Tran Nga N, Liu James, Bullock Tyler, Flowers David
Simulation Center, Edward Via College of Osteopathic Medicine, Auburn, USA.
Medicine, Kirksville College of Osteopathic Medicine, Kirksville, USA.
Cureus. 2024 Apr 30;16(4):e59405. doi: 10.7759/cureus.59405. eCollection 2024 Apr.
The objective of this case report is to describe and document a case of respiratory syncytial virus (RSV) in a pediatric patient with Dravet syndrome (DS), also known as severe myoclonic epilepsy of infancy. Febrile seizures are often a complication in a patient with DS and can lead to status epilepticus, necessitating measures to prevent triggers such as fever, electrolyte imbalance, or dehydration. An increased awareness and understanding of DS can facilitate the identification of warning signs. A two-year-old female with a past medical history of DS with focal and generalized features presented to the pediatric emergency department (ED) with a five-day history of cough, fever, and decreased oral intake. The patient's parents accompanied her and expressed concerns regarding the risk of seizures associated with a rise in body temperature, as they had been alternating between acetaminophen and ibuprofen to manage her fever with a maximum recorded temperature of 101.5℉. She exhibited signs of increased work of breathing, necessitating the administration of supplemental oxygen via nasal cannula. Blood samples were obtained and resulted in the development of metabolic acidosis. A respiratory panel confirmed the presence of an RSV infection, promoting the administration of breathing treatment with albuterol and ipratropium bromide. The patient was admitted for dehydration and was started on ½ normal saline/potassium chloride 20 mEq at 40 mL/hr. Additionally, her home medication regimen was resumed to minimize the risk of seizures. Given the patient's complications and increased risk of seizure, she was transferred to higher-level care where her status improved after the placement of a percutaneous endoscopic gastrostomy (PEG). This case underscores the complexities involved in managing patients with DS, particularly when complicated by respiratory illness and electrolyte imbalances that can lower the seizure threshold. This patient received a combination of diet and medications to prevent seizures, as well as allow for recovery and correction of the underlying metabolic acidosis. The transfer to a higher level of care in this case was necessary to allow for the specialized resources and expertise needed to handle this case.
本病例报告的目的是描述和记录一例患有德雷维特综合征(DS,又称婴儿严重肌阵挛性癫痫)的儿科患者感染呼吸道合胞病毒(RSV)的情况。热性惊厥在DS患者中通常是一种并发症,可导致癫痫持续状态,因此需要采取措施预防发热、电解质失衡或脱水等诱发因素。提高对DS的认识和理解有助于识别警示信号。一名两岁女性,有DS病史,具有局灶性和全身性特征,因咳嗽、发热和口服摄入量减少五天而到儿科急诊科就诊。患者父母陪同,表达了对体温升高相关癫痫发作风险的担忧,因为他们一直在交替使用对乙酰氨基酚和布洛芬来控制她的发热,最高记录体温为101.5℉。她表现出呼吸做功增加的迹象,需要通过鼻导管给予补充氧气。采集血样后出现代谢性酸中毒。呼吸道检查确认存在RSV感染,并因此给予沙丁胺醇和异丙托溴铵进行呼吸治疗。患者因脱水入院,并开始以40毫升/小时的速度输注1/2生理盐水/20毫当量氯化钾。此外恢复其家庭用药方案以尽量降低癫痫发作风险。鉴于患者的并发症和癫痫发作风险增加,她被转至更高水平护理机构,在那里经皮内镜下胃造口术(PEG)置入后病情有所改善。本病例强调了管理DS患者所涉及的复杂性,尤其是当合并呼吸系统疾病和电解质失衡从而降低癫痫发作阈值时更为复杂。该患者接受饮食和药物联合治疗以预防癫痫发作,并促进潜在代谢性酸中毒的恢复和纠正。在这种情况下转至更高水平护理机构是必要的,以便获得处理该病例所需的专业资源和专业知识。