نمایش مختصر رکورد

dc.contributor.authorمحمود کيوان‌آراen_US
dc.contributor.authorمعصومه صادقيen_US
dc.contributor.authorسکينه سقائيان‌نژاد ‌اصفهانيen_US
dc.contributor.authorحميدرضا تدينen_US
dc.date.accessioned1399-12-04T14:12:23Zfa_IR
dc.date.accessioned2021-02-22T14:12:33Z
dc.date.available1399-12-04T14:12:23Zfa_IR
dc.date.available2021-02-22T14:12:33Z
dc.date.issued2012-06-06en_US
dc.date.issued1391-03-17fa_IR
dc.date.submitted2012-06-06en_US
dc.date.submitted1391-03-17fa_IR
dc.identifier.citation(1391). مدیریت اطلاعات سلامت, 9(2)fa_IR
dc.identifier.issn1735-7853
dc.identifier.issn1735-9813
dc.identifier.urihttp://him.mui.ac.ir/index.php/him/article/view/613
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/765467
dc.description.abstractIntroduction: Acute coronary syndrome (ACS) includes ST segment elevation myocardial infarction (STEMI), non- ST segment elevation myocardial infarction (NSTEMI), and unstable angina. It is among the leading causes of death. Registry systems are designed and implemented to collect and analyze the data related to a specific disease. Decreasing the burden ACS would need some strategies such as designing and implementing a registry system. This study tried to compare ACS registry systems in selected countries. Methods: This comparative descriptive research used an applied approach. The data was collected from the national registry of ACS in the USA, Switzerland, and Malaysia and myocardial infarction (MI) registry in Isfahan (as the first MI registry in Iran). Data was mainly collected from articles, journals, websites, and other written documents using a checklist which was designed based on the minimum requirements of a registry system. The validity of the checklist was confirmed by specialists. Since most resources were in English, translations were performed by an expert team to maximize the concordance with the source. Data was analyzed using comparative tables. Results: In all three countries, there were national registries for ACS. They registered all stages including gathering and analyzing data and distribution of information. Although there is no national registry in Iran, an MI registry has been implemented in Isfahan which only covers data collection. The registry systems in the USA and Switzerland are supervised by specialty associations relevant to coronary disease. In Malaysia however, the database is under the control of Ministry of Health. The American ACS had the highest level of experience and the best features among the studied registry systems. Conclusion: Overall, according to the large burden of heart diseases in Iran, designing and implementing a national registry is essential. It could bring a better management for controlling and preventing diseases. Keywords: Acute Coronary Syndrome; Information Systems; Registry.en_US
dc.languageEnglish
dc.language.isoen_US
dc.publisherدانشگاه علوم پزشکی اصفهانfa_IR
dc.relation.ispartofمدیریت اطلاعات سلامتfa_IR
dc.titleبررسی مقایسه‌ای کلیات نظام ملی ثبت سندروم حاد کرونری در کشورهای منتخبen_US
dc.typeTexten_US
dc.contributor.departmentدانشيار، جامعه‌شناسي پزشکي، مرکز تحقيقات سياست‌گذاري سلامت، دانشگاه علوم پزشکي شيراز، شيراز، ايرانen_US
dc.contributor.departmentدانشيار، بيماري‌هاي قلب و عروق، مرکز تحقيقات قلب و عروق، دانشگاه علوم پزشکي اصفهان، اصفهان، ايرانen_US
dc.contributor.departmentمربي، مدارک پزشکي، مرکز تحقيقات مديريت و اقتصاد سلامت، دانشگاه علوم پزشکي اصفهان، اصفهان، ايرانen_US
dc.contributor.departmentکارشناس ارشد، مدارک پزشکي، دانشگاه علوم پزشکي اصفهان، اصفهان، ايرانen_US
dc.citation.volume9
dc.citation.issue2


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