Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Le Bonheur Children's Hospital, University of Tennessee Health Science Center, Memphis, Tennessee, USA.
Epilepsia. 2022 Apr;63(4):836-843. doi: 10.1111/epi.17177. Epub 2022 Feb 2.
An exploratory analysis from a long-term, phase 3, open-label, repeat-dose safety study of diazepam nasal spray for acute treatment of seizure clusters assessed the use of a second dose up to 24 hours after the initial dose and effectiveness in potentially reducing the number of seizures.
Seizures and doses were recorded in diaries.
Of 175 patients enrolled, 163 received ≥1 dose of diazepam nasal spray and were included in the safety population; those patients received a total of 4390 doses for a total of 3853 seizure clusters. Less than half of these patients used a second dose a least once during the study (79 patients [48.5%]), with a total of 485 second doses for seizure clusters (12.6% of all seizure clusters). Among these 79 patients, 33 (41.8%) used only one second dose during the study (range: 1-82). The proportion of seizure clusters treated with a second dose over time was consistently low across 24 h: 0-4 h, 152 (3.9%); 4-6 h, 72 (1.9%); 6-8 h, 39 (1.0%); 8-12 h, 55 (1.4%); 12-16 h, 42 (1.1%); 16-20 h, 42 (1.1%); 20-24 h, 83 (2.2%). Rates of treatment-emergent adverse events (TEAEs) and treatment-related TEAEs occurring within 1 day of a second dose were low (15.2% and 5.1%, respectively).
Patients with epilepsy may experience seizure clusters lasting up to 24 hours, and little is known about the effectiveness of rescue therapies for that duration. The current labeling of the US Food and Drug Administration (FDA)-approved outpatient treatments for seizure clusters (rectal diazepam, intranasal midazolam, and diazepam nasal spray) allows for a second dose, if needed, for control. These findings support the safety profile of second doses, and the low use supports the effectiveness of diazepam nasal spray across 24 hours.
从一项长期、3 期、开放标签、重复剂量的地西泮鼻喷剂治疗急性癫痫发作的安全性研究中进行探索性分析,评估初始剂量后 24 小时内使用第二剂以及潜在减少癫痫发作次数的效果。
通过日记记录癫痫发作和剂量。
在纳入的 175 例患者中,163 例患者至少接受了 1 剂地西泮鼻喷剂,纳入安全性人群;这些患者共接受了 4390 剂,共治疗了 3853 次癫痫发作。在研究期间,不到一半的患者至少使用了一剂第二剂(79 例患者[48.5%]),总共治疗了 485 次癫痫发作(所有癫痫发作的 12.6%)。在这 79 例患者中,有 33 例(41.8%)在研究期间仅使用了一剂第二剂(范围:1-82)。随着时间的推移,使用第二剂治疗的癫痫发作比例一直很低:24 小时内 0-4 小时 152 例(3.9%);4-6 小时 72 例(1.9%);6-8 小时 39 例(1.0%);8-12 小时 55 例(1.4%);12-16 小时 42 例(1.1%);16-20 小时 42 例(1.1%);20-24 小时 83 例(2.2%)。第二剂治疗后出现的治疗中出现的不良事件(TEAEs)和与治疗相关的 TEAEs 发生率较低(分别为 15.2%和 5.1%)。
癫痫患者可能会经历长达 24 小时的癫痫发作,而对于该持续时间的抢救治疗效果知之甚少。目前,美国食品和药物管理局(FDA)批准的癫痫发作门诊治疗药物(直肠地西泮、鼻内咪达唑仑和地西泮鼻喷剂)允许按需使用第二剂,如果需要,可控制病情。这些发现支持了第二剂的安全性,且低使用率表明地西泮鼻喷剂在 24 小时内具有有效性。