• 제목/요약/키워드: International healthcare standard

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의료의 질 개선 전문가의 자격 시스템에 대한 현황 (The review of qualifying systems of quality improvement specialists in healthcare)

  • 박성희;황정해;최윤경;이순교
    • 한국의료질향상학회지
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    • 제19권2호
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    • pp.14-34
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    • 2013
  • Objectives: The purpose of this study is to provide comprehensive information of qualification systems of developed countries needed to establish our national system for QI(Quality improvement) specialists. Methods: All articles related to any applicable domestic or foreign countries' laws, operational status, and detailed programs for professional qualification system of QI were reviewed. Result: In the United States, a non-profit organization, Healthcare Quality Certification Commission (HQCC) has set the policies, procedures and standards in the field of health care quality. And qualification system of CPHQ (certified professional in healthcare quality) has been operated in order to authenticate the qualifications in the field of quality management. IBQH(international Board for quality in healthcare), a qualification system of experts in the United Kingdom, was designed to assist the qualification of professionals to improve the quality of healthcare. In addition, Health Research Center of Feinberg School of Medicine in Northwestern University has been operating Master's and doctoral degree programs in the field of the quality of care and patient safety and IHI (institute for healthcare improvement) open school was operating a professional training course related to the quality of care and patient safety. Conclusion: Quantity and complexity of information of the quality of care and patient safety have been increased. For reform of the health care system, a special training course of the expertise and leadership are needed. So far, there is no national professional certification courses in our nation. Therefore essential job skill should be acquired individually. For systematic and effective quality improvement activities, the educational and certification system with professional development model are needed.

유비쿼터스 헬스케어 서비스를 위한 SIP 기반 혈액관리 시스템에 관한 연구 (A Study on Blood Management System based on SIP for Ubiquitous Healthcare service)

  • 박용민;오영환
    • 한국통신학회논문지
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    • 제36권10B호
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    • pp.1222-1232
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    • 2011
  • RFID/USN은 유비쿼터스 컴퓨팅을 위한 핵심 기술로써 다양한 센서기술과 프로세서 집적기술 그리고 무선 네트워크 기술을 이용해서 실제 물리적 환경 정보를 원격에서 손쉽게 수집하고 모니터링 하는 것이 가능하다. 특히 의료분야는 U-Healthcare와 결합된 보건의료산업과 서비스에서 국제적인 경쟁력을 확보한 수 있을 것으로 기대되고 있다. 하지만 USN은 RFID의 표준 관리 시스템인 EPCglobal 아키텍처와 갚은 표준 프레임워크의 부재로 상호 운영 및 글로벌 센서 네트워크 구현에 문제점이 있다. 따라서 본 논문에서는 USN의 센서 노드를 관리하는 시스템인 SIP 기반의 USN 관리 시스템 (UMS)을 제안한다. UMS는 세션 관리 기능 및 이동성 지원을 제공하는 SIP(Session Initiation Protocol)라는 인터넷 표준 프로토콜에 기반을 두고 있다. UMS 아키텍처는 기존의 SIP 아키텍처에 UUA(USN User Agent)와 UNS(USN Name Server)를 추가함으로써 이동성을 고려한 센서 노도의 위치 및 상태를 관리하게 된다. UUA는 제한된 능력의 센서 노드를 대신해 위치 등록과정을 수행하고 UNS는 센서 노드의 위치 추적을 위해 이름 변환 서비스를 제공한다. 제안하는 관리 시스템은 하나의 통일된 규격이 존재하지 않는 현재의 센서 네트워크를 통합 및 연동을 쉽게 히여 인터넷을 기반한 글로벌한 센서 네트워크 구축을 가능하게 한다. 또한, 인터넷 표준 프로토콜인 SIP를 사용하기 때문에 다른 서비스 및 프로토콜과의 연동이 쉽고 SIP 기반의 기존 자원을 재활용 활 수 있는 장점을 가진다. 본 논문에서는 제안하는 UMS를 기반으로 혈액관리 시스템의 시나리오를 통해 타당성을 검증한다.

Validation of the mobile wireless digital automatic blood pressure monitor using the cuff pressure oscillometric method, for clinical use and self-management, according to international protocols

  • Yoo, Sooyoung;Baek, Hyunyoung;Doh, Kibbeum;Jeong, Jiyeoun;Ahn, Soyeon;Oh, Il-Young;Kim, Kidong
    • Biomedical Engineering Letters
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    • 제8권4호
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    • pp.399-404
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    • 2018
  • The purpose of this study was to evaluate the accuracy of a mobile wireless digital automatic blood pressure monitor for clinical use and mobile health (mHealth). In this study, a manual sphygmomanometer and a digital blood pressure monitor were tested in 100 participants in a repetitive and sequential manner to measure blood pressure. The guidelines for measurement used the Korea Food & Drug Administration protocol, which reflects international standards, such as the American National Standard Institution/Association for the Advancement of Medical Instrumentation SP 10: 1992 and the British Hypertension Society protocol. Measurements were generally consistent across observers according to the measured mean ${\pm}SD$, which ranged in $0.1{\pm}2.6mmHg$ for systolic blood pressure (SBP) and $0.5{\pm}2.2mmHg$ for diastolic blood pressure (DBP). For the device and the observer, the difference in average blood pressure (mean${\pm}$SD) was $2.3{\pm}4.7mmHg$ for SBP and $2.0{\pm}4.2mmHg$ for DBP. The SBP and DBP measured in this study showed accurate measurements that satisfied all criteria, including an average difference that did not exceed 5 mmHg and a standard deviation that did not exceed 8 mmHg. The mobile wireless digital blood pressure monitor has the potential for clinical use and managing one's own health.

정신보건서비스 유형 및 시설기준 수립을 위한 관련 법제도 분석 연구 (A Study on the Regulation for Type and Design Guideline of Mental Health Service)

  • 문하늬;윤우용;채철균
    • 의료ㆍ복지 건축 : 한국의료복지건축학회 논문집
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    • 제22권2호
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    • pp.25-33
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    • 2016
  • Purpose : The information of mental health facilities in Korean law is so unclear that people hardly enable to understand what sort of proper mental health service is prepared for them. Futhermore, there is not enough regulation and standard to classify each type of facilities in the law. Therefore the purpose of this study is to provide data on the basis for classification and facility standards by analysing Korean law and policies. Methods : This study was conducted by a research on law and regulation of mental health facility. Results : The result of this study can be summarized into three points. The first one, current law and policy do not reflect a change in community mental health services paradigm. The second one, the classified facility should be designed to fit the community mental health services. The third one, overall, it requires more detailed guidelines to enhance the quality of mental health services. Besides, the treatment as well as the function of the prevention and rehabilitation are necessary criteria that can also be enhanced. Implications : This study looked at the classification and facility standard of mental health facility by the change in community mental health services paradigm. Forward according to these changes, there is a need for specific guidelines for mental health facility.

A Pilot Establishment of the Job-Exposure Matrix of Lead Using the Standard Process Code of Nationwide Exposure Databases in Korea

  • Ju-Hyun Park;Sangjun Choi;Dong-Hee Koh;Dae Sung Lim;Hwan-Cheol Kim;Sang-Gil Lee;Jihye Lee;Ji Seon Lim;Yeji Sung;Kyoung Yoon Ko;Donguk Park
    • Safety and Health at Work
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    • 제13권4호
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    • pp.493-499
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    • 2022
  • Background: The purpose of this study is to construct a job-exposure matrix for lead that accounts for industry and work processes within industries using a nationwide exposure database. Methods: We used the work environment measurement data (WEMD) of lead monitored nationwide from 2015 to 2016. Industrial hygienists standardized the work process codes in the database to 37 standard process and extracted key index words for each process. A total of 37 standardized process codes were allocated to each measurement based on an automated key word search based on the degree of agreement between the measurement information and the standard process index. Summary statistics, including the arithmetic mean, geometric mean, and 95th percentile level (X95), was calculated according to industry, process, and industry process. Using statistical parameters of contrast and precision, we compared the similarity of exposure groups by industry, process, and industry process. Results: The exposure intensity of lead was estimated for 583 exposure groups combined with 128 industry and 35 process. The X95 value of the "casting" process of the "manufacture of basic precious and non-ferrous metals" industry was 53.29 ㎍/m3, exceeding the occupational exposure limit of 50 ㎍/m3. Regardless of the limitation of the minimum number of samples in the exposure group, higher contrast was observed when the exposure groups were by industry process than by industry or process. Conclusion: We evaluated the exposure intensities of lead by combination of industry and process. The results will be helpful in determining more accurate information regarding exposure in lead-related epidemiological studies.

도시철도 역사 환승구간의 유니버설 디자인 기준에 관한 연구 (A Study on Universal Design Guideline of the Urban Railway Station: Transit Zone)

  • 강병근;이주연
    • 의료ㆍ복지 건축 : 한국의료복지건축학회 논문집
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    • 제22권2호
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    • pp.35-44
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    • 2016
  • Purpose: Recently, Universal design has been applied to a variety of concepts of social integration in the national legislation and institutions, however, the applying to urban railway station is not satisfied. Most of cases, the handicapped can not work continuously, universal design must be provided. Methods: This study derives the detailed criteria through comparing and analyzing an national and international universal design-related system in transit zone. And the status is investigated in transit zone of domestic urban railway station. Improved national standard requirements are derived considering the type of the handicapped and universal design principles. Result: The domestic status shows that the most lacking entry criteria is not specified in national standards or the design is a lowest-level required by criteria through comparing detailed criteria drawn into domestic analysis. Therefore, in order to provide a pedestrian environment to meet the universal design principles and requirements for the handicapped, there is a need to re-establish with a specific national standards. Implications: This study will draw on universal design standards for seamless transfer in transit zone of urban railway station. The next studies are needed to target the overall paths ranging from outside to landing in urban railway station.

호흡보조의료기기의 사용목적 및 대상에 따른 규격적용 방안 및 성능에 관한 연구 (A Study for Application of Standard and Performance Test According to Purpose and Subject of Respiratory Medical Device)

  • 박준현;호예지;이덕희;최재순
    • 대한의용생체공학회:의공학회지
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    • 제40권5호
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    • pp.215-221
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    • 2019
  • The respiratory medical device is a medical device that delivers optimal oxygen or a certain amount of humidification to a patient by delivering artificial respiration to a patient through a machine when the patient has lost the ability to breathe spontaneously. These include respirators for use in chronic obstructive pulmonary disease and anesthesia or emergency situations, and positive airway pressure devices for treating sleep apnea, and as the population of COPD (chronic obstructive pulmonary disease) and elderly people worldwide surge, the market for the respiratory medical devices it is getting bigger. As the demand for both airway pressure devices, there is a problem that the ventilator standard is applied because the reference standard has not been established. Therefore, the boundaries between the items are blurred due to the purpose, intended use, and method of use overlapping similar items in a respiratory medical device. In addition, for both airway pressure devices, there is a problem that the ventilator standard is applied because the reference standard has not been established. Therefore, in this study, we propose clear classification criteria for the respiratory medical devices according to the purpose, intended use, and method of use and provide safety and performance evaluation guidelines for those items to help quality control of the medical devices. And to contribute to the rapid regulating and improvement of public health. This study investigated the safety and performance test methods through the principles of the respiratory medical device, national and international standards, domestic and international licensing status, and related literature surveys. The results of this study are derived from the safety and performance test items in the individual ventilator(ISO 80601-2-72), the International Standard for positive airway pressure device (ISO 80601-2-70), The safety and performance of humidifiers (ISO 80601-2-74) and the safety evaluation items related to home healthcare environment (IEC 60601-1-11), In addition, after reviewing the guidelines drawn up through expert consultation bodies including manufacturers and importers, certified test inspection institutions, academia, etc., the final guidelines were established through revision and supplementation. Therefore, in this study, we propose guidelines for evaluating the safety and performance of the respiratory medical device in accordance with growing technology development.

Natural Standard Methodology를 이용한 암 보완대체의학의 근거 및 권고수준에 대한 연구 (Study on Level of Evidence and Recommendations of Complementary and Alternative Medicine for Cancer by Using Natural Standard Methodology)

  • 김정선;유화승;조종관;손창규;조정효;이연월
    • 대한한방내과학회지
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    • 제29권1호
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    • pp.160-176
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    • 2008
  • Objective : We designed this study to analyse the Natural Standard methodology and apply the results to new study and evaluation methods. Methods : We investigated the main stream of complementary and alternative medicine (CAM), the methodology of Natural Standard, guideline in CAM, and concrete 35 cancer-related herbs and dietary supplements in 98 ones. Results : There are 35 graded herbs and supplements associated with cancer in natural standard contents: 9 foods, 17 herbs, 7 amino acids, enzymes and vitamins, and 2 herbal mixture formulas. Most of them get a grade of C: unclear or conflicting scientific evidence. Conclusion : Natural Standard aims to provide high-quality, reliable information about CAM therapies to clinicians, patients, and healthcare institutions. The more demands for and use of CAM grows, the more the needs for related studies increases. According to this international and multidisciplinary collaborative effort, we have to develop how to study and evaluate the results. We need guidelines in association with the evidence and recommendations of CAM.

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HL7 버전 3 기반의 투약관리시스템을 위한 임상문서구조의 생성 (Health Level 7 Version 3 based Generating Clinical Document Architecture for Medication Administration System)

  • 김근희;조수미;이은주;김화선;조훈
    • 한국멀티미디어학회논문지
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    • 제11권3호
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    • pp.386-397
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    • 2008
  • 본 연구는 HL7 버전 3의 객체지향 분석 및 개발 방법론인 HL7 개발 프레임워크(HDF)를 이용하여 투약관리의 임상문서구조의 개발을 통해 임상활동의 표준화 데이터 모델을 구현하는 것을 제안한다. 투약관리는 의료현장에서 임상전문가가 행하는 가장 중요한 업무이다. 표준화 된 데이터 모델 및 구조화된 병원정보시스템은 근거기반 임상 활동을 이루기 위해 상당히 중요한 과제이다. 임상문서구조를 생성하기 위해서 HDF와 제공된 도구들을 사용하였다. 본 연구자들은 투약관리활동에서 HDF의 각 단계의 다이어그램을 생성할 수 있었다. 그 결과, 임상 활동 중 하나인 투약관리에 대한 표준화 정보모델을 생성하였다. 이 모델은 보건의료정보시스템을 모델링하기 위한 정보통신개발자들에게 국제 표준방법론을 이해하기 위한 기본적 개념모델이 될 것이다.

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보건의료 빅데이터 플랫폼에서 LOD를 활용한 데이터 연계 방안 (Data Linkage Method Using LOD in the Healthcare Big Data Platform)

  • 이경희;김기남;조완섭
    • 한국빅데이터학회지
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    • 제4권2호
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    • pp.195-205
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    • 2019
  • LOD(Linked Open Data)는 데이터 공개방식 중에서 가장 우수한 수준으로 평가받고 있으며, 인터넷 상에서 서로 관련있는 데이터를 표준방식으로 연결하여 하나의 거대한 데이터베이스처럼 검색할 수 있도록 한다. 글로벌 환경에서 관련있는 데이터들이 LOD 형태로 구축되는 사례가 증가하고 있으나 국내 보건의료 분야에서 LOD 형태의 데이터 공개는 아직 초보적인 수준에 머물러 있다. 본 논문에서는 한국의학연구논문 데이터와 보건의료 빅데이터 연계 플랫폼 데이터를 중심으로 국내외 관련있는 DB들을 LOD 방식으로 연계하여 서비스하는 LOD 플랫폼 구축사례를 소개한다. 각 DB의 모든 데이터를 LOD로 연계하는 것은 시간과 노력이 많이 필요하며, 기본적으로 민간보다 국가나 공공기관이 담당해야 하는 인프라성 연구이다. 본 연구에서는 각 DB의 일부만을 대상으로 하여 LOD국내외 10개 사이트를 연계하였으며, 이를 통해 사용자는 편리한 방식으로 국내외 여러 기관의 데이터를 연계하여 검색할 수 있게 된다.

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