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Structured electronic template for histopathology reports on colorectal carcinomas: a joint project by the Cancer Registry of Norway and the Norwegian Society for Pathology.

机译:用于结直肠癌的组织病理学报告的结构化电子模板:挪威癌症登记处和挪威病理学会的联合项目。

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摘要

Both individual patient treatment and cancer registries depend on adequate histopathology reports. To ensure the quality of these reports, professional organizations have published guidelines on minimum data sets for various cancer types. Norway has a population of 4.6 million, and all individuals have a unique identification number. As required by law, relevant information on cancer is submitted to the Cancer Registry of Norway. A closed, national health data network has been established facilitating electronic transferal between various institutions. The Cancer Registry and the Norwegian Society for Pathology have jointly established a nationwide project to (i) develop standardized templates in database format for histopathology reports on cancer resection specimens and (ii) develop an Extensible Markup Language (XML) standard to facilitate future electronic transfer of cancer reports from hospitals to the Cancer Registry. A minimum data set template for reporting colorectal carcinoma resection specimens and the Extensible Markup Language standard have been established. The template is based on international guidelines and classification systems. For most key parameters, pull-down menus with predefined alternatives have been constructed. The template is fully integrated into software being used by all pathology laboratories in Norway. Since the introduction of the template in April 2005, the template had been used for reporting 430 (93%) of 462 colorectal resections at 2 pilot laboratories (Akershus University Hospital [Lorenskog, Norway] and Stavanger, University Hospital [Stavanger, Norway]), demonstrating that high and consistent quality can be ascertained. Pathologists have found the template both time saving and user friendly. The template is now gradually implemented nationwide.
机译:个体患者的治疗和癌症登记都取决于足够的组织病理学报告。为了确保这些报告的质量,专业组织已经发布了有关各种癌症类型的最低数据集的指南。挪威人口460万人,所有个人都有唯一的身份证号码。根据法律要求,有关癌症的相关信息将提交给挪威癌症登记处。建立了一个封闭的国家卫生数据网络,以促进各机构之间的电子传输。癌症注册机构和挪威病理学会共同建立了一个全国性项目,以(i)以数据库格式开发标准化模板,以用于癌症切除标本的组织病理学报告,以及(ii)开发可扩展标记语言(XML)标准,以促进未来的电子传输从医院到癌症登记处的癌症报告。已经建立了报告结直肠癌切除标本的最小数据集模板和可扩展标记语言标准。该模板基于国际准则和分类系统。对于大多数关键参数,已经构建了带有预定义替代项的下拉菜单。该模板已完全集成到挪威所有病理实验室使用的软件中。自从2005年4月引入该模板以来,该模板已用于报告2个试验实验室(阿克斯胡斯大学医院[挪威洛伦斯科格]和斯塔万格大学医院[挪威斯塔万格])中462个大肠切除术中的430个(93%) ,表明可以确定高质量和一致的质量。病理学家发现该模板既节省时间又便于用户使用。该模板现已在全国范围内逐步实施。

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