Division of Epilepsy and Clinical Neurophysiology, Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
Epilepsia Open. 2021 Dec;6(4):714-719. doi: 10.1002/epi4.12540. Epub 2021 Oct 19.
There is no consensus on the type or duration of the posttreatment EEG needed for assessing treatment response for infantile spasms (IS). We assessed whether outpatient electroencephalograms (EEGs) are sufficient to confirm infantile spasms (IS) treatment response.
Three-year retrospective review identified new-onset IS patients. Only presumed responder to IS treatment at 2 weeks with a prolonged (>90 minutes) outpatient EEG to assess treatment response and at least 3-month follow-up were included. Hypsarrhythmia, electroclinical spasms, and sleep were evaluated for the first hour and for the duration of the EEG.
We included 37 consecutive patients with new-onset IS and presumed clinical response at 2 weeks posttreatment. Follow-up outpatient prolonged EEGs (median: 150 minutes, range: 90-240 minutes) were obtained 14 days (IQR: 13-17) after treatment initiation. EEGs detected ongoing IS in 11 of 37 (30%) presumed early responders. Prolonged outpatient EEG had a sensitivity of 85% (confidence interval [CI] 55%-98%) for detecting treatment failure. When hypsarrhythmia and/or electroclinical spasms were not seen, EEG had a negative predictive value 92% (CI: 75%-99%) for confirming continued IS resolution. Outpatient EEG combined with clinical assessment, however, identified all treatment failures at 2 weeks. Compared with the entire prolonged EEG, the first-hour recording missed IS in 45% (5/11). While sleep was captured in 95% (35/37) of the full EEG recording, the first hour of recording captured sleep in only 54% (20/37).
Infantile spasms treatment response can be confirmed with a clinical history of spasm freedom and an outpatient prolonged EEG without evidence for ongoing spasms (hypsarrhythmia/electroclinical spams on EEG). Outpatient prolonged EEG, but not routine EEGs, represents an alternative to inpatient long-term monitoring for IS posttreatment EEG follow-up.
目前对于评估婴儿痉挛症(IS)治疗反应所需的治疗后脑电图(EEG)类型或时长尚无共识。我们评估了门诊 EEG 是否足以确认婴儿痉挛症(IS)的治疗反应。
对新诊断的 IS 患者进行了为期 3 年的回顾性研究。仅纳入在治疗后 2 周内有延长(>90 分钟)门诊 EEG 以评估治疗反应和至少 3 个月随访,且被认为对 IS 治疗有反应的患者。评估了发作后第 1 小时和 EEG 持续时间的高度失律、电临床痉挛和睡眠。
共纳入 37 例新诊断为 IS 且在治疗后 2 周内被认为有临床反应的患者。在开始治疗后 14 天(IQR:13-17)获得了中位数为 150 分钟(范围:90-240 分钟)的门诊延长 EEG。在 37 例被认为是早期反应者中,有 11 例(30%)经 EEG 检测到持续的 IS。延长的门诊 EEG 检测治疗失败的敏感性为 85%(置信区间 [CI] 55%-98%)。当未观察到高度失律和/或电临床痉挛时,EEG 对确认 IS 持续缓解具有 92%(CI:75%-99%)的阴性预测值。然而,门诊 EEG 结合临床评估可在 2 周时识别所有治疗失败。与整个延长的 EEG 相比,第 1 小时的记录错过了 45%(5/11)的 IS。虽然在整个 EEG 记录中,95%(35/37)记录到了睡眠,但第 1 小时的记录仅记录到了 54%(20/37)的睡眠。
可通过痉挛消失的临床病史和无持续痉挛(EEG 上的高度失律/电临床痉挛)的门诊延长 EEG 来确认婴儿痉挛症的治疗反应。门诊延长 EEG 而不是常规 EEG 代表了婴儿痉挛症治疗后 EEG 随访替代住院长期监测的方法。