全身免疫炎症指数作为预测急性肺栓塞的潜在生物标志物:系统综述

Andrew Suwadi, Kevin Tandarto, Sidhi Laksono
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引用次数: 0

摘要

背景急性肺栓塞(APE)是一种威胁生命的疾病,死亡率很高。其病理生理学涉及各种复杂的过程。全身免疫炎症指数(SII)是一种著名的生物标志物,它反映了促炎和抗炎免疫成分之间错综复杂的平衡。在这篇系统性综述中,我们旨在确定 SII 作为 APE 潜在生物标志物的意义。我们使用纽卡斯尔-渥太华量表(NOS)评估了偏倚风险。我们研究的结果包括院内和长期死亡率、APE 的严重程度以及 SII 预测 APE 的敏感性和特异性。这些研究讨论了 SII 在预测 APE 严重程度、APE 死亡率、高危 APE 和 APE 发生率方面的应用。SII 在预测上述每个变量方面都取得了重大成果。此外,每项研究都确定了不同的 SII 临界值。具体来说,截断值为 1161 时,预测大规模 APE 事件的灵敏度为 91%,特异度为 90%。>1235.35 临界值可区分高风险 APE,灵敏度为 87.32%,特异度为 68.85%。>1111x109 临界值可预测总死亡率,灵敏度为 72%,特异度为 51%。最后,以 1839.91 为临界值预测 APE 事件,灵敏度为 75.8%,特异度为 61.9%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systemic Immune-Inflammation Index as a Potential Biomarker for Predicting Acute Pulmonary Embolism: A Systematic Review.
BACKGROUND Acute pulmonary embolism (APE) is a life-threatening condition with a high mortality rate. The pathophysiology involves various complex processes. The systemic immune-inflammatory index (SII) is a well-known biomarker that reflects the intricate balance between pro-inflammatory and anti-inflammatory immune components. In this systematic review, we aim to determine the significance of SII as a potential biomarker for APE. METHOD We utilized PubMed, ProQuest, EBSCOHost, and Google Scholar to search for articles. We assessed bias risk using the Newcastle Ottawa Scale (NOS). The outcomes we examined included in-hospital and long-term mortality, the severity of APE, and the sensitivity and specificity of the SII in predicting APE. RESULTS Four studies, involving 2,038 patients, were included for analysis. These studies discuss the use of SII in predicting APE severity, APE mortality, high-risk APE, and the occurrence of APE. SII demonstrates significant results in predicting each of these variables. Furthermore, each study establishes different SII cut-off values. Specifically, a cut-off of 1161 predicts massive APE events with a sensitivity of 91% and a specificity of 90%. A cut-off of >1235.35 differentiates high-risk APE with a sensitivity of 87.32% and a specificity of 68.85%. A cut-off of >1111x109 predicts overall mortality with a sensitivity of 72% and a specificity of 51%. Finally, a cut-off at 1839.91 predicts APE events with a sensitivity of 75.8% and a specificity of 61.9%. CONCLUSION The SII can be employed as a potential new biomarker to predict outcomes in APE patients, particularly the occurrence, severity, and mortality of APE.
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