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Analysis of a novel field dilution method for testing samples that exceed the analytic range of point-of-care blood lead analyzers

机译:分析一种新的现场稀释方法,用于检测超出现场即时血铅分析仪分析范围的样品

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Investigators developed and evaluated a dilution method for the LeadCare II analyzer (LCII) for blood lead levels > 65 (.ig/dL, the analyzer's maximum reporting value. Venous blood samples from lead-poisoned children were initially analyzed in the field using the dilution method. Split samples were analyzed at the US Centers for Disease Control and Prevention (CDC) laboratory using both the dilution method and inductively coupled plasma-mass spectrometry (ICP-MS). The concordance correlation coefficient of CDC LCII vs. ICP-MS values (N= 211) was 0.976 (95% confidence interval (CI) 0.970-0.981); of Field LCII vs. ICP-MS (N= 68) was 0.910 (95% CI 0.861-0.942), and CDC LCII vs. Field LCII (N=53) was 0.721 (95% CI 0.565-0.827). Sixty percent of CDC and 54 % of Field LCII values were within ±10 % of the ICP-MS value. Results from the dilution method approximated ICP-MS values and were useful for field-based decision-making. Specific recommendations for additional evaluation are provided.
机译:研究人员开发并评估了LeadCare II分析仪(LCII)的血铅水平> 65(.ig / dL,分析仪的最大报告值)的稀释方法。最初使用稀释液在现场对铅中毒儿童的静脉血样本进行了分析方法:使用稀释方法和电感耦合等离子体质谱法(ICP-MS)在美国疾病控制与预防中心(CDC)实验室分析分离的样品,CDC LCII与ICP-MS值的一致性相关系数(N = 211)为0.976(95%置信区间(CI)0.970-0.981);现场LCII与ICP-MS(N = 68)为0.910(95%CI 0.861-0.942),而CDC LCII与现场LCII(N = 53)为0.721(95%CI 0.565-0.827)。CDC的60%和Field LCII值的54%在ICP-MS值的±10%之内。稀释法得出的结果近似于ICP-MS值并为基于现场的决策提供了帮助,并提供了用于进一步评估的具体建议。

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