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Using Clinical Alerts to Decrease Inappropriate Medication Prescribing

2015年3月7日 更新者:Linda Canty, MD、Baystate Medical Center

Using Clinical Alerts in a Computerized Provider Order Entry System to Decrease Inappropriate Medication Prescribing Among Hospitalized Elders

Introduction:

The Beers list identifies medications that should be avoided in persons 65 years or older because they are ineffective, pose an unnecessarily high risk, or a safer alternative is available. In a recent study, we found a high rate of prescribing of Beers list medications to hospitalized patients. At Baystate, 41% of medical patients received at least one Beers list drug classified as "high severity," meaning it carried a high risk for an adverse drug reaction, while 5% received 3 or more. Some Beers drugs have been associated with delirium and falls. When compared to Baystate patients who did not receive a high severity medication, those who did had an increased risk of mortality (7.8% vs. 5.2%), longer length of stay (5.5 days vs. 3.9 days) and higher costs ($11,240 vs. 6243).

Specific Aims:

  1. Quantify the impact of synchronous electronic alerts on physician prescribing of high-severity Beers' list drugs to hospitalized patients over the age of 65 years.
  2. Compare physician reactions to each drug-specific alert

Project Description:

We will develop a series of clinical alerts in CIS, Baystate's computerized provider order entry system, to reduce the use of potentially inappropriate medications among hospitalized elders. We will randomize providers to electronic alerts or usual care. Whenever a provider randomized to alerts attempts to place an order for a high-risk medication on the Beers list and the intended recipient is over 65 years of age, a synchronous alert (i.e. a "pop-up") will inform the physician about the risks associated with the medication and will propose safer alternatives.

We will collect data on physician ordering and patient outcomes comparing the number of Beers list prescriptions from providers receiving electronic alerts to those not receiving alerts. Our anticipated outcome is a decrease in inappropriate prescribing during the period when the electronic alerts are activated. Other potential outcomes include decrease in length of stay and a decrease in falls.

研究概览

地位

完全的

条件

研究类型

介入性

注册 (实际的)

719

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Massachusetts
      • Springfield、Massachusetts、美国、01199
        • Baystate Medical Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

65年 及以上 (年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Hospitalized patients with Age > 65

Exclusion Criteria:

  • None

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
无干预:日常护理
实验性的:Pop-up alerts
Providers will receive pop-up alerts in the electronic medical record when prescribing one of the specified medications from the Beers list.
Pop-up alert in the electronic medical record whenever the provider enters an order for a specified high risk medication from the Beers list.

研究衡量的是什么?

主要结果指标

结果测量
大体时间
The percentage of elderly patients who receive a specified high-risk medication from the Beer's list.
大体时间:Earlier of hospital stay or end of study
Earlier of hospital stay or end of study

次要结果测量

结果测量
大体时间
The average number of specified high risk medications prescribed per patient.
大体时间:Earlier of hospital stay or end of study
Earlier of hospital stay or end of study
Restraint use
大体时间:Earlier of hospital stay or end of study
Earlier of hospital stay or end of study
Falls
大体时间:Earlier of hospital stay or end of study
Earlier of hospital stay or end of study
Length of stay
大体时间:Earlier of hospital stay or end of study
Earlier of hospital stay or end of study
Total Cost
大体时间:Earlier of hospital stay or end of study
Earlier of hospital stay or end of study
Discharge status
大体时间:6 months
6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Linda J Canty, MD、Baystate Medical Center

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2013年4月1日

初级完成 (实际的)

2013年6月1日

研究完成 (实际的)

2013年6月1日

研究注册日期

首次提交

2009年12月15日

首先提交符合 QC 标准的

2009年12月16日

首次发布 (估计)

2009年12月17日

研究记录更新

最后更新发布 (估计)

2015年3月10日

上次提交的符合 QC 标准的更新

2015年3月7日

最后验证

2015年3月1日

更多信息

与本研究相关的术语

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

Pop-up alert的临床试验

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