Data analysis

数据分析
  • 文章类型: Journal Article
    目的:息肉和症状的准确诊断和量化对于制定慢性鼻窦炎伴鼻息肉病(CRSwNP)的治疗策略至关重要。这项初步研究旨在开发一种基于人工智能(AI)的图像分析系统,该系统能够从鼻内窥镜检查视频中分割鼻息肉。
    方法:回顾性分析2019年至2022年间52例CRSwNP患者的鼻内窥镜检查记录。提取的图像在Web应用程序Roboflow上手动分割。生成了342张图像的数据集,并将其分为训练(80%),验证(10%),和测试(10%)集。UltralyticsYOLOv8.0.28模型用于自动分割。
    结果:YOLOv8s-seg模型由195层组成,需要42.4GFLOP进行操作。当针对验证集进行测试时,该算法的精度为0.91,召回率为0.839,在50%IoU时的平均精度(mAP50)为0.949。对于分段任务,观察到类似的指标,包括50%到95%的IoU的mAP范围从0.675到0.679。
    结论:研究表明,经过精心训练的AI算法可以有效地识别和描绘CRSwNP患者的鼻息肉。尽管存在某些限制,例如专注于CRSwNP特定样品,该算法为现有的诊断方法提供了一个有前途的补充工具。
    OBJECTIVE: Accurate diagnosis and quantification of polyps and symptoms are pivotal for planning the therapeutic strategy of Chronic rhinosinusitis with nasal polyposis (CRSwNP). This pilot study aimed to develop an artificial intelligence (AI)-based image analysis system capable of segmenting nasal polyps from nasal endoscopy videos.
    METHODS: Recorded nasal videoendoscopies from 52 patients diagnosed with CRSwNP between 2019 and 2022 were retrospectively analyzed. Images extracted were manually segmented on the web application Roboflow. A dataset of 342 images was generated and divided into training (80%), validation (10%), and testing (10%) sets. The Ultralytics YOLOv8.0.28 model was employed for automated segmentation.
    RESULTS: The YOLOv8s-seg model consisted of 195 layers and required 42.4 GFLOPs for operation. When tested against the validation set, the algorithm achieved a precision of 0.91, recall of 0.839, and mean average precision at 50% IoU (mAP50) of 0.949. For the segmentation task, similar metrics were observed, including a mAP ranging from 0.675 to 0.679 for IoUs between 50% and 95%.
    CONCLUSIONS: The study shows that a carefully trained AI algorithm can effectively identify and delineate nasal polyps in patients with CRSwNP. Despite certain limitations like the focus on CRSwNP-specific samples, the algorithm presents a promising complementary tool to existing diagnostic methods.
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  • 文章类型: Journal Article
    目的:本研究旨在使用韩国医学检查中的真实和模拟数据,比较和评估两种停止规则(SEM0.3和0.25)下的计算机自适应测试(CAT)的效率和准确性。
    方法:本研究采用事后模拟和真实数据分析来探索医学检查中CAT的最佳停止规则。真实数据来自哈勒姆大学医学院2020年考试期间三年级医学生的反应。模拟数据是使用R中真实项目库的估计参数生成的。结果变量包括通过或失败的受试者数量,SEM值为0.25和0.30,管理的项目数,和相关性。通过基于0.0的切分检查通过或失败的一致性来评估真实CAT结果的一致性。通过比较两种停止规则下管理的物品的平均数量来评估所有CAT设计的效率。
    结果:SEM0.25和SEM0.30均在CAT中提供了准确性和效率之间的良好平衡。实际数据显示,两种SEM条件之间的通过/失败结果差异最小,能力估计之间的相关性很高(r=0.99)。模拟结果证实了这些发现,表示真实数据和模拟数据之间相似的平均项目编号。
    结论:研究结果表明,在Rasch模型的背景下,SEM0.25和0.30都是有效的终止标准,在CAT中平衡准确性和效率。
    OBJECTIVE: This study aimed to compare and evaluate the efficiency and accuracy of computerized adaptive testing (CAT) under two stopping rules (SEM 0.3 and 0.25) using both real and simulated data in medical examinations in Korea.
    METHODS: This study employed post-hoc simulation and real data analysis to explore the optimal stopping rule for CAT in medical examinations. The real data were obtained from the responses of 3rd-year medical students during examinations in 2020 at Hallym University College of Medicine. Simulated data were generated using estimated parameters from a real item bank in R. Outcome variables included the number of examinees\' passing or failing with SEM values of 0.25 and 0.30, the number of items administered, and the correlation. The consistency of real CAT result was evaluated by examining consistency of pass or fail based on a cut score of 0.0. The efficiency of all CAT designs was assessed by comparing the average number of items administered under both stopping rules.
    RESULTS: Both SEM 0.25 and SEM 0.30 provided a good balance between accuracy and efficiency in CAT. The real data showed minimal differences in pass/fail outcomes between the 2 SEM conditions, with a high correlation (r = 0.99) between ability estimates. The simulation results confirmed these findings, indicating similar average item numbers between real and simulated data.
    CONCLUSIONS: The findings suggest that both SEM 0.25 and 0.30 are effective termination criteria in the context of the Rasch model, balancing accuracy and efficiency in CAT.
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  • 文章类型: Journal Article
    COVID-19的严重结局与年龄增长和合并症有关。我们研究的具体目的是确定COVID-19对肝硬化患者临床病程和预后的影响。
    我们从VA国家资料库检索数据,并确定了患有肝硬化的SARS-CoV-2RNA测试患者。根据人口统计学和合并症,每位病毒阳性患者与病毒阴性受试者的倾向匹配。主要终点是COVID-19诊断后30天内的死亡,次要终点是14天内的住院。
    在1,115,037名接受SARS-CoV-2RNA检测的个体中,31,680患有肝硬化。这些病人中,4456名病毒阳性患者与8752名病毒阴性受试者倾向匹配。在这个13,208人的队列中,中位年龄为67岁,95%为男性。大多数有多种合并症。酒精使用,丙型肝炎和MASH是肝硬化的主要病因。在基线,MELD中位数为6%,21%有肝功能失代偿.高龄是住院和死亡率的最重要决定因素。合并症,饮酒和MELD增加了住院的可能性,而SARS-CoV-2阳性降低了第14天的住院风险.MELD与较高的死亡风险相关,而疫苗接种降低了住院和死亡的风险。SARS-CoV-2阳性使第30天的死亡风险增加了72%,第90天的死亡风险增加了26%。
    尽管发生COVID-19的肝硬化患者住院的可能性较小,与病毒阴性者相比,他们更有可能在30天内死亡。接种疫苗可有效减少住院和死亡。
    UNASSIGNED: Severe outcomes of COVID-19 are associated with advancing age and comorbidities. The specific aim of our study was to determine the impact of COVID-19 on the clinical course and outcome of patients with cirrhosis.
    UNASSIGNED: We retrieved data from VA national repository and identified patients tested for SARS-CoV-2 RNA who had cirrhosis. Each virus positive patient was propensity-matched with virus negative subjects by demographics and comorbidities. Primary endpoint was death within 30 days of COVID-19 diagnosis and secondary endpoint was hospitalization within 14 days.
    UNASSIGNED: Among 1,115,037 individuals tested for SARS-CoV-2 RNA, 31,680 had cirrhosis. Of those patients, 4456 virus positive patients were propensity-matched with 8752 virus negative subjects. In this cohort of 13,208, median age was 67 years and 95% were male. Most had multiple comorbidities. Alcohol use, hepatitis C and MASH were the dominant etiologies of cirrhosis. At baseline, median MELD was 6% and 21% had hepatic decompensation. Advanced age was the most significant determinant of hospitalization and mortality. Comorbidities, alcohol use and MELD increased the likelihood of hospitalization whereas SARS-CoV-2 positivity had lower Day-14 hospitalization hazard. MELD was associated with higher mortality hazard whereas vaccination reduced the hazard of hospitalization and death. SARS-CoV-2 positivity increased the hazard of death at Day-30 by 72% and at Day-90 by 26%.
    UNASSIGNED: Although patients with cirrhosis who developed COVID-19 were less likely to be hospitalized, they were more likely to die within 30 days compared to their virus negative counterparts. Vaccination was effective in reducing both hospitalization and death.
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  • 文章类型: Journal Article
    分布式分析平台的开发是由满足各种治理相关或法律约束的日益增长的需求推动的。在这些平台中,所谓的个人健康培训(PHT)是近年来出现的代表之一。然而,在需要来自具有不同PHT基础设施的站点的数据的项目中,机构面临着多种PHT生态系统组合带来的挑战,包括数据治理,法规遵从性,或修改现有工作流。在这些场景中,平台的互操作性更好。在这项工作中,我们介绍了PHT技术互操作性的概念框架,涵盖了五个基本要求:数据集成,统一车站标识符,相互元数据,一致的安全协议,商业逻辑。我们在一项可行性研究中评估了我们的概念,该研究涉及两个不同的PHT基础设施:PHT-meDIC和PADME。我们分析了蒂宾根大学医院和莱比锡大学医院患者的脑白质营养不良数据,和亚琛大学医院的鉴别诊断患者。我们的研究结果证明了这两个PHT基础设施之间的技术互操作性,允许研究人员在参与机构中进行分析。与多归属策略相比,我们的方法更节省空间,它只显示了一个最小的时间开销。
    The development of platforms for distributed analytics has been driven by a growing need to comply with various governance-related or legal constraints. Among these platforms, the so-called Personal Health Train (PHT) is one representative that has emerged over the recent years. However, in projects that require data from sites featuring different PHT infrastructures, institutions are facing challenges emerging from the combination of multiple PHT ecosystems, including data governance, regulatory compliance, or the modification of existing workflows. In these scenarios, the interoperability of the platforms is preferable. In this work, we introduce a conceptual framework for the technical interoperability of the PHT covering five essential requirements: Data integration, unified station identifiers, mutual metadata, aligned security protocols, and business logic. We evaluated our concept in a feasibility study that involves two distinct PHT infrastructures: PHT-meDIC and PADME. We analyzed data on leukodystrophy from patients in the University Hospitals of Tübingen and Leipzig, and patients with differential diagnoses at the University Hospital Aachen. The results of our study demonstrate the technical interoperability between these two PHT infrastructures, allowing researchers to perform analyses across the participating institutions. Our method is more space-efficient compared to the multi-homing strategy, and it shows only a minimal time overhead.
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  • 文章类型: Journal Article
    获取个人层面的健康数据对于获得新见解和推进科学发展至关重要。特别是,基于人工智能的现代方法依赖于对大型数据集的可用性和访问。在卫生部门,由于隐私问题,访问个人级别的数据通常具有挑战性。一个有希望的替代方案是生成完全合成的数据,即,通过与原始数据具有相似统计特性的随机过程生成的数据,但与原始的个人级别记录没有一对一的对应关系。在这项研究中,我们使用最先进的合成数据生成方法,并针对营养领域的特定用例对生成的数据进行深入的质量分析。我们证明了需要对超越描述性统计的合成数据进行仔细分析,并为如何实现合成数据集的全部潜力提供有价值的见解。通过扩展方法,而且通过彻底分析从训练模型中采样的效果,我们能够在所选用例中大量重现重要的现实分析结果。
    Access to individual-level health data is essential for gaining new insights and advancing science. In particular, modern methods based on artificial intelligence rely on the availability of and access to large datasets. In the health sector, access to individual-level data is often challenging due to privacy concerns. A promising alternative is the generation of fully synthetic data, i.e., data generated through a randomised process that have similar statistical properties as the original data, but do not have a one-to-one correspondence with the original individual-level records. In this study, we use a state-of-the-art synthetic data generation method and perform in-depth quality analyses of the generated data for a specific use case in the field of nutrition. We demonstrate the need for careful analyses of synthetic data that go beyond descriptive statistics and provide valuable insights into how to realise the full potential of synthetic datasets. By extending the methods, but also by thoroughly analysing the effects of sampling from a trained model, we are able to largely reproduce significant real-world analysis results in the chosen use case.
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  • 文章类型: Journal Article
    背景:鼓励性肺活量计是一种基本且通用的医疗设备,无法从中直接收集电子医疗保健数据。因此,尽管有大量研究调查临床应用,对于最佳器械使用,目前尚无共识,且支持其预期益处的证据很少,如预防术后呼吸系统并发症.
    目的:该研究的目的是开发和测试用于激励肺活量计数据捕获的附加硬件设备。
    方法:设计了一种附加设备,已建成,并使用反射式光学传感器进行测试,以识别普通激励肺活量计的容积活塞和流量线轴的实时位置。调查人员使用数字流量计手动测试了传感器液位精度和触发范围校准。创建并测试了有效的呼吸分类算法,以从无效的呼吸尝试中确定有效。为了评估实时使用情况,使用激励肺活量计和附加设备作为使用AppleiPad的控制器开发了一个视频游戏。
    结果:在用户测试中,以99%(SD1.4%)的体积准确度和100%的流量准确度捕获传感器位置.中值和平均体积在目标体积传感器水平的7.5%(SD6%)内,和最大传感器触发值很少超过预期的传感器水平,在2种相似但不同的激励肺活量计设计上显示出与放置良好的相关性。呼吸分类算法在用户测试中显示出100%的灵敏度和99%的特异性,并且该设备作为视频游戏控制器实时操作而没有明显的干扰或延迟。
    结论:创建了一种用于激励肺活量计的有效且可重复使用的附加设备,以允许收集以前无法访问的激励肺活量计数据,并演示物联网在普通医院设备上的使用。该设计显示出高传感器精度和在实时应用中使用数据的能力,显示出捕获当前无法访问的临床数据的能力的希望。进一步使用该设备可以促进对激励肺活量计的改进研究,以提高采用率,激励坚持,并探讨其临床效果,有助于指导临床护理。
    BACKGROUND: The incentive spirometer is a basic and common medical device from which electronic health care data cannot be directly collected. As a result, despite numerous studies investigating clinical use, there remains little consensus on optimal device use and sparse evidence supporting its intended benefits such as prevention of postoperative respiratory complications.
    OBJECTIVE: The aim of the study is to develop and test an add-on hardware device for data capture of the incentive spirometer.
    METHODS: An add-on device was designed, built, and tested using reflective optical sensors to identify the real-time location of the volume piston and flow bobbin of a common incentive spirometer. Investigators manually tested sensor level accuracies and triggering range calibrations using a digital flowmeter. A valid breath classification algorithm was created and tested to determine valid from invalid breath attempts. To assess real-time use, a video game was developed using the incentive spirometer and add-on device as a controller using the Apple iPad.
    RESULTS: In user testing, sensor locations were captured at an accuracy of 99% (SD 1.4%) for volume and 100% accuracy for flow. Median and average volumes were within 7.5% (SD 6%) of target volume sensor levels, and maximum sensor triggering values seldom exceeded intended sensor levels, showing a good correlation to placement on 2 similar but distinct incentive spirometer designs. The breath classification algorithm displayed a 100% sensitivity and a 99% specificity on user testing, and the device operated as a video game controller in real time without noticeable interference or delay.
    CONCLUSIONS: An effective and reusable add-on device for the incentive spirometer was created to allow the collection of previously inaccessible incentive spirometer data and demonstrate Internet-of-Things use on a common hospital device. This design showed high sensor accuracies and the ability to use data in real-time applications, showing promise in the ability to capture currently inaccessible clinical data. Further use of this device could facilitate improved research into the incentive spirometer to improve adoption, incentivize adherence, and investigate the clinical effectiveness to help guide clinical care.
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  • 文章类型: Journal Article
    VIVID(通过创新设计解决植入式心脏复律除颤器治疗中种族差异的视频)研究是一项多中心研究,随机对照试验旨在评估基于视频的决策支持工具在符合一级预防ICD指南标准的Black患者中增强植入式心律转复除颤器(ICD)植入的知情同意方面的有效性.在更广泛的VIVID随机试验中,我们进行了一项定性调查,以阐明考虑植入ICD作为心脏骤停一级预防的黑人个体的决定因素.
    在2016年10月至2019年7月之间,在随机分组的2个时间点进行了深入访谈,≈7天(决定的时间间隔)和90天;确定ICD植入的时间间隔。访谈结果按随机分组进行分类,那些分配给2个基于遭遇的视频决策支持工具或标准护理(无视频)中的1个。面试参与者是有目的地选择的,以确保跨性别的多样性,年龄,教育背景,研究地点,和随机分组;参与者来自美国14个学术和社区的电生理学诊所。数据分析采用了主题分析技术。
    在1周时采访了不同的黑人个体样本(n=59;女性,37.3%)和90天(n=48;女性,39.6%)。影响黑人个体考虑一级预防ICD植入的决定的主要因素是(1)他们的临床医生对ICD植入的建议;(2)他们对自己心脏健康状况的看法;(3)为了家人延长生命的愿望。
    这些发现提供了有价值的见解,可以指导临床医生在与ICD植入相关的共同决策过程中与Black患者进行沟通。
    UNASSIGNED: The VIVID (Videos for Addressing Racial Disparities in Implantable Cardioverter Defibrillator Therapy via Innovative Designs) study was a multicenter, randomized controlled trial aimed at evaluating the effectiveness of a video-based decision support tool in enhancing informed consent for implantable cardioverter defibrillator (ICD) implantation among Black patients who met guideline criteria for primary prevention ICDs. Within the broader VIVID randomized trial, a qualitative investigation was conducted to elucidate the decisional factors among Black individuals considering ICD implantation for the primary prevention of sudden cardiac arrest.
    UNASSIGNED: Between October 2016 and July 2019, in-depth interviews were conducted at 2 time points from randomization, ≈7 days (time interval for the decision) and at 90 days; the time interval for determining ICD implantation. Interview findings were categorized by randomized groups, those assigned to 1 of the 2 encounter-based video decision support tools or standard care (without video). Interview participants were purposefully selected to ensure diversity across gender, age, educational background, research site, and randomization group; participants were sampled from 14 academic and community-based electrophysiology clinics in the United States. Data analysis employed applied thematic analysis techniques.
    UNASSIGNED: A diverse sample of Black individuals were interviewed at 1 week (n=59; female, 37.3%) and 90 days (n=48; female, 39.6%). The primary factors influencing the decisions of Black individuals considering a primary prevention ICD implantation were (1) their clinicians\' recommendations for ICD implantation; (2) their perception of their cardiac health status; and (3) a desire to prolong their lives for the sake of their families.
    UNASSIGNED: These findings offer valuable insights that may guide clinicians in their communication with Black patients during shared decision-making encounters related to ICD implantation.
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  • 文章类型: Journal Article
    血块形成,止血和血栓形成的关键过程,它在各种医疗条件下的影响引起了广泛的关注。血凝块的显微镜检查提供了对其组成和结构的重要见解,帮助了解血凝块病理生理学和制定有针对性的治疗策略。这项研究探讨了使用拓扑数据分析(TDA)来评估血浆凝块的微观特征,专注于元素组件的识别,洞和Wasserstein距离。这种方法应该使研究人员能够根据其拓扑结构对纤维蛋白网络进行客观分类。我们在静态条件下从猪和人柠檬酸化血浆样品中形成的血浆凝块上测试了这种数学表征方法,其中研究了稀释和直接凝血酶抑制的效果。分析显示荧光标记的纤维蛋白网络的共聚焦显微镜图像。两种治疗都导致血浆凝块结构的视觉差异,这可以用TDA量化。基线和稀释样品之间的显着差异,以及用阿加曲班抗凝血的血液,被数学检测到。因此,TDA可能指示稳定性受损的凝块,为血栓形成风险评估提供了有价值的工具。总之,血浆凝块的显微镜检查,再加上拓扑数据分析,为全面表征凝块微观结构提供了一条有前途的途径。这种方法可以有助于更深入地了解凝块病理生理学,从而完善我们评估凝块特征的能力。
    Blood clot formation, a crucial process in hemostasis and thrombosis, has garnered substantial attention for its implications in various medical conditions. Microscopic examination of blood clots provides vital insights into their composition and structure, aiding in the understanding of clot pathophysiology and the development of targeted therapeutic strategies. This study explores the use of topological data analysis (TDA) to assess plasma clot characteristics microscopically, focusing on the identification of the elements components, holes and Wasserstein distances. This approach should enable researchers to objectively classify fibrin networks based on their topologic architecture. We tested this mathematical characterization approach on plasma clots formed in static conditions from porcine and human citrated plasma samples, where the effect of dilution and direct thrombin inhibition was explored. Confocal microscopy images showing fluorescence labeled fibrin networks were analyzed. Both treatments resulted in visual differences in plasma clot architecture, which could be quantified using TDA. Significant differences between baseline and diluted samples, as well as blood anticoagulated with argatroban, were detected mathematically. Therefore, TDA could be indicative of clots with compromised stability, providing a valuable tool for thrombosis risk assessment. In conclusion, microscopic examination of plasma clots, coupled with Topological Data Analysis, offers a promising avenue for comprehensive characterization of clot microstructure. This method could contribute to a deeper understanding of clot pathophysiology and thereby refine our ability to assess clot characteristics.
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  • 文章类型: Journal Article
    背景:使用嵌入式单案例研究设计来探索新西兰农村男性获得心理健康服务的经验。研究人员必须承认案例研究中的定位性,并且主要作者使用反身实践来承认他的价值观和信念。
    目的:探讨和论证第一作者作为内部研究者的反身过程。
    结论:三组参与了这项研究:有心理健康挑战的男性,他们的合作伙伴,和心理健康临床医生。本文通过备忘录和日记在当前文献的背景下进行了初步研究。
    结论:反身性对于确保研究过程完成和确定偏差至关重要。定位存在于一个连续统一体上,研究人员对自己诚实是至关重要的,被调查的主题和小组,为了尊重参与者和他们所代表的人,以及致力于揭示真相。
    结论:内幕研究有可能弥合学术界和实践之间的差距。它促进了研究知识直接向从业人员的转移,导致更多的循证决策和实践。
    BACKGROUND: An embedded single case-study design was used to explore the experiences of men in rural New Zealand accessing mental health services. It is essential for researchers to acknowledge positionality in case study research and the lead author used reflexive practice to acknowledge his values and beliefs.
    OBJECTIVE: To explore and demonstrate the reflexive process of the lead author\'s position as an inside researcher.
    CONCLUSIONS: Three groups were involved in the research: men with mental health challenges, their partners, and mental health clinicians. The article presents the initial research through memos and diarying in the context of current literature.
    CONCLUSIONS: Reflexivity is essential for ensuring the research process is complete and biases are identified. Positionality exists on a continuum and it is critical for researchers to be honest with themselves, the topic and the group being investigated, to show respect for the participants and the people they represent, as well as to be committed to revealing the truth.
    CONCLUSIONS: Insider research has the potential to bridge the gap between academia and practice. It facilitates the transfer of research knowledge directly to practitioners, leading to more evidence-informed decision-making and practice.
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  • 文章类型: Journal Article
    背景:许多国家的医疗保健监管机构对医疗保健提供者进行检查并公布检查结果,旨在提高护理质量。2014年,医疗质量委员会首次开始对英格兰的一般做法进行全面检查。假定检查和评级将提高标准并改善护理,但任何改善的存在和程度是未知的。我们的目标是确定实践检查评级是否与处方指标的过去表现相关,以及检查后处方行为是否发生变化。
    方法:使用英格兰6771个一般实践的数据集进行纵向研究。实践检查日期和得分与每月关于抗生素处方指标的实践水平数据挂钩,催眠药和非甾体抗炎药。该样本涵盖2014年9月至2018年12月期间接受首次检查的实践。使用回归分析和检查的差异时间来确定对处方的影响。
    结果:在检查开始之前,评级较高的实践具有更好的处方。在检查后的六个月里,未观察到处方的总体变化.然而,最佳和较差评级做法之间的差异有所减少,但并不完全。从长远来看也是如此。几乎没有证据表明,一旦评级公开,实践对检查的预期做出了反应,或者做出了不同的反应。
    结论:虽然观察到的处方行为的一些历史变化由于检查和评级过程而有所减少,我们发现这种变化很小,似乎来自评级较低的做法的改善和评级较高的做法的恶化。虽然检查和评级无疑会产生其他影响,这些处方指标基本没有变化.
    BACKGROUND: Healthcare regulators in many countries undertake inspections of healthcare providers and publish inspection outcomes with the intention of improving quality of care. Comprehensive inspections of general practices in England by the Care Quality Commission began for the first time in 2014. It is assumed that inspection and rating will raise standards and improve care, but the presence and extent of any improvements is unknown. We aim to determine if practice inspection ratings are associated with past performance on prescribing indicators and if prescribing behaviour changes following inspection.
    METHODS: Longitudinal study using a dataset of 6771 general practices in England. Practice inspection date and score was linked with monthly practice-level data on prescribing indicators relating to antibiotics, hypnotics and non-steroidal anti-inflammatory drugs. The sample covers practices receiving their first inspection between September 2014 and December 2018. Regression analysis and the differential timing of inspections is used to identify the impact on prescribing.
    RESULTS: Better-rated practices had better prescribing in the period before inspections began. In the six months following inspections, no overall change in prescribing was observed. However, the differences between the best and worse rated practices were reduced but not fully. The same is also true when taking a longer-term view. There is little evidence that practices responded in anticipation of inspection or reacted differently once the ratings were made public.
    CONCLUSIONS: While some of the observed historic variation in prescribing behaviour has been lessened by the process of inspection and ratings, we find this change is small and appears to come from both improvements among lower-rated practices and deteriorations among higher-rated practices. While inspection and rating no doubt had other impacts, these prescribing indicators were largely unchanged.
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