLES

Figure 1.

Efficacy rates of different Levetiracetam loading doses.

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Figure 2.

Relative efficacy rates in comparison to 20 mg/kg Phenytoin of different Levetiracetam loading doses.

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REFERENCES

  1. Appleton R.E., Rainford N.E.A., Gamble C., Messahei S., Humphreys A., Hickey H. et al. Levetiracetam as an alternative to phenytoin for second-line emergency treatment of children with convulsive status epilepticus: the EcLiPSE RCT. Health Technology Assessment, 2020, 2020 (58), 1–96. doi: 10.3310/hta24580
    [CROSSREF]
  2. Arrigo A., Raiteri U., Ardizzone G. Levetiracetam monotherapy for treatment of partial status epilepticus in a patient following a liver transplant. Epilepsia, 2004, 2004 (Suppl. 3), 145.
  3. Chakravarthi S., Goyal M.K., Modi M., Bhalla A., Singh P. Levetriacetam versus phenytoin in management of status epilepticus. Journal of Clinical Neuroscience, 2015, 2015, 959–963. doi: 10.1016/j.jocn.2014.12.013.
    [CROSSREF]
  4. Chamberlain J.M., Kapur J., Shinnar S., Elm J., Holsti M., Babcock L. Efficacy of levetiracetam, fosphenytoin, and valproate for established status epilepticus by age group (ESETT): a double-blind, responsive-adaptive, randomized controlled trial. Lancet, 2020, 2020 (10231), 1217–1224. doi: 10.1017/S01406736(20)30611–5.
    [CROSSREF]
  5. Dalziel S.R., Borland M.L., Furyk J., Bonisch M., Neutze J., Donath S. et al. Levetiracetam versus phenytoin for second-line treatment of convulsive status epilepticus in children (Con-SEPT): an open-labe, multicentre, randomized controlled trial. Lancet, 2019, 2019 (10186): 2135–2145. doi 10.1016/S01406736(19)30722–6
    [CROSSREF]
  6. Gujjar A.R., Nandhagopal R., Jacob P.C., Al-Hashim A., Al-Amrani K., Ganguly S.S. et al. Intravenous levetiracetam vs phenytoin for status epilepticus and cluster seizures: A prospective, randomized study. Seizure: European Journal of Epileptology, 2017, 2017, 8–12. doi: 10.1016/j.seizure.2017.05.001
    [CROSSREF]
  7. Handral A., Veerappa B.G., Gowda S.K., Benakappa N., Benakappa A. Levetiracetam versus Fosphenytoin in pediatric convulsive status epilepticus: a randomized controlled trail. Journal of Pediatric Neurosciences, 2020, 2020, 252–256. doi: 10.4103/jpn.JPN_109_19
  8. Kapur J., Elm J., Chamberlain J.M., Barsan W., Cloyd J., Lowenstein D. et al. Randomized trial of three anticonvulsant medications for status epilepticus. New England Journal of Medicine, 2019, 2019, 2103–2113. doi: 10.1056/NEJMoal1905795
    [CROSSREF]
  9. Lyttle M.D., Rainford N.E.A., Gamble C., Messahel S., Humphreys A., Hickey H. et al. Levetiracetam versus phenytoin for second-line treatment of paediatric convulsive status epilepticus (EcLiPSE): a multicentre, open-label, randomised trial. Lancet, 2019, 2019 (10186), 2125–2134. doi: 10.1016/S01406736(19)30724-x
    [CROSSREF]
  10. Misra U.K., Kalita J., Maurya P.K. Levetiracetam versus lorazepam in status epilepticus: a randomized, open labelled pilot study. Journal of Neurology, 2012, 2012, 645–648. doi: 10.1007/s00415-011-6227-2
    [CROSSREF]
  11. Mundlamuri R.C., Sinha S., Subbakrishna D.K., Prathyusha P.V., Nagappa M., Bindu P.S. et al. Management of generalised convulsive status epilepticus (SE): A prospective randomized controlled study of combined treatment with intravenous lorazepam with either phenytoin, sodium valproate or levetiracetam – Pilot study. Epilepsy Research, 2015, 2015, 52–58. doi: 10.1016/j.eplepsyres.2015.04.013
    [CROSSREF]
  12. Nalisetty S., Kandasamy S., Sridharan B., Vijayakumar V., Sangaralingam T., Krishnamoorthi N. Clinical effectiveness of Levetiracetam compared to Fosphenytoin in the treatment of benzodiazepine refractory convulsive status epilepticus. The Indian Journal of Pediatrics, 2020, 2020, 512–519. doi: 10.1007/s12098-020-03221-2
    [CROSSREF]
  13. Navarro V., Dagron C., Elie C., Lamhaut L., Demeret S., Urien S. Prehospital treatment with levetiracetam plus clonazepam or placebo plus clonacepam in status epilepticus (SAMUKeppra): a randomized, double-blind, phase 3 trial. Lancet Neurology, 2016, 2016, 47–55. doi: 10.1016/S1474-442(15)00296-3
    [CROSSREF]
  14. Nazir M., Rayees A.T., Asimi R., Syed W.A. Comparative efficacy of IV phenytoin, IV valproate, and IV levetiracetam in childhood status epilepticus. Journal of Epilepsy Research, 2020, 2020, 69–73. doi: 10.14581/jer.20011
    [CROSSREF]
  15. Nene D., Mundlamuri R.C., Satishchandra P., Prathyusha P.V., Nagappa M., Bindu P.S. et al. Comparing the efficacy of sodium valproate and levetiracetam following initial lorazepam in elderly patients with genralized convulsive status epilepticus (GCSE): A prospective randomized controlled pilot study. Seizure: European Journal of Epileptology, 2019, 2019, 111–117. doi: 10.1016/j.seizure.2019.01.015
    [CROSSREF]
  16. Nicolas J.-M., Hannestad J., Holden D., Kervyn S., Nabulsi N., Tytgat D. et al. Brivaracetam, a selective high-affinity synaptic vesicle protein 2A (SV2A) ligand with preclinical evidence of high brain permeability and fast onset of action. Epilepsia, 2016, 2016, 201–209. doi: 10.1111/epi.13267
    [CROSSREF]
  17. Noureen N., Khan S., Khursheed A., Iqbal I., Maryam M., Sharib S.M. et al. Clinical efficacy and safety of injectable levetiracetam versus phenytoin as second-line therapy in the management of generalized convulsive status epilepticus in children: an open-label randomized controlled trial. Journal of Clinical Neurology, 2019, 2019, 468–472. doi: 10.3988/jcn.2019.15.4.468
    [CROSSREF]
  18. Redecker J., Wittstock M., Rösche J. The efficacy of different kinds of intravenously applied antiepileptic drugs in the treatment of status epilepticus. How can it be determined? Epilepsy & Behavior, 2017, 71, 35–38. doi: 10.1016/j.yebeh.2017.03.18
    [CROSSREF]
  19. Rösche J., Dudek M., Teleki A., Godau J., Bösel J. Levetiracetam in der Behandlung des Status Epilepticus – ein update. Fortschritte der Neurologie – Psychiatrie, 2019, 2019, 357–363. doi: 10.1055/a-0832-8652
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