The Impact of Electroencephalographic (EEG) Seizure Treatment in Near Term ≥ 36 Weeks Gestation and Term Infants With Neonatal Encephalopathy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 69
- 试验地点
- 2
- 主要终点
- Presence of a single combined event: death in the first two years of life or moderate or severe disability at 18-24 months
研究概览
简要总结
This is a prospective, randomized, single-center pilot trial of term and near term (≥ 36 weeks gestation) infants with encephalopathy or seizures comparing a "EEG Seizure Treatment Group" or ESG with a "Clinical Seizure Treatment Group" or CSG.
The investigators hypothesize that the accurate detection and treatment of EEG seizures will decrease the seizure burden and improve outcomes in newborn infants with seizures and/or hypoxic-ischemic encephalopathy (HIE).
详细描述
This is a prospective, randomized, pilot trial of term and near term (≥ 36 weeks gestation) infants with encephalopathy or seizures comparing a "EEG Seizure Treatment Group" or ESG with a "Clinical Seizure Treatment Group" or CSG. Eligibility is based on clinical criteria for moderate/severe encephalopathy or seizures. We will recruit near term or term infants (≥ 36 weeks gestation) with a diagnosis of seizures or encephalopathy admitted to the neonatal intensive care unit (NICU) at St. Louis Children's Hospital within the first 72 hours of life. Infants will be randomized into an EEG Seizure Treatment Group (ESG) or a Clinical Seizure Treatment Group (CSG) (n=20 in each group). Patients in both groups will have EEG monitoring. While treating physicians will have access to EEG data in the ESG, no EEG data in the CSG will be available to the clinician for treatment of seizures. AED treatment will be initiated/escalated using stringent EEG seizure criteria (EST) or clinical criteria (CST) with the goal being seizure cessation. The specific AED, dosage, and duration of treatment is standardized in both groups. Monitoring will continue for a period of upto 96 hours in both arms. Other than the anticonvulsant drugs, treatment thresholds and dosing schedules, treatment in both arms will be at the discretion of the bedside physician.All infants will undergo an assessment of neuromotor disability and neurodevelopmental evaluation at 18 to 24 months.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 1 Hour 至 72 Hours（Child）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Term or near term infants ≥ 36 weeks gestation admitted to the neonatal intensive care unit
- •≤ 72 hours of age
- •Screening for the "at risk" infant by the clinical team to include any one of the following:
- •Apgar score <5 at 5 min
- •Cord blood or postnatal gas with pH <7.0 or BE > -12
- •Need for respiratory support at 10 min of life
- •Suspected or definite seizures
- •Encephalopathy defined by recognition of altered neurological behavior
- •Infants identified in the above screen will be examined by the research team and will be eligible if they satisfy at least one of the following:
- •Moderate-severe neonatal encephalopathy (3 out of 6 criteria)
- •Suspected or definite neonatal seizures
- •Exclusion criteria:
- •Infants < 36 weeks gestation
- •> 72 hours of age
- •Infants with congenital anomalies of the central nervous system
- •Moribund infants for whom no further aggressive treatment is planned
- •Metabolic disorders or documented CNS infection
- •Neuro-muscular blockade
排除标准
- 未提供
结局指标
主要结局
Presence of a single combined event: death in the first two years of life or moderate or severe disability at 18-24 months
时间窗: first two years of life; 18-24 months
Seizure burden
时间窗: 2 to 3 years
次要结局
- EEG background state(2 to 3 years)
- Number, duration of anticonvulsants used and cumulative dose(2 to 3 years)
- Duration of hospital stay(2 to 3 years)
- MRI measures from the Day #7-10 MRI in survivors(2 to 3 years)
- Time to all per oral feeding(2 to 3 years)
- Time to seizure cessation(2 to 3 years)