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用于一氧化碳中毒院前分诊的便携式血气分析仪评估:仪器验证研究

Evaluation of a Portable Blood Gas Analyzer for Prehospital Triage in Carbon Monoxide Poisoning: Instrument Validation Study.

作者信息

Lyon Matthieu, Fehlmann Christophe Alain, Augsburger Marc, Schaller Thomas, Zimmermann-Ivol Catherine, Celi Julien, Gartner Birgit Andrea, Lorenzon Nicolas, Sarasin François, Suppan Laurent

机构信息

Division of Emergency Medicine, Department of Anesthesiology, Clinical Pharmacology, Intensive Care and Emergency Medicine, University of Geneva Hospitals and Faculty of Medicine, Geneva, Switzerland.

School of Epidemiology and Public Health, University of Ottawa, Ottawa, ON, Canada.

出版信息

JMIR Form Res. 2023 Oct 6;7:e48057. doi: 10.2196/48057.

Abstract

BACKGROUND

Carbon monoxide (CO) poisoning is an important cause of morbidity and mortality worldwide. Symptoms are mostly aspecific, making it hard to identify, and its diagnosis is usually made through blood gas analysis. However, the bulkiness of gas analyzers prevents them from being used at the scene of the incident, thereby leading to the unnecessary transport and admission of many patients. While multiple-wavelength pulse oximeters have been developed to discriminate carboxyhemoglobin (COHb) from oxyhemoglobin, their reliability is debatable, particularly in the hostile prehospital environment.

OBJECTIVE

The main objective of this pilot study was to assess whether the Avoximeter 4000, a transportable blood gas analyzer, could be considered for prehospital triage.

METHODS

This was a monocentric, prospective, pilot evaluation study. Blood samples were analyzed sequentially with 2 devices: the Avoximeter 4000 (experimental), which performs direct measurements on blood samples of about 50 µL by analyzing light absorption at 5 different wavelengths; and the ABL827 FLEX (control), which measures COHb levels through an optical system composed of a 128-wavelength spectrophotometer. The blood samples belonged to 2 different cohorts: the first (clinical cohort) was obtained in an emergency department and consisted of 68 samples drawn from patients admitted for reasons other than CO poisoning. These samples were used to determine whether the Avoximeter 4000 could properly exclude the diagnosis. The second (forensic) cohort was derived from the regional forensic center, which provided 12 samples from documented CO poisoning.

RESULTS

The mean COHb level in the clinical cohort was 1.7% (SD 1.8%; median 1.2%, IQR 0.7%-1.9%) with the ABL827 FLEX versus 3.5% (SD 2.3%; median 3.1%, IQR 2.2%-4.1%) with the Avoximeter 4000. Therefore, the Avoximeter 4000 overestimated COHb levels by a mean difference of 1.8% (95% CI 1.5%-2.1%). The consistency of COHb readings by the Avoximeter 4000 was excellent, with an intraclass correlation coefficient of 0.97 (95% CI 0.93-0.99) when the same blood sample was analyzed repeatedly. Using prespecified cutoffs (5% in nonsmokers and 10% in smokers), 3 patients (4%) had high COHb levels according to the Avoximeter 4000, while their values were within the normal range according to the ABL827 FLEX. Therefore, the specificity of the Avoximeter 4000 in this cohort was 95.6% (95% CI 87%-98.6%), and the overtriage rate would have been 4.4% (95% CI 1.4%-13%). Regarding the forensic samples, 10 of 12 (83%) samples were positive with both devices, while the 2 remaining samples were negative with both devices.

CONCLUSIONS

The limited difference in COHb level measurements between the Avoximeter 4000 and the control device, which erred on the side of safety, and the relatively low overtriage rate warrant further exploration of this device as a prehospital triage tool.

摘要

背景

一氧化碳(CO)中毒是全球发病和死亡的重要原因。症状大多是非特异性的,难以识别,其诊断通常通过血气分析进行。然而,气体分析仪体积庞大,无法在事故现场使用,从而导致许多患者被不必要地转运和收治。虽然已经开发出多波长脉搏血氧仪来区分碳氧血红蛋白(COHb)和氧合血红蛋白,但它们的可靠性存在争议,尤其是在恶劣的院前环境中。

目的

这项初步研究的主要目的是评估便携式血气分析仪Avoximeter 4000是否可用于院前分诊。

方法

这是一项单中心、前瞻性、初步评估研究。血液样本依次用两种设备进行分析:Avoximeter 4000(实验设备),通过分析5个不同波长的光吸收对约50微升血液样本进行直接测量;以及ABL827 FLEX(对照设备),通过由128波长分光光度计组成的光学系统测量COHb水平。血液样本属于两个不同的队列:第一个(临床队列)在急诊科获得,由68份从因非CO中毒入院的患者采集的样本组成。这些样本用于确定Avoximeter 4000是否能正确排除诊断。第二个(法医)队列来自地区法医中心,该中心提供了12份记录在案的CO中毒样本。

结果

使用ABL827 FLEX时,临床队列中COHb的平均水平为1.7%(标准差1.8%;中位数1.2%,四分位间距0.7%-1.9%),而使用Avoximeter 4000时为3.5%(标准差2.3%;中位数3.1%,四分位间距2.2%-4.1%)。因此,Avoximeter 4000高估了COHb水平,平均差异为1.8%(95%置信区间1.5%-2.1%)。当对同一血液样本进行重复分析时,Avoximeter 4000的COHb读数一致性极佳,组内相关系数为0.97(95%置信区间0.93-0.99)。根据预先设定的临界值(非吸烟者为5%,吸烟者为10%),根据Avoximeter 4000,3名患者(4%)的COHb水平较高,而根据ABL827 FLEX,他们的值在正常范围内。因此,该队列中Avoximeter 4000的特异性为95.6%(95%置信区间87%-98.6%),过度分诊率为4.4%(95%置信区间1.4%-13%)。关于法医样本,12份样本中有10份(83%)两种设备检测均为阳性,而其余2份样本两种设备检测均为阴性。

结论

Avoximeter 4000与对照设备在COHb水平测量上的差异有限,且偏向安全一方,同时过度分诊率相对较低,这使得有必要进一步探索将该设备用作院前分诊工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3164/10589834/5d2b6794413e/formative_v7i1e48057_fig1.jpg

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