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床边即时检测在危急重症患者中的准确性。

Accuracy of bedside point of care testing in critical emergency department patients.

机构信息

Department of Emergency Medicine, Stony Brook University, Stony Brook, NY, United States.

Department of Clinical Pathology, Stony Brook University, Stony Brook, NY, United States.

出版信息

Am J Emerg Med. 2018 Apr;36(4):567-570. doi: 10.1016/j.ajem.2017.09.018. Epub 2017 Sep 14.

Abstract

BACKGROUND

Point-of-care (POC) testing reduces laboratory turn-around having the potential to improve timely diagnosis and management. We compared the accuracy of nurse performed POC and core laboratory testing and determined whether deviations between the two were clinically meaningful.

METHODS

We performed a prospective, observational study on a convenience sample of 50 critical care ED patients in whom a POC chemistry and hematocrit was ordered. Blood samples were divided into 2 aliquots; one sample was tested by the treating nurse using a handheld POC device and the other sample was tested in the core laboratory. Paired comparisons of test results were performed using Pearson's correlation coefficients, Lin concordance coefficients, and Bland Altman plots.

RESULTS

Mean patient age was 67, 50% were male, 82% were admitted. Pearson's correlation and Lin concordance coefficients were excellent (0.84-1.00) for all 8 analytes. Mean (95%CI) paired differences between POC and core laboratory measurements were Na 0.30 (-0.22 to 0.82) mmol/L, K-0.12 (-0.14 to - 0.09) mmol/L, Cl 2.10 (1.41 to 2.78) mmol/L, TCO-1.68 (-2.06 to -1.30) mmol/L, glucose 2.46 (1.46 to 3.46) mg/dL, BUN, 1.69 (0.95 to 2.42) mg/dL, creatinine 0.13 (0.08 to 0.17) mg/dL, and hematocrit -0.39 (-0.93 to 0.15) %. In 3 of 400 measurements, the difference between POC and core lab exceeded the maximal clinically acceptable deviation based on physician surveys.

CONCLUSIONS

Bedside POC by ED nurses is reliable and accurate and does not deviate significantly from core laboratory testing by trained technicians.

摘要

背景

即时检测(POC)可减少实验室检测周转时间,从而有可能改善及时诊断和管理。我们比较了护士进行的即时检测和核心实验室检测的准确性,并确定两者之间的差异是否具有临床意义。

方法

我们对便利样本中的 50 例重症监护 ED 患者进行了前瞻性、观察性研究,这些患者的即时检测需要进行化学和血细胞比容检测。将血液样本分成 2 份样本;一份样本由主治护士使用手持式即时检测设备进行检测,另一份样本在核心实验室进行检测。使用 Pearson 相关系数、Lin 一致性系数和 Bland-Altman 图对测试结果进行配对比较。

结果

患者平均年龄为 67 岁,50%为男性,82%为入院患者。所有 8 种分析物的 Pearson 相关系数和 Lin 一致性系数均为优秀(0.84-1.00)。POC 和核心实验室测量之间的平均(95%CI)配对差异为:Na 0.30(-0.22 至 0.82)mmol/L,K-0.12(-0.14 至-0.09)mmol/L,Cl 2.10(1.41 至 2.78)mmol/L,TCO-1.68(-2.06 至-1.30)mmol/L,葡萄糖 2.46(1.46 至 3.46)mg/dL,BUN 1.69(0.95 至 2.42)mg/dL,肌酐 0.13(0.08 至 0.17)mg/dL,血细胞比容-0.39(-0.93 至 0.15)%。在 400 次测量中的 3 次中,POC 和核心实验室之间的差异超过了根据医生调查确定的最大临床可接受偏差。

结论

ED 护士床边即时检测可靠准确,与训练有素的技术人员的核心实验室检测无显著差异。

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