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印度一家公立医院临床化学实验室的分析前误差发生率。

Preanalytical error occurrence rate in clinical chemistry laboratory of a public hospital in India.

作者信息

Singla Parul, Parkash Anuj Anand, Bhattacharjee Jayshree

机构信息

Department of Biochemistry, Lady Hardinge Medical College & S.S.K. Hospital, New Delhi, India.

出版信息

Clin Lab. 2011;57(9-10):749-52.

Abstract

BACKGROUND

The pre and post analytical phase in a testing cycle contributes up to 93% of total laboratory errors. Hence, it is of utter importance for the laboratory to study error occurrence rates during the testing cycle and implement a quality improvement plan to release an accurate result.

METHODS

The present study was conducted during the period 2008 - 2009 in the clinical biochemistry lab in Lady Hardinge Medical College and associated hospitals. During a 6 month period 32,589 samples were monitored for major preanalytical problems at the receiving counter of the laboratory.

RESULTS

Out of all laboratory problems, up to 61% are associated with the preanalytical phase in the lab. Out of this, 33% of the errors are associated with the test request forms, 18% errors with sample collection in glass vials, and 3% errors associated with sample processing in the laboratory. As per Quality Improvement policy of the lab, a closed blood evacuation system (vacutainers) has been implemented for sample collection. Post implementation, preanalytical error rate has been reduced to 48%, however, tube filling errors still remain the major problem noted.

CONCLUSIONS

Based on these observations, transcription errors related to test request forms is of great concern and needs corrective measures via proper educational programs. If this area is compromised it can lead to adverse patient outcome. However, with the use of vacutainers a better specimen quality and health care worker safety is achieved. It also decreases inconvenience to the patient.

摘要

背景

检测周期中的分析前和分析后阶段占实验室总误差的93%。因此,对于实验室来说,研究检测周期中的误差发生率并实施质量改进计划以发布准确结果至关重要。

方法

本研究于2008年至2009年期间在哈丁夫人医学院及相关医院的临床生物化学实验室进行。在6个月的时间里,在实验室接收柜台对32589份样本的主要分析前问题进行了监测。

结果

在所有实验室问题中,高达61%与实验室的分析前阶段有关。其中,33%的误差与检测申请表有关,18%的误差与玻璃小瓶中的样本采集有关,3%的误差与实验室中的样本处理有关。根据实验室的质量改进政策,已实施封闭式血液采集系统(真空采血管)进行样本采集。实施后,分析前误差率已降至48%,然而,试管灌装误差仍然是主要问题。

结论

基于这些观察结果,与检测申请表相关的转录错误备受关注,需要通过适当的教育计划采取纠正措施。如果这一领域出现问题,可能会导致患者不良后果。然而,使用真空采血管可以提高样本质量,保障医护人员安全。它还减少了患者的不便。

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