Rocamora R, Kurthen M, Lickfett L, Von Oertzen J, Elger C E
Department of Epileptology, University of Bonn, Bonn, Germany.
Epilepsia. 2003 Feb;44(2):179-85. doi: 10.1046/j.1528-1157.2003.15101.x.
Cardiac asystole provoked by epileptic seizures is a rare but important complication in epilepsy and is supposed to be relevant to the pathogenesis of sudden unexplained death in epilepsy (SUDEP). We sought to determine the frequency of this complication in a population of patients with medically intractable epilepsy and to analyze the correlation between EEG, electrocardiogram (ECG), and clinical features obtained from long-term video-EEG monitoring.
Retrospective analysis of the clinical records of hospitalized patients from May 1992 to June 2001 who underwent long-term video-/EEG monitoring.
Of a total of 1,244 patients, five patients had cardiac asystole in the course of ictal events. In these patients, 11 asystolic events, between 4 and 60 s long in a total of 19 seizures, were registered. All seizures had a focal origin with simple partial seizures (n = 13), complex partial seizures (n = 4), and secondarily generalized seizures (n = 2). One patient showed the longest asystole ever reported (60 s) because of a seizure. Cardiac asystole occurred in two patients with left-sided temporal lobe epilepsy (TLE) and in three patients with frontal lobe epilepsy (FLE; two left-sided, one bifrontal). Two patients reported previous cardiac disease, but only one had a pathologic ECG by the time of admission. Two patients had a simultaneous central ictal apnea during the asystole. None of the patients had ongoing deficits due to the asystole.
These findings confirm that seizure-induced asystole is a rare complication. The event appeared only in focal epilepsies (frontal and temporal) with a lateralization to the left side. A newly diagnosed or known cardiac disorder could be a risk factor for ictal asystole. Abnormally long postictal periods with altered consciousness might point to reduced cerebral perfusion during the event because of ictal asystole. Central ictal apnea could be a frequent associated phenomenon.
癫痫发作诱发的心搏骤停是癫痫中一种罕见但重要的并发症,被认为与癫痫不明原因猝死(SUDEP)的发病机制相关。我们试图确定在药物难治性癫痫患者群体中这种并发症的发生率,并分析脑电图(EEG)、心电图(ECG)与长期视频脑电图监测获得的临床特征之间的相关性。
对1992年5月至2001年6月期间住院并接受长期视频/EEG监测的患者的临床记录进行回顾性分析。
在总共1244例患者中,有5例患者在发作事件过程中出现心搏骤停。在这些患者中,共记录到11次心搏骤停事件,时长在4至60秒之间,发作次数总计19次。所有发作均起源于局灶性,包括单纯部分性发作(n = 13)、复杂部分性发作(n = 4)和继发性全身性发作(n = 2)。一名患者因发作出现了有记录以来最长的心搏骤停(60秒)。心搏骤停发生在2例左侧颞叶癫痫(TLE)患者和3例额叶癫痫(FLE;2例左侧,1例双侧额叶)患者中。2例患者报告有既往心脏病史,但入院时只有1例心电图异常。2例患者在心搏骤停期间同时出现中枢性发作性呼吸暂停。所有患者均未因心搏骤停而遗留持续性功能缺损。
这些发现证实发作诱发的心搏骤停是一种罕见的并发症。该事件仅出现在局灶性癫痫(额叶和颞叶)中,且以左侧为主。新诊断或已知的心脏疾病可能是发作性心搏骤停的一个危险因素。发作后意识改变且持续时间异常延长可能表明发作期间因发作性心搏骤停导致脑灌注减少。中枢性发作性呼吸暂停可能是一种常见的伴随现象。