NeuroCure Clinical Research Center, Charité Universitätsmedizin Berlin, Berlin, Germany.
J Transl Med. 2013 Jun 27;11:157. doi: 10.1186/1479-5876-11-157.
2-8% of all children aged between 6 months and 5 years have febrile seizures. Often these seizures cease spontaneously, however depending on different national guidelines, 20-40% of the patients would need therapeutic intervention. For seizures longer than 3-5 minutes application of rectal diazepam, buccal midazolam or sublingual lorazepam is recommended. Benzodiazepines may be ineffective in some patients or cause prolonged sedation and fatigue. Preclinical investigations in a rat model provided evidence that febrile seizures may be triggered by respiratory alkalosis, which was subsequently confirmed by a retrospective clinical observation. Further, individual therapeutic interventions demonstrated that a pCO2-elevation via re-breathing or inhalation of 5% CO2 instantly stopped the febrile seizures. Here, we present the protocol for an interventional clinical trial to test the hypothesis that the application of 5% CO2 is effective and safe to suppress febrile seizures in children.
The CARDIF (CARbon DIoxide against Febrile seizures) trial is a monocentric, prospective, double-blind, placebo-controlled, randomized study. A total of 288 patients with a life history of at least one febrile seizure will be randomized to receive either carbogen (5% CO2 plus 95% O2) or placebo (100% O2). As recurrences of febrile seizures mainly occur at home, the study medication will be administered by the parents through a low-pressure can fitted with a respiratory mask. The primary outcome measure is the efficacy of carbogen to interrupt febrile seizures. As secondary outcome parameters we assess safety, practicability to use the can, quality of life, contentedness, anxiousness and mobility of the parents.
The CARDIF trial has the potential to develop a new therapy for the suppression of febrile seizures by redressing the normal physiological state. This would offer an alternative to the currently suggested treatment with benzodiazepines. This study is an example of academic translational research from the study of animal physiology to a new therapy.
ClinicalTrials.gov identifier: NCT01370044.
6 个月至 5 岁的儿童中,有 2-8%会出现热性惊厥。这些惊厥通常会自行停止,但根据不同的国家指南,20-40%的患者需要治疗干预。对于持续时间超过 3-5 分钟的惊厥,建议直肠给予地西泮、口腔给予咪达唑仑或舌下给予劳拉西泮。在一些患者中,苯二氮䓬类药物可能无效或导致长时间镇静和疲劳。在大鼠模型中的临床前研究提供了证据,表明热性惊厥可能由呼吸性碱中毒触发,随后通过回顾性临床观察得到证实。此外,个体治疗干预表明,通过再呼吸或吸入 5%CO2 来升高 pCO2 可立即停止热性惊厥。在此,我们提出了一项干预性临床试验的方案,以检验以下假设:应用 5%CO2 可有效且安全地抑制儿童热性惊厥。
CARDIF(CARbon DIoxide against Febrile seizures)试验是一项单中心、前瞻性、双盲、安慰剂对照、随机研究。共有 288 例至少有一次热性惊厥病史的患者将被随机分为接受碳氧混合气(5%CO2 加 95%O2)或安慰剂(100%O2)组。由于热性惊厥的复发主要发生在家庭中,研究药物将由父母通过配备呼吸面罩的低压罐给予。主要结局测量指标是碳氧混合气中断热性惊厥的疗效。作为次要结局参数,我们评估安全性、使用罐的可行性、父母的生活质量、满意度、焦虑和活动能力。
CARDIF 试验有可能通过纠正正常生理状态来开发一种新的热性惊厥抑制疗法。这将为目前建议的苯二氮䓬类药物治疗提供替代方案。这项研究是从动物生理学研究到新疗法的学术转化研究的一个范例。
ClinicalTrials.gov 标识符:NCT01370044。