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Brief report of real-world evidence development (RWD/RWE) in 2021: United States, Russia, and the Eurasian Economic Union (EAEU) 2021年现实世界证据发展(RWD/RWE)简要报告:美国、俄罗斯和欧亚经济联盟(EAEU)
Pub Date : 2022-01-31 DOI: 10.37489/2782-3784-myrwd-6.
A. Kolbin, D. Belousov
The article provides a brief overview of the main trends in the development of the real-world data and real-world evidence (RWD/RWE) paradigm in the United States, Russia, and the Eurasian Economic Union (EAEU) in 2021. The review is compiled in calendar sequence. First, events in the United States are presented, sourced from the information resource, ‘The Evidence Base’. Following this, data for the Russian Federation and the EAEU is collected and stored on the ‘myRWD — Real Clinical Practice’ Facebook page, and in the journal, ‘Real-World Data & Evidence’. The information is summarized and a complete picture of the development of real clinical practice and its evidence in the indicated countries is given.
本文简要概述了2021年美国、俄罗斯和欧亚经济联盟(EAEU)真实世界数据和真实世界证据(RWD/RWE)范式发展的主要趋势。评论是按日历顺序编写的。首先,介绍了来自信息资源“证据库”的美国事件。在此之后,俄罗斯联邦和欧亚经济联盟的数据被收集并存储在“myRWD -真实临床实践”Facebook页面和“真实世界数据与证据”杂志上。总结了这些信息,并给出了实际临床实践发展的完整图景及其在指定国家的证据。
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引用次数: 6
Resolution based on the results of the conference: "RWD/ RWE – Research Tools of Real-World Clinical Practice Today and Tomorrow" 基于会议结果的决议:“RWD/ RWE -现实世界临床实践的研究工具的今天和明天”
Pub Date : 2021-10-25 DOI: 10.37489/2782-3784-myrwd-5
A. Kolbin
On September 16, 2021, the Association of Health Technology Assessment Professionals, the Association of Russian Clinical Pharmacologists, St. Petersburg Branch of ISPOR organized the II annual scientific and practical conference with international participation: "RWD/RWE – Research Tools of Real-World Clinical Practice Today and Tomorrow". The topic of the conference brought together leading Russian and world experts in the field of RWD/RWE. 
2021年9月16日,卫生技术评估专业人员协会,俄罗斯临床药理学家协会,ISPOR圣彼得堡分会组织了第二届国际参与的年度科学和实践会议:“RWD/RWE -现实世界临床实践的研究工具今天和明天”。会议的主题汇集了RWD/RWE领域的俄罗斯和世界领先专家。
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引用次数: 7
Applying real-world data to justify requirements to purchased drugs in public procurement 在公共采购中应用真实数据来证明购买药品的要求
Pub Date : 2021-09-16 DOI: 10.37489/2782-3784-myrwd-4
M. Borzova
The article describes the approaches of law enforcement practice in relation to the regulatory limits within which a medical institution may exercise it's right to establish requirements for purchased drugs based on purchaser's clinical practice and its own clinical experience.
本文介绍了医疗机构根据购买者的临床实践和自身的临床经验,在一定的监管限制范围内行使对采购药品建立要求的权利的执法实践方法。
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引用次数: 1
Registers as the basis for data collection and evidence building 登记册作为数据收集和证据建立的基础
Pub Date : 2021-09-01 DOI: 10.37489/2782-3784-myrwd-3
Российская Федерация, V. IvanovA., Zao
The development of medical science requires a constant increase in the effectiveness and safety of treatment. Collection of real-world data (RWD) is one way of solving these problems. Clinical registries are one of the most important parts of this process. Clinical registries allow collecting data on the use of medical technologies and monitoring the results of therapy in real clinical practice. The introduction of patient registers and the collection of RWD data into widespread medical practice can help to optimize costs in the treatment of high-cost diseases and to better plan the budget.
医学的发展要求不断提高治疗的有效性和安全性。收集实际数据(RWD)是解决这些问题的一种方法。临床登记是这一过程中最重要的部分之一。临床登记可以收集有关医疗技术使用的数据,并在实际临床实践中监测治疗结果。在广泛的医疗实践中引入患者登记和收集RWD数据可以帮助优化高成本疾病的治疗成本,并更好地规划预算。
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引用次数: 4
Paracetamol safety in COVID-19 对乙酰氨基酚在COVID-19中的安全性
Pub Date : 2021-09-01 DOI: 10.37489/2782-3784-myrwd-2
B. Romanov
The relevance of paracetamol safety assessment is associated with broad recommendations for its use as a symptomatic agent in COVID-19 and an agent for adverse events following vaccination to prevent COVID-19.Objectives. Conducting a review of global paracetamol safety data during the initial period of COVID-19 pandemic (in 2020 and in the first half of 2021).Materials and methods. 2,356 scientific articles and their abstracts on paracetamol safety in electronic libraries; data on 2,272 clinical trials of paracetamol in ClinicalTrials.gov and the State Register of Medicines of the Ministry of Health of the Russian Federation; 173,707 individual reports of adverse drugs reactions of paracetamol in the international pharmacovigilance database VigiBase. The data were evaluated by statistical methods in the VigiLyze analytical system (authorized expert access).Results. No publications and completed clinical trials were found on the safety issue of paracetamol use in COVID-19. During the initial period of COVID-19 pandemic (from January 1, 2020 to July 31, 2021), the number of reports of paracetamol safety issues included in VigiBase decreased by 22,1%, which may be due to a decrease in the number of specialists sending reports on safety, with an increase of their duties and with a switching attention of these specialists and patients to other problems associated with the COVID-19 pandemic. No changes have been identified in the sources of safety data and trade names for paracetamol medicinal products. It has been established that the main part (99,4% of cases) of side effects associated with paracetamol develops outside the use of vaccines for the prevention of COVID-19. Pre-COVID and COVID data include information on 2,692 and 2,527 names of various paracetamol safety concerns, respectively. These data overlap the list of side effects specified in instructions for medical use and include new symptoms not described in instructions for medical use.Conclusions. The lack of safety signals may be due to the lack of alertness of specialists and marketing authorization holders regarding paracetamol. During the COVID period, the structure and frequency of paracetamol safety concerns codified in terms of MedDRA (version 24.0) have changed, which can be studied in future studies of paracetamol, ibuprofen and other medicinal products.
扑热息痛安全性评估的相关性与广泛建议将其用作COVID-19的症状药物和预防疫苗接种后不良事件的药物有关。对2019冠状病毒病大流行初期(2020年和2021年上半年)全球扑热息痛安全性数据进行审查。材料和方法。2356篇电子图书馆扑热息痛安全性科学论文及其摘要;关于临床试验网站和俄罗斯联邦卫生部国家药品注册的2,272项扑热息痛临床试验的数据;国际药物警戒数据库VigiBase中有173,707例扑热息痛不良反应的个人报告。在VigiLyze分析系统(授权专家访问)中采用统计方法对数据进行评估。没有关于COVID-19使用扑热息痛安全性问题的出版物和已完成的临床试验。在COVID-19大流行初期(2020年1月1日至2021年7月31日),VigiBase中包含的扑热息痛安全问题报告数量减少了22.1%,这可能是由于发送安全报告的专家数量减少,他们的职责增加,这些专家和患者的注意力转向了与COVID-19大流行相关的其他问题。在扑热息痛药品的安全数据来源和商品名称方面没有发现任何变化。已经确定,与扑热息痛相关的主要副作用(99.4%的病例)是在预防COVID-19的疫苗使用之外发生的。COVID前和COVID数据分别包括2,692和2,527个各种扑热息痛安全问题的信息。这些数据与医疗使用说明书中规定的副作用列表重叠,并包括医疗使用说明书中未描述的新症状。缺乏安全信号可能是由于专家和上市许可持有人对扑热息痛缺乏警惕性。在COVID期间,根据MedDRA(24.0版本)编纂的扑热息痛安全问题的结构和频率发生了变化,可以在未来对扑热息痛、布洛芬和其他药品的研究中进行研究。
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引用次数: 0
Why do we need "Real-World Data & Evidence", the new scientific electronic journal? 为什么我们需要新的科学电子期刊《真实世界的数据与证据》?
Pub Date : 2021-08-03 DOI: 10.37489/2782-3784-myrwd-1
A. Kolbin
The modern request of the global healthcare system is the collection and analysis of the information obtained during the analysis of data collected in research of routine medical practice, namely real-world data (RWD), and the evidence based on it, real-world evidence (RWE).
全球卫生保健系统的现代要求是收集和分析在日常医疗实践研究中收集的数据分析过程中获得的信息,即真实世界数据(RWD),以及基于它的证据,即真实世界证据(RWE)。
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引用次数: 1
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Real-World Data & Evidence
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