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D-二聚体水平与急性缺血性卒中患者的预后、梗死面积及美国国立卫生研究院卒中量表评分相关。

D-dimer Level is Correlated with Prognosis, Infarct Size, and NIHSS in Acute Ischemic Stroke Patients.

作者信息

Abbas Nora I, Sayed Osama, Samir Sherif, Abeed Nashwa

机构信息

Critical Care Medicine Department, Faculty of Medicine, Cairo University, Cairo, Egypt.

出版信息

Indian J Crit Care Med. 2021 Feb;25(2):193-198. doi: 10.5005/jp-journals-10071-23744.

DOI:10.5005/jp-journals-10071-23744
PMID:33707899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7922437/
Abstract

UNLABELLED

Stroke ranks the fourth leading disease causing adult mortality and disability. D-dimer (D-D) is the ultimate product of plasmin-mediated degradation of fibrin-rich thrombi. D-D is a simple readily accessible biomarker employed within the diagnostic algorithms for the exclusion of venous thromboembolism. The correlation between D-D infarct size in MRI brain, APACHE II score, and the National Institute of Health Stroke Scale (NIHSS) score in critically ill acute stroke patients has not been fully investigated before.

OBJECTIVE

We aimed to investigate the diagnostic and prognostic value of elevated plasma D-D in critically ill patients admitted with acute cerebrovascular accidents. As far as we know, we are the first to investigate the correlation between plasma D-D levels and the ischemic lesion size in MRI brain and also APACHE II score and NIHSS in critically ill acute ischemic cerebrovascular patients.

SETTING AND PARTICIPANTS

A prospective, observational cohort study inside the Critical Care Medicine Department. Thirty patients with AIS were enrolled additionally to 1 healthy age- and sex-matched controls.

INTERVENTIONS

We employed particle-enhanced, immunoturbidimetric assay to detect plasma D-D concentrations. D-D levels D0 and D1 were measured upon admission and 24 hours later, respectively. We reviewed the patient' s health records; additionally, demographic, clinical, laboratory, and neuroimaging information was abstracted.

RESULTS

D-D concentrations were significantly higher in acute stroke patients compared to healthy controls. ROC curve analysis showed that elevated D-D level more than 310 ng/mL can predict infarct lesion size >1.5 cm in diffusion-weighted MRI brain with sensitivity and specificity (100 and 83%, respectively) and also admission D-D (D0) at cutoff concentration 350 ng/mL and D1 at cutoff value 370 ng/mL are predictors of complicated course with sensitivity and specificity (100 and 84.6%, respectively). There was no significant difference between D0 and D1 D-D levels (-value >0.05).

CONCLUSION

The plasma D-D biomarker can be a simple readily available test reliable predictor of infarct lesion size >1.5 cm in DW-MRI and outcome in union with the common practice instrumental tests.

HOW TO CITE THIS ARTICLE

Abbas NI, Sayed O, Samir S, Abeed N. D-dimer Level is Correlated with Prognosis, Infarct Size, and NIHSS in Acute Ischemic Stroke Patients. Indian J Crit Care Med 2021;25(2):193-198.

摘要

未标注

中风是导致成人死亡和残疾的第四大主要疾病。D - 二聚体(D - D)是纤溶酶介导的富含纤维蛋白血栓降解的最终产物。D - D是一种简单且易于获取的生物标志物,用于静脉血栓栓塞排除诊断算法中。此前,重症急性中风患者的D - D与MRI脑梗死大小、急性生理与慢性健康状况评分系统(APACHE II)评分以及美国国立卫生研究院卒中量表(NIHSS)评分之间的相关性尚未得到充分研究。

目的

我们旨在研究急性脑血管意外入院的重症患者血浆D - D升高的诊断和预后价值。据我们所知,我们是首个研究重症急性缺血性脑血管病患者血浆D - D水平与MRI脑缺血性病变大小、APACHE II评分以及NIHSS之间相关性的研究。

设置与参与者

在重症医学科进行的一项前瞻性观察队列研究。另外纳入30例急性缺血性卒中患者以及1名年龄和性别匹配的健康对照。

干预措施

我们采用颗粒增强免疫比浊法检测血浆D - D浓度。分别在入院时和24小时后测量D - D水平D0和D1。我们查阅了患者的健康记录;此外,提取了人口统计学、临床、实验室和神经影像学信息。

结果

与健康对照相比,急性卒中患者的D - D浓度显著更高。ROC曲线分析表明,D - D水平升高超过310 ng/mL可预测扩散加权MRI脑梗死病变大小>1.5 cm,敏感性和特异性分别为100%和83%,入院时D - D(D0)截断浓度为350 ng/mL以及D1截断值为370 ng/mL是病情复杂的预测指标,敏感性和特异性分别为100%和84.6%。D0和D1的D - D水平之间无显著差异(P值>0.05)。

结论

血浆D - D生物标志物可以是一种简单易用的检测方法,是DW - MRI中梗死病变大小>1.5 cm以及联合常规器械检查结果的可靠预测指标。

如何引用本文

Abbas NI, Sayed O, Samir S, Abeed N. D - 二聚体水平与急性缺血性卒中患者的预后、梗死大小及NIHSS相关。《印度重症医学杂志》2021;25(2):193 - 198。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a977/7922437/7defa47e6bf2/ijccm-25-193-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a977/7922437/22ed2be6d651/ijccm-25-193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a977/7922437/b3d2831e4c70/ijccm-25-193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a977/7922437/7defa47e6bf2/ijccm-25-193-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a977/7922437/22ed2be6d651/ijccm-25-193-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a977/7922437/b3d2831e4c70/ijccm-25-193-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a977/7922437/7defa47e6bf2/ijccm-25-193-g003.jpg

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