The predictive utility of cytokines, procalcitonin and C-reactive protein among febrile pediatric hematology and oncology patients with severe sepsis or septic shock.

IF 1.2 4区 医学 Q4 HEMATOLOGY Pediatric Hematology and Oncology Pub Date : 2024-01-01 Epub Date: 2023-07-15 DOI:10.1080/08880018.2023.2233567
Shu-Peng Lin, Xiao-Jun Xu, Chan Liao, Ning Zhao, Yuan-Yuan Chen, Hua Song, Wei-Qun Xu, Juan Liang, Di-Ying Shen, Jing-Ying Zhang, He-Ping Shen, Fen-Ying Zhao, Yong-Min Tang
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Abstract

Severe sepsis and septic shock are life-threatening for pediatric hematology and oncology patient receiving chemotherapy. Th1/Th2 cytokines, C-reactive protein (CRP), and procalcitonin (PCT) are all thought to be associated with disease severity. The aim of this study was to prospectively verify the utility of Th1/Th2 cytokines and compare them with PCT and CRP in the prediction of adverse outcomes. Data on patients were collected from January 1, 2011, to December 31, 2020. Blood samples were taken for Th1/Th2 cytokine, CRP, and PCT measurements at the initial onset of infection. Severe infection (SI) was defined as severe sepsis or septic shock. Th1/Th2 cytokine levels were determined by using flow cytometric bead array technology. In total, 7,735 febrile episodes were included in this study. For SI prediction, the AUCs of IL-6, IL-10 and TNF-α were 0.814, 0.805 and 0.624, respectively, while IL-6 and IL-10 had high sensitivity and specificity. IL-6 > 220.85 pg/ml and IL-10 > 29.95 pg/ml had high odds ratio (OR) values of approximately 3.5 in the logistic regression. Within the subgroup analysis, for bloodstream infection (BSI) prediction, the AUCs of IL-10 and TNF-α were 0.757 and 0.694, respectively. For multiorgan dysfunction syndrome (MODS) prediction, the AUC of CRP was 0.606. The AUC of PCT for mortality prediction was 0.620. In conclusion, IL-6 and IL-10 provide good predictive value for the diagnosis of SI. For children with SI, IL-10 and TNF-α are associated with BSI, while CRP and PCT are associated with MODS and death, respectively.

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细胞因子、降钙素原和 C 反应蛋白对严重败血症或脓毒性休克的发热儿科血液病和肿瘤病人的预测作用。
严重脓毒症和脓毒性休克对接受化疗的儿科血液病和肿瘤病人有生命危险。Th1/Th2细胞因子、C反应蛋白(CRP)和降钙素原(PCT)都被认为与疾病的严重程度有关。本研究旨在前瞻性地验证 Th1/Th2 细胞因子的效用,并将其与 PCT 和 CRP 在预测不良预后方面进行比较。研究收集了 2011 年 1 月 1 日至 2020 年 12 月 31 日期间的患者数据。在感染初期抽取血液样本进行 Th1/Th2 细胞因子、CRP 和 PCT 测量。严重感染(SI)定义为严重败血症或脓毒性休克。Th1/Th2细胞因子水平通过流式细胞计数珠阵列技术进行测定。本研究共纳入了 7735 例发热病例。在预测 SI 方面,IL-6、IL-10 和 TNF-α 的 AUC 分别为 0.814、0.805 和 0.624,而 IL-6 和 IL-10 具有较高的灵敏度和特异性。在逻辑回归中,IL-6 > 220.85 pg/ml和IL-10 > 29.95 pg/ml的几率比(OR)值高达约3.5。在亚组分析中,对于血流感染(BSI)预测,IL-10 和 TNF-α 的 AUC 分别为 0.757 和 0.694。在预测多器官功能障碍综合征(MODS)时,CRP 的 AUC 为 0.606。PCT 预测死亡率的 AUC 为 0.620。总之,IL-6 和 IL-10 对 SI 的诊断具有良好的预测价值。对于 SI 患儿,IL-10 和 TNF-α 与 BSI 相关,而 CRP 和 PCT 分别与 MODS 和死亡相关。
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来源期刊
CiteScore
2.60
自引率
5.90%
发文量
71
审稿时长
6-12 weeks
期刊介绍: PHO: Pediatric Hematology and Oncology covers all aspects of research and patient management within the area of blood disorders and malignant diseases of childhood. Our goal is to make PHO: Pediatric Hematology and Oncology the premier journal for the international community of clinicians and scientists who together aim to define optimal therapeutic strategies for children and young adults with cancer and blood disorders. The journal supports articles that address research in diverse clinical settings, exceptional case studies/series that add novel insights into pathogenesis and/or clinical care, and reviews highlighting discoveries and challenges emerging from consortia and conferences. Clinical studies as well as basic and translational research reports regarding cancer pathogenesis, genetics, molecular diagnostics, pharmacology, stem cells, molecular targeting, cellular and immune therapies and transplantation are of interest. Papers with a focus on supportive care, late effects and on related ethical, legal, psychological, social, cultural, or historical aspects of these fields are also appreciated. Reviews on important developments in the field are welcome. Articles from scientists and clinicians across the international community of Pediatric Hematology and Oncology are considered for publication. The journal is not dependent on or connected with any organization or society. All submissions undergo rigorous peer review prior to publication. Our Editorial Board includes experts in Pediatric Hematology and Oncology representing a wide range of academic and geographic diversity.
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