中风引起的免疫抑制和吞咽困难独立预测中风相关肺炎——predict研究

S. Hoffmann, H. Harms, L. Ulm, D. Nabavi, B. Mackert, I. Schmehl, G. Jungehulsing, J. Montaner, A. Bustamante, M. Hermans, F. Hamilton, Jos Göhler, U. Malzahn, C. Malsch, P. Heuschmann, C. Meisel, A. Meisel
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引用次数: 130

摘要

卒中相关性肺炎是卒中后常见的并发症,预后较差。吞咽困难是卒中相关肺炎的已知危险因素,但越来越多的证据表明卒中诱导免疫抑制状态增加卒中相关肺炎的易感性。我们的目的是通过研究单核细胞HLA-DR表达作为免疫抑制标志物以及炎症(白细胞介素-6)和感染(脂多糖结合蛋白)的生物标志物的预测特性,证实卒中诱导的免疫抑制综合征与卒中相关性肺炎独立于吞咽困难相关。这是一项前瞻性、多中心研究,在德国和西班牙的11个研究地点,包括486例急性缺血性卒中患者。每日筛查卒中相关肺炎、吞咽困难和生物标志物。卒中相关性肺炎发生率为5.2%。在多变量回归分析中,吞咽困难和单核细胞HLA-DR下降是卒中相关肺炎的独立预测因子。肺炎的比例在单核细胞HLA-DR高四分位数(≥21876 mAb/细胞)中为0.9%,在低四分位数(≤12369 mAb/细胞)中为8.5%。出现吞咽困难时,肺炎的比例分别上升至5.9%和18.8%。没有吞咽困难和单核细胞HLA-DR表达正常的患者没有卒中相关肺炎的风险。我们证明吞咽困难和脑卒中引起的免疫抑制综合征是脑卒中相关肺炎的独立危险因素。免疫抑制和吞咽困难筛查可能有助于识别卒中相关性肺炎高危患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stroke-induced immunodepression and dysphagia independently predict stroke-associated pneumonia – The PREDICT study
Stroke-associated pneumonia is a frequent complication after stroke associated with poor outcome. Dysphagia is a known risk factor for stroke-associated pneumonia but accumulating evidence suggests that stroke induces an immunodepressive state increasing susceptibility for stroke-associated pneumonia. We aimed to confirm that stroke-induced immunodepression syndrome is associated with stroke-associated pneumonia independently from dysphagia by investigating the predictive properties of monocytic HLA-DR expression as a marker of immunodepression as well as biomarkers for inflammation (interleukin-6) and infection (lipopolysaccharide-binding protein). This was a prospective, multicenter study with 11 study sites in Germany and Spain, including 486 patients with acute ischemic stroke. Daily screening for stroke-associated pneumonia, dysphagia and biomarkers was performed. Frequency of stroke-associated pneumonia was 5.2%. Dysphagia and decreased monocytic HLA-DR were independent predictors for stroke-associated pneumonia in multivariable regression analysis. Proportion of pneumonia ranged between 0.9% in the higher monocytic HLA-DR quartile (≥21,876 mAb/cell) and 8.5% in the lower quartile (≤12,369 mAb/cell). In the presence of dysphagia, proportion of pneumonia increased to 5.9% and 18.8%, respectively. Patients without dysphagia and normal monocytic HLA-DR expression had no stroke-associated pneumonia risk. We demonstrate that dysphagia and stroke-induced immunodepression syndrome are independent risk factors for stroke-associated pneumonia. Screening for immunodepression and dysphagia might be useful for identifying patients at high risk for stroke-associated pneumonia.
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