University of Minnesota College of Pharmacy, Minneapolis, Minnesota, USA.
Montefiore Hospital, Bronx, New York, USA.
Epilepsia. 2021 Apr;62(4):846-856. doi: 10.1111/epi.16847. Epub 2021 Feb 22.
Seizure clusters must be treated quickly and effectively to prevent progression to prolonged seizures and status epilepticus. Rescue therapy for seizure clusters has focused on the use of benzodiazepines. Although intravenous benzodiazepine administration is the primary route in hospitals and emergency departments, seizure clusters typically occur in out-of-hospital settings, where a more portable product that can be easily administered by nonmedical caregivers is needed. Thus, other methods of administration have been examined, including rectal, intranasal, intramuscular, and buccal routes. Following US Food and Drug Administration (FDA) approval in 1997, rectal diazepam became the mainstay of out-of-hospital treatment for seizure clusters in the United States. However, social acceptability and consistent bioavailability present limitations. Intranasal formulations have potential advantages for rescue therapies, including ease of administration and faster onset of action. A midazolam nasal spray was approved by the FDA in 2019 for patients aged 12 years or older. In early 2020, the FDA approved a diazepam nasal spray for patients aged 6 years or older, which has a different formulation than the midazolam nasal product and enhances aspects of bioavailability. Benzodiazepines, including diazepam, present significant challenges in developing a suitable intranasal formulation. Diazepam nasal spray contains dodecyl maltoside (DDM) as an absorption enhancer and vitamin E to increase solubility in an easy-to-use portable device. In a Phase 1 study, absolute bioavailability of the diazepam nasal spray was 97% compared with intravenous diazepam. Subsequently, the nasal spray demonstrated less variability in bioavailability than rectal gel (percentage of geometric coefficient of variation of area under the curve = 42%-66% for diazepam nasal spray compared with 87%-172% for rectal gel). The diazepam nasal spray safety profile is consistent with that expected for rectal diazepam, with low rates of nasal discomfort (≤6%). To further improve the efficacy of rescue therapy, investigation of novel intranasal benzodiazepine formulations is underway.
癫痫发作群必须迅速有效地治疗,以防止进展为长时间发作和癫痫持续状态。癫痫发作群的抢救治疗集中在使用苯二氮䓬类药物上。虽然静脉内苯二氮䓬给药是医院和急诊科的主要途径,但癫痫发作群通常发生在院外环境中,需要一种更便携的产品,以便非医疗照护者易于给药。因此,已经研究了其他给药途径,包括直肠、鼻内、肌肉内和颊部途径。在美国食品和药物管理局(FDA)于 1997 年批准后,直肠地西泮成为美国院外治疗癫痫发作群的主要药物。然而,社会可接受性和一致的生物利用度存在局限性。鼻内制剂对于抢救疗法具有潜在优势,包括给药方便和起效更快。咪达唑仑鼻喷雾剂于 2019 年获得 FDA 批准,适用于 12 岁及以上的患者。2020 年初,FDA 批准了一种用于 6 岁及以上患者的地西泮鼻喷雾剂,其配方与咪达唑仑鼻用产品不同,增强了生物利用度的某些方面。苯二氮䓬类药物,包括地西泮,在开发合适的鼻内制剂方面存在重大挑战。地西泮鼻喷雾剂含有十二烷基麦芽糖苷(DDM)作为吸收增强剂和维生素 E,以增加在易于使用的便携式设备中的溶解度。在一项 1 期研究中,与静脉内地西泮相比,地西泮鼻喷雾剂的绝对生物利用度为 97%。随后,与直肠凝胶(地西泮鼻喷雾剂的曲线下面积几何变异系数的百分比=42%-66%,直肠凝胶=87%-172%)相比,鼻喷雾剂的生物利用度变异性更小。地西泮鼻喷雾剂的安全性与直肠地西泮一致,鼻腔不适的发生率较低(≤6%)。为了进一步提高抢救治疗的疗效,正在研究新型鼻内苯二氮䓬制剂。