• The Journal of the Korea Contents Association
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• v.20 no.5
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• pp.236-242
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• 2020

Big data technology has been rising as a leading technology in the healthcare paradigm. As a world-class big data nation including National Health Insurance data, Korea has been focused on health policies and sustainability through database forecasting and policy establishment. So the need for education of big data by public officials in healthcare sector is increasing. However, there has not yet been National Competency Standards(NCS) or education modules, in this study, healthcare big data education module and content have been developed for the public servants with confidence.

• The Korean Society of Law and Medicine
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• v.22 no.4
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• pp.3-35
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• 2021

Inmitten der Flut der privaten und öffentlichen Information gilt die riesige Informationsmenge als Schlüsselressource im Zeitalter der 4. industriellen Revolution, repräsentiert durch Big-Data. Das Interesse an diesen wächst weltweit. Es gibt eine aktive Diskussion darüber, wie man Daten sichert und akkumuliert und wie man die gesammelten Daten sicher und effektiv nutzt. Gesundheitsdaten werden vor allem als die wertvollste Ressource bewertet, für die Big-DataTechnologie eingesetzt wird. Um Gesundheitsdaten sinnvoll zu nutzen, müssen verteilte Gesundheitsdaten integriert und den Benutzern in einer Form zur Verfügung gestellt werden, die für Forschung oder Inspektion verwendet werden kann. In einer Situation, in der große Länder um den Aufbau bzw. die Führung der Datenwirtschaft konkurrieren, wurden im August 2020 auch in Südkorea die sog. „3-Daten-Gesetze" geändert, die das Datenschutzgesetz(DSG) enthälten. Das DSG führte das Konzept der pseudonymen Informationen ein und baute eine Rechtsgrundlage für deren Verwendung auf. Als Folgemaßnahme kündigte die, Kommission für den Schutz personenbezogener Daten(Personal Information Protection Commission: PIPC)' die „Richtlinien für die Bahandlung mit pseudonymen Informationen" und, Ministerium für Gesundheit und Wohlfahrt' die „Richtlinien für die Verwendung von Gesundheitsdaten" an. Gesundheitsdaten stehen direkt in Zusammenhang mit Leben und Körper des Menschen und damit enthalten viele sensible Daten. Es handelt sich also um ein System, das aus einer vorsichtigeren und konservativeren Sicht unter der Voraussetzung verwendet werden kann, personenbezogene Daten sicherer zu schützen. Um die Hauptinhalte der „Richtlinien für Verwendung von Gesundheitsdaten" zu analysieren, überprüften wir zunächst die Hauptinhalte des überarbeiteten DSG. Danach durch die Analyse der wesentlichen Inhalte der „Richtlinien für Verwendung von Gesundheitsdaten" wurden Probleme wie Konflikte mit anderen Gesetzen und Verbesserungsmaßnahmen überprüft.

• Proceedings of the Korea Information Processing Society Conference
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• 2022.11a
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• pp.318-321
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• 2022

최근 의료데이터 표준화에 대한 중요성이 보건의료 빅데이터 구축과 맞물려 보건의료데이터 표준화와 마이데이터 생태계 조성을 추진하고 있다. 그리고 개인들의 휴대용 기기 이용증가와 모바일 환경으로 전반적인 디지털헬스의 패러다임 변화에 따라 HL7 FHIR의 사용이 점차 확대될 것으로 예측된다. 본 논문에서는 의료정보 표준인 HL7 FHIR와 의료영상 표준인 DICOM으로 환자 정보를 전달하기 위한 다중 의료 정보 중재 플랫폼에 대해서 기술한다. 이를 구현하기 위해 HL7 FHIR의 Patient, Observation, DiagnosticReport, Bundle 리소스를 활용하여 환자 정보와 임상 리포트 정보를 전달하여 StudyList에서 보여줄 수 있도록 구현하였다. 현재 구현된 내용은 FHIR 기반의 임상데이터로 의료영상을 포함한 표준화된 정보로 제공하여 마이데이터 실증 플랫폼으로 활용될 것으로 기대된다.

• Information and Communications Magazine
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• v.32 no.1
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• pp.63-75
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• 2014

정보통신기술의 발전과 생산되는 데이터의 양적 증가에 따라 빅데이터에 대한 관심이 증대되고 있다. 빅데이터(Big Data)란 기존 데이터베이스의 데이터 저장 관리 분석 능력을 초과하는 다양한 형식을 가진 대량의 데이터를 의미한다. 여러 분야에서 빅데이터가 생성, 분석, 활용되고 있는데, 특히 보건의료 및 바이오 분야에서의 빅데이터 분석은 사회경제적으로 큰 영향력을 발휘할 수 있기 때문에 크게 주목 받고 있다. 본 연구에서는 보건의료 분야에서 생성되는 데이터의 특징과 빅데이터 분석 프로세스에 대해서 조사하였고, 국내 외 빅데이터 정책 및 활용사례를 분석하였다. 그리고 현재의 빅데이터 활용 장벽을 극복할 수 있는 몇 가지 전략을 제시하였다. 대량의 데이터에서 유용한 정보를 생성해내는 빅데이터 분석 기술은 보건의료 및 바이오 분야에서 국가경쟁력을 향상시키는 중요한 기반이 될 것이다.

• Journal of the Health Care and Life Science
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• v.8 no.2
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• pp.83-93
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• 2020

In this study, a practical model for health information management education using the EMR education system at universities for nurturing health care information managers was studied. Currently, there is no practical training course for health care information management in the standards for evaluation and certification of health care information management education introduced to strengthen the job competency of health care information managers. Accordingly, the program was constructed so that the practice program suggested as an educational environment in the Health and Medical Information Management Education Evaluation and Certification Manual can be practiced in the EMR education system. In addition, a practical model that can be performed according to the on-site practice guidelines for health and medical information management for each program was studied. Using the health care information management education EMR system, master data management, patient registration, doctor prescription, medical cost calculation, health insurance claim management, form management, discharge registration, cancer registration, unrecorded management, health care data management, health care statistics, A practice model was studied so that practice on information protection/security management can be performed. It will be possible to play a role as a health care information management expert by raising the quality level of health care information management education through systematic and standardized health care information management practice courses at universities. Accordingly, it is necessary to cultivate health care information management experts who develop and manage medical services based on medical data analysis through practical training of health care information managers.

• Information and Communications Magazine
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• v.32 no.11
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• pp.3-7
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• 2015

최근 활발히 연구되고 있는 빅데이터와 의료 영역이 융합되면서, 보건의료서비스 분야에서는 데이터 집약적이고 공간을 초월한 새로운 서비스패러다임의 움직임이 진행되고 있다. 본고에서는 이러한 빅데이터를 활용하여 건강증진 및 예방을 위하여 생활 속에서 제공되고 있는 생활환경 및 보건 데이터 기반의 라이프케어 서비스동향과 기술에 관하여 알아본다.

• The Korean Society of Law and Medicine
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• v.22 no.4
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• pp.117-157
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• 2021

This research reviewed the HIPAA/HITECH, 21st Century Cures Act, Common Law, and private Guidances from the perspectives in protecting and utilitizing the medical data, while implications were followed. First, the standards for protection and utilization are relatively clearly regulated through single law on personal medical information in the United States. The HIPAA has been introduced in 1996 as fundamental act on protection of medical data. Medical data was divided into personally identifiable information, non-identifying information, and limited dataset under HIPAA. Regulations on de-identification measures for medical information, objects for deletion of limited data sets, and agreement on prohibition of data re-identification were stipulated. Moreover, in the 21st Century Cures Act regulated mutual compatibility for data sharing, prohibition of data blocking, and strengthening of accessibility of data subjects. Common Law introduced comprehensive consent system and clearly stipulates procedures. Second, the regulatory system is relatively simplified and clearly stipulated in the United States. To be specific, the expert consensus and the safe harbor system were introduced as an anonymity measure for identifiable medical information, which clearly defines the process while increasing trust. Third, the protection of the rights of the data subject is specified, the duty of explanation is specified in detail, while the information right of the consumer (opt-out procedure) for identification information is specified. For instance, the HHS rule and FDA regulations recognize the comprehensive consent system for human research, but the consent procedure, method, and requirements are stipulated through the common rule. Fourth, in the case of the United States, a trust-based system is being used throughout the health and medical data legislation. To be specific, Limited Data Sets are allowed to use in condition to the researcher's agreement to prohibit re-identification, and de-identification or consent process is simplified under the system.

• Proceedings of the Korean Institute of Information and Commucation Sciences Conference
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• 2017.10a
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• pp.375-377
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• 2017

전 세계적으로 공공데이터를 민간에 개방하고자 하는 노력으로 오픈데이터(Open Data) 정책을 도입하고 있다. 최근 보건의료에서는 삶의 방식과 환경의 변화로 인해 다양한 질병에 노출될 가능성이 증가하면서 예방과 진료를 목적으로 의료기관을 이용하려는 고객의 수 또한 지속적으로 증가하고 있는 추세이다. 이에 이 논문에서는 공공데이터 심사평가원에서 제공하는 보건의료 공공데이터를 활용하여 의료기관 정보에 대한 대용량 데이터를 활용하여 앱을 개발하였다. 개발된 내용은 심사평가원의 의료기관별 정보와 구글 맵 Open API를 통해 병원 위치를 지도를 통해 제공하며, 추가적으로 각 병원별 진료과목, 시설 정보 등의 상세정보를 제공한다.

• The Korean Society of Law and Medicine
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• v.17 no.2
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• pp.315-346
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• 2016

With the development of big data processing technology, the potential value of healthcare big data has attracted much attention. In order to realize these potential values, various research using the healthcare big data are essential. However, the big data regulatory system centered on the Personal Information Protection Act does not take into account the aspect of big data as an economic material and causes many obstacles to utilize it as a research purpose. The regulatory system of healthcare information, centered on the primary purpose of patient treatment, should be improved in a way that is compatible with the development of technology and easy to use for public interest. To this end, it is necessary to examine the trends of overseas legal system reflecting the concerns about the balance of protection and utilization of personal information. Based on the implications of the overseas legal system, we can derive improvement points in the following directions from our legal system. First, a legal system that specializes in healthcare information and encompasses protection and utilization is needed. De-identification, which is an exception to the Privacy Act, should also clearly define its level. It is necessary to establish a legal basis for linking healthcare big data to create synergy effects in research. It is also necessary to examine the introduction of the opt-out system on the basis of the discussion on the foreign debate and social consensus. But most importantly, it is the people's trust in these systems.

• The Korean Society of Law and Medicine
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• v.22 no.3
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• pp.31-55
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• 2021

The Personal Information Protection Act, one of the revised 3 Data Laws, established a special cases concerning pseudonymous data. As a result, a personal information controller may process pseudonymized information without the consent of data subjects for statistical purposes, scientific research purposes, and archiving purposes in the public interest, etc. In addition, as a follow-up to the revised Personal Information Protection Act, a 'Guidelines for Utilization of Healthcare Data' was prepared, which deals with the pseudonymization in the medical sector. The guidelines are meaningful in that they provide practical criteria for accomplices by defining specific interpretations and examples that take into account the characteristics of healthcare data. However, the guidelines need to clarify the purpose of using pseudonymous data and strengthen the fairness of the composition of the data deliberation committee. The guidelines also require establishing a healthcare data compensation framework and strengthening the protection of rights for vulnerable subjects. In addition, the guidelines need to be adjusted for inconsistency with the Bioethics and Safety Act and the Medical Service Act. It is expected that this study will contribute to the creation of a safe environment for the utilization of healthcare data as well as the improvement of related laws and systems.