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Addressing Origins of the Opioid Epidemic by Improving Prescribing for Opioid-Naive Patients

Not Applicable
Completed
Conditions
Opioid-Related Disorders
Opioid Abuse
Prescription Drug Abuse and Dependency
Opioid Use
Interventions
Other: Default Prescribing Change
Registration Number
NCT03377855
Lead Sponsor
Weill Medical College of Cornell University
Brief Summary

Risk of long-term opioid dependence increases with initial opioid dose/duration, but despite recent Centers for Disease Control and Prevention (CDC)-endorsed minimum doses for initial opioid prescription, primary care providers are likely to overprescribe. In this quality improvement project, primary care departments at Weill Cornell and the Institute for Family Health (federally qualified health center in New York City) will implement an unobtrusive "nudge" in their electronic prescribing software to promote the CDC-endorsed low doses for all opioids. In the evaluation, we will employ a quasi-experimental design with rigorous interrupted time series analysis methods to assess the effect of the "nudge" on prescribing rates. The analysis will be performed at the provider level, with deidentified physician data and a limited data set (fully deidentified except for date of prescription) of patient-level data.

Detailed Description

The two participating institutions, WCMC (Weill Cornell Medical College) and IFH (Institute for Family Health), intend to redesign the e-prescribing interface to create a minor "nudge" to encourage prescribers to prescribe the minimum dose set by the 2016 CDC guideline for opioid-naive patients in 2018. The change to the e-prescribing system is that after a prescriber chooses the drug they wish to prescribe, the minimum recommended dosage from the CDC guidelines will be displayed. The prescriber can choose to change the dosage by overwriting in the field box. The changes to the prescriber system will be implemented at two Weill Cornell clinical organizations: Weill Cornell Internal Medicine Associates (WCIMA) and Weill Cornell Medical Associates (CMA), and at all locations at our collaborating institution IFH (Institute for Family Health). Weill Cornell and IFH will provide data for the analysis, which will be conducted by the co-investigators on this protocol. The project will assess data pre- and post- implementation to study prescribing patterns.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
948
Inclusion Criteria
  • Prescriber - practices internal medicine at WCMC OR family practice at IFH and has prescribed opioids since 11/1/2015
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Exclusion Criteria
  • Prescriber - has not written any opioid prescriptions during the study period
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Default Prescribing ChangeDefault Prescribing ChangeIn the e-prescribing system, the default opioid dosage/duration is changed to the minimum recommended dosage from the CDC guidelines for short acting opioids.
Primary Outcome Measures
NameTimeMethod
Change in the proportion of opioid prescriptions for opioid-naïve patients that comply with CDC recommendations before and after the interventionTwo years prior to and six months after implementation

Change in the proportion of opioid prescriptions for opioid-naïve patients that comply with CDC recommendations before and after the intervention

Secondary Outcome Measures
NameTimeMethod
Change in the average days of supply of opioids for opioid naive patientsTwo years prior to and six months after implementation

Change in the average days of supply of opioids for opioid naive patients

Trial Locations

Locations (2)

Weill Medical College of Cornell University

🇺🇸

New York, New York, United States

The Institute for Family Health

🇺🇸

New York, New York, United States

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