国家器官移植科学登记:数据需求和使用。

Topics in health record management Pub Date : 1990-12-01
D K Hearington, B J Ettner, T Breen, R White
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引用次数: 0

摘要

通过科学登记还有很多工作要完成,通过将信息整合到特定于患者的文件中,而不是现有的“按表格归档”的设置,将使其更有效率。此外,用户将能够直接输入数据,消除移植和随访日期以及实际使用表格之间的时间延迟问题。随着数据库的增长,注册表数据也将变得更加有用。长期移植和患者生存的数据将直接影响未来的政策决定和移植实践。移植的临床结果也会受到供体管理和器官保存技术的影响,所有这些都可以通过使用注册数据来解决。最终的目标是使移植更可靠、更可预测、更广泛的可用性和更便宜。国家综合数据库实现了这一目标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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National scientific registry of organ transplantation: data needs and uses.

There is a lot of work yet to be accomplished through the scientific registry, which will be made more efficient by the consolidation of information into patient-specific files rather than the existing "file by form" set-up. Additionally, users will be able to input data directly, eliminating the problem of the time delays between transplant and follow-up dates and the actual use of the forms. The registry data also will become more useful as the database grows. The data on long-term graft and patient survival will directly influence future policy decisions and transplant practices. The clinical outcomes of transplantation also will be influenced by donor management and organ preservation techniques, all of which can be addressed through the use of registry data. The ultimate goal is to make transplantation more reliable, more predictable, more widely available, and less expensive. The national, comprehensive database accomplishes that goal.

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