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Promising biomarkers for the prediction of catheter‐related venous thromboembolism in hospitalized children: An exploratory study

机译:有前途的生物标志物,用于预测住院儿童的导管相关静脉血栓栓塞,探索性研究

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Abstract Background Pediatric venous thromboembolism (VTE) has increased over the past 10 years, with central venous catheters (CVC) being the strongest risk factor. Current tools are not sufficient to predict VTE risk. The utility of biomarkers in predicting CVC‐related VTE has been minimally explored. Our objective is to determine the utility of microparticles (MPs), factor VIII (FVIII) activity, and thrombin generation (TG) in prospectively predicting VTE occurrence in hospitalized children with CVCs. Procedure In this nested case‐control pilot study, consecutive hospitalized children needing CVC placement (1 month to 21 years) were enrolled. Venous samples were collected prior to or within 24?h of CVC placement. MPs were measured using factor Xa initiated clot‐based assay. FVIII was measured using a one‐stage clot‐based assay. TG was measured using calibrated automated thrombogram. Results There were three CVC‐related VTE events (7%) in our cohort of 42 subjects. Xa clotting time (XaCT) ratio was lower (0.68 ± 0.07?vs 0.95 ± 0.21, P ?=?.4), while FVIII (461 ± 120?vs 267 ± 130, P ?=?.02), peak thrombin (418 ± 89?vs 211 ± 101, P ?=?.001), endogenous thrombin potential (ETP) (1828 ± 485?vs 1282 ± 394, P ?=?.03), and velocity index (VI) (182 ± 28?vs 75 ± 53, P ?=?.001) were higher in subjects with CVC‐related VTE compared to those without CVC‐related VTE. Sensitivity/specificity analysis revealed optimal cutoff values for XaCT ratio (0.75), FVIII (370), ETP (1680), peak (315), and VI (130), with receiver operating characteristic area under the curve values?0.9. Conclusion MPs, FVIII, and TG can potentially predict pediatric CVC‐related VTE in a prospective fashion. Stratification according to VTE risk may aid in guiding preventative efforts in future studies.
机译:摘要背景小子静脉血栓栓塞(VTE)在过去10年中增加,中央静脉导管(CVC)是最强的风险因素。目前的工具不足以预测VTE风险。探讨了生物标志物预测CVC相关VTE的效用。我们的目的是确定微粒(MPS),因子VIIII(FVIII)活性和凝血酶生成(TG)的效用,以预测CVC的住院儿童的VTE发生。在这种嵌套案例控制试验研究中,连续住院儿童需要CVC放置(1个月至21岁)。在CVC放置之前或在24μmH中收集静脉样品。使用因子Xa引发的基于克罗特的测定测量MPS。使用基于单级凝块的测定测量FVIII。使用校准的自动血栓图测量TG。结果我们的42个科目中有三个相关的相关VTE事件(7%)。 XA凝血时间(XACT)比率较低(0.68±0.07?vs 0.95±0.21,p?=Δ.4),而FVIII(461±120?与267±130,p?=β.02),峰凝血酶( 418±89?vs 211±101,p?=α.001),内源性凝血酶潜力(ETP)(1828±485〜1282±394,p?=Δ.03)和速度指数(VI)(182±与没有CVC相关VTE的人相比,28?= 75±53,p?= 001)与CVC相关VTE的受试者较高。灵敏度/特异性分析显示了XACT比率(0.75),FVIII(370),ETP(1680),峰(315)和VI(130)的最佳截止值,接收器在曲线值下的接收器操作特征区域?& 0.9。结论MPS,FVIII和TG可能以潜在的方式预测儿科CVC相关的VTE。根据VTE风险的分层可能有助于指导未来研究的预防努力。

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