Analytical performance specifications and quality assurance of point-of-care testing in primary healthcare.

IF 6.6 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY Critical reviews in clinical laboratory sciences Pub Date : 2024-05-01 Epub Date: 2023-10-01 DOI:10.1080/10408363.2023.2262029
Anne Stavelin, Sverre Sandberg
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引用次数: 0

Abstract

Point-of-care testing (POCT) is the fastest-growing segment of laboratory medicine. This review focuses on the essential aspects of setting analytical performance specifications (APS) and performing quality assurance for POCT in primary healthcare. In-vitro diagnostic medical devices for POCT are typically small and easy to operate. Users often have little to no laboratory experience and may not necessarily see the value of conducting quality assurance on their devices. Therefore, training, guidance, and motivation should be integral parts of the total quality management system, as they are vital for managing errors and ensuring reliable results. It is common to believe that the analytical quality of POCT should be comparable to that of laboratory testing, and as a result, APS should be the same. This paper challenges this concept. The APS for POCT can often be less stringent compared to those used in a central laboratory because the requester is closer to both the analytical and clinical situation. Point-of-care instruments should be selected based on clinical needs, the required analytical quality and user-friendliness in the intended usage setting.Quality assurance should include both internal quality control (IQC) and external quality assessment (EQA). It is recommended that IQC protocols should be dependent on the complexity of the POCT device. A scoring system to determine how frequent IQC should be analyzed in primary healthcare on different types of POCT devices has been suggested. The main challenge in EQA for POCT involves using suitable control materials that reflect instrument performance on patient samples. Obtaining commutable control materials for POCT is difficult since the matrix often is whole blood. An essential aspect of EQA for POCT is that feedback reports should be easily interpretable. Users should receive advice from the EQA organizer regarding the root causes of deviating results. Quality assurance for POCT is not an easy task and presents numerous challenges. However, there is evidence that quality assurance improves the quality of POCT measurements and, consequently, can enhance patient outcomes.

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初级保健中护理点检测的分析性能规范和质量保证。
护理点检测(POCT)是实验室医学发展最快的领域。这篇综述的重点是在初级保健中制定分析性能规范(APS)和执行POCT质量保证的基本方面。用于POCT的体外诊断医疗设备通常很小并且易于操作。用户通常几乎没有实验室经验,也不一定看到对其设备进行质量保证的价值。因此,培训、指导和激励应该是全面质量管理体系的组成部分,因为它们对于管理错误和确保可靠的结果至关重要。人们普遍认为,POCT的分析质量应与实验室测试的分析质量相当,因此,APS应相同。本文对这一概念提出了挑战。与中央实验室使用的APS相比,POCT的APS通常不那么严格,因为请求者更接近分析和临床情况。应根据临床需求、所需的分析质量和预期使用环境中的用户友好性来选择护理点仪器。质量保证应包括内部质量控制(IQC)和外部质量评估(EQA)。建议IQC协议应取决于POCT设备的复杂性。有人提出了一种评分系统,以确定在不同类型的POCT设备上的初级医疗保健中应分析IQC的频率。POCT在EQA中的主要挑战涉及使用合适的对照材料,以反映患者样本的仪器性能。获得用于POCT的可换向控制材料是困难的,因为基质通常是全血。POCT EQA的一个重要方面是反馈报告应该易于解释。用户应收到EQA组织者关于偏离结果的根本原因的建议。POCT的质量保证不是一项容易的任务,它带来了许多挑战。然而,有证据表明,质量保证可以提高POCT测量的质量,从而提高患者的预后。
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来源期刊
CiteScore
20.00
自引率
0.00%
发文量
25
审稿时长
>12 weeks
期刊介绍: Critical Reviews in Clinical Laboratory Sciences publishes comprehensive and high quality review articles in all areas of clinical laboratory science, including clinical biochemistry, hematology, microbiology, pathology, transfusion medicine, genetics, immunology and molecular diagnostics. The reviews critically evaluate the status of current issues in the selected areas, with a focus on clinical laboratory diagnostics and latest advances. The adjective “critical” implies a balanced synthesis of results and conclusions that are frequently contradictory and controversial.
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