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全国临床生物化学检验报告适宜性调查

National survey on appropriateness of clinical biochemistry reporting in China.

出版信息

Clin Chem Lab Med. 2015 Oct;53(11):1745-51. doi: 10.1515/cclm-2015-0127.

Abstract

BACKGROUND

Accurate and reliable testing reports play an important role in the prevention, diagnosis, treatment and prognosis of disease. However, little is known about the appropriateness of laboratory testing reporting in China. This national survey takes clinical biochemistry as an example to investigate the state of reporting appropriateness in our country.

METHODS

An electronic questionnaire was sent to 1209 laboratories. The participants were asked to retrospectively evaluate the error rates of the following quality indicators: report template integrity, report content filling integrity, report delay, report recall, non-conformities between instrument and laboratory information system (LIS) data, non-conformities between report and request, report notification error, and report modification. Mann-Whitney and Kruskal-Wallis tests were used to identify the potential impacts of reporting appropriateness.

RESULTS

A total of 662 of the 1209 laboratories (55%) submitted the survey results, with three returning incomplete data. For the integrity of the report, only 31% of the laboratories had a complete report template that contained all of 21 elements. In addition, the overall error rate of content filling integrity was 45.9% for 19,770 pieces of reports. The overall σ-values of other six quality indicators were all >4, and no significant difference was found among different departments. Group comparison suggested that reporting electronically had a better performance.

CONCLUSIONS

The laboratory reporting system in China needs to improve, particularly the integrity of the report. Strengthening information technology will not only promote reporting appropriateness, but also guarantee accurate, standardized and traceable data collection and long-term monitoring.

摘要

背景

准确可靠的检测报告在疾病的预防、诊断、治疗和预后中起着重要作用。然而,目前对于中国实验室检测报告的适宜性知之甚少。本全国性调查以临床生物化学为例,调查我国报告适宜性的状况。

方法

向 1209 个实验室发送电子问卷。要求参与者回顾性评估以下质量指标的错误率:报告模板完整性、报告内容填写完整性、报告延迟、报告召回、仪器与实验室信息系统(LIS)数据之间的不一致、报告与请求之间的不一致、报告通知错误和报告修改。使用 Mann-Whitney 和 Kruskal-Wallis 检验来识别报告适宜性的潜在影响。

结果

在 1209 个实验室中,共有 662 个(55%)实验室提交了调查结果,其中 3 个实验室返回的数据不完整。对于报告的完整性,只有 31%的实验室有完整的报告模板,其中包含 21 个元素。此外,内容填写完整性的整体错误率为 19770 份报告的 45.9%。其他六个质量指标的整体 σ 值均>4,不同科室之间没有发现显著差异。组间比较表明,电子报告表现更好。

结论

中国的实验室报告系统需要改进,特别是报告的完整性。加强信息技术不仅可以促进报告的适宜性,还可以保证准确、规范和可追溯的数据收集和长期监测。

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