Service d'Urgences Neuro-Vasculaires, Assistance Publique-Hôpitaux de Marseille (APHM), CHU de la Timone, Marseille, France.
AJNR Am J Neuroradiol. 2013 Jan;34(1):107-14. doi: 10.3174/ajnr.A3174. Epub 2012 Jul 5.
Recent studies highlight the role of CC in preserving ischemic penumbra. Some authors suggested the quality of CC could also impact recanalization. The purpose of this study is to test this hypothesis in patients who were treated with i.v. thrombolysis for MCA-M1 occlusion.
A normalized index derived from Tmax maps (MR-PWI) was defined to quantify the CC deficit (nCCD) in 64 patients with stroke who underwent i.v. thrombolysis. Correlations between nCCD and parameters that may be altered by CC quality were tested (baseline NIHSS, volume of diffusion abnormalities, modified Rankin Scale at 3 months). The correlation between baseline nCCD and MCA-M1 recanalization rate at 24 hours was tested.
The nCCD is significantly correlated with NIHSS and with lesional volume (Pearson correlation test, positive correlations, respectively, 0.40, 0.57; P = .00089, P = 8.7e-07). The nCCD also has a significant predictive value on the full recanalization at 24 hours that decreases as TTT increases (logistic regression, P = .021). Furthermore, among patients who were treated within 3 hours, nCCD and recanalization are significantly correlated (correlation ratio test, eta2 = 0.23, P = .0023): Patients who did not achieve full recanalization have significantly higher nCCD than fully recanalized patients (Mann-Whitney U test, P = .007). In addition, the probability of full recanalization decreases as the nCCD increases (P = .021). nCCD (OR 0.988, 95% CI 0.977-0.999, P = .042) and full recanalization at 24 hours (OR 4.539, 95% CI 1.252-16.456, P = .021) are independent predictors of functional independence at 3 months.
The nCCD index is a predictor of full MCA-M1 recanalization in patients treated with i.v. thrombolysis.
最近的研究强调了 CC 在保护缺血半暗带中的作用。一些作者还提出,CC 的质量也可能影响再通。本研究旨在测试该假说在接受静脉溶栓治疗 MCA-M1 闭塞的患者中是否成立。
在 64 例接受静脉溶栓治疗的卒中患者中,通过 Tmax 图(MR-PWI)定义了一个归一化指数来量化 CC 缺陷(nCCD)。测试了 nCCD 与可能因 CC 质量而改变的参数之间的相关性(基线 NIHSS、弥散异常体积、3 个月时改良 Rankin 量表)。还测试了基线 nCCD 与 24 小时时 MCA-M1 再通率之间的相关性。
nCCD 与 NIHSS 和病灶体积呈显著正相关(Pearson 相关检验,分别为 0.40,0.57;P=0.00089,P=8.7e-07)。nCCD 对 24 小时时完全再通也有显著的预测价值,随着 TTT 的增加而降低(logistic 回归,P=0.021)。此外,在 3 小时内接受治疗的患者中,nCCD 与再通呈显著相关性(相关比检验,eta2=0.23,P=0.0023):未达到完全再通的患者的 nCCD 明显高于完全再通的患者(Mann-Whitney U 检验,P=0.007)。此外,随着 nCCD 的增加,完全再通的概率降低(P=0.021)。nCCD(OR 0.988,95%CI 0.977-0.999,P=0.042)和 24 小时时的完全再通(OR 4.539,95%CI 1.252-16.456,P=0.021)是 3 个月时功能独立的独立预测因子。
nCCD 指数是接受静脉溶栓治疗的患者 MCA-M1 完全再通的预测因子。