Department of Neurology, Johns Hopkins School of Medicine, 600 North Wolfe St. Phipps 446C, Baltimore, MD, 21287, USA.
Neurocrit Care. 2020 Oct;33(2):582-586. doi: 10.1007/s12028-019-00889-z.
Stroke patients are currently monitored for neurological deterioration for 24 h following treatment with intravenous tissue plasminogen activator (IV tPA) or mechanical thrombectomy. This requires low nursing ratios and an intensive-care-like setting. As the half-life of IV tPA is short, many patients may not require such prolonged intensive monitoring and could be downgraded much earlier. We evaluate the frequency of neurological deterioration in the 0-12 and 12-24 h post-treatment windows.
Patients presenting with acute ischemic stroke treated with IV tPA and/or thrombectomy at our institution from 2016-2018 were prospectively followed per protocol for 24 h post-therapy (examinations every 15 min for 2 h, every 30 min for 6 h, and hourly thereafter). Neurological deteriorations were recorded along with interventions and complications. Frequency of deterioration within the 0-12 and 12-24 h post-treatment windows was determined, along with factors associated with decline at each time point.
A total of 172 patients were treated (IV:135, IA:65, both:30). Thirty-six (21%) experienced a documented neurologic deterioration [8 due to intracerebral hemorrhage (4.7%)]. Five patients deteriorated in the 12-24 h window; all but one had experienced earlier examination changes. Elevated NIHSS was associated with a higher likelihood of deterioration overall. Early fluctuation was associated with decline after 12 h.
New onset of neurologic deterioration is rare 12-24 h after treatment of acute stroke. Stable patients with low NIHSS scores and no ICU needs may not require intensive monitoring greater than 12 h post-treatment.
目前,接受静脉注射组织型纤溶酶原激活剂(IV tPA)或机械取栓治疗的中风患者在治疗后 24 小时内需要进行神经恶化监测,这需要低护理比例和类似重症监护的环境。由于 IV tPA 的半衰期较短,许多患者可能不需要如此长时间的密集监测,并且可以更早降级。我们评估了治疗后 0-12 小时和 12-24 小时治疗窗口内神经恶化的频率。
我们对 2016 年至 2018 年期间在我们机构接受 IV tPA 和/或取栓治疗的急性缺血性中风患者进行前瞻性随访,根据方案在治疗后 24 小时内进行监测(治疗后每 15 分钟进行一次检查,持续 2 小时,每 30 分钟进行一次检查,持续 6 小时,之后每小时进行一次检查)。记录神经恶化情况以及干预措施和并发症。确定治疗后 0-12 小时和 12-24 小时内恶化的频率,并确定每个时间点与下降相关的因素。
共治疗了 172 名患者(IV:135 名,IA:65 名,两者均:30 名)。36 名(21%)患者出现了有记录的神经恶化[8 名因颅内出血(4.7%)]。5 名患者在 12-24 小时治疗窗口内恶化;除 1 名患者外,所有患者均在较早的检查中发生了变化。较高的 NIHSS 评分与整体恶化的可能性更高相关。早期波动与 12 小时后下降相关。
急性中风治疗后 12-24 小时新发生的神经恶化很少见。NIHSS 评分较低且不需要 ICU 护理的稳定患者可能不需要在治疗后超过 12 小时进行密集监测。