On the Usage of Combined Data Structures to Study COVID-19 in Understudied Populations.
On the Usage of Combined Data Structures to Study COVID-19 in Understudied Populations.
复制标题
关于使用组合数据结构研究未受研究人群中的 COVID-19。
DOI:
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发表时间:
2021
影响因子:
13.8
通讯作者:
David J. Schlueter
中科院分区:
文献类型:
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作者:
David J. Schlueter
In Bourgeois et al,1 the authors demonstrate the utility of electronic health record (EHR) data structures to systematically study an otherwise understudied population in the context of an ongoing pandemic. Furthermore, they provide an example of how to perform such analyses using data stored in different data models across different countries. Through the Consortium for Clinical Characterization of COVID-19 by EHR (4CE), data from 27 hospitals in 6 countries (from a larger consortium of global data from 351 hospitals from 7 countries) were combined to study COVID-19– associated clinical outcomes in the pediatric population, uncovering findings of elevated markers of inflammation, evidence of abnormalities in coagulation, cardiac arrhythmias, viral pneumonia, and respiratory failure. This work adds further knowledge to the manifestations of COVID-19 in children and youth that have been previously studied in systematic reviews.2,3 The ongoing COVID-19 pandemic has affected how we live and work in unprecedented ways. From widespread stay-at-home orders and mask mandates to working and instructing our children from home, the COVID-19 outbreak has profoundly affected every part of the globe. One notable facet of this pandemic is the amount of research that has been undertaken to address COVID-19. As of April 2021, a PubMed search for COVID-19 returned more than 110 000 indexed results, elucidating the vast amount of COVID-19–related research undertaken in the past several months. Much of this research is cooperative among disparate entities; from the release of the initial genetic sequence of SARS-CoV-2 to the public to collaborative development of vaccinations, collaboration has the potential to save lives in a timely manner. Collaborative research at a national or global scale can assist not only in the development of therapeutics but also in understanding the natural course of disease in otherwise understudied populations. For example, in Bourgeois et al,1 much is unknown about how COVID-19 affects children and youth because it is difficult to study the disease because of the challenges associated with including minors in clinical trials.1 In a narrative synthesis of pediatric COVID-19 evidence, Metha et al2 note that clinical data are scarce among much of the current literature, which illustrates a muchneeded area of study among pediatric patients with COVID-19. Despite being difficult, it is important to study the clinical course of disease in all populations. One natural data source for studying clinical outcomes among understudied populations is EHRs, which comprise structured and unstructured data collected as part of routine clinical care. Bourgeois et al1 write that “sites executed queries on local clinical data warehouses containing patient-level EHR data. To construct the required data files, sites used the Informatics for Integrating Biology & the Bedside platform, the Observational Medical Outcomes Partnership (OMOP) Common Data Model (CDM), Epic Clarity, or other clinical data warehouses.”1 EHR standards, such as OMOP, provide a common, standardized abstraction of medical concepts that translates site-specific medical concepts to a common vocabulary so that researchers may leverage data from multiple contributing sources. For example, in the case of OMOP, site-specific source condition concepts (eg, International Statistical Classification of Diseases and Related Health Problems, Tenth Revision [ICD10], or even nonstandard hospital-specific codes) are converted to the systemized nomenclature of medicine, or SNOMED, ontology as a common vocabulary. However, there is an inherent difficulty in the merging of data sources at such a scale at the row level because individual countries may have + Related article
DOI:
10.1056/nejmsr1809937
发表时间:
2019-08-15
期刊:
The New England journal of medicine
影响因子:
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作者:
All of Us Research Program Investigators;Denny JC;Rutter JL;Goldstein DB;Philippakis A;Smoller JW;Jenkins G;Dishman E
通讯作者:
Dishman E