ArticleBMC health services research2019
Evaluating the demographic and clinical minimum data sets of Iranian National Electronic Health Record.
Article in BMC health services research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
8 citing papers in PubMed.
- Determining the minimum data set of the tuberculosis information management system.Journal of education and health promotion · 2025Article
- Development of a minimum data set for a blockchain-based personal health records (PHRs), for patient/physician interaction in family medicine.Journal of education and health promotion · 2024Article
- Designing a minimum data set for the information management system (registry) of spinal canal stenosis: An applied-descriptive study.Health science reports · 2023Article
- Evaluating the success of Iran Electronic Health Record System (SEPAS) based on the DeLone and McLean model: a cross-sectional descriptive study.BMC medical informatics and decision making · 2023Article
- Article
- Identifying a minimum data set as a necessity to design a web-based personal health record for patients under chronic dialysis.Journal of family medicine and primary care · 2022Article
- A study to design minimum data set of COVID-19 registry system.BMC infectious diseases · 2021Article
- Minimum Data Set for a Poisoning Registry: A Systematic Review.Iranian journal of pharmaceutical research : IJPR · 2021Review
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Authors and funding
3 authors.
Funding
Abstract
backgroundDesigning a standard data set is necessary to overcome the dispersion of data among different health information systems. The objective of this study was to evaluate the current demographic and clinical minimum data sets (MDSs) of Iranian National Electronic Health Record (known as SEPAS) and to identify most necessary data elements.
methodsData were collected using a list of current demographic and clinical data of SEPAS and a self-administered questionnaire. All faculty members of six health related fields and the hospital authorities, and IT and HIM administrators of 6 hospitals in Kerman University of Medical Sciences were invited to participate in this study. The content validity of the questionnaire was confirmed by six medical informatics and HIM experts and the reliability was determined by Cronbach's alpha (α =0.95). SPSS v18 was used to generate descriptive statistics.
resultsSurvey results indicated that 15 data elements should become mandatory elements of MDS for communicating data to SEPAS. These elements include patient's name, surname, father's name, nationality, cell number, job, residential address, residence place, passport number (for non-Iranian patients), diagnosis date, death time, death place and the unit of the hospital where the patient died. Moreover, participants suggested 33 additional demographic and clinical data elements to be communicated mandatorily to SEPAS.
conclusionThe results of this study showed that the minimum data sets of Iranian national electronic health record needs to be revised. Using the proposed MDSs by this study can improve the quality and efficiency of information and reduce redundancy by adding necessary data and preventing communication of unnecessary data. The method employed in this study can be used for investigating, refining and completing the MDSs of other health information systems.
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