automated testing

自动化测试
  • 文章类型: Journal Article
    表面增强拉曼散射(SERS)技术,作为一种重要的分析工具,在化学和生物医学传感领域有着广泛的应用。自动测试通常与生化分析技术相结合,以缩短检测时间并最大程度地减少人为错误。目前用于样品检测的SERS基底耗时且容易受到高人为误差的影响。不利于SERS与自动化测试的结合。这里,一种新颖的蜂巢式SERS微阵列设计用于唾液样品中尿素酶的大面积自动化测试,以缩短检测时间并最大程度地减少人为错误。蜂巢风格的SERS微阵列装饰有六边形微孔和均匀分布的银纳米星。与其他四种常见的SERS基底相比,最佳的蜂巢式SERS微阵列表现出最佳的SERS性能。连续采集唾液样本的100个SERS光谱的RSD为6.56%,并且一次检测的时间从5分钟减少到10秒。SERS强度和脲酶浓度之间的R2为0.982,存在值得注意的线性关系。表明唾液样品中脲酶活性的定量检测能力。蜂巢风格的SERS微阵列,结合自动化测试,为SERS技术在生物医学领域的广泛应用提供了新的途径。
    Surface-enhanced Raman scattering (SERS) technology, as an important analytical tool, has been widely applied in the field of chemical and biomedical sensing. Automated testing is often combined with biochemical analysis technologies to shorten the detection time and minimize human error. The present SERS substrates for sample detection are time-consuming and subject to high human error, which are not conducive to the combination of SERS and automated testing. Here, a novel honeycomb-inspired SERS microarray is designed for large-area automated testing of urease in saliva samples to shorten the detection time and minimize human error. The honeycomb-inspired SERS microarray is decorated with hexagonal microwells and a homogeneous distribution of silver nanostars. Compared with the other four common SERS substrates, the optimal honeycomb-inspired SERS microarray exhibits the best SERS performance. The RSD of 100 SERS spectra continuously collected from saliva samples is 6.56%, and the time of one detection is reduced from 5 min to 10 s. There is a noteworthy linear relationship with a R2 of 0.982 between SERS intensity and urease concentration, indicating the quantitative detection capability of the urease activity in saliva samples. The honeycomb-inspired SERS microarray, combined with automated testing, provides a new way in which SERS technology can be widely used in biomedical applications.
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  • 文章类型: Journal Article
    我们先前证明了符号数字模态测试(VR-SDMT)的全自动语音识别模拟的收敛有效性,用于评估多发性硬化症(pwMS)患者的处理速度。
    我们的目标是在54pwMS和18个健康对照(HC)中复制这些结果,展示了VR-SDMT的可靠性。
    在多发性硬化症(MS)(r=-0.771,p<0.001)和HC(r=-0.785,p<0.001)组中,VR-SDMT与传统口服SDMT之间存在显着相关性。
    统称为,我们的两项研究证明了VR-SDMT评估pwMS处理速度的可靠性和有效性.
    UNASSIGNED: We previously demonstrated the convergent validity of a fully automated voice recognition analogue of the Symbol Digit Modalities Test (VR-SDMT) for evaluating processing speed in people with multiple sclerosis (pwMS).
    UNASSIGNED: We aimed to replicate these results in 54 pwMS and 18 healthy controls (HCs), demonstrating the VR-SDMT\'s reliability.
    UNASSIGNED: Significant correlations were found between the VR-SDMT and the traditional oral SDMT in the multiple sclerosis (MS) (r = -0.771, p < 0.001) and HC (r = -0.785, p < 0.001) groups.
    UNASSIGNED: Taken collectively, our two studies demonstrate the reliability and validity of the VR-SDMT for assessing processing speed in pwMS.
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  • 文章类型: English Abstract
    呼吸机是一种重要的人工替代自主通气功能的医疗器械。其安全性和可靠性关系到患者的健康乃至生命安全。随着呼吸机新国家标准和国际标准的发布,对检测和评价提出了更高的要求。本研究主要介绍了一种呼吸机性能自动测试系统。该测试系统是基于PF-300气流分析仪Imtmedical和标准模拟肺。开发了模拟肺自动开关模块,利用基于Python的软件开发平台设计了呼吸机自动测试系统。它不仅可以自动测试呼吸机的所有通风控制参数和监测参数,还可以实现数据的自动记录,表单报告和数据分析,提高检查效率和质量,检测和质量控制。
    Ventilator is an important medical instrument which can replace the function of autonomous ventilation artificially. Its safety and reliability are related to the health and even life safety of patients. With the publishing of the new national standard and international standard for ventilators, higher requirements are put forward for the detection and evaluation. This study mainly introduces an automatic test system for ventilator performance. The test system is based on PF-300 air-flow analyzer of Imtmedical and standard simulation lung. The automatic switch module of simulation lung is developed, and the automatic test system of ventilator is designed using the software development platform based on Python. It can not only automatically test all ventilation control parameters and monitoring parameters of the ventilator, but also realize automatic data recording, form reports and data analysis, and improve the efficiency and quality of inspection, detection and quality control.
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  • 文章类型: Journal Article
    传统上,非人类灵长类动物的认知灵活性是通过概念集转移任务(CSST)来衡量的。在我们的实验室里,几内亚狒狒(N=24)在大约10年的时间内通过CSST任务进行了连续测试。我们的任务涉及在触摸屏上呈现三种刺激,所有刺激都由3种可能的颜色和3种形状制成。受试者必须触摸包含刺激维度的刺激(例如,绿色)一直得到奖励,直到刺激维度发生变化。分析坚持的反应,在过去两年的测试(大约160万次试验)中收集的分数和响应时间表明(1)狒狒已经发展出一种“专家”形式的认知灵活性,以及(2)它们的表现与年龄有关,它在青少年中处于发展阶段,在成年人中最佳,在中年下降,在最老的年龄组中严重受损。与Bonté收集的数据进行直接比较,Flemming&Fagot(2011)对一些与当前研究相同的狒狒和相同的任务表明,(3)经过10年的训练,所有年龄组的表现都有所改善,即使是现在的老人。所有这些数据验证了使用非人灵长类动物作为人类认知灵活性的模型,并表明人类的认知灵活性具有悠久的进化历史。
    Cognitive flexibility in non-human primates is traditionally measured with the conceptual set shifting task (CSST). In our laboratory, Guinea baboons (N = 24) were continuously tested with a CSST task during approximately 10 years. Our task involved the presentation of three stimuli on a touch screen all made from 3 possible colours and 3 shapes. The subjects had to touch the stimulus containing the stimulus dimension (e.g., green) that was constantly rewarded until the stimulus dimension changed. Analysis of perseveration responses, scores and response times collected during the last two years of testing (approximately 1.6 million trials) indicate (1) that the baboons have developed an \"expert\" form of cognitive flexibility and (2) that their performance was age-dependent, it was at a developing stage in juveniles, optimal in adults, declining in middle-aged, and strongly impaired in the oldest age group. A direct comparison with the data collected by Bonté , Flemming & Fagot (2011) on some of the same baboons and same task as in the current study indicates that (3) the performance of all age groups has improved after 10 years of training, even for the now old individuals. All these data validate the use of non-human primates as models of human cognitive flexibility and suggest that cognitive flexibility in humans has a long evolutionary history.
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  • 文章类型: Journal Article
    组合交互测试,这是一种验证具有许多输入参数的系统的技术,使用称为覆盖数组的数学对象作为测试输入。该技术生成有限数量的测试用例,同时保证给定的组合覆盖。虽然这个领域已经被广泛的研究,处理输入参数之间的约束仍然是一个重大挑战,这可能显著增加生成覆盖阵列的成本。在这项工作中,我们提出了一个数学运算,称为“基于弱化乘积的组合联接”,从两个现有的覆盖阵列构造一个新的覆盖阵列。该操作通过在生成期间增加并行性来重用现有覆盖阵列以节省计算资源,而不损失原始阵列的组合覆盖。根据用例场景,我们提出的方法将覆盖阵列生成时间显着减少了13-96%。
    Combinatorial interaction testing, which is a technique to verify a system with numerous input parameters, employs a mathematical object called a covering array as a test input. This technique generates a limited number of test cases while guaranteeing a given combinatorial coverage. Although this area has been studied extensively, handling constraints among input parameters remains a major challenge, which may significantly increase the cost to generate covering arrays. In this work, we propose a mathematical operation, called \"weaken-product based combinatorial join\", which constructs a new covering array from two existing covering arrays. The operation reuses existing covering arrays to save computational resource by increasing parallelism during generation without losing combinatorial coverage of the original arrays. Our proposed method significantly reduce the covering array generation time by 13-96% depending on use case scenarios.
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  • 文章类型: Journal Article
    背景:概念2(C2)划船测功机在全球范围内用于基于家庭的训练,官方比赛,以及体育和科学方面的绩效评估。先前的研究报告了机械动力输出的完全低估与不清楚定义的中风变异性正相关。这项研究的目的是量化C2的准确性,同时通过使用用于空气制动划船测功机的测试台来控制划船行程的潜在影响变量,从而排除生物变异性。
    方法:采用了一种用于划船测力计的独特电动试验台。准确性被评估为在稳定期间C2和参考系统之间的机械功率输出差异(即,行程功率在一系列50个空间内的最小变化,无笔划)和不稳定的模拟划船(即,测量系列期间的持续变化),同时操纵冲程变量形状,力,或费率。
    结果:在稳定的模拟划船过程中,C2和参考系统之间的差异在2.9-4.3%之间。差异不受中风形状的影响(P=0.153),但按卒中发生率为22-28min-1(P<0.001)。在不稳定的模拟划船过程中,随着行程力和速度的变化,2.5-3.9%的平均差异与稳定模拟划船期间相似,但随机误差增加了18倍。C2低估了前五个冲程的机械动力输出10-70%。他们的排除将平均差异降低到0.2-1.9%。
    结论:由于对起始行程的极大低估,C2的标称精度取决于所考虑的笔划的总数。范围为0.2-1.9%,一旦飞轮被充分加速。划船不均匀会增加不准确性,但中风的形状有边际影响。因此,划船者应尽可能均匀地划船,并更喜欢更高的划水率以优化C2读数。我们建议使用外部参考系统进行科学和高性能评估,特别是对于短测试设计,其中的开始行程将产生重大影响。
    BACKGROUND: The Concept 2 (C2) rowing ergometer is used worldwide for home-based training, official competitions, and performance assessment in sports and science. Previous studies reported a disparate underestimation of mechanical power output positively related to an unclearly defined stroke variability. The aim of this study was to quantify the accuracy of the C2 while controlling for the potentially influencing variables of the rowing stroke by using a test rig for air-braked rowing ergometers and thus excluding biological variability.
    METHODS: A unique motorized test rig for rowing ergometers was employed. Accuracy was assessed as the difference in mechanical power output between C2 and a reference system during steady (i.e., minimal variations of stroke power within a series of 50 spacemark, no -strokes) and unsteady simulated rowing (i.e., persistent variations during measurement series) while manipulating the stroke variables shape, force, or rate.
    RESULTS: During steady simulated rowing, differences between C2 and the reference system ranged 2.9-4.3%. Differences were not significantly affected by stroke shapes (P = 0.153), but by stroke rates ranging 22-28 min-1 (P < 0.001). During unsteady simulated rowing with alterations of stroke force and rate, mean differences of 2.5-3.9% were similar as during steady simulated rowing, but the random error increased up to 18-fold. C2 underestimated mechanical power output of the first five strokes by 10-70%. Their exclusion reduced mean differences to 0.2-1.9%.
    CONCLUSIONS: Due to the enormous underestimation of the start strokes, the nominal accuracy of the C2 depends on the total number of strokes considered. It ranges 0.2-1.9%, once the flywheel has been sufficiently accelerated. Inaccuracy increases with uneven rowing, but the stroke shape has a marginal impact. Hence, rowers should row as even as possible and prefer higher stroke rates to optimize C2 readings. We recommend external reference systems for scientific and high-performance assessments, especially for short tests designs where the start strokes will have a major impact.
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  • 文章类型: Journal Article
    Chronic liver disease (CLD) is a significant health problem affecting millions of people worldwide. In Scotland, CLD is a major cause of premature mortality. Liver function tests (LFTs) are a panel of frequently requested blood tests which may indicate liver disease. However, LFTs commonly contain at least one abnormal result, and abnormalities are rarely investigated to the extent recommended by national guidelines. The intelligent Liver Function Testing (iLFT) pathway is a novel, automated system designed to improve early diagnosis of liver disease. Initial abnormal LFT results trigger a cascade of reflexive testing to help identify the cause of any liver dysfunction. Algorithms combine these results with demographic and clinical data (such as patient age, body mass index, and alcohol intake) and fibrosis estimates to produce an electronic diagnosis and management plan. The pilot trial demonstrated that iLFT increased diagnosis of liver disease whilst remaining cost-effective. As such, iLFT has been fully operational across our region (NHS Tayside, Scotland) since August 2018. In the first year, iLFT generated over 2000 diagnoses from 1824 patient samples with an abnormality in the initial LFTs. The majority of these patients could be safely managed in primary care. iLFT allows maximal value to be obtained from liver blood tests across biochemistry, virology, immunology, and hematology with only minor changes to working practices. \'Intelligent\', algorithm-led testing pathways break down the barrier between clinical and laboratory medicine and offer solutions to many of the challenges experienced in modern healthcare systems.
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  • 文章类型: Journal Article
    罗氏Cobas化学分析仪的溶血指数(HI)检查功能可以直接报告血红蛋白(Hb)浓度。我们旨在验证HI检查功能,以测量血浆无细胞Hb。
    通过分析仪采集血浆样品(6μl)并在生理盐水中稀释以测量570和600nm处Hb的吸光度。基于摩尔消光系数计算Hb浓度。不精确,定量下限(LLOQ),和分析测量范围(AMR)进行了评估。通过比较新方法与现有分光光度法之间的结果来确定准确性。我们进一步研究了黄疸,血脂和结转的干扰。还评估了该测定在能力测试中的性能。参考范围从现有方法转移。
    运行内和总简历分别为1.7%-4.2%和2.1%-7.0%,分别(n=20)。LLOQ为11mg/dL(CV=8.1%),AMR的上限为506mg/dL。新方法的结果与现有的参考测定具有良好的相关性:Y(新方法)=0.974x(参考方法)4.9,r=0.9990,n=52。浓度高达60mg/dL的胆红素和高达389的血脂指数未显示出明显的干扰。没有检测到显著的残留。能力测试的平均标准偏差指数为0.03±0.29。参考范围为<22mg/dL。
    使用HI检查功能的无血浆细胞Hb测量满足无血浆细胞Hb测定的分析要求。它简单且具有成本效益。
    The Roche Cobas chemistry analyzer\'s hemolysis index (HI) check function can directly report hemoglobin (Hb) concentrations. We aimed to validate the HI check function for the measurement of plasma cell-free Hb.
    Plasma samples (6 μl) were taken by the analyzer and diluted in normal saline to measure the absorbance for Hb at 570 and 600 nm. Hb concentrations were calculated based on the molar extinction coefficient. Imprecision, lower limit of quantification (LLOQ), and analytical measurement range (AMR) of the assay were evaluated. The accuracy was determined by comparing the results between the new method and an existing spectrophotometric method. We further studied interference of icterus and lipemia and carryover. The performance of the assay in proficiency testing was also evaluated. The reference range was transferred from the existing method.
    Within-run and total CVs were 1.7%-4.2% and 2.1%-7.0%, respectively (n = 20). The LLOQ was 11 mg/dL (CV = 8.1%) with the upper limit of AMR of 506 mg/dL. The results of the new method correlated well with the existing reference assay: Y (new method) = 0.974 x (reference method) + 4.9, r = 0.9990, n = 52. Bilirubin with a concentration up to 60 mg/dL and lipemic index up to 389 did not show significant interference. No significant carryover was detected. The average standard deviation index in proficiency testing was 0.03 ± 0.29. The reference range was <22 mg/dL.
    Plasma cell-free Hb measurement using the HI check function meets the analytical requirements of the plasma cell-free Hb assays. It is simple and cost-effective.
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  • 文章类型: Journal Article
    Liver function tests (LFTs) are frequently requested blood tests which may indicate liver disease. LFTs are commonly abnormal, the causes of which can be complex and are frequently under investigated. This can lead to missed opportunities to diagnose and treat liver disease at an early stage. We developed an automated investigation algorithm, intelligent liver function testing (iLFT), with the aim of increasing the early diagnosis of liver disease in a cost-effective manner.
    We developed an automated system that further investigated abnormal LFTs on initial testing samples to generate a probable diagnosis and management plan. We integrated this automated investigation algorithm into the laboratory management system, based on minimal diagnostic criteria, liver fibrosis estimation, and reflex testing for causes of liver disease. This algorithm then generated a diagnosis and/or management plan. A stepped-wedged trial design was utilised to compare LFT outcomes in general practices in the 6 months before and after introduction of the iLFT system. Diagnostic outcomes were collated and compared.
    Of eligible patients with abnormal LFTs, 490 were recruited to the control group and 64 were recruited to the intervention group. The primary diagnostic outcome was based on the general practitioner diagnosis, which agreed with the iLFT diagnosis in 67% of cases. In the iLFT group, the diagnosis of liver disease was increased by 43%. Additionally, there were significant increases in the rates of GP visits after diagnosis and the number of referrals to secondary care in the iLFT group. iLFT was cost-effective with a low initial incremental cost-effectiveness ratio of £284 per correct diagnosis, and a saving to the NHS of £3,216 per patient lifetime.
    iLFT increases liver disease diagnoses, improves quality of care, and is highly cost-effective. This can be achieved with minor changes to working practices and exploitation of functionality existing within modern laboratory diagnostics systems.
    There is a growing epidemic of advanced liver disease, this could be offset by early detection and management. Checking liver blood tests (LFTs) should be an opportunity to diagnose liver problems, but abnormal results are often incompletely investigated. In this study we were able to substantially increase the diagnostic yield of the abnormal LFTs using the automated intelligent LFT system. With the addition of referral recommendations and management plans, this strategy provides optimum investigation and management of LFTs and is cost saving to the NHS.
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  • 文章类型: Journal Article
    One factor hindering the widespread use of cognitive testing for people with multiple sclerosis (pwMS) is the need for a tester to administer tests.
    To undertake a proof of concept study assessing the feasibility of a fully automated speech recognition version of the Symbol Digit Modalities Test (auto-SDMT) in detecting abnormalities in processing speed in pwMS.
    A sample of 50 pwMS and 32 matched healthy control (HC) subjects was tested with the auto-SDMT and the Brief International Cognitive Assessment for MS (BICAMS).
    The percentages of MS participants impaired on the auto-SDMT and the traditional oral SDMT were 34% and 32%, respectively. Excellent convergent validity was found between the two tests (MS: r = -0.806, p < 0.001 and HC: r = -0.629, p < 0.001). The auto-SDMT had a similar sensitivity and specificity to the traditional oral SDMT in predicting overall impairment on the BICAMS.
    The auto-SDMT is a sensitive measure for detecting processing speed deficits in pwMS. The test, the first entirely computer administrated oral response version of the SDMT, uses speech recognition technology, thereby eliminating the need for a human tester. Replication of the results is required in a larger representative sample of pwMS.
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