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A quick inexpensive laboratory method in acute paracetamol poisoning could improve risk assessment, management and resource utilization

机译:一种快速廉价的急性对乙酰氨基酚中毒实验室方法可以改善风险评估,管理和资源利用

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Objectives: Acute paracetamol poisoning is an emerging problem in Sri Lanka. Management guidelines recommend ingested dose and serum paracetamol concentrations to assess the risk. Our aim was to determine the usefulness of the patient's history of an ingested dose of >150 mg/kg and paracetamol concentration obtained by a simple colorimetric method to assess risk in patients with acute paracetamol poisoning. Materials and Methods: Serum paracetamol concentrations were determined in 100 patients with a history of paracetamol overdose using High Performance Liquid Chromatography (HPLC); (reference method). The results were compared to those obtained with a colorimetric method. The utility of risk assessment by reported dose ingested and colorimetric analysis were compared. Results: The area under the receiver operating characteristic curve for the history of ingested dose was 0.578 and there was no dose cut-off providing useful risk categorization. Both analytical methods had less than 5% intra-and inter-batch variation and were accurate on spiked samples. The time from blood collection to result was six times faster and ten times cheaper for colorimetry (30 minutes, US$2) than for HPLC (180 minutes, US$20). The correlation coefficient between the paracetamol levels by the two methods was 0.85. The agreement on clinical risk categorization on the standard nomogram was also good (Kappa = 0.62, sensitivity 81%, specificity 89%). Conclusions: History of dose ingested alone greatly over-estimated the number of patients who need antidotes and it was a poor predictor of risk. Paracetamol concentrations by colorimetry are rapid and inexpensive. The use of these would greatly improve the assessment of risk and greatly reduce unnecessary expenditure on antidotes.
机译:目的:急性对乙酰氨基酚中毒在斯里兰卡是一个新出现的问题。管理指南建议摄入剂量和血清对乙酰氨基酚浓度以评估风险。我们的目的是确定摄入剂量> 150 mg / kg的患者病史和通过简单比色法获得的对乙酰氨基酚浓度以评估急性对乙酰氨基酚中毒患者的风险的有用性。材料和方法:采用高效液相色谱法(HPLC)测定100名有扑热息痛过量史的患者的血清扑热息痛浓度; (参考方法)。将结果与通过比色法获得的结果进行比较。通过报告的摄入剂量和比色分析比较了风险评估的效用。结果:接收器工作特性曲线下的摄入剂量历史记录区域为0.578,并且没有剂量截止值可提供有用的风险分类。两种分析方法的批内和批间差异均小于5%,并且对加标样品的分析准确。比起HPLC(180分钟,US $ 20),从血液采集到结果的时间比色法(30分钟,US $ 2)快六倍,便宜十倍。两种方法中对乙酰氨基酚水平之间的相关系数为0.85。在标准诺模图上对临床风险分类的一致性也很好(Kappa = 0.62,敏感性81%,特异性89%)。结论:单独摄入剂量的病史大大高估了需要解毒剂的患者人数,这是风险的不良预测指标。通过比色法测定扑热息痛的浓度是快速且廉价的。使用这些将大大改善风险评估,并大大减少解毒剂的不必要支出。

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