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在使用全球触发工具时,增加每两周记录样本的大小是否会影响结果?一项对两种不同样本量的回顾性记录审查的观察性研究。

Does increasing the size of bi-weekly samples of records influence results when using the Global Trigger Tool? An observational study of retrospective record reviews of two different sample sizes.

作者信息

Mevik Kjersti, Griffin Frances A, Hansen Tonje E, Deilkås Ellen T, Vonen Barthold

机构信息

Regional Patient Safety Resource Center, Nordland Hospital Trust, Bodø, Norway.

Fran Griffin & Associates, LLC, Neptune, New Jersey, USA.

出版信息

BMJ Open. 2016 Apr 25;6(4):e010700. doi: 10.1136/bmjopen-2015-010700.

Abstract

OBJECTIVES

To investigate the impact of increasing sample of records reviewed bi-weekly with the Global Trigger Tool method to identify adverse events in hospitalised patients.

DESIGN

Retrospective observational study.

SETTING

A Norwegian 524-bed general hospital trust.

PARTICIPANTS

1920 medical records selected from 1 January to 31 December 2010.

PRIMARY OUTCOMES

Rate, type and severity of adverse events identified in two different samples sizes of records selected as 10 and 70 records, bi-weekly.

RESULTS

In the large sample, 1.45 (95% CI 1.07 to 1.97) times more adverse events per 1000 patient days (39.3 adverse events/1000 patient days) were identified than in the small sample (27.2 adverse events/1000 patient days). Hospital-acquired infections were the most common category of adverse events in both the samples, and the distributions of the other categories of adverse events did not differ significantly between the samples. The distribution of severity level of adverse events did not differ between the samples.

CONCLUSIONS

The findings suggest that while the distribution of categories and severity are not dependent on the sample size, the rate of adverse events is. Further studies are needed to conclude if the optimal sample size may need to be adjusted based on the hospital size in order to detect a more accurate rate of adverse events.

摘要

目的

采用全球触发工具法,调查增加每两周审查的住院患者病历样本量对识别不良事件的影响。

设计

回顾性观察研究。

地点

挪威一家拥有524张床位的综合医院信托机构。

参与者

从2010年1月1日至12月31日选取的1920份病历。

主要结局

每两周选取10份和70份病历这两种不同样本量中识别出的不良事件的发生率、类型和严重程度。

结果

在大样本中,每1000患者日识别出的不良事件比小样本多1.45倍(95%可信区间为1.07至1.97)(39.3起不良事件/1000患者日),小样本为(27.2起不良事件/1000患者日)。医院获得性感染是两个样本中最常见的不良事件类型,其他不良事件类型在两个样本中的分布无显著差异。两个样本中不良事件严重程度的分布无差异。

结论

研究结果表明,虽然不良事件的类型和严重程度分布不依赖于样本量,但不良事件的发生率依赖于样本量。是否需要根据医院规模调整最佳样本量以更准确地检测不良事件发生率,还需要进一步研究来得出结论。

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