Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Mar 10;21(6):1535759721999670.
doi: 10.1177/1535759721999670. Online ahead of print.

Treatment of Super-Refractory Status Epilepticus: A Review

Affiliations

Treatment of Super-Refractory Status Epilepticus: A Review

Juan G Ochoa et al. Epilepsy Curr. .

Abstract

Purpose: Super-refractory status epilepticus (SRSE) presents management challenges due to the absence of randomized controlled trials and a plethora of potential medical therapies. The literature on treatment options for SRSE reports variable success and quality of evidence. This review is a sequel to the 2020 American Epilepsy Society (AES) comprehensive review of the treatment of convulsive refractory status epilepticus (RSE).

Methods: We sought to determine the effectiveness of treatment options for SRSE. We performed a structured literature search (MEDLINE, Embase, CENTRAL, CINAHL) for studies on reported treatments of SRSE. We excluded antiseizure medications (ASMs) covered in the 2016 AES guideline on the treatment of established SE and the convulsive RSE comprehensive review of the 2020 AES. Literature was reviewed on the effectiveness of vagus nerve stimulation, ketogenic diet (KD), lidocaine, inhalation anesthetics, brain surgery, therapeutic hypothermia, perampanel, pregabalin (PGB), and topiramate in the treatment of SRSE. Two authors reviewed each therapeutic intervention. We graded the level of the evidence according to the 2017 classification scheme of the American Academy of Neurology.

Results: For SRSE (level U; 39 class IV studies total), insufficient evidence exists to support that perampanel, PGB, lidocaine, or acute vagus nerve stimulation (VNS) is effective. For children and adults with SRSE, insufficient evidence exists to support that the KD is effective (level U; 5 class IV studies). For adults with SRSE, insufficient evidence exists that brain surgery is effective (level U, 7 class IV studies). For adults with SRSE insufficient, evidence exists that therapeutic hypothermia is effective (level C, 1 class II and 4 class IV studies). For neonates with hypoxic-ischemic encephalopathy, insufficient evidence exists that therapeutic hypothermia reduces seizure burden (level U; 1 class IV study). For adults with SRSE, insufficient evidence exists that inhalation anesthetics are effective (level U, 1 class IV study) and that there is a potential risk of neurotoxicity.

Conclusion: For patients with SRSE insufficient, evidence exists that any of the ASMs reviewed, inhalational anesthetics, ketogenic diet, acute VNS, brain surgery, and therapeutic hypothermia are effective treatments. Data supporting the use of these treatments for SRSE are scarce and limited mainly to small case series and case reports and are confounded by differences in patients' population, and comedications, among other factors.

Keywords: SRSE; adults; children; super-refractory status epilepticus; treatment effectiveness.

PubMed Disclaimer

Conflict of interest statement

Declaration of Conflicting Interests: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: J. Ochoa: Consultant for Compumedics. M. Dougherty: Employment at Neurotech, LLC; Owner, cEEG Monitoring Company. A. Papanastassious: Co-owner, unpaid, for Cerenovum; partial ownership, unpaid, for Druksys; patent for device to treat chronic subdural hematomas, in process, currently held by institution employer. B. Gidal: Consultant for Aquestive, Eisai Inc., Greenwich, and SK Life Science; End Point Review Committee for Sunovion Pharmaceuticals Inc; and grant/contract with UCB Inc. I. Mohamed: PI with expected research support from Marinus Pharmaceuticals; travel compensation as sub-PI for research study meeting for UCB GmBH. D. Vossler: PI with research support to institution for Accorda, Biogen, Eisai, Pfizer, SK Life Science, UCB, and Vertex; consultant or speaker’s bureau for Greenwich Biosciences, Neurelis, Otsuka, SK Life Sciences, Sunovion, and UCB Biosciences.

References

    1. Trinka E, Cock H, Hesdorffer D, et al. A definition and classification of status epilepticus – report of the ILAE task force on classification of status epilepticus. Epilepsia. 2015;56(10):1515–1523. doi:10.1111/epi.13121 - PubMed
    1. Shorvon S, Ferlisi M. The treatment of super-refractory status epilepticus: a critical review of available therapies and a clinical treatment protocol. Brain. 2011;134(10):2802–2818. doi:10.1093/brain/awr215 - PubMed
    1. Brophy GM, Bell R, Claassen J, et al. Guidelines for the evaluation and management of status epilepticus. Neurocrit Care. 2012;17(1):3–23. doi:10.1007/s12028-012-9695-z - PubMed
    1. Bayrlee A, Ganeshalingam N, Kurczewski L, Brophy GM. Treatment of super-refractory status epilepticus. Curr Neurol Neurosci Rep. 2015;15(10). doi:10.1007/s11910-015-0589-2 - PubMed
    1. Dubey D, Kalita J, Misra UK. Status epilepticus: refractory and super-refractory. Neurology India. 2017;65(7):12. doi:10.4103/neuroindia.NI_958_16 - PubMed

LinkOut - more resources