Division of Neurology, Department of Medicine, Udon Thani Hospital, Udon Thani, Thailand.
Integrated Epilepsy Research Group, Khon Kaen University, Khon Kaen, Thailand; Division of Neurology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Clin Neurol Neurosurg. 2020 Nov;198:106206. doi: 10.1016/j.clineuro.2020.106206. Epub 2020 Sep 8.
A good functional response at 24 h from an intravenous recombinant tissue plasminogen activator (rtPA) treatment is associated with 3-month ischemic stroke outcome. The criterion for 24 -h neurological improvement is varied from 4 to 8 point the National Institutes of Health Stroke Scale (NIHSS) score reduction. This study aimed to evaluate the smaller difference of the NIHSS at 2 points on long term functional status.
The inclusion criteria were adult patients diagnosed as acute ischemic stroke and received the rtPA treatment. There were two stroke outcomes comprised of immediate 24 -hs and 3 month long term outcomes. Favorable 24 -h outcome defined by improvement of the NIHSS at 24 h after the rtPA treatment at least 2 points or equal to 0. At 3 months, the outcome was evaluated by using the modified Rankin scale (mRS). The mRS of 0-1 and 2-6 defined as favorable and poor outcome, respectively. Factors associated with poor outcomes at 24 h and 3 months after the rtPA treatment were calculated by logistic regression analysis.
There were 618 patients met the study criteria. Of those, 403 patients (65.2 %) received the rtPA treatment at the tertiary care hospital. At 24 h after the rtPA treatment, 163 patients (26.38 %) had poor outcome. After adjusted, age and atrial fibrillation had adjusted odds ratios (95 % confidence interval) for poor outcome at 24 h after the rtPA treatment of 1.026 (1.009, 1.043) and 1.725 (1.119, 2.658). At 3 months after the rtPA treatment, the poor outcome at 24 h after rtPA treatment had the highest adjusted odds ratio at 42.876 (95 % confidence interval of 21.500, 85.501).
The NIHSS differences of 2 points at 24 -h after the rtPA treatment from baseline may be an additional tool to predict the 3-month functional outcome of acute ischemic stroke patients.
静脉注射重组组织纤溶酶原激活剂(rtPA)治疗后 24 小时的良好功能反应与 3 个月的缺血性卒中风结局相关。24 小时神经改善的标准是 NIHSS 评分降低 4 至 8 分。本研究旨在评估 NIHSS 在 2 点的较小差异对长期功能状态的影响。
纳入标准为诊断为急性缺血性脑卒中并接受 rtPA 治疗的成年患者。有两个卒中结局,包括即时 24 小时和 3 个月的长期结局。24 小时后 NIHSS 改善至少 2 分或等于 0 定义为 24 小时时的有利结局。3 个月时,采用改良 Rankin 量表(mRS)进行评估。mRS 为 0-1 和 2-6 分别定义为有利和不良结局。通过 logistic 回归分析计算 rtPA 治疗后 24 小时和 3 个月不良结局的相关因素。
符合研究标准的患者有 618 名。其中,403 名(65.2%)患者在三级医疗机构接受 rtPA 治疗。rtPA 治疗后 24 小时,163 名(26.38%)患者预后不良。调整后,年龄和心房颤动是 rtPA 治疗后 24 小时不良结局的调整比值比(95%置信区间)为 1.026(1.009,1.043)和 1.725(1.119,2.658)。rtPA 治疗后 3 个月,rtPA 治疗后 24 小时的不良预后的调整比值比最高,为 42.876(95%置信区间为 21.500,85.501)。
rtPA 治疗后 24 小时 NIHSS 基线差异 2 分可能是预测急性缺血性脑卒中患者 3 个月功能结局的附加工具。