Testing

Testing
  • 文章类型: Journal Article
    目的:头孢菌素类药物是全球处方最多的抗生素之一,与多种超敏反应(HSR)有关。这篇综述总结了头孢菌素超敏反应的最新进展,重点是诊断测试。
    结果:报告的评估不同即时和延迟头孢菌素HSR的测试策略包括皮肤测试,体外试验,和诊断药物挑战。然而,体内和体外试验在不同超敏反应内型中的诊断性能仍不清楚;需要足够有力的研究来调查这些诊断方式的真阳性和阴性预测值,使用药物挑战的参考标准来定义头孢菌素超敏反应.诊断测试的完善应以我们对头孢菌素抗原决定因素的理解增长为指导。这种增长对于进一步澄清头孢菌素之间的交叉反应性至关重要,并可能描述简化的评估过程,从而减少不必要的抗生素回避。
    OBJECTIVE: Cephalosporins are one of the most prescribed antibiotics worldwide and are implicated in a wide range of hypersensitivity reactions (HSR). This review summarizes recent updates in cephalosporin hypersensitivity with a focus on diagnostic testing.
    RESULTS: Reported testing strategies to evaluate different immediate and delayed cephalosporin HSR have included skin testing, in vitro testing, and diagnostic drug challenges. However, the diagnostic performance of in vivo and in vitro tests remains unclear across different hypersensitivity endotypes; adequately powered studies investigating the true positive and negative predictive value of these diagnostic modalities are needed using the reference standard of drug challenges to define cephalosporin hypersensitivity. Refinement of diagnostic testing should be guided by growth in our understanding of cephalosporin antigenic determinants. This growth will be crucial in driving further clarification of cross-reactivity between cephalosporins, and potentially delineating streamlined evaluation processes resulting in reduced unnecessary antibiotic avoidance.
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  • 文章类型: Journal Article
    Powassan病毒是一种蜱传黄病毒,可引起严重的神经侵袭性疾病,在美国东北部和中西部的地方性地区,加拿大,和俄罗斯。诊断是具有挑战性的,它依赖于高度的怀疑指数,并根据感染持续时间和患者的免疫状态选择正确的检测方法。这篇综述涵盖了Powassan病毒的实验室测试,包括历史考虑,现代选择,以及研究领域正在开发的方法。
    Powassan virus is a tick-borne flavivirus that can cause severe neuroinvasive disease, with areas of endemicity in the Northeast and Midwest United States, Canada, and Russia. Diagnosis is challenging and relies on a high index of suspicion and choosing the right test based on duration of infection and the patient\'s immune status. This review covers laboratory testing for Powassan virus, including historical considerations, modern options, and methods being developed in the research space.
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  • 文章类型: Journal Article
    正确强度的有氧运动可以减轻帕金森病(PD)的运动和非运动症状,提高生活质量。然而,一个具体的,已验证,非侵入性,并且不存在评估生理变量以规定PD患者最佳有氧运动强度的实验室协议。因此,这项研究旨在提出一个协议,帕金森临界心率测试(帕金森-CHR测试),为了确定PD患者的临界心率(CHR)并验证其有效性,可靠性,和敏感性。15名特发性PD患者,能够练习练习的人,被招募参加研究(71.1±6.6年)。该研究包括两个实验:i)第一个旨在评估协议的有效性和可靠性,参与者以一周的间隔进行两次测试;ii)第二个实验旨在调查协议的敏感性,在为期8周的训练计划之前和之后,根据Parkinson-CHR强度对个体进行评估。在实验1中,在覆盖距离(400、800和1200m)的时间上没有观察到测试和重新测试之间的差异,总心率,临界心率,临界转速(p>0.05)。在实验2中,经过8周的训练计划后,覆盖400和800m的时间以及所有距离的总心率都减少了。帕金森-CHR测试是可靠的,可重复,便宜,和非侵入性协议来评估,开处方,并监测PD患者的有氧运动强度。
    Aerobic exercise with the correct intensity can attenuate motor and non-motor symptoms of Parkinson\'s disease (PD) and improve the quality of life. However, a specific, validated, non-invasive, and outside the laboratory protocol that assesses physiological variables to prescribe optimal aerobic exercise intensity for people with PD is nonexistent. Therefore, this study aimed to propose a protocol, the Parkinson\'s critical heart rate test (Parkinson-CHR test), to determine the critical heart rate (CHR) in individuals with PD and verify its validity, reliability, and sensitivity. Fifteen people with idiopathic PD, who were able to practice exercises, were recruited to participate in the study (71.1 ± 6.6 years). The study consisted of two experiments: i) the first one aimed to assess the validity and reliability of the protocol, with participants performing the test twice at a one-week interval; ii) the second experiment aimed to investigate the protocol sensitivity, with individuals being evaluated before and after an 8-week training program according to Parkinson-CHR intensity. In experiment 1, no differences between test and retest were observed in the time to cover the distances (400, 800 and 1200 m), the total heart rate, the critical heart rate, and critical speed (p > 0.05). In experiment 2, there was a reduction in time to cover 400 and 800 m as well as in the total heart rate for all distances after the 8-week training program. The Parkinson-CHR test is a reliable, reproducible, inexpensive, and non-invasive protocol to assess, prescribe, and monitor aerobic exercise intensity in people with PD.
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  • 文章类型: Journal Article
    冰球需要两个级别的特定敏捷性,涉及不同的能力,其中敏捷性水平及其约束可能因性能水平而异。因此,本研究旨在比较青年曲棍球运动员在两个成绩水平上的冰上和非冰上方向速度(COD)变化之间的关系水平。这项研究是在曲棍球赛季进行的,包括U16精英玩家(n=40)和U16次精英玩家(n=23)。两组都进行了特定的冰上适应性测试(4-m加速度,30米冲刺,和6x54-m测试,有和没有冰球的伊利诺伊州冰上敏捷性测试)和非冰上测试,包括非臂摆动反向跳跃(CMJ),广泛的跳跃,和引体向上。皮尔逊相关性显示,精英球员的加速表现与CMJ(r=-0.46)和跳远(r=-0.31)有关。次精英球员表现出对CMJ(r=-0.77)和跳远(r=-0.43)的30米冲刺的更强依赖性,拉升(r=-0.62)和CMJ(r=-0.50)与6x54-m试验的关系,但与加速度无关。精英玩家在非冰上和冰上性能限制之间存在差异,与次精英选手相比,他们的滑冰冲刺与垂直和水平起飞能力的关系较小。亚精英玩家\'冰外力量决定了他们的冲刺和重复冲刺表现。精英和次精英玩家的COD表现基于不同的条件约束。
    Ice hockey requires two levels of specific agility, involving different abilities, where the level of agility and their constraints might vary by the performance level. Therefore, this study aimed to compare the relationship level between on-ice and off-ice change of directional speed (COD) of youth hockey players at two performance levels. The study was conducted during the hockey season, including U16 elite players (n = 40) and U16 sub-elite players (n = 23). Both groups performed specific on-ice fitness tests (4-m acceleration, 30-m sprint, and 6 x 54-m tests, an on-ice Illinois agility test with and without a puck) and off-ice tests consisting of non-arm swing countermovement jumps (CMJs), broad jumps, and pull-ups. Pearson correlation showed that the acceleration performance of elite players was related to the CMJ (r = -0.46) and the broad jump (r = -0.31). Sub-elite players showed stronger dependence of the 30-m sprint on the CMJ (r = -0.77) and the broad jump (r = -0.43), the relation of pulls ups (r = -0.62) and the CMJ (r = -0.50) to the 6 x 54-m test, yet no association to acceleration. Elite players differ between off-ice and on-ice performance constraints, where their skating sprint is less related to their vertical and horizontal take-off abilities than in sub-elite players. Sub-elite players\' off-ice power determines their sprint and repeated sprint performance. COD performance of elite and sub-elite players is based on different conditioning constraints.
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  • 文章类型: Journal Article
    背景:严重急性呼吸综合征冠状病毒2(SARS-CoV-2)可能由不知道感染的个体传播。这种传播增加了癌症患者的后果,他们可能需要经常去医疗机构,暴露于免疫受损的疗法,并面临2019年冠状病毒病(COVID-19)的更高发病率。我们确定了(1)无症状,临床诊断,和(2)血清学记录但临床未诊断的SARS-CoV-2感染肺癌个体。
    方法:在多中心注册中心中,肺癌患者(无论以前是否接种过SARS-CoV-2疫苗或有记录的感染)接受了临床数据和系列血液样本的收集,测试了抗核衣壳蛋白抗体(抗NAb)或IgG(N)水平。我们使用多变量逻辑回归模型来研究首次感染SARS-CoV-2的患者中与症状的存在或不存在以及临床诊断的存在或不存在相关的临床特征。
    结果:在有血清学证据或临床记录的SARS-CoV-2感染的患者中,80/142(56%)在首次感染时没有报告症状,61/149(40%)从未诊断。无症状感染在老年人和早期肺癌中更为常见。在多变量分析中,SARS-CoV-2血清学阳性的非白种人被临床诊断的可能性降低了70%(P=.002).
    结论:在多中心肺癌人群中,相当比例的SARS-CoV-2感染没有相关症状或从未被临床诊断.因为这类病例似乎在可能面临更高的COVID-19相关发病率的人群中更频繁发生,限制疾病传播和严重程度的措施仍然至关重要。
    BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may be spread by individuals unaware they are infected. Such dissemination has heightened ramifications in cancer patients, who may need to visit healthcare facilities frequently, be exposed to immune-compromising therapies, and face greater morbidity from coronavirus disease 2019 (COVID-19). We determined characteristics of (1) asymptomatic, clinically diagnosed, and (2) serologically documented but clinically undiagnosed SARS-CoV-2 infection among individuals with lung cancer.
    METHODS: In a multicenter registry, individuals with lung cancer (regardless of prior SARS-CoV-2 vaccination or documented infection) underwent collection of clinical data and serial blood samples, which were tested for antinucleocapsid protein antibody (anti-N Ab) or IgG (N) levels. We used multivariable logistic regression models to investigate clinical characteristics associated with the presence or absence of symptoms and the presence or absence of a clinical diagnosis among patients with their first SARS-CoV-2 infection.
    RESULTS: Among patients with serologic evidence or clinically documented SARS-CoV-2 infection, 80/142 (56%) had no reported symptoms at their first infection, and 61/149 (40%) were never diagnosed. Asymptomatic infection was more common among older individuals and earlier-stage lung cancer. In multivariable analysis, non-white individuals with SARS-CoV-2 serologic positivity were 70% less likely ever to be clinically diagnosed (P = .002).
    CONCLUSIONS: In a multicenter lung cancer population, a substantial proportion of SARS-CoV-2 infections had no associated symptoms or were never clinically diagnosed. Because such cases appear to occur more frequently in populations that may face greater COVID-19-associated morbidity, measures to limit disease spread and severity remain critical.
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  • 文章类型: Journal Article
    背景:ChatGPT(OpenAI),最先进的大型语言模型,在各种专业应用中表现出卓越的性能。尽管人工智能越来越受欢迎和有效,很少有研究使用Rasch分析的KIDMAP来评估ChatGPT解决多项选择题(MCQ)的能力,这是一种用于评估ChatGPT在MCQ回答中的表现的网站工具。
    目的:本研究旨在(1)展示网站的实用性(Rasch分析,特别是RaschOnline),和(2)确定ChatGPT与正常样品相比所达到的等级。
    方法:使用2023年台湾高考英语考试的10个项目评估了ChatGPT的能力。在Rasch模型下,对300名正态分布的模拟学生进行了模拟,以与ChatGPT的回答进行竞争。RaschOnline用于生成5个视觉演示,包括项目困难,差分项目功能,项目特性曲线,赖特地图,还有KIDMAP,为了实现研究目标。
    结果:研究结果表明:(1)10个项目的难度以单调的方式从更容易到更难增加,用logits(-2.43,-1.78,-1.48,-0.64,-0.1,0.33,0.59,1.34,1.7和2.47)表示;(2)在第5项的性别组之间观察到不同项目功能的证据(P=.04);(3)第5项显示出与Rasch模型的良好拟合(P=.61);(4)由Infit均方误差低于阈值1.5表示;(5)性别组之间获得的测量结果没有显着差异(P=.83);(6)能力等级之间存在显着差异(P<.001);(7)ChatGPT的能力等级为A,超越等级B到E。
    结论:通过使用RaschOnline,这项研究提供的证据表明,与正常样本相比,ChatGPT具有达到A级的能力。它在回答2023年台湾高考英语考试的MCQ方面表现出出色的能力。
    BACKGROUND: ChatGPT (OpenAI), a state-of-the-art large language model, has exhibited remarkable performance in various specialized applications. Despite the growing popularity and efficacy of artificial intelligence, there is a scarcity of studies that assess ChatGPT\'s competence in addressing multiple-choice questions (MCQs) using KIDMAP of Rasch analysis-a website tool used to evaluate ChatGPT\'s performance in MCQ answering.
    OBJECTIVE: This study aims to (1) showcase the utility of the website (Rasch analysis, specifically RaschOnline), and (2) determine the grade achieved by ChatGPT when compared to a normal sample.
    METHODS: The capability of ChatGPT was evaluated using 10 items from the English tests conducted for Taiwan college entrance examinations in 2023. Under a Rasch model, 300 simulated students with normal distributions were simulated to compete with ChatGPT\'s responses. RaschOnline was used to generate 5 visual presentations, including item difficulties, differential item functioning, item characteristic curve, Wright map, and KIDMAP, to address the research objectives.
    RESULTS: The findings revealed the following: (1) the difficulty of the 10 items increased in a monotonous pattern from easier to harder, represented by logits (-2.43, -1.78, -1.48, -0.64, -0.1, 0.33, 0.59, 1.34, 1.7, and 2.47); (2) evidence of differential item functioning was observed between gender groups for item 5 (P=.04); (3) item 5 displayed a good fit to the Rasch model (P=.61); (4) all items demonstrated a satisfactory fit to the Rasch model, indicated by Infit mean square errors below the threshold of 1.5; (5) no significant difference was found in the measures obtained between gender groups (P=.83); (6) a significant difference was observed among ability grades (P<.001); and (7) ChatGPT\'s capability was graded as A, surpassing grades B to E.
    CONCLUSIONS: By using RaschOnline, this study provides evidence that ChatGPT possesses the ability to achieve a grade A when compared to a normal sample. It exhibits excellent proficiency in answering MCQs from the English tests conducted in 2023 for the Taiwan college entrance examinations.
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  • 文章类型: Journal Article
    产志贺毒素的大肠杆菌(STEC)是一种重要的水传播病原体,能够引起严重的胃肠道感染,并伴有潜在的致命并发症。包括溶血性尿毒综合征.所有STEC血清群都有编码至少一种志贺毒素(stx1和/或stx2)的基因,构成STEC的主要毒力因子。环介导等温扩增(LAMP)能够以高度的特异性和灵敏度实现快速实时病原体检测。这项研究的目的是开发和验证采用LAMP技术的现场便携式诊断工作站,以允许对环境水样进行快速实时STEC检测。从地下水井(n=13)收集水样(n=28),河流(n=12),戈尔韦Corrib集水区的一个沟谷(n=2)和一个农业排水沟(n=1)。水样(100毫升)通过0.22微米的过滤器,并加入缓冲液洗脱捕获的细胞。过滤后,使用靶向stx1、stx2和大肠杆菌phoA基因的LAMP测定直接测试洗脱物。便携式诊断工作站用于现场研究,以证明仪器的现场测试能力。使用靶向stx1和stx2基因的实时PCR测定来确认结果。stx1,stx2和phoALAMP测定的检测限为2、2和6个拷贝,分别。总的来说,LAMP在15/28(53.6%)中检测到stx1、stx2和phoA基因,9/28(32.2%)和24/28(85.7%)样本,分别。为了确认,stx1和stx2的LAMP结果与使用PCR获得的结果完全相关(100%)。便携式诊断工作站在整个现场操作中表现出高灵敏度,从样品收集到最终结果的平均时间为40分钟。我们描述了一个简单的,可转移和有效的诊断技术,用于各种水源的现场分子分析。这种方法可以对饮用水进行现场检测,使公共卫生和水管理当局能够做出基于证据的决策。
    Shiga toxin-producing Escherichia coli (STEC) is an important waterborne pathogen capable of causing serious gastrointestinal infections with potentially fatal complications, including haemolytic-uremic syndrome. All STEC serogroups harbour genes that encode at least one Shiga toxin (stx1 and/or stx2), which constitute the primary virulence factors of STEC. Loop-mediated isothermal amplification (LAMP) enables rapid real-time pathogen detection with a high degree of specificity and sensitivity. The aim of this study was to develop and validate an on-site portable diagnostics workstation employing LAMP technology to permit rapid real-time STEC detection in environmental water samples. Water samples (n=28) were collected from groundwater wells (n=13), rivers (n=12), a turlough (n=2) and an agricultural drain (n=1) from the Corrib catchment in Galway. Water samples (100 ml) were passed through a 0.22 µm filter, and buffer was added to elute captured cells. Following filtration, eluates were tested directly using LAMP assays targeting stx1, stx2 and E. coli phoA genes. The portable diagnostics workstation was used in field studies to demonstrate the on-site testing capabilities of the instrument. Real-time PCR assays targeting stx1 and stx2 genes were used to confirm the results. The limit of detection for stx1, stx2 and phoA LAMP assays were 2, 2 and 6 copies, respectively. Overall, stx1, stx2 and phoA genes were detected by LAMP in 15/28 (53.6 %), 9/28 (32.2 %) and 24/28 (85.7 %) samples, respectively. For confirmation, the LAMP results for stx1 and stx2 correlated perfectly (100 %) with those obtained using PCR. The portable diagnostics workstation exhibited high sensitivity throughout the on-site operation, and the average time from sample collection to final result was 40 min. We describe a simple, transferable and efficient diagnostic technology for on-site molecular analysis of various water sources. This method allows on-site testing of drinking water, enabling evidence-based decision-making by public health and water management authorities.
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  • 文章类型: Journal Article
    计算机神经认知测试是脑震荡多领域评估的一个组成部分。然而,计算机化神经认知测试的使用仅限于11岁及以上的患者,使临床医生几乎没有选择来评估年幼儿童。
    为了检查儿童脑震荡后即刻评估和认知测试的变化(Impact儿科)(Impact应用,2021)脑震荡后5-9岁儿童的得分和与表现相关的因素。
    参与者包括脑震荡30(M=8.5±5.9)天内63名5-9(M=7.5±1.0)岁的儿童(42%[n=27]名女性)。所有参与者在初次就诊时完成了ImPACT儿科检查,并在医疗许可后返回活动(RTA)就诊。IMPACT儿科测试是一种计算机化的神经认知电池,其中包括5项评估记忆和视觉处理速度的测试。使用多变量和单变量方差分析和配对t检验来比较从初次就诊到就诊的ImPACT儿科评分。协方差和多元线性回归的多变量和单变量分析检查了与ImPACT儿科表现相关的因素。
    参与者表现出从初次就诊到医疗许可就诊的总体表现(F(4,59)=3.08,p=0.02,Wilks\'Λ=0.83,ηp2=0.17),快速处理速度显著提高(F(1,62)=7.48,p<0.01,ηp2=0.11)。当控制年龄时,性别,多动症的历史,几天到诊所,整体性能的改善仍然显着(F(4,51)=2.99,p=0.03,Wilks\'Λ=0.81,ηp2=0.19)。年龄与初次就诊时的快速处理综合评分显着相关(F(4,59)=5.9,p<0.001,Adj。R2=0.25)和医疗许可访问(F(4,59)=3.8,p=0.008,Adj。R2=0.16),年龄较大的儿童在两个时间点都表现更好(初次就诊:B=8.17,p<0.001;医疗许可:B=3.62,p=0.03)。
    我们的主要发现表明,5-9岁儿童在从初次就诊到医疗许可的ImPACT儿科快速处理方面显着改善。然而,ImPACT儿科的记忆成分没有发现差异.年龄较大的孩子在处理速度上也比年龄较小的孩子表现更好。研究结果表明,ImPACT儿科的处理速度组件可用于监测5-9岁儿童脑震荡后神经认知功能的改善,但是在解释表现时需要考虑年龄差异。
    UNASSIGNED: Computerized neurocognitive testing is one component of a multidomain assessment of concussion. However, the use of computerized neurocognitive testing has been limited to patients aged 11 years and up, leaving clinicians with few options to evaluate younger children.
    UNASSIGNED: To examine the change in Immediate Post-concussion Assessment and Cognitive Testing Pediatric (ImPACT Pediatric) (ImPACT Applications, 2021) scores and factors associated with performance in children aged 5-9 years following a concussion.
    UNASSIGNED: Participants included 63 children (42% [n = 27] female) aged 5-9 (M = 7.5 ± 1.0) years within 30 (M = 8.5 ± 5.9) days of a concussion. All participants completed the ImPACT Pediatric at their initial visit and at medical clearance for their return to activity (RTA) visit. The ImPACT Pediatric test is a computerized neurocognitive battery that includes 5 tests that assess memory and visual processing speed. Multivariate and univariate analyses of variance and paired t-tests were used to compare ImPACT Pediatric scores from the initial visit to medical clearance. Multivariate and univariate analyses of covariance and multiple linear regression examined factors associated with ImPACT Pediatric performance.
    UNASSIGNED: Participants demonstrated improved overall performance from the initial visit to the medical clearance visit (F(4, 59)=3.08, p = 0.02, Wilks\' Λ = 0.83, ηp2=0.17), with significant improvement in Rapid Processing Speed (F(1, 62)=7.48, p < 0.01, ηp2=0.11). When controlling for age, sex, history of ADHD, and days to clinic, the improvement in overall performance remained significant (F(4, 51)=2.99, p = 0.03, Wilks\' Λ = 0.81, ηp2=0.19). Older age was significantly associated with the Rapid Processing composite score at the initial visit (F(4, 59)=5.9, p < 0.001, Adj. R2=0.25) and medical clearance visit (F(4, 59)=3.8, p = 0.008, Adj. R2=0.16), with older children associated with better performance at both time points (Initial visit: B = 8.17, p < 0.001; Medical Clearance: B = 3.62, p = 0.03).
    UNASSIGNED: Our main findings suggest that children aged 5-9 years improved significantly in Rapid Processing on the ImPACT Pediatric from the initial visit to medical clearance. However, no differences were found for the memory components of the ImPACT Pediatric. Older children also performed better on processing speed than younger children. The findings suggest that the processing speed components of ImPACT Pediatric are useful for monitoring improvements in neurocognitive functioning following concussion in children aged 5-9 years, but that age differences need to be considered when interpreting performance.
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  • 文章类型: Journal Article
    标准参考材料(SRM)2806:液压油中的介质测试粉尘代表一系列由国家标准与技术研究所(NIST)认证的参考材料,用于校准液体光学(或自动)颗粒计数器,适用于广泛的工业,航空航天,和军事应用。该系列,包括SRM2806b,和SRM2806d,由IFTS为NIST制造,国际过滤器测试服务公司,在法国。材料接受认证的一个重要因素是瓶对瓶的均匀程度,由IFTS和NIST评估。开发了一种统计图形方法,该方法可提供即时的视觉和定量统计指标,以表征SRM。这种NIST开发的方法用于四项研究,以评估材料在其生产阶段和成品瓶装产品阶段的同质性。IFTS使用光学颗粒计数器进行测量以进行在线质量保证,并对成品400瓶系列的40瓶进行采样,以根据粒度分布确定均匀性。NIST还测定成品材料的粒度分布并进行显微镜检查以寻找悬浮液中可能的污染物。对两种材料(2806b和2806d)进行加速老化实验以验证它们的稳定性。
    Standard Reference Material (SRM) 2806: Medium Test Dust in Hydraulic Fluid represents a series of reference materials certified by the National Institute of Standards and Technology (NIST) used to calibrate liquid-borne optical (or automatic) particle counters applied in a wide range of industrial, aerospace, and military applications. The series, including SRM 2806b, and SRM 2806d, was manufactured for NIST by IFTS, Institut de la Filtration et des Techniques Séparatives International Filter Testing Services, in France. An important factor for the acceptance of the material for certification was the degree of bottle-to-bottle homogeneity, which was evaluated by both IFTS and NIST. A statistical graphics methodology was developed that provided immediate visual as well as quantitative statistical metrics with which to characterize the SRM. This NIST-developed approach was used in four studies to assess the homogeneity of the material during both its production stage and its finished bottled-product stage. IFTS performed measurements using an optical particle counter for on-line quality assurance and sampled 40 bottles of the finished 400 bottle series to determine homogeneity from the particle size distribution. NIST also determined the particle size distribution of the finished material and performed microscopy to look for possible contaminant material in the suspension. An accelerated aging experiment was conducted on both materials (2806b and 2806d) to verify their stability.
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  • 文章类型: Journal Article
    COVID-19大流行对美洲印第安人和阿拉斯加原住民(AI/AN)社区产生了重大影响。感染率,住院治疗,相对于非西班牙裔白人,死亡率很高。虽然AI/AN社区的COVID-19疫苗接种水平最高,利用率仍然不理想,需要确定检测和疫苗接种的促进因素和障碍。
    我们检查了2021年1月至5月的横断面调查数据,其中包括来自五个部落卫生组织的619名AI/AN患者(AK,CO,KS,NM,西澳)。暴露包括感知到的压力,凯斯勒遇险,PTSD筛查,和AUDIT-C酒精滥用屏幕。泊松回归用于估计与COVID-19检测和疫苗接种流行率的关联。
    超过四分之三的参与者接受了COVID-19测试,近一半的参与者接种了疫苗。感知压力和PTSD筛查阳性与疫苗接种流行率降低相关,患病率(PR)0.83(0.73,0.93)和PR0.80(0.66,0.98),分别。在报告的心理弹性和创伤后应激障碍较低的亚组中,COVID-19测试的患病率降低,PR0.78(0.64,0.95)。
    过去一个月的感知压力和PTSD筛查阳性与城市AI/AN人群中COVID-19疫苗接种流行率降低有关。报告有限韧性和PTSD症状的亚组COVID-19检测的患病率较低。心理健康与COVID-19检测和疫苗接种之间的复杂关系值得进一步探索,以确定改善城市AI/AN人群健康的干预措施,已知在心理健康和COVID-19结局方面存在差异的人群。
    UNASSIGNED: The COVID-19 pandemic has substantially impacted American Indian and Alaska Native (AI/AN) communities. Rates of infection, hospitalization, and mortality have been severe relative to non-Hispanic whites. While AI/AN communities have had some of the highest levels of COVID-19 vaccination, utilization rates remain suboptimal and there is a need to identify facilitators and barriers to testing and vaccination.
    UNASSIGNED: We examined cross-sectional survey data from January to May 2021, among 619 AI/AN patients from five tribal health organizations (AK, CO, KS, NM, WA). Exposures include perceived stress, Kessler distress, PTSD screening, and AUDIT-C alcohol misuse screen. Poisson regression was used to estimate associations with prevalence of COVID-19 testing and vaccination.
    UNASSIGNED: Over three-quarters of participants were tested for COVID-19 and nearly half were vaccinated. Perceived stress and positive PTSD screening were associated with reduced vaccination prevalence, Prevalence Ratio (PR) 0.83 (0.73, 0.93) and PR 0.80 (0.66, 0.98), respectively. There was reduced prevalence of COVID-19 testing in subgroups with lower reported psychological resilience and PTSD, PR 0.78 (0.64, 0.95).
    UNASSIGNED: Past-month perceived stress and positive PTSD screening are associated with reduced prevalence of COVID-19 vaccination in urban AI/AN people. Subgroups reporting limited resilience and PTSD symptoms had lower prevalence of COVID-19 testing. The complex relationship between mental health and COVID-19 testing and vaccination warrants further exploration to identify interventions to improve health among urban AI/AN people, a population with known disparities in both mental health and COVID-19 outcomes.
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