THE POSSIBILITY OF USING ELECTRONIC MEDICAL RECORDS FOR CLINICAL OBSERVATION

Currently, healthcare practice generates data exchange and stores a huge amount of patient-specific information in electronic medical records (EMC) and auxiliary databases. EMC used in normal clinical practice, can now be used for clinical research. The various methods available for obtaining data d...

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Main Authors: R. D. Kurbanov, R. Kh. Trigulova
Format: Article
Language:Russian
Published: InterMedservice 2021-05-01
Series:Евразийский Кардиологический Журнал
Subjects:
Online Access:https://www.heartj.asia/jour/article/view/6268
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author R. D. Kurbanov
R. Kh. Trigulova
author_facet R. D. Kurbanov
R. Kh. Trigulova
author_sort R. D. Kurbanov
collection DOAJ
description Currently, healthcare practice generates data exchange and stores a huge amount of patient-specific information in electronic medical records (EMC) and auxiliary databases. EMC used in normal clinical practice, can now be used for clinical research. The various methods available for obtaining data during research projects, in particular from integrated EMCs, have some unique capabilities. Of course, there are problems and obstacles to expanding the use of EMC, and one of the solutions to these obstacles is to address issues of semantic compatibility, privacy, and security. The collective efforts of numerous international associations involved in the development of standards have led to the emergence of standards for both the structure and the semantics of clinical information that provide semantic compatibility between different systems. It is always necessary to remember that when using EMC for clinical trials, it is first necessary to integrate various types of information, in accordance with the criteria for acceptability of the protocol, elements of clinical trial data, EMC data for only one purpose – to enable cohort identification. Electronic control systems should be able to exchange information through the use of recently published international standards for their compatibility and clinically proven information structures to ensure consistent complete recording and data exchange between different patient groups. Such systems eliminate obstacles when using various clinical languages and documentation styles, as well as recognized incomplete routine entries. Under these conditions, research projects can use data on patients from various EMC systems from various medical institutions, as well as in international multilingual environments.
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spelling doaj-art-411ff64227ae4027b3bc8245bd5b03be2025-08-20T03:58:56ZrusInterMedserviceЕвразийский Кардиологический Журнал2225-16852305-07482021-05-0102788210.38109/2225-1685-2021-2-78-826236THE POSSIBILITY OF USING ELECTRONIC MEDICAL RECORDS FOR CLINICAL OBSERVATIONR. D. Kurbanov0R. Kh. Trigulova1Republican Specialized Scientific Practical Medical Center of CardiologyRepublican Specialized Scientific Practical Medical Center of CardiologyCurrently, healthcare practice generates data exchange and stores a huge amount of patient-specific information in electronic medical records (EMC) and auxiliary databases. EMC used in normal clinical practice, can now be used for clinical research. The various methods available for obtaining data during research projects, in particular from integrated EMCs, have some unique capabilities. Of course, there are problems and obstacles to expanding the use of EMC, and one of the solutions to these obstacles is to address issues of semantic compatibility, privacy, and security. The collective efforts of numerous international associations involved in the development of standards have led to the emergence of standards for both the structure and the semantics of clinical information that provide semantic compatibility between different systems. It is always necessary to remember that when using EMC for clinical trials, it is first necessary to integrate various types of information, in accordance with the criteria for acceptability of the protocol, elements of clinical trial data, EMC data for only one purpose – to enable cohort identification. Electronic control systems should be able to exchange information through the use of recently published international standards for their compatibility and clinically proven information structures to ensure consistent complete recording and data exchange between different patient groups. Such systems eliminate obstacles when using various clinical languages and documentation styles, as well as recognized incomplete routine entries. Under these conditions, research projects can use data on patients from various EMC systems from various medical institutions, as well as in international multilingual environments.https://www.heartj.asia/jour/article/view/6268electronic medical recordintegrated electronic medical record systemclinical studies, semantic compatibility
spellingShingle R. D. Kurbanov
R. Kh. Trigulova
THE POSSIBILITY OF USING ELECTRONIC MEDICAL RECORDS FOR CLINICAL OBSERVATION
Евразийский Кардиологический Журнал
electronic medical record
integrated electronic medical record system
clinical studies, semantic compatibility
title THE POSSIBILITY OF USING ELECTRONIC MEDICAL RECORDS FOR CLINICAL OBSERVATION
title_full THE POSSIBILITY OF USING ELECTRONIC MEDICAL RECORDS FOR CLINICAL OBSERVATION
title_fullStr THE POSSIBILITY OF USING ELECTRONIC MEDICAL RECORDS FOR CLINICAL OBSERVATION
title_full_unstemmed THE POSSIBILITY OF USING ELECTRONIC MEDICAL RECORDS FOR CLINICAL OBSERVATION
title_short THE POSSIBILITY OF USING ELECTRONIC MEDICAL RECORDS FOR CLINICAL OBSERVATION
title_sort possibility of using electronic medical records for clinical observation
topic electronic medical record
integrated electronic medical record system
clinical studies, semantic compatibility
url https://www.heartj.asia/jour/article/view/6268
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