Antoniazzi Aldana M, Unda Santiago R, Klyde Daniel M, Miller Raphael, Lam Sharon, Fluss Rose, Altschul David J
Neurological Surgery, Montefiore Medical Center, New York, USA.
Neurological Surgery, Montefiore Medical Center, Bronx, USA.
Cureus. 2021 May 11;13(5):e14973. doi: 10.7759/cureus.14973.
Hemorrhage transformation (HT) is a known complication of arterial ischemic stroke (AIS). In addition, it is known that the increase of proinflammatory immune cells in the brain tissue after AIS predict worse outcomes. However, it is not clear whether inflammation due to preceding or post-stroke infections affect outcomes and moreover, if systemic inflammatory markers could be useful as a clinical prediction tool for HT post-stroke. Therefore, our objective was to assess the association between systemic pro-inflammatory profile in AIS patients with HT and in-hospital mortality that did not course with acute infections during hospitalization.
This study was conducted using the 2016 and 2017 National Inpatient Sample (NIS) with International Classification of Diseases (ICD-10) codes. Multivariate logistic regression was used to examine the association between HT and in-hospital mortality with pro-inflammatory anomalies of white blood cells (WBCs) in AIS patients. Exclusion criteria comprised patients with under 18 years old, and with a diagnosis of gastrointestinal, urogenital, respiratory infection, bacteremia, viral infection, sepsis, or fever.
A total of 212,356 patients with AIS were included in the analysis. 422 (0.2%) patients had a HT and 10,230 (4.8%) patients died during hospitalization. The most common WBC pro-inflammatory marker was leukocytosis with 6.9% (n=29/422) of HT and 5.5% (n=560/10,230) of patients that died during hospitalization. After adjusting for socio-demographic, comorbidities and treatment factors, leukocytosis was found to be an independent risk factor for both outcomes, HT [OR = 1.5, 95% CI: 1-2.3, p=0.024] and, in-hospital mortality [OR = 1.5, 95% CI: 1.3-1.6, p < 0.001].
Sterile leukocytosis is a potential clinical prediction tool to determine which patients are at higher risk of developing HT and die during hospitalization.
出血转化(HT)是动脉缺血性卒中(AIS)的一种已知并发症。此外,已知AIS后脑组织中促炎免疫细胞增加预示着更差的预后。然而,尚不清楚卒中前或卒中后感染引起的炎症是否会影响预后,以及全身炎症标志物是否可作为卒中后HT的临床预测工具。因此,我们的目的是评估AIS患者中全身促炎状态与HT及住院期间未并发急性感染的住院死亡率之间的关联。
本研究使用2016年和2017年全国住院患者样本(NIS)及国际疾病分类(ICD - 10)编码进行。多变量逻辑回归用于检验AIS患者中HT及住院死亡率与白细胞(WBC)促炎异常之间的关联。排除标准包括18岁以下患者,以及诊断为胃肠道、泌尿生殖道、呼吸道感染、菌血症、病毒感染、脓毒症或发热的患者。
共有212,356例AIS患者纳入分析。422例(0.2%)患者发生HT,10,230例(4.8%)患者在住院期间死亡。最常见的WBC促炎标志物是白细胞增多,HT患者中有6.9%(n = 29/422),住院期间死亡患者中有5.5%(n = 560/10,230)。在调整社会人口统计学、合并症和治疗因素后,发现白细胞增多是两种结局的独立危险因素,即HT [比值比(OR)= 1.5,95%置信区间(CI):1 - 2.3,p = 0.024]以及住院死亡率[OR = 1.5,95% CI:1.3 - 1.6,p < 0.001]。
无菌性白细胞增多是一种潜在的临床预测工具,可用于确定哪些患者发生HT及住院期间死亡的风险更高。