Predicting risk of symptomatic intracerebral hemorrhage and mortality after treatment with recombinant tissue-plasminogen activator using SEDAN score

被引:13
作者
Al-Khaled, M. [1 ]
Langner, B. [1 ]
Bruening, T. [1 ]
机构
[1] Med Univ Lubeck, Dept Neurol, D-23564 Lubeck, Germany
来源
ACTA NEUROLOGICA SCANDINAVICA | 2016年 / 133卷 / 04期
关键词
acute ischemic stroke; thrombolysis; recombinant tissue-plasminogen activator; hemorrhage; SEDAN Score; mortality; ACUTE ISCHEMIC-STROKE; INTRACRANIAL HEMORRHAGE; INTRAVENOUS ALTEPLASE; THROMBOLYTIC THERAPY; TRIAL; ECASS;
D O I
10.1111/ane.12447
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purposeThe most feared complication after treatment with recombinant tissue-plasminogen activator (rt-PA) is the occurrence of symptomatic intracerebral hemorrhage (sICH). The aims of the study were to predict the risk of sICH (ECASS II definition) after a therapy with rt-PA and to examine whether associations exist between SEDAN score and the early mortality in patients with acute ischemic stroke in a monocenter study. MethodsDuring a 6-year period (2008-2013), 542 consecutive stroke patients (mean age, 733years; 51.1% women; median NIHSS score, 11) treated with IV thrombolysis were included in a monocenter study. SICH was diagnosed in according to the with ECASS II definition. ResultsThe absolute risk for sICH revealed 9.2% (95% CI, 6.5-11.4) of patients treated with IV thrombolysis and was 0%, 4.6% (95% CI, 1.3-7.9), 6.6% (95% CI, 3.3-10.5), 13.5% (95% CI, 6.7-19.2), 23.6% (95% CI, 12.7-34.5), and 26.7% (95% CI, 12.7-34.5) for 0, 1, 2, 3, 4, and 5 SEDAN points. Logistic regression revealed that sICH was associated with increasing SEDAN scores (OR, 1.93 per SEDAN point; 95% CI, 1.51-2.46; P<0.001). The predictive performance was assessed with area under a receiver operating characteristic curve (0.73; 95% CI, 0.65-0.80; P<0.001). During hospitalization (median, 9days), 53 patients (9.8%; 95% CI, 7.4-12.45) died. In-hospital mortality was higher in patients with than those without sICH (30 vs 7.7%; P<0.001), and it was increased with increasing SEDAN score (OR, 1.45 per point; 95% CI, 1.12-1.89; P=0.005). ConclusionsHigher SEDAN score was associated with an increased risk of sICH and early mortality in this monocenter study.
引用
收藏
页码:239 / 244
页数:6
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