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Prevalence of hemolytic specimens referred for arterial blood gas analysis.

机译:溶血标本的发生率用于动脉血气分析。

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Laboratory diagnostics is essential to clinical decision-making, assisting in the diagnosis, therapeutic drug monitoring and follow-up of the vast majority of human disorders. Nevertheless, laboratory testing is often delivered in a pressurized and complex environment, so that it appears to be no safer than other areas of diagnostics and healthcare. Although major efforts have been introduced for increasing both quality and safety throughout the total testing process over the past decades (1), there is evidence that laboratory errors still occur, especially in those processes that fall outside the direct jurisdiction of the laboratory personnel, and that conventionally belong to the "preanalytical phase" (2-4). Several studies have documented the burden and the type of preanalytical errors in different realities worldwide, but most of them have focused on errors related to clinical chemistry, immunochemistry, coagulation and hematological testing (5). Unfortunately, no reliable information has been provided to date on preanalytical errors related to arterial blood gas (ABG) analysis. In particular, considering that in vitro hemolysis is the leading source of unsuitable specimens in clinical laboratories (5), no data are available on the prevalence of hemolyzed specimens referred for ABG testing.
机译:实验室诊断对于临床决策,协助诊断,治疗药物监测以及对绝大多数人类疾病的随访至关重要。但是,实验室测试通常是在加压且复杂的环境中进行的,因此它似乎比诊断和医疗保健的其他领域更安全。尽管在过去几十年中为提高整个测试过程的质量和安全性做出了巨大努力(1),但有证据表明,实验室错误仍然会发生,尤其是那些不在实验室人员直接管辖范围内的过程,以及通常属于“分析前阶段”(2-4)。几项研究记录了全球不同现实中的分析错误的负担和类型,但大多数研究都集中在与临床化学,免疫化学,凝血和血液学检测有关的错误(5)。不幸的是,迄今为止,尚未提供有关与动脉血气(ABG)分析相关的分析前错误的可靠信息。特别是,考虑到体外溶血是临床实验室中不适当标本的主要来源(5),因此尚无用于ABG测试的溶血标本的患病率数据。

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