评估中性粒细胞与淋巴细胞比率、血小板与淋巴细胞比率和全身免疫炎症指数,作为新生儿败血症的诊断指标。

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Journal of International Medical Research Pub Date : 2024-08-01 DOI:10.1177/03000605241270696
Shanshan Zhu, Qian Zhou, Zhonghua Hu, Junsheng Jiang
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引用次数: 0

摘要

目的评估作为新生儿败血症诊断指标的中性粒细胞与淋巴细胞比值(NLR)、血小板与淋巴细胞比值(PLR)和全身免疫炎症指数(SII):这项回顾性研究以患有败血症的新生儿和健康新生儿为对照。结果:共有 60 名新生儿患有败血症:结果:研究共涉及 60 名败血症新生儿和 60 名健康对照组。与对照组相比,败血症组的 NLR、PLR 和 SII 值较高。逻辑回归分析表明,NLR、PLR 和 SII 是新生儿败血症的独立风险因素。此外,接收器操作特征曲线(ROC)分析表明,NLR、PLR 和 SII 是预测新生儿败血症的可靠指标,其中 SII 的预测价值最高:结论:NLR、PLR 和 SII 似乎是预测新生儿败血症的有用指标。
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Assessment of neutrophil to lymphocyte ratio, platelet to lymphocyte ratio and systemic immune-inflammatory index, as diagnostic markers for neonatal sepsis.

Objective: To assess the neutrophil to lymphocyte ratio (NLR), platelet to lymphocyte ratio (PLR) and systemic immune-inflammatory index (SII), as diagnostic markers for neonatal sepsis.

Methods: This retrospective study involve neonates with sepsis and healthy neonates as controls. NLR, PLR, and SII were compared between groups.

Result: In total, 60 neonates with sepsis and 60 healthy controls were involved in the study. Compared with controls, the sepsis group had higher values for NLR, PLR and SII. Logistic regression analysis suggested that the NLR, PLR and SII were independent risk factors for neonatal sepsis. In addition, receiver operating characteristic (ROC) curve analysis indicated that the NLR, PLR and SII were reliable predictors of neonatal sepsis and SII had the best predictive value.

Conclusions: NLR, PLR and SII appear to be useful indicators for predicting neonatal sepsis.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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