Hemmen Thomas M, Raman Rema, Guluma Kama Z, Meyer Brett C, Gomes Joao A, Cruz-Flores Salvador, Wijman Christine A, Rapp Karen S, Grotta James C, Lyden Patrick D
Department of Neuroscience, University of California, San Diego, CA 92103-8466, USA.
Stroke. 2010 Oct;41(10):2265-70. doi: 10.1161/STROKEAHA.110.592295. Epub 2010 Aug 19.
Induced hypothermia is a promising neuroprotective therapy. We studied the feasibility and safety of hypothermia and thrombolysis after acute ischemic stroke.
Intravenous Thrombolysis Plus Hypothermia for Acute Treatment of Ischemic Stroke (ICTuS-L) was a randomized, multicenter trial of hypothermia and intravenous tissue plasminogen activator in patients treated within 6 hours after ischemic stroke. Enrollment was stratified to the treatment time windows 0 to 3 and 3 to 6 hours. Patients presenting within 3 hours of symptom onset received standard dose intravenous alteplase and were randomized to undergo 24 hours of endovascular cooling to 33°C followed by 12 hours of controlled rewarming or normothermia treatment. Patients presenting between 3 and 6 hours were randomized twice: to receive tissue plasminogen activator or not and to receive hypothermia or not. Results- In total, 59 patients were enrolled. One patient was enrolled but not treated when pneumonia was discovered just before treatment. All 44 patients enrolled within 3 hours and 4 of 14 patients enrolled between 3 to 6 hours received tissue plasminogen activator. Overall, 28 patients randomized to receive hypothermia (HY) and 30 to normothermia (NT). Baseline demographics and risk factors were similar between groups. Mean age was 65.5±12.1 years and baseline National Institutes of Health Stroke Scale score was 14.0±5.0; 32 (55%) were male. Cooling was achieved in all patients except 2 in whom there were technical difficulties. The median time to target temperature after catheter placement was 67 minutes (Quartile 1 57.3 to Quartile 3 99.4). At 3 months, 18% of patients treated with hypothermia had a modified Rankin Scale score of 0 or 1 versus 24% in the normothermia groups (nonsignificant). Symptomatic intracranial hemorrhage occurred in 4 patients (68); all were treated with tissue plasminogen activator <3 hours (1 received hypothermia). Six patients in the hypothermia and 5 in the normothermia groups died within 90 days (nonsignificant). Pneumonia occurred in 14 patients in the hypothermia and in 3 of the normothermia groups (P=0.001). The pneumonia rate did not significantly adversely affect 3 month modified Rankin Scale score (P=0.32).
This study demonstrates the feasibility and preliminary safety of combining endovascular hypothermia after stroke with intravenous thrombolysis. Pneumonia was more frequent after hypothermia, but further studies are needed to determine its effect on patient outcome and whether it can be prevented. A definitive efficacy trial is necessary to evaluate the efficacy of therapeutic hypothermia for acute stroke.
诱导性低温是一种很有前景的神经保护疗法。我们研究了急性缺血性卒中后低温治疗与溶栓治疗的可行性及安全性。
急性缺血性卒中静脉溶栓加低温治疗(ICTuS-L)是一项针对缺血性卒中发病6小时内接受治疗的患者进行的低温治疗与静脉注射组织型纤溶酶原激活剂的随机多中心试验。入组根据治疗时间窗分为0至3小时和3至6小时两组。症状发作3小时内就诊的患者接受标准剂量静脉注射阿替普酶,并随机分为接受24小时血管内降温至33°C,随后12小时控制性复温或常温治疗。3至6小时内就诊的患者进行两次随机分组:是否接受组织型纤溶酶原激活剂治疗以及是否接受低温治疗。结果:共入组59例患者。1例患者在治疗前发现肺炎,入组但未接受治疗。3小时内入组的44例患者以及3至6小时内入组的14例患者中的4例接受了组织型纤溶酶原激活剂治疗。总体而言,28例患者随机接受低温治疗(HY),30例接受常温治疗(NT)。两组间基线人口统计学特征和危险因素相似。平均年龄为65.5±12.1岁,基线美国国立卫生研究院卒中量表评分为14.0±5.0;32例(55%)为男性。除2例因技术困难未成功外,所有患者均实现了降温。导管置入后达到目标温度的中位时间为67分钟(四分位数间距Q1 57.3至Q3 99.4)。在3个月时,接受低温治疗的患者中18%的改良Rankin量表评分为0或1,而常温治疗组为24%(无显著差异)。4例患者发生症状性颅内出血(68例中);所有这些患者均在<3小时接受了组织型纤溶酶原激活剂治疗(1例接受了低温治疗)。低温治疗组6例患者和常温治疗组5例患者在90天内死亡(无显著差异)。低温治疗组14例患者发生肺炎,常温治疗组3例发生肺炎(P = 0.001)。肺炎发生率对3个月时的改良Rankin量表评分无显著不良影响(P = 0.32)。
本研究证明了卒中后血管内低温联合静脉溶栓的可行性和初步安全性。低温治疗后肺炎更常见,但需要进一步研究以确定其对患者预后的影响以及是否可以预防。有必要进行一项确定性疗效试验来评估治疗性低温对急性卒中的疗效。