Van Ness P C
Department of Neurology, UCLA School of Medicine.
Epilepsia. 1990 Jan-Feb;31(1):61-7. doi: 10.1111/j.1528-1157.1990.tb05361.x.
Seven patients with complex partial or secondarily generalized tonic-clonic status epilepticus (SE) refractory to benzodiazepines (BZDs) and phenytoin (PHT) were treated with pentobarbital (PTB) coma with an EEG burst suppression (BSP) pattern. PTB administered by continuous intravenous (i.v.) infusion pump at a loading dose of 6-8 mg/kg in 40-60 min was usually sufficient to produce BSP activity and seizure control. PTB was continued 0-24 h at 1-4 mg/kg/h, adjusted to maintain blood pressure (BP) and BSP. Infusion rate was decreased if systolic BP (SBP) was less than 90 mm Hg. Normal saline fluid challenge was occasionally used to elevate BP, but in no case was it necessary to discontinue PTB infusion or use pressors. Other antiepileptic drugs (AEDs) were maintained at therapeutic levels for chronic seizure protection. Seizures were stopped in all cases. Four patients attained premorbid neurologic status, two patients briefly survived in vegetative states with recurring seizures after PTB withdrawal, and one patient died of asystole after receiving PTB for 7 h. Patients who had poor outcomes had prolonged seizures (16 h to 3 weeks) before institution of PTB anesthesia, and all had significant underlying central nervous system (CNS) pathology. PTB-induced BSP appears to be safe and effective for refractory SE if it is started soon after failure of a BZD and PHT. Ultimate prognosis depends on SE etiology.
7例复杂部分性或继发性全身性强直-阵挛性癫痫持续状态(SE)患者,对苯二氮䓬类药物(BZDs)和苯妥英(PHT)治疗无效,采用戊巴比妥(PTB)昏迷疗法并伴有脑电图爆发抑制(BSP)模式进行治疗。通过持续静脉(i.v.)输注泵以6 - 8mg/kg的负荷剂量在40 - 60分钟内给予PTB,通常足以产生BSP活动并控制癫痫发作。PTB以1 - 4mg/kg/h的速度持续输注0 - 24小时,根据血压(BP)和BSP进行调整。如果收缩压(SBP)低于90mmHg,则降低输注速率。偶尔使用生理盐水补液来升高血压,但在任何情况下都无需停止PTB输注或使用升压药。其他抗癫痫药物(AEDs)维持在治疗水平以提供慢性癫痫保护。所有病例的癫痫发作均停止。4例患者恢复到病前神经状态,2例患者在停用PTB后短暂存活于植物人状态且癫痫复发,1例患者在接受PTB治疗7小时后死于心搏停止。预后不良的患者在开始PTB麻醉前癫痫发作持续时间较长(16小时至3周),且均有明显的潜在中枢神经系统(CNS)病变。如果在BZD和PHT治疗失败后不久开始使用,PTB诱导的BSP对于难治性SE似乎是安全有效的。最终预后取决于SE的病因。