Electronic Defaults to Reduce Opioid Prescribing in Dentistry Practices
A Cluster-randomized Trial of Modifying Electronic Health Record Defaults to Reduce the Prescribed Quantity of Opioid Analgesics in Dentistry Practices
1 other identifier
interventional
10,000
0 countries
N/A
Brief Summary
The goal of this research is to investigate the impact of changing opioid analgesic prescribing defaults on the quantity of opioids prescribed for acute non-cancer pain in adult dentistry settings. We will change prescribing defaults for select short-acting opioid analgesics including immediate release oxycodone and hydrocodone as well as codeine and tramadol, including their co-formulations with acetaminophen. In a cluster-randomized trial of three Montefiore Medical Center dentistry sites, we will evaluate the impact of this intervention on patient-level outcomes using 18 months of data (6 months pre-intervention and 12 months post-intervention).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Dec 2016
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2016
CompletedFirst Submitted
Initial submission to the registry
December 19, 2016
CompletedFirst Posted
Study publicly available on registry
January 25, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 13, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
July 13, 2018
CompletedAugust 14, 2018
August 1, 2018
1.6 years
December 19, 2016
August 13, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
Initial prescription number of pills to dispense
From the electronic health record
Through study completion (18 months)
Secondary Outcomes (7)
Initial prescription morphine milligram equivalents to dispense
Through study completion (18 months)
Opioid analgesic reorder (y/n)
Within 30 days after the initial prescription
Total opioid analgesic pills to dispense, including re-orders
Within 30 days after the initial prescription
Total morphine milligram equivalents to dispense, including re-orders
Within 30 days after the initial prescription
Outpatient visits
Within 30 days after the index prescription
- +2 more secondary outcomes
Study Arms (3)
10-pill default
EXPERIMENTALThe intervention condition consists of a change to the electronic health record so that new opioid analgesic prescriptions automatically default to 10 pills (i.e., the "quantity dispensed" field is pre-populated). This value is modifiable by providers who can tailor the prescription based on clinical factors.
5-pill default
EXPERIMENTALNew opioid analgesic prescriptions will automatically default to 5 pills.
Standard of care
NO INTERVENTIONThe control condition will be the usual electronic health record interface. The default number of pills varies by medication, most medications currently have either a blank default or a default of 30 pills.
Interventions
Eligibility Criteria
You may qualify if:
- Dentistry clinic within Montefiore Medical Center
- Received a new opioid analgesic prescription, defined as no opioid analgesic prescription in the preceding 6 months
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Montefiore Medical Centerlead
- Albert Einstein College of Medicinecollaborator
Related Publications (1)
Bachhuber MA, Nash D, Southern WN, Heo M, Berger M, Schepis M, Sugarman OK, Cunningham CO. Reducing Opioid Analgesic Prescribing in Dentistry Through Prescribing Defaults: A Cluster-Randomized Controlled Trial. Pain Med. 2023 Jan 4;24(1):1-10. doi: 10.1093/pm/pnac106.
PMID: 35792881DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Marcus Bachhuber, MD
Montefiore Medical Center
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
December 19, 2016
First Posted
January 25, 2017
Study Start
December 1, 2016
Primary Completion
July 13, 2018
Study Completion
July 13, 2018
Last Updated
August 14, 2018
Record last verified: 2018-08