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在中国实施 ISBT 128。

Implementation of ISBT 128 in China.

机构信息

Blood Center of Zhejiang Province, Key Laboratory of Blood Safety Research, Ministry of Health, Hangzhou, Zhejiang, China.

出版信息

Transfusion. 2010 Jan;50(1):80-4. doi: 10.1111/j.1537-2995.2009.02370.x. Epub 2009 Aug 27.

DOI:10.1111/j.1537-2995.2009.02370.x
PMID:19712062
Abstract

BACKGROUND

In 2001, the blood collection agencies of Zhejiang Province adopted a unified information system, but when a blood product was transferred from the collection and processing facility inventory to some other inventories, because of lacking the unique identifying ability between facilities, the numbers might be overlapped. The exchange of blood units between agencies needed change of labels, and it was very complicated. The SARS outbreak in 2003 made this problem more prominent. Therefore, we decided to redevelop a new information system based on ISBT 128 to solve this problem.

STUDY DESIGN AND METHODS

We registered with ICCBBA and obtained the technical documentation and database. We requested the new product description code from ICCBBA and properly adjusted the incompatibility between ISBT 128 and the national standards. We redesigned the information system and labels and validated some related equipment and the laboratory information system.

RESULTS

In May 2005, we completed the development of the new information system based on ISBT 128, and by the end of 2005, all the blood collection agencies of the Zhejiang Province began to use ISBT 128. As a result, the product information in blood collection agencies of Zhejiang Province can be shared, and the exchange of blood products between agencies became safe and rapid. It was highly praised by the nation's Ministry of Health.

CONCLUSIONS

ISBT 128 was successfully implemented in Zhejiang Province.

摘要

背景

2001 年,浙江省各血液采集机构采用了统一的信息系统,但当血液制品从采集和处理机构的库存转移到其他一些库存时,由于缺乏机构之间的唯一识别能力,数量可能会重复。机构之间的血液单位交换需要更改标签,这非常复杂。2003 年的 SARS 爆发使这个问题更加突出。因此,我们决定基于 ISBT 128 重新开发一个新的信息系统来解决这个问题。

研究设计和方法

我们向 ICCBBA 注册并获得了技术文档和数据库。我们向 ICCBBA 请求新产品描述代码,并适当调整了 ISBT 128 与国家标准之间的不兼容性。我们重新设计了信息系统和标签,并验证了一些相关设备和实验室信息系统。

结果

2005 年 5 月,我们完成了基于 ISBT 128 的新信息系统的开发,到 2005 年底,浙江省所有的血液采集机构都开始使用 ISBT 128。因此,浙江省血液采集机构的产品信息可以共享,机构之间的血液产品交换变得安全快捷。这得到了国家卫生部的高度评价。

结论

ISBT 128 在浙江省成功实施。

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