Department of Pediatrics and Intensive Care, 42705Fundación Cardioinfantil-Instituto de Cardiología, Universidad de La Sabana, Bogotá, Colombia.
113097Universidad CES Graduate School, Medellín, Colombia.
J Intensive Care Med. 2023 Jan;38(1):95-105. doi: 10.1177/08850666221109186. Epub 2022 Jun 19.
Sepsis is one of the main causes of morbidity and mortality worldwide. Microcirculatory impairment, especially damage to the endothelium and glycocalyx, is often not assessed. The objective of this systematic review and meta-analysis was to summarize the available evidence of the risk of unsatisfactory outcomes in patients with sepsis and elevated glycocalyx injury and endothelial activation biomarkers.
A systematic search was carried out on PubMed/MEDLINE, Embase, Cochrane and Google Scholar up to December 31, 2021, including studies in adults and children with sepsis which measured glycocalyx injury and endothelial activation biomarkers within 48 hours of hospital admission. The primary outcome was the risk of mortality from all causes and the secondary outcomes were the risk of developing respiratory failure (RF) and multiple organ dysfunction syndrome (MODS) in patients with elevations of these biomarkers.
A total of 17 studies (3,529 patients) were included: 11 evaluated syndecan-1 (n=2,397) and 6 endocan (n=1,132). Syndecan-1 was higher in the group of patients who died than in those who survived [255 ng/mL (IQR: 139-305) vs. 83 ng/mL (IQR:40-111); p=0.014]. Patients with elevated syndecan-1 had a greater risk of death (OR 2.32; 95% CI 1.89, 3.10: p<0.001), MODS (OR 3.3; 95% CI 1.51, 7.25: p=0.003;), or RF (OR 7.53; 95% CI 1.86-30.45: p=0.005). Endocan was higher in patients who died [3.1 ng/mL (IQR 2.3, 3.7) vs. 1.62 ng/mL (IQR 1.2, 5.7); OR 9.53; 95% CI 3.34, 27.3; p<0.001], who had MODS (OR 8.33; 95% CI 2.07, 33.58; p=0.003) and who had RF (OR 9.66; 95% CI 2.26, 43.95; p=0.002).
Patients with sepsis and abnormal glycocalyx injury and endothelial activation biomarkers have a greater risk of developing respiratory failure, multiple organ failure, and death. Microcirculatory impairment should be routinely evaluated in patients with sepsis, using biomarkers to stratify risk groups.
脓毒症是全球发病率和死亡率的主要原因之一。微循环损伤,尤其是内皮细胞和糖萼的损伤,往往未被评估。本系统评价和荟萃分析的目的是总结脓毒症患者糖萼损伤和内皮激活生物标志物升高与不良结局风险相关的现有证据。
系统检索了 PubMed/MEDLINE、Embase、Cochrane 和 Google Scholar 数据库,截至 2021 年 12 月 31 日,纳入了评估脓毒症成人和儿童患者糖萼损伤和内皮激活生物标志物的研究,这些标志物在入院后 48 小时内进行了测量。主要结局是所有原因导致的死亡率风险,次要结局是这些生物标志物升高的患者发生呼吸衰竭(RF)和多器官功能障碍综合征(MODS)的风险。
共纳入 17 项研究(3529 例患者):11 项研究评估了 syndecan-1(n=2397),6 项研究评估了 endocan(n=1132)。死亡组患者的 syndecan-1 水平高于存活组[255ng/mL(IQR:139-305)vs. 83ng/mL(IQR:40-111);p=0.014]。高水平 syndecan-1 的患者死亡风险更高(OR 2.32;95%CI 1.89,3.10:p<0.001)、MODS(OR 3.3;95%CI 1.51,7.25:p=0.003)或 RF(OR 7.53;95%CI 1.86-30.45:p=0.005)的风险更高。死亡患者的 endocan 水平更高[3.1ng/mL(IQR:2.3,3.7)vs. 1.62ng/mL(IQR:1.2,5.7);OR 9.53;95%CI 3.34,27.3;p<0.001],MODS(OR 8.33;95%CI 2.07,33.58;p=0.003)和 RF(OR 9.66;95%CI 2.26,43.95;p=0.002)的风险更高。
脓毒症患者糖萼损伤和内皮激活生物标志物异常与呼吸衰竭、多器官衰竭和死亡风险增加相关。应使用生物标志物对脓毒症患者进行常规的微循环损伤评估,以对风险组进行分层。