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改善分诊时生命体征记录:一项急诊科质量改进项目。

Improving vital sign documentation at triage: an emergency department quality improvement project.

机构信息

Tuscan Emergency Medicine Intervention, Florence, Italy.

出版信息

J Patient Saf. 2011 Mar;7(1):26-9. doi: 10.1097/PTS.0b013e31820c9895.

Abstract

BACKGROUND

Improving the quality and safety of patients seen in an emergency department (ED) has become a priority in Italy. The Tuscan Regional Health Ministry has supported quality improvement projects in several Tuscan EDs in cooperation with Harvard Medical International and Harvard Medical School.

OBJECTIVE

To improve the triage process, we assessed the completeness of documenting the vital signs of patients seen at triage in the ED of the University Hospital Santa Chiara, Pisa, Italy. At the University Hospital of Pisa's ED, triage is based on 5 categories, each identified by a color: white (lowest priority), blue, green, yellow, and red (highest priority). For patients triaged as "yellow," blood pressure, heart rate, and oxygen saturation are considered mandatory vital signs and important components of a complete patient record. The aims of this project were as follows: 1) to assess the percentage of patients seen during ED triage in whom vital signs were recorded in the clinical record, 2) to analyze the reasons for missing vital sign data, and 3) to design and implement a strategy to improve the percentage of patients in whom vital signs were recorded.

METHODS

This project began in November 2005 with the identification of a multidisciplinary ED Quality Team. Faculty from Harvard Medical School provided a 2-day training course on the methods and tools of clinical quality improvement. After the training, the team defined their improvement project. The clinical quality improvement project followed a Plan-Do-Study-Act cycle. Preintervention and postintervention data collection consisted of a retrospective analysis of one-third of all patients triaged in the "yellow" category who were admitted to the ED during 1 month, randomly selected using a computer-generated list.

RESULTS

A total of 245 clinical records in the preintervention (March 2006) and 251 (April-May 2007) during the postintervention were included. We found that in 77.9% (191/245) of these records, vital signs were correctly recorded during the preintervention period. Patients with limb trauma and those with abdominal complaints represented the vast majority of patients in whom vital sign data were missing. The postintervention data revealed an improvement in the documentation of mandatory vital signs from 77.9% to 87.9%.

CONCLUSIONS

Creating a multidisciplinary team and implementing a formal quality improvement project improved vital sign documentation at triage for a group of patients seen during ED triage in 1 Italian hospital.

摘要

背景

提高急诊科(ED)就诊患者的质量和安全性已成为意大利的首要任务。托斯卡纳地区卫生部与哈佛医学国际和哈佛医学院合作,在多家托斯卡纳 ED 支持质量改进项目。

目的

为了改善分诊流程,我们评估了意大利比萨圣基娅拉大学医院 ED 分诊中记录患者生命体征的完整性。在比萨大学医院的 ED,分诊基于 5 个类别,每个类别都用颜色标识:白色(最低优先级)、蓝色、绿色、黄色和红色(最高优先级)。对于分诊为“黄色”的患者,血压、心率和血氧饱和度被视为强制性生命体征,是完整患者记录的重要组成部分。该项目的目的如下:1)评估 ED 分诊中记录生命体征的患者比例,2)分析缺失生命体征数据的原因,3)设计并实施一项提高记录生命体征患者比例的策略。

方法

该项目于 2005 年 11 月开始,成立了一个多学科 ED 质量团队。哈佛医学院的教员提供了为期两天的关于临床质量改进方法和工具的培训课程。培训后,团队确定了他们的改进项目。临床质量改进项目遵循计划-执行-研究-行动(Plan-Do-Study-Act)循环。干预前和干预后数据收集包括对在 ED 接受治疗的“黄色”类别中随机选择的一个月内分诊的三分之一患者进行回顾性分析,使用计算机生成的列表。

结果

共纳入干预前(2006 年 3 月)和干预后(2007 年 4-5 月)的 245 份临床记录。我们发现,在这些记录中,77.9%(191/245)正确记录了生命体征。肢体创伤和腹部不适的患者是生命体征数据缺失的绝大多数患者。干预后数据显示,强制性生命体征的记录从 77.9%提高到了 87.9%。

结论

创建多学科团队并实施正式的质量改进项目,改善了意大利一家医院 ED 分诊中一组患者的分诊生命体征记录。

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