Epilepsy Center Frankfurt Rhine-Main and Department of Neurology, Center of Neurology and Neurosurgery, Goethe-University Frankfurt, Schleusenweg 2-16, 60528, Frankfurt am Main, Germany.
LOEWE Center for Personalized Translational Epilepsy Research (CePTER), Goethe-University Frankfurt, Frankfurt am Main, Germany.
CNS Drugs. 2022 Sep;36(9):951-975. doi: 10.1007/s40263-022-00940-2. Epub 2022 Aug 16.
Status epilepticus (SE) is an acute, life-threatening medical condition that requires immediate, effective therapy. Therefore, the acute care of prolonged seizures and SE is a constant challenge for healthcare professionals, in both the pre-hospital and the in-hospital settings. Benzodiazepines (BZDs) are the first-line treatment for SE worldwide due to their efficacy, tolerability, and rapid onset of action. Although all BZDs act as allosteric modulators at the inhibitory gamma-aminobutyric acid (GABA) receptor, the individual agents have different efficacy profiles and pharmacokinetic and pharmacodynamic properties, some of which differ significantly. The conventional BZDs clonazepam, diazepam, lorazepam and midazolam differ mainly in their durations of action and available routes of administration. In addition to the common intravenous, intramuscular and rectal administrations that have long been established in the acute treatment of SE, other administration routes for BZDs-such as intranasal administration-have been developed in recent years, with some preparations already commercially available. Most recently, the intrapulmonary administration of BZDs via an inhaler has been investigated. This narrative review provides an overview of the current knowledge on the efficacy and tolerability of different BZDs, with a focus on different routes of administration and therapeutic specificities for different patient groups, and offers an outlook on potential future drug developments for the treatment of prolonged seizures and SE.
癫痫持续状态(SE)是一种危及生命的急性疾病,需要立即进行有效的治疗。因此,无论是在院前还是院内环境中,医护人员都需要不断应对长时间癫痫发作和 SE 的急性护理这一挑战。由于苯二氮䓬类药物(BZDs)具有疗效确切、耐受性好和起效迅速等特点,目前已在全球范围内将其作为 SE 的一线治疗药物。尽管所有 BZDs 均作为变构调节剂作用于抑制性γ-氨基丁酸(GABA)受体,但各药物的疗效谱和药代动力学及药效动力学特性存在差异,其中一些差异非常显著。传统的 BZDs(如氯硝西泮、地西泮、劳拉西泮和咪达唑仑)主要在作用持续时间和可用给药途径方面存在差异。除了在 SE 急性治疗中长期确立的常见静脉、肌肉和直肠给药途径外,近年来还开发了其他 BZD 给药途径,如鼻内给药途径,其中一些制剂已上市。最近,还研究了通过吸入器经肺内给予 BZDs。本综述概述了不同 BZD 的疗效和耐受性方面的现有知识,重点介绍了不同给药途径和不同患者群体的治疗特异性,并对治疗长时间癫痫发作和 SE 的潜在未来药物研发进行了展望。