Clinical Trials Directory

Trials / Completed

CompletedNCT01034761

Using Clinical Alerts to Decrease Inappropriate Medication Prescribing

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
719 (actual)
Sponsor
Baystate Medical Center · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPop-up alertPop-up alert in the electronic medical record whenever the provider enters an order for a specified high risk medication from the Beers list.

Timeline

Start date
2013-04-01
Primary completion
2013-06-01
Completion
2013-06-01
First posted
2009-12-17
Last updated
2015-03-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01034761. Inclusion in this directory is not an endorsement.