Chumnanvej Sorayouth, Dunn Ian F, Kim Dong H
Department of Neurosurgery, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Neurosurgery. 2007 Jan;60(1):99-102; discussion 102-3. doi: 10.1227/01.NEU.0000249207.66225.D9.
Phenytoin (PHT) is widely administered after subarachnoid hemorrhage, often for several weeks or months. In addition to known side effects, PHT use has been correlated with cognitive disability and poor outcome. To reduce the rate of PHT complications, we converted from a multi-week prophylactic regimen to a 3-day course of treatment. This study evaluates the changes in seizure rates and adverse events.
From July 1998 to June 2002, 453 patients with spontaneous subarachnoid hemorrhage were treated. In the first 9 months, 79 patients were administered PHT until discharged from the hospital, unless a drug reaction occurred first. In the last 39 months, PHT was discontinued 3 days after admission (370 patients), unless there was a history of epilepsy (four patients). This study represents a retrospective analysis of prospectively collected data, with follow-up periods of 3 to 12 months after discharge.
The 3-day PHT regimen produced a statistically significant reduction (P = 0.002) in the rate of PHT complications. In the first period, seven (8.8%) out of 79 patients experienced a hypersensitivity reaction, compared with two (0.5%) out of 370 patients in the second period. The percentage of patients having seizures, both short- and long-term, did not change significantly. In the first period, the seizure rate during hospitalization was 1.3%; in the second period, it was 1.9% (P = 0.603). At an average follow-up period of 6.7 months, three (5.7%) out of 53 survivors in the first period experienced a seizure (including those who had a seizure during hospitalization). In the second period, 12 (4.6%) out of 261 survivors experienced a seizure at an average follow-up period of 5.4 months (P = 0.573).
A 3-day regimen of PHT prophylaxis is adequate to prevent seizures in subarachnoid hemorrhage patients. Drug reactions are significantly reduced, but seizure rates do not change. Short-term PHT administration may be a superior treatment paradigm.
苯妥英钠(PHT)在蛛网膜下腔出血后广泛应用,通常持续数周或数月。除了已知的副作用外,使用PHT还与认知障碍和不良预后相关。为降低PHT并发症的发生率,我们从多周预防方案改为3天疗程的治疗。本研究评估癫痫发作率和不良事件的变化。
1998年7月至2002年6月,对453例自发性蛛网膜下腔出血患者进行治疗。在最初的9个月里,79例患者接受PHT治疗直至出院,除非先出现药物反应。在最后的39个月里,370例患者在入院3天后停用PHT(4例有癫痫病史者除外)。本研究是对前瞻性收集数据的回顾性分析,出院后随访3至12个月。
3天PHT方案使PHT并发症发生率有统计学意义的降低(P = 0.002)。在第一阶段,79例患者中有7例(8.8%)出现过敏反应,而在第二阶段,370例患者中有2例(0.5%)出现过敏反应。短期和长期癫痫发作患者的百分比没有显著变化。在第一阶段,住院期间的癫痫发作率为1.3%;在第二阶段,为1.9%(P = 0.603)。在平均随访6.7个月时,第一阶段53例幸存者中有3例(5.7%)出现癫痫发作(包括住院期间发作的患者)。在第二阶段,261例幸存者中有12例(4.6%)在平均随访5.4个月时出现癫痫发作(P = 0.573)。
3天的PHT预防方案足以预防蛛网膜下腔出血患者的癫痫发作。药物反应显著减少,但癫痫发作率没有变化。短期使用PHT可能是一种更好的治疗模式。