reliability and validity

信度和效度
  • 文章类型: Journal Article
    钩端螺旋体病是一种具有重大全球影响和挑战性诊断的人畜共患疾病。使用经过充分验证的快速测试对于及时识别疾病和降低死亡率至关重要。本研究分析了由OswaldoCruz基金会(Fiocruz)在巴西生产的用于诊断钩端螺旋体病的双路径平台(DPP)测定法的准确性和可靠性。首先,使用巴西六个州的参考实验室常规处理的样本,在巴西钩端螺旋体病参考实验室中建立了血清学小组。它由150个钩端螺旋体病阳性(根据MAT和IgM-ELISA)和250个阴性样品组成。随后,小组样本一式三份分发给参考实验室进行DPP测定.在评估诊断质量时使用了不同的措施。对于不同的测试前概率设置估计预测值。在各州,灵敏度在67.33%和74.00%之间变化,特异性在93.20%和98.40%之间变化,他们之间有足够的协议。对于症状少于7天的患者样本,准确性较低。在患病率高达25%左右的情况下,阳性和阴性预测值约为90%.然而,在高预测试概率的情况下,NPV很低。这项研究提高了对DPP在钩端螺旋体病诊断中的应用的理解。特别是它在医疗机构中的应用。只要对结果的解释充分考虑了症状发作的时间以及临床和流行病学背景,DPP是钩端螺旋体病诊断程序中使用的有效选项。
    Leptospirosis is a zoonotic disease with significant global impact and a challenging diagnosis. The utilization of adequately validated rapid tests is relevant for the opportune identification of the disease and for reduction in fatality rates. The present study analyzes the accuracy and reliability of the Dual Path Platform (DPP) assay -produced in Brazil by the Oswaldo Cruz Foundation (Fiocruz)- for diagnosing leptospirosis. Firstly, a serological panel was constructed in the Brazilian Reference Laboratory for Leptospirosis using samples routinely handled by reference laboratories of six Brazilian states. It consisted of 150 positive (according to MAT and IgM-ELISA) and 250 negative samples for leptospirosis. Subsequently, the panel samples were distributed to the reference laboratories for the performance of DPP assays in triplicate. Different measures were used in the assessment of diagnostic quality. Predictive values were estimated for different pre-test probability settings. Sensitivities varied between 67.33 % and 74.00 % and specificities between 93.20 % and 98.40 % in the states, and there were adequate agreements between them. Accuracies were lower for the samples of patients with less than 7 days of symptoms. In contexts of prevalence values up to around 25 %, positive and negative predictive values were around 90 %. However, in situations of high pre-test probabilities, NPVs were low. This study improves understanding of the use of DPP in diagnosing leptospirosis, particularly its application in healthcare settings. As long as the time of symptoms onset and clinical and epidemiological contexts are adequately considered for the interpretation of results, DPP is a valid option to be used in the leptospirosis diagnostic routine.
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  • 文章类型: Journal Article
    与美国和欧洲国家相比,日本的老龄化社会正在迅速发展。老龄化限制了老年人的日常生活活动(ADL),在家里降低他们的生活和功能。因此,改善他们的ADL以尽可能长时间有效地支持他们在家中的运作至关重要。因此,支持者需要有共同的理解,及时意识到ADL的下降,并迅速引入康复。功能独立性测量(FIM)和Barthel指数(BI)是用于定量评估ADL的主要量表。然而,以前的研究报告说,FIM需要专业知识来进行评估,并且BI不能适当地捕获ADL的变化。自我评估负担量表(SAB-M)被开发为家庭护理人员适当评估老年人ADL变化的量表。先前使用SAB-M的研究已经证实了其在住院患者中的可靠性和有效性,由其家庭护理人员评估。因此,本研究旨在调查由家庭照顾者评估的社区居住老年人SAB-M的信度和效度.
    这项研究包括社区居住的老年人,他们在2020年10月至2020年12月在日本的第一作者的设施接受了家访康复。根据以前的研究,家庭护理人员使用SAB-M两次评估20名老年人的内部可靠性.此外,家庭护理人员使用SAB-M评估了168名老年人的内部一致性。对于标准有效性,SAB-M用于家庭护理人员的评估,和治疗师使用FIM电机(FIM-M)。这项研究使用加权卡帕,Cronbach的阿尔法,和Spearman的等级相关系数,用于评估员内部可靠性的统计分析,内部一致性,和标准有效性,分别。
    总分的加权卡帕系数为0.98(p<0.01),喂食为0.93(p<0.01),洗澡为0.91(p<0.01),敷料为0.98(p<0.01),转移为0.94(p<0.01),步行/轮椅为0.94(p<0.01),楼梯为0.95(p<0.01),膀胱管理为0.96(p<0.01)。克朗巴赫的七个项目的阿尔法为0.93。SAB-M和FIM-M评分的Spearman等级相关系数为0.91(p<0.01)。
    SAB-M在社区居住的老年人中具有足够的信度和效度。家庭护理人员可以使用SAB-M常规评估社区居住老年人的ADL变化,使他们能够在老年人ADL下降时及时考虑引入康复。因此,实施SAB-M有助于老年人尽可能长时间地在家生活和功能。
    UNASSIGNED: The aging society in Japan is progressing rapidly compared with that in the United States and European countries. Aging limits activities of daily living (ADL) in older adults, declining their lives and functions at home. Therefore, improving their ADL to effectively support their functioning at home for as long as possible is vital. Consequently, supporters need to have a common understanding, be promptly aware of the decline in ADL, and quickly introduce rehabilitation. The Functional Independence Measure (FIM) and Barthel Index (BI) are the main scales used to quantitatively assess ADL. However, previous studies have reported that FIM requires specialized knowledge for evaluation, and BI does not appropriately capture changes in ADL. The Self-Assessment Burden Scale-Motor (SAB-M) was developed as a scale for family caregivers to appropriately assess changes in ADL in older adults. Previous studies using the SAB-M have confirmed its reliability and validity in hospitalized patients as assessed by their family caregivers. Therefore, this study aimed to investigate the reliability and validity of the SAB-M among community-dwelling older adults as assessed by their family caregivers.
    UNASSIGNED: This study included community-dwelling older adults who received home-visit rehabilitation at the first author\'s facility between October 2020 and December 2020 in Japan. Following previous studies, the SAB-M was used by family caregivers to assess 20 older adults twice for intra-rater reliability. Furthermore, 168 older adults were evaluated by family caregivers for internal consistency using the SAB-M. For criterion validity, the SAB-M was used for the assessment by family caregivers, and therapists used the FIM-Motor (FIM-M). This study used the weighted kappa, Cronbach\'s alpha, and Spearman\'s rank correlation coefficients for the statistical analysis of intra-rater reliability, internal consistency, and criterion validity, respectively.
    UNASSIGNED: The weighted kappa coefficient for the total score was 0.98 (p < 0.01) and individual item, it was 0.93 for feeding (p < 0.01), 0.91 for bathing (p < 0.01), 0.98 for dressing (p < 0.01), 0.94 for transfer (p < 0.01), 0.94 for walking/wheelchair (p < 0.01), 0.95 for stairs (p < 0.01), and 0.96 for bladder management (p < 0.01). The Cronbach\'s alpha was 0.93 for the seven items. The Spearman\'s rank correlation coefficient between the SAB-M and FIM-M scores was 0.91 (p < 0.01).
    UNASSIGNED: The SAB-M has sufficient reliability and validity among community-dwelling older adults. Family caregivers can routinely assess changes in the ADL of community-dwelling older adults using the SAB-M, enabling them to promptly consider introducing rehabilitation when older adults\' ADL declines. Therefore, implementing SAB-M helps older adults live and function at home for as long as possible.
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  • 文章类型: Journal Article
    目的:我们检查了参加人类免疫缺陷病毒研究的730名性少数(SM)和跨性别和性别多样化(TGD)青年的性少数青少年压力量表(SMASI)的心理测量特性和标准有效性。方法:我们测试了全球量表和子量表的因子结构以及跨年龄的测量不变性,性别认同,出生时分配的性别,性认同,种族身份,和城市。对于标准有效性,我们在全球范围内回归了心理健康和药物使用措施。结果:总体量表具有良好的拟合度(比较拟合指数=0.95)和较高的可靠性(omega=0.89)。亚尺度模型拟合足够。我们通过性别认同和年龄确认了不变性,并建立了标准有效性。结论:SMASI在SM新兴成年人和TGD青年中表现出很强的心理测量特性。修改可以增强SMASI,以更好地捕捉少数民族青年中的性和性别压力。
    Purpose: We examined the psychometric properties and criterion validity of the Sexual Minority Adolescent Stress Inventory (SMASI) among 730 sexual minority (SM) and transgender and gender-diverse (TGD) youth aged 14 to 24 years who participated in a human immunodeficiency virus study. Methods: We tested the factor structure of the global scale and subscales and measurement invariance across age, gender identity, sex assigned at birth, sexual identity, ethnoracial identity, and city. For criterion validity, we regressed mental health and substance use measures on the global scale. Results: The global scale had excellent fit (comparative fit index = 0.95) and high reliability (omega = 0.89). Subscale model fit was adequate. We confirmed invariance by gender identity and age and established criterion validity. Conclusion: The SMASI exhibits strong psychometric properties among SM emerging adults and TGD youth. Modifications could enhance the SMASI to better capture both sexual and gender minority stress among ethnoracial minority youth.
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  • 文章类型: Journal Article
    我们的目标是检查ICD-10操作标准应用程序是否改变为非操作,在现实生活中获得的基于原型的诊断。
    精神病学住院医师将ICD-10的诊断标准作为“诊断测试”应用于他们已经关注的五名门诊患者,这些患者具有基于原型的诊断。使用测试来确定意见的变化是否显着,以及任何诊断组比其他诊断组更容易发生变化。本文是UTNU1111-1260-1212研究的一部分。
    十七个居民回顾了他们最近的五个案例档案,检索85对诊断的非基于操作的与基于操作的诊断。Stuart-Maxwell检验除了30%的诊断变化外,没有显著的意见变化(χ2=5.25,p=0.39;功率=0.94)。尽管没有统计学意义,20.2%的评价结果导致了影响治疗选择的变化。使用ICD-10操作标准略微增加了观察到的诊断数量,但可能与临床无关.所有非手术诊断都没有随着手术标准的应用而有更高的变化趋势(χ2=11.6,p=0.07)。女性与较高的诊断变化趋势相关。
    应用ICD-10操作标准作为诊断测试不会在居民中引起统计学上显著的诊断意见改变,没有诊断组似乎对诊断改变更明智。诊断意见变化中与性别相关的差异可能是沉没成本偏差的证据。虽然没有统计学意义,在诊断完善后使用操作标准可能有助于处理没有足够治疗反应的受试者。
    UNASSIGNED: Our objective was to check if the ICD-10 operational criteria application changes non-operational, prototype-based diagnoses obtained in a real-life scenario.
    UNASSIGNED: Psychiatry residents applied the diagnostic criteria of the ICD-10 as a \"diagnostic test\" to five outpatient patients they were already following who had a prototype-based diagnosis. Tests were used to ascertain whether changes in opinion were significant and if any of the diagnostic groups were more prone to change than others. The present paper is part of the study with UTN U1111-1260-1212.
    UNASSIGNED: Seventeen residents reviewed their last five case files, retrieving 85 diagnostic pairs of non-operational-based vs. operational-based diagnoses. The Stuart-Maxwell test did not indicate a significant opinion change (χ2 = 5.25, p = 0.39; power = 0.94) besides 30% of diagnostic changes. Despite not being statistically significant, 20.2% of all evaluations resulted in a change that would affect treatment choices. Using ICD-10 operational criteria slightly increased the number of observed diagnoses, but probably without clinical relevance. None of the non-operational diagnoses have a higher tendency to change with operational criteria application (χ2 = 11.6, p = 0.07). The female gender was associated with a higher diagnostic change tendency.
    UNASSIGNED: Applying ICD-10 operational criteria as a diagnostic test does not induce a statistically significant diagnostic opinion change in residents and no diagnostic group seems more sensible to diagnostic change. Gender-related differences in diagnostic opinion changes might be evidence of sunk cost bias. Although not statistically significant, using operational criteria after diagnostic elaboration might help to deal with subjects without adequate treatment response.
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  • 文章类型: Journal Article
    目标:尽管教育要求评估住院医师的教学能力,为此目的,存在有限的具有有效性证据的工具。现有的工具不允许教师以大型小组形式评估居民主导的教学,或者教学是否互动。本研究收集了关于使用居民主导的大型团体教学评估工具(Relate)的有效性证据,教师用来评估住院医师教学能力的工具。关系包括23种行为,分为六个要素:学习环境,目标和目标,谈话内容,促进理解和保留,会话管理,和关闭。
    方法:本研究采用梅西克统一的有效性框架。研究人员使用了来自三个儿科住院医师计划的居民主导教学的视频记录来开发Relate和评估者指南。通过参考框架培训对教师进行了仪器使用培训。在2018-2019年期间,所有站点的居民教学都进行了视频录制。两名训练有素的教师评估员评估了每个视频。获得了有关性能的描述性统计数据。有效性证据来源包括:评估者训练效果(反应过程),可靠性和可变性(内部结构),以及对里程碑评估的影响(与其他变量的关系)。
    结果:48个视频,来自16位居民,进行了分析。评估者培训将评估者间的可靠性从0.04提高到0.64。Φ系数可靠性为0.50。整体关系表现与儿科教学里程碑之间存在显着相关性,r=0.34,P=0.019。
    结论:关联提供了具有足够可靠性的有效性证据来衡量居民主导的大型小组教学能力。
    Despite educational mandates to assess resident teaching competence, limited instruments with validity evidence exist for this purpose. Existing instruments do not allow faculty to assess resident-led teaching in a large group format or whether teaching was interactive. This study gathers validity evidence on the use of the Resident-led Large Group Teaching Assessment Instrument (Relate), an instrument used by faculty to assess resident teaching competency. Relate comprises 23 behaviors divided into six elements: learning environment, goals and objectives, content of talk, promotion of understanding and retention, session management, and closure.
    Messick\'s unified validity framework was used for this study. Investigators used video recordings of resident-led teaching from three pediatric residency programs to develop Relate and a rater guidebook. Faculty were trained on instrument use through frame-of-reference training. Resident teaching at all sites was video-recorded during 2018-2019. Two trained faculty raters assessed each video. Descriptive statistics on performance were obtained. Validity evidence sources include: rater training effect (response process), reliability and variability (internal structure), and impact on Milestones assessment (relations to other variables).
    Forty-eight videos, from 16 residents, were analyzed. Rater training improved inter-rater reliability from 0.04 to 0.64. The Φ-coefficient reliability was 0.50. There was a significant correlation between overall Relate performance and the pediatric teaching Milestone, r = 0.34, P = .019.
    Relate provides validity evidence with sufficient reliability to measure resident-led large-group teaching competence.
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  • 文章类型: Journal Article
    NAPinICU问卷,专门用于评估重症监护病房中老年患者的需求,作为理解和解决其独特需求的宝贵工具。本研究应用了跨文化翻译过程,随后进行横断面调查,以测量患者的需求,并评估阿拉伯语翻译版本的NAPinICU问卷的心理测量特性。老年人翻译的问卷表现出很高的内容效度,良好的测试-重测可靠性和可接受的内部一致性。辨别效度证实了大学和私立医院患者之间需求评级的显着差异。这个经过翻译和验证的工具可以帮助评估重症监护病房老年人的需求。对这些患者需求的评估有助于提高护士和其他医疗保健提供者提供给他们的护理质量。
    The NAPinICU questionnaire, specifically designed to assess the needs of older adult patients in intensive care units, serves as a valuable tool for understanding and addressing their unique requirements. This study applied a cross-cultural translation process, followed by a cross-sectional survey to measure patients\' needs and evaluate the psychometric properties of the Arabic-translated version of the NAPinICU questionnaire. The older adults\' translated questionnaire demonstrated high content validity, good test-retest reliability and acceptable internal consistency. Discriminative validity confirmed significant differences in needs ratings between university and private hospital patients. This translated and validated tool can help in assessing the needs of older adults in intensive care units. Assessment of these patients\' needs assists in enhancing the quality of care delivered to them by nurses and other healthcare providers.
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  • 文章类型: Journal Article
    目的:参与者招募一直是临床试验中的主要挑战。本研究旨在开发和验证加入临床试验问卷(JoinCT),探讨患者参与临床试验的意愿及相关因素。
    方法:这项问卷开发研究涉及四个阶段:(i)探索和理解主题,(二)问卷编制,(三)内容效度测试,最后,(iv)问卷的实地测试。对于现场测试阶段,我们在具有不同社会人口统计学背景和医疗条件的癌症患者中进行了JoinCT的横断面自我管理调查.除了内容有效性,Cronbach的α用于评估域的内部一致性,并采用验证性因子分析评价JoinCT框架的模型拟合度。
    结果:共有389名受访者参与了调查。根据从现场数据收集阶段获得的结果,JoinCT由四个独立变量域组成,即“知识”,“对福利的感知”,“对风险的感知”,和“信心”。唯一的因变量是参与临床试验的意愿。Cronbach的最小α为0.937,与JoinCT整体框架的模型拟合也很好,比较拟合指数(>0.90),均方根误差近似(<0.08),和标准化均方根残差(<0.08)。
    结论:联合临床试验问卷(JoinCT)已成功验证,具有出色的信度和效度,和一个很好的模型。参与临床试验的意愿的主要因素是知识,感知的好处,对风险的感知,和信心。
    OBJECTIVE: Participant recruitment has always been a major challenge in clinical trials. This study aimed to develop and validate the Join Clinical Trial Questionnaire (JoinCT), exploring the willingness to join a clinical trial and associated factors in patients.
    METHODS: This questionnaire development study involved four phases: (i) exploring and understanding the subject matter, (ii) questionnaire development, (iii) content validity testing, and lastly, (iv) field-testing of the questionnaire. For the field-testing phase, a cross-sectional self-administered survey of JoinCT was conducted among cancer patients with various socio-demographic backgrounds and medical conditions. Besides content validity, Cronbach\'s alpha was used to evaluate the internal consistency of domains, and confirmatory factor analysis was used to evaluate the model fit of the JoinCT framework.
    RESULTS: A total of 389 respondents participated in the survey. Based on the results obtained from a field data collection phase, JoinCT consisted of four independent variables domains, namely \"knowledge\", \"perception of benefits\", \"perception of risks\", and \"confidence\". The only dependent variable was the willingness to participate in a clinical trial. The minimum Cronbach\'s alpha was 0.937, and the model fit for the overall framework of JoinCT is also excellent with Comparative Fit Index (> 0.90), root mean square error approximation (< 0.08), and Standardized Root Mean Square Residual (< 0.08).
    CONCLUSIONS: The Join Clinical Trial Questionnaire (JoinCT) was successfully validated with excellent reliability and validity, and a good model fit. The main factors that contribute to willingness to participate in clinical trials are knowledge, perception of benefits, perception of risks, and confidence.
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  • 文章类型: Journal Article
    背景:恶性热疗(MH)在中国是一种罕见的麻醉急症,死亡率很高。我们开发了基于微信小程序的恶性高热国家远程应急系统(MH-NRES),以提供实时应急系统,帮助中国麻醉师应对MH危机。然而,必须密切关注小程序的可用性。
    目的:本研究的目的是(1)评估基于小程序的MH-NRES对麻醉医师的可用性;(2)测试改良的mHealthapp可用性问卷的有效性和可靠性。
    方法:设计了移动应用程序评级量表(uMARS)的修改用户版本。连同系统可用性量表(SUS)和研究后系统可用性问卷(PSSUQ),另外两份经过验证的问卷,然后使用uMARS来评估MH-NRES的可用性。计算总分和uMARS子量表的Cronbachα以评估内部一致性。计算了3份问卷的相关系数。
    结果:在这项研究中,118名麻醉师对问卷做出了回应。整体平均uMARS评分为4.43±0.61,范围为3至5。平均PSSUQ评分在良好到良好的范围内,平均值为6.02±0.97,范围为3.19至7。总体SUS评分为76.0±17.6,范围为45至100。总uMARS评分具有优异的内部一致性(Cronbachα=0.984)。uMARS及其分量表与PSSUQ(系数0.758-0.819,P<0.001)和SUS(系数0.535-0.561,P<0.001)密切相关,分别。
    结论:从本研究的可用性评估问卷中获得的数据表明,MH-NRES在易用性方面的质量很高,满意度和感知有用性,这表明该系统可能是麻醉医师教育和管理MH危机的有用工具。未来需要来自高保真模拟和临床场景的反馈,以进一步评估该系统的可用性。
    Malignant hyperthermia (MH) is a rare anesthetic emergency with a high mortality rate in China. We developed a WeChat applet-based National Remote Emergency System for Malignant Hyperthermia (MH-NRES) to provide a real-time emergency system to help Chinese anesthesiologists deal with MH crises. However, it is imperative that close attention should be paid to the usability of the applet.
    The objectives of this study were to (1) evaluate the usability of the applet-based MH-NRES for anesthesiologists; and (2) to test the validity and reliability of a modified mHealth app usability questionnaire.
    A modified User Version of the Mobile Application Rating Scale (uMARS) was designed. Together with System Usability Scale (SUS) and Post-Study System Usability Questionnaire (PSSUQ), another two well-validated questionnaires, uMARS were then used to evaluate the usability of MH-NRES. The Cronbach alpha of the total score and the subscales of uMARS was calculated to evaluate the internal consistency. The correlation coefficients among three questionnaires were calculated.
    In this study, 118 anesthesiologists provided responses to the questionnaire. The overall mean uMARS score was 4.43 ± 0.61, which ranged from 3 to 5. The mean PSSUQ score were in good to excellent range with mean of 6.02 ± 0.97, which ranged from 3.19 to 7. The overall SUS score was 76.0 ± 17.6, which ranged from 45 to 100. The total uMARS score had excellent internal consistency (Cronbach alpha = 0.984). uMARS and its subscales were strongly correlated with PSSUQ (coefficient 0.758-0.819, P < 0.001) and SUS (coefficient 0.535-0.561, P < 0.001), respectively.
    Data obtained from the usability evaluation questionnaires in this study indicated a high quality of the MH-NRES on the ease of use, satisfaction and perceived usefulness, which suggest this system might be a useful tool for anesthesiologists\' education and management of MH crises. Future feedback from high-fidelity simulation and clinical scenarios are need for further usability evaluation of this system.
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  • 文章类型: Journal Article
    医学博士课程的教育已经转向强调临床能力,委托的专业活动提供了学习目标和结果的框架,在临床环境中进行评估。虽然目标和结果的确定和结构化定义已经发展,许多评估职员学生临床技能的方法相对保持不变。应用先进的统计设计和分析技术来研究临床技能评估的有效性的医学教育研究很少。一种稳健的统计方法,多特征多方法矩阵分析,可用于调查跨多个评估工具和设置的结构效度。四个特征被操作化,以代表关键临床技能的构建(专业性,数据收集,数据合成,和数据交付)。使用三种方法评估了这些特征(教师教练的直接观察,基于工作场所的临床评估,和客观结构化临床考试类型临床实践考试)。四个性状和三种方法相互关联,用于多性状-多方法矩阵分析。结果表明,三种方法的可靠性值在足够的范围内,大多数有效性系数具有统计学意义。收敛和发散有效性的最明显证据是具有专业特质。相同方法/不同性状分析的相关性表明方法效果很大;特别是在基于临床工作场所的评估中。多特征多方法矩阵方法,目前在医学教育中利用不足,可用于探索复杂结构的有效性证据,如临床技能。这些结果可以告知教师发展计划,以提高临床环境中评估的可靠性和有效性。
    Education in Doctor of Medicine programs has moved towards an emphasis on clinical competency, with entrustable professional activities providing a framework of learning objectives and outcomes to be assessed within the clinical environment. While the identification and structured definition of objectives and outcomes have evolved, many methods employed to assess clerkship students\' clinical skills remain relatively unchanged. There is a paucity of medical education research applying advanced statistical design and analytic techniques to investigate the validity of clinical skills assessment. One robust statistical method, multitrait-multimethod matrix analysis, can be applied to investigate construct validity across multiple assessment instruments and settings. Four traits were operationalized to represent the construct of critical clinical skills (professionalism, data gathering, data synthesis, and data delivery). The traits were assessed using three methods (direct observations by faculty coaches, clinical workplace-based evaluations, and objective structured clinical examination type clinical practice examinations). The four traits and three methods were intercorrelated for the multitrait-multimethod matrix analysis. The results indicated reliability values in the adequate to good range across the three methods with the majority of the validity coefficients demonstrating statistical significance. The clearest evidence for convergent and divergent validity was with the professionalism trait. The correlations on the same method/different traits analyses indicated substantial method effect; particularly on clinical workplace-based assessments. The multitrait-multimethod matrix approach, currently underutilized in medical education, could be employed to explore validity evidence of complex constructs such as clinical skills. These results can inform faculty development programs to improve the reliability and validity of assessments within the clinical environment.
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  • 文章类型: Journal Article
    背景:通常通过自我报告来评估心脑血管危险因素的存在。然而,在老龄化研究中,自我报告的心脑血管危险因素的信度和效度仍然不一致.
    目的:为了确定最常见的自我报告的血管危险因素的信度和效度:高血压,糖尿病,还有心脏病.
    方法:1,870名65岁或以上的非裔美国人,加勒比海西班牙裔,和非西班牙裔白人个体被招募作为衰老和痴呆的社区研究的一部分.我们评估了可靠性,有效性,灵敏度,特异性,和自我报告的高血压的百分比一致性,糖尿病,还有心脏病,与直接测量血压相比,血红蛋白A1c(HbA1c),和药物使用。分析随后按年龄分层,性别,教育,和种族群体。
    结果:高血压自我报告的可靠性,糖尿病,心脏病非常好。自我报告和临床措施之间的协议是中等的高血压(kappa:0.58),对糖尿病有好处(卡帕:0.76-0.79),中度心脏病(卡帕:0.45)因年龄而异,性别,教育,和种族群体。对高血压的敏感性和特异性为88.6%-78.1%,糖尿病患者为87.7%-92.0%(HbA1c≥6.5%)或92.7%-92.8%(HbA1c≥7%),心脏病的发生率为85.8%-75.5%。对于高血压,自我报告的一致性百分比为87.0%,91.6%-92.6%为糖尿病患者,心脏病占77.4%。
    结论:确定自我报告的高血压病史,糖尿病,与直接测量或药物使用相比,心脏病是可靠和有效的。
    Queries for the presence of cardiovascular and cerebrovascular risk factors are typically assessed through self-report. However, the reliability and validity of self-reported cardiovascular and cerebrovascular risk factors remain inconsistent in aging research.
    To determine the reliability and validity of the most frequently self-reported vascular risk factors: hypertension, diabetes, and heart disease.
    1,870 individuals aged 65 years or older among African Americans, Caribbean Hispanics, and white non-Hispanic individuals were recruited as part of a community study of aging and dementia. We assessed the reliability, validity, sensitivity, specificity, and percent agreement of self-reported hypertension, diabetes, and heart disease, in comparison with direct measures of blood pressure, hemoglobin A1c (HbA1c), and medication use. The analyses were subsequently stratified by age, sex, education, and ethnic group.
    Reliability of self-reported hypertension, diabetes, and heart disease was excellent. Agreement between self-reports and clinical measures was moderate for hypertension (kappa: 0.58), good for diabetes (kappa: 0.76-0.79), and moderate for heart disease (kappa: 0.45) differing slightly by age, sex, education, and ethnic group. Sensitivity and specificity for hypertension was 88.6% -78.1%, for diabetes was 87.7% -92.0% (HbA1c ≥6.5%) or 92.7% -92.8% (HbA1c ≥7%), and for heart disease was 85.8% -75.5%. Percent agreement of self-reported was 87.0% for hypertension, 91.6% -92.6% for diabetes, and 77.4% for heart disease.
    Ascertainment of self-reported histories of hypertension, diabetes, and heart disease are reliable and valid compared to direct measurements or medication use.
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