严重围手术期不良事件的漏报:静脉浸润和外渗。

IF 2.2 Q2 HEALTH CARE SCIENCES & SERVICES
Drug, Healthcare and Patient Safety Pub Date : 2020-11-13 eCollection Date: 2020-01-01 DOI:10.2147/DHPS.S271832
George Tewfik
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引用次数: 0

摘要

了解和预防围手术期潜在的灾难性并发症的关键一步是准确记录其发生和随后的分析。然而,由于以下几个因素,静脉浸润和外渗的记录可能不准确:与浸润/外渗相关的罕见严重并发症,ICD-10编码描述损伤的局限性,依赖编码器在可搜索的数据库中记录这些事件,以及麻醉学记录这些事件的质量措施有限。尽管目前文献引用的研究结果发现静脉浸润率为16%甚至更高,但新泽西州纽瓦克大学医院的一项有限的内部审查发现,该机构在18个月内仅记录了14例静脉浸润率明显较低。这使作者得出结论,需要采取干预措施,以便更好地跟踪这些事件,包括工作人员教育和更有效/更容易使用的报告系统等步骤。准确记录和分析与不良事件有关的数据,特别是关于浸润和外渗的数据,需要修订和重新解释,以获得其发生率的准确情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Under-Reporting of a Critical Perioperative Adverse Event: Intravenous Infiltration and Extravasation.

A critical step in understanding and preventing potentially disastrous complications in the perioperative period is the accurate recording of their occurrence and subsequent analysis. However, the recording of intravenous infiltration and extravasation is likely inaccurate due to several factors: rare serious complications associated with infiltration/extravasation, limitation in ICD-10 codes to describe the injury, reliance on coders to record these events in searchable databases, and limited quality measures in anesthesiology to record these events. Although current literature cites results of studies that found rates of 16% and higher for intravenous infiltration, a limited internal review at University Hospital in Newark, NJ found significantly lower rates with only 14 instances recorded in an 18-month period across the institution. This leads the author to conclude that interventions are required to better track these events including such steps as staff education and more efficient/accessible reporting systems. The accurate recording and analyzing of data related to adverse events, and in particular regarding infiltration and extravasation, require revision and reinterpretation to gain an accurate picture of their rates.

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来源期刊
Drug, Healthcare and Patient Safety
Drug, Healthcare and Patient Safety HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.10
自引率
0.00%
发文量
24
审稿时长
16 weeks
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