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在急性门诊环境中,三种即时护理静脉血检测平台的分析前误差:一项混合方法服务评估。

Pre-analytical error for three point of care venous blood testing platforms in acute ambulatory settings: A mixed methods service evaluation.

机构信息

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.

Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.

出版信息

PLoS One. 2020 Feb 3;15(2):e0228687. doi: 10.1371/journal.pone.0228687. eCollection 2020.

Abstract

INTRODUCTION

Point of care blood testing to aid diagnosis is becoming increasingly common in acute ambulatory settings and enables timely investigation of a range of diagnostic markers. However, this testing allows scope for errors in the pre-analytical phase, which depends on the operator handling and transferring specimens correctly. The extent and nature of these pre-analytical errors in clinical settings has not been widely reported.

METHODS

We carried out a convergent parallel mixed-methods service evaluation to investigate pre-analytical errors leading to a machine error reports in a large acute hospital trust in the UK. The quantitative component comprised a retrospective analysis of all recorded error codes from Abbott Point of Care i-STAT 1, i-STAT Alinity and Abbott Rapid Diagnostics Afinion devices to summarise the error frequencies and reasons for error, focusing on those attributable to the operator. The qualitative component included a prospective ethnographic study and a secondary analysis of an existing ethnographic dataset, based in hospital-based ambulatory care and community ambulatory care respectively.

RESULTS

The i-STAT had the highest usage (113,266 tests, January 2016-December 2018). As a percentage of all tests attempted, its device-recorded overall error rate was 6.8% (95% confidence interval 6.6% to 6.9%), and in the period when reliable data could be obtained, the operator-attributable error rate was 2.3% (2.2% to 2.4%). Staff identified that the most difficult step was the filling of cartridges, but that this could be improved through practice, with a perception that cartridge wastage through errors was rare.

CONCLUSIONS

In the observed settings, the rate of errors attributable to operators of the primary point of care device was less than 1 in 40. In some cases, errors may lead to a small increase in resource use or time required so adequate staff training is necessary to prevent adverse impact on patient care.

摘要

介绍

在急性门诊环境中,床边即时检测(POCT)辅助诊断的应用越来越普遍,这使得及时检测一系列诊断标志物成为可能。然而,这种检测为分析前阶段的错误提供了空间,而分析前阶段的准确性取决于操作人员是否正确处理和转移样本。目前尚未广泛报道临床环境中这些分析前错误的程度和性质。

方法

我们采用收敛平行混合方法进行了服务评估,以调查英国一家大型急性医院信托中导致机器错误报告的分析前错误。定量部分包括对 Abbott Point of Care i-STAT 1、i-STAT Alinity 和 Abbott Rapid Diagnostics Afinion 设备所有记录的错误代码进行回顾性分析,以总结错误频率和原因,重点关注归因于操作人员的错误。定性部分包括前瞻性民族志研究和对分别基于医院门诊和社区门诊的现有民族志数据集的二次分析。

结果

i-STAT 的使用率最高(2016 年 1 月至 2018 年 12 月期间进行了 113,266 次测试)。按所有尝试测试的百分比计算,其设备记录的总错误率为 6.8%(95%置信区间为 6.6%至 6.9%),在可获得可靠数据的期间,归因于操作人员的错误率为 2.3%(2.2%至 2.4%)。工作人员发现最困难的步骤是加样,但通过练习可以提高这一步骤的熟练度,并且他们认为因错误而导致的试剂盒浪费很少。

结论

在所观察的环境中,归因于主要 POCT 设备操作人员的错误率低于每 40 次 1 次。在某些情况下,错误可能会导致资源使用或所需时间略有增加,因此需要进行充分的员工培训,以防止对患者护理产生不利影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/6996845/acfd301e05a9/pone.0228687.g001.jpg

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