Minnesota Epilepsy Group, Saint Paul, MN, USA.
University of California, San Francisco, CA, USA.
CNS Drugs. 2024 Feb;38(2):125-140. doi: 10.1007/s40263-023-01060-1. Epub 2024 Feb 15.
Patients with epilepsy may experience seizure clusters, which are described by the US Food and Drug Administration (FDA) as intermittent, stereotypic episodes of frequent seizure activity that are distinct from a patient's usual seizure pattern. Untreated seizure clusters may increase the risk for status epilepticus, as well as decrease quality of life and increase burden on patients and care partners. Benzodiazepine therapies are the mainstay for acute treatment of seizure clusters and are often administered by nonmedical care partners outside a healthcare facility. Three rescue therapies are currently FDA-approved for this indication, with diazepam rectal gel being the first in 1997, for patients aged ≥ 2 years. Limitations of rectal administration (e.g., positioning and disrobing the patient, which may affect ease of use and social acceptability; interpatient variation in bioavailability) led to the investigation of the potential for nasal administration as an alternative. Midazolam nasal spray (MDS) was approved by the FDA in 2019 for patients aged ≥ 12 years and diazepam nasal spray (DNS) in 2020 for patients aged ≥ 6 years; these two intranasal therapies have differences in their formulations [e.g., organic solvents (MDS) vs. Intravail and vitamin E for absorption and solubility (DNS)], effectiveness (e.g., proportion of seizure clusters requiring only one dose), and safety profiles. In clinical studies, the proportion of seizure clusters for which only one dose of medication was used varied between the three approved rescue therapies with the highest single-dose rate for any time period for DNS; however, although studies for all three preparations enrolled patients with highly intractable epilepsy, inclusion and exclusion criteria varied, so the three cannot be directly compared. Treatments that have been used off-label for seizure clusters in the USA include midazolam for injection as an intranasal spray (indicated for sedation/anxiolysis/amnesia and anesthesia) and tablet forms of clonazepam (indicated for treatment for seizure disorders) and lorazepam (indicated for anxiety). In the European Union, buccal and intranasal midazolam are used for treating the indication of prolonged, acute convulsive seizures and rectal diazepam solution for the indication of epileptic and febrile convulsions; duration of effectiveness for these medications for the treatment of seizure clusters has not been established. This paper examines the literature context for understanding seizure clusters and their treatment and provides effectiveness, safety, and administration details for the three FDA-approved rescue therapies. Additionally, other medications that are used for rescue therapy in the USA and globally are discussed. Finally, the potential benefits of seizure action plans and candidates for their use are addressed. This paper is intended to provide details about the unique characteristics of rescue therapies for seizure clusters to help clarify appropriate treatment for individual patients.
癫痫患者可能会经历癫痫发作群,美国食品和药物管理局(FDA)将其描述为频繁发作的间歇性、刻板发作,与患者通常的发作模式不同。未经治疗的癫痫发作群可能会增加癫痫持续状态的风险,降低生活质量,并增加患者和护理伙伴的负担。苯二氮䓬类治疗是治疗癫痫发作群的主要方法,通常由非医疗护理伙伴在医疗机构外使用。目前有三种救援疗法被 FDA 批准用于该适应症,其中,地西泮直肠凝胶于 1997 年首次获批,适用于≥2 岁的患者。直肠给药的局限性(例如,患者的体位和脱衣,这可能会影响使用的便利性和社会可接受性;患者之间生物利用度的差异)导致人们研究将鼻腔给药作为替代方法的可能性。咪达唑仑鼻喷雾剂(MDS)于 2019 年被 FDA 批准用于≥12 岁的患者,而地西泮鼻喷雾剂(DNS)于 2020 年被批准用于≥6 岁的患者;这两种鼻腔内治疗方法在配方[例如,有机溶剂(MDS)与 Intravail 和维生素 E 用于吸收和溶解(DNS)]、疗效(例如,仅需一剂药物即可控制的癫痫发作群比例)和安全性方面存在差异。在临床研究中,三种批准的救援疗法中,只有一种剂量的药物即可控制癫痫发作群的比例各不相同,任何时间段的最高单剂量率均为 DNS;然而,尽管所有三种制剂的研究都纳入了高度难治性癫痫患者,但纳入和排除标准存在差异,因此不能直接进行比较。在美国,用于癫痫发作群的标签外治疗药物包括咪达唑仑注射剂作为鼻内喷雾(用于镇静/焦虑/健忘和麻醉)和氯硝西泮片剂(用于治疗癫痫发作障碍)和劳拉西泮(用于焦虑)。在欧盟,口腔和鼻腔内咪达唑仑用于治疗延长性、急性惊厥性癫痫发作,直肠地西泮溶液用于治疗癫痫和热性惊厥;这些药物治疗癫痫发作群的有效性持续时间尚未确定。本文研究了理解癫痫发作群及其治疗的文献背景,并提供了三种 FDA 批准的救援疗法的有效性、安全性和给药细节。此外,还讨论了在美国和全球用于救援治疗的其他药物。最后,还讨论了癫痫行动计划的潜在好处及其使用的候选者。本文旨在提供有关癫痫发作群救援疗法的独特特征的详细信息,以帮助澄清对个体患者的适当治疗。