Using Clinical Alerts to Decrease Inappropriate Medication Prescribing
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Purpose
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:
- 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.
- 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.
| Condition | Intervention |
|---|---|
|
Elderly Inappropriate Medication Prescribing |
Behavioral: Pop-up alert |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Using Clinical Alerts in a Computerized Provider Order Entry System to Decrease Inappropriate Medication Prescribing Among Hospitalized Elders |
- The percentage of elderly patients who receive a specified high-risk medication from the Beer's list. [ Time Frame: Earlier of hospital stay or end of study ] [ Designated as safety issue: Yes ]
- The average number of specified high risk medications prescribed per patient. [ Time Frame: Earlier of hospital stay or end of study ] [ Designated as safety issue: Yes ]
- Restraint use [ Time Frame: Earlier of hospital stay or end of study ] [ Designated as safety issue: Yes ]
- Falls [ Time Frame: Earlier of hospital stay or end of study ] [ Designated as safety issue: Yes ]
- Length of stay [ Time Frame: Earlier of hospital stay or end of study ] [ Designated as safety issue: No ]
- Total Cost [ Time Frame: Earlier of hospital stay or end of study ] [ Designated as safety issue: No ]
- Discharge status [ Time Frame: 6 months ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 7500 |
| Study Start Date: | March 2013 |
| Estimated Study Completion Date: | September 2013 |
| Estimated Primary Completion Date: | September 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 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.
|
Behavioral: Pop-up alert
Pop-up alert in the electronic medical record whenever the provider enters an order for a specified high risk medication from the Beers list.
|
| No Intervention: Usual care |
Eligibility| Ages Eligible for Study: | 65 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Hospitalized patients with Age > 65
Exclusion Criteria:
- None
Contacts and Locations| Contact: Linda J Canty, MD | 413-794-3895 | Linda.CantyMD@baystatehealth.org |
| United States, Massachusetts | |
| Baystate Medical Center | Not yet recruiting |
| Springfield, Massachusetts, United States, 01199 | |
| Contact: Linda J Canty, MD 413-794-3895 Linda.CantyMD@baystatehealth.org | |
| Principal Investigator: | Linda J Canty, MD | Baystate Medical Center |
More Information
No publications provided
| Responsible Party: | Linda Canty, MD, Assistant Clinical Professor of Medine, Baystate Medical Center |
| ClinicalTrials.gov Identifier: | NCT01034761 History of Changes |
| Other Study ID Numbers: | 132454 |
| Study First Received: | December 15, 2009 |
| Last Updated: | March 5, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Baystate Medical Center:
|
Electronic prescribing Inappropriate medications Patient safety Elderly patients in the hospital |
ClinicalTrials.gov processed this record on May 16, 2013