Mojarrab Shahnaz, Rafei Ali, Akhondzadeh Shahin, Jeddian Alireza, Jafarpour Maryam, Zendehdel Kazem
Deputy of Research, Ministry of Health and Medical Education, I.R. Iran.
Information Technology Department, Ministry of Health and Medical Education, I.R. Iran.
Arch Iran Med. 2017 Nov 1;20(11):696-703.
Registration systems for diseases and other health outcomes provide important resource for biomedical research, as well as tools for public health surveillance and improvement of quality of care. The Ministry of Health and Medical Education (MOHME) of Iran launched a national program to establish registration systems for different diseases and health outcomes. Based on the national program, we organized several workshops and training programs and disseminated the concepts and knowledge of the registration systems. Following a call for proposals, we received 100 applications and after thorough evaluation and corrections by the principal investigators, we approved and granted about 80 registries for three years. Having strong steering committee, committed executive and scientific group, establishing national and international collaboration, stating clear objectives, applying feasible software, and considering stable financing were key components for a successful registry and were considered in the evaluation processes. We paid particulate attention to non-communicable diseases, which constitute an emerging public health problem. We prioritized establishment of regional population-based cancer registries (PBCRs) in 10 provinces in collaboration with the International Agency for Research on Cancer. This initiative was successful and registry programs became popular among researchers and research centers and created several national and international collaborations in different areas to answer important public health and clinical questions. In this paper, we report the details of the program and list of registries that were granted in the first round.
疾病及其他健康结果登记系统为生物医学研究提供了重要资源,同时也是公共卫生监测及改善医疗质量的工具。伊朗卫生与医学教育部发起了一项建立不同疾病及健康结果登记系统的国家计划。基于该国家计划,我们组织了多次研讨会和培训项目,并传播登记系统的概念和知识。在发布提案征集通知后,我们收到了100份申请,经过主要研究者的全面评估和修正,我们批准并授予了约80个登记处为期三年的许可。拥有强大的指导委员会、敬业的执行和科学团队、建立国内和国际合作、明确目标、应用可行的软件以及考虑稳定的资金是成功建立登记处的关键要素,并在评估过程中予以考量。我们特别关注构成新出现公共卫生问题的非传染性疾病。我们优先与国际癌症研究机构合作,在10个省份建立基于区域人口的癌症登记处(PBCR)。这一举措取得了成功,登记项目在研究人员和研究中心中受到欢迎,并在不同领域促成了多项国内和国际合作,以解答重要的公共卫生和临床问题。在本文中,我们报告该项目的详细情况以及第一轮获批的登记处名单。