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De-Implementing Opioids for Dental Extractions

Not Applicable
Completed
Conditions
Tooth Extraction
Interventions
Other: Clinical Decision Support
Other: Patient education
Registration Number
NCT03584789
Lead Sponsor
HealthPartners Institute
Brief Summary

The overarching goal of this project is to de-implement the reliance on opioid analgesics and to implement reliance on non-opioid analgesics to manage postoperative pain following dental extractions. Using a prospective, provider-level, 3-arm cluster randomized trial design, the investigators will compare different strategies to reduce the reliance on opioids and increase the use of alternative pain management approaches utilizing information support tools aimed at both providers and their patients.

Detailed Description

The primary objective of this project is to de-implement the use of opioid analgesics for the management of postoperative pain following dental extractions and to implement effective alternative pain management. The investigators propose a cluster-randomized trial design in which dental practitioners will be randomly assigned to 1 of 3 conditions involving different implementation strategies. The first condition, Standard Practice, will serve as a control condition. The second condition will implement a clinical decision support (CDS) tool that will extract patient history and interface with the state prescription drug monitoring program to provide personalized recommendations for analgesic prescribing and offer language for discussing optimal, evidence-based non-opioid pain management with dental extraction patients. The third condition will involve an enhanced version of the CDS (CDS-E) that will also include information regarding optimal, evidence-based, non-opioid pain management delivered directly to the patient both before and following the dental extraction visit. The investigators will examine opioid and non-opioid prescribing data from the electronic health record across study arms as well as other provider- and patient-focused outcomes using mixed methods.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
5722
Inclusion Criteria
  • Have a dental extraction of a permanent teeth performed by an eligible HealthPartners provider during the intervention period
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Exclusion Criteria
  • Patients who have opted out of research at HealthPartners
  • Meet above age criteria
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Clinical Decision SupportClinical Decision SupportA clinical decision support system designed to assist dentists in providing optimal pain management for patients without resorting to opioids when a non-opioid alternative would suffice. It provides pertinent clinical information to the dentist, including point-of-care access to the Prescription Drug Monitoring Program.
Clinical Decision Support + EducationClinical Decision SupportPatient education regarding pain management before and after dental extraction, including information about the risks and benefits of various strategies.
Clinical Decision Support + EducationPatient educationPatient education regarding pain management before and after dental extraction, including information about the risks and benefits of various strategies.
Primary Outcome Measures
NameTimeMethod
Opioid Prescribing at the Extraction EncounterAt the extraction encounter

Number of participants prescribed an opioid.

Secondary Outcome Measures
NameTimeMethod
Compare the Study Arm Differences in Patient Experiences of Post-extraction Pain3-6 days after the extraction encounter

Study arm comparison of the average patient-reported pain 3 days following the extraction encounter. (Numeric Rating Scale, 0 'no pain at all' - 10 'worst pain imaginable')

Compare the Study Arm Differences in Shared Decision-making3-6 days after the extraction encounter

The CollaboRATE scale measures shared decision making and consists of the mean of three items, each rated on a 0 ("no effort was made") to 4 ("every effort was made") scale. The possible range for the composite score is 0-4, with a higher score on the scale indicating that more shared decision-making occurred.

Exclusive Non-opioid Prescribing or Recommendations at the Extraction EncounterAt the extraction encounter

Number of participants prescribed or recommended non-opioid analgesics (ibuprofen, naproxen, aspirin, or acetaminophen) and did not prescribe opioids (at the time of the extraction encounter).

Trial Locations

Locations (1)

HealthPartners Dental Group

🇺🇸

Bloomington, Minnesota, United States

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