Evaluating real-world effectiveness of tele-buprenorphine: A mixed-methods study to develop clinical guidance
Project Number1R01DA060942-01
Contact PI/Project LeaderLIN, LEWEI ALLISON Other PIs
Awardee OrganizationUNIVERSITY OF MICHIGAN AT ANN ARBOR
Description
Abstract Text
Project Summary/Abstract
Buprenorphine is a life-saving treatment for people with opioid use disorder (OUD), yet only 1 in 5
people with OUD receive this medication. Telehealth-delivered buprenorphine (tele-buprenorphine) is one of
the most promising interventions to increase treatment and retention, yet there is limited data on comparative
effectiveness and no prior randomized controlled trials (RCTs) to support implementation. This dearth of
evidence represents a major challenge for clinicians and policymakers when weighing questions around risks
versus benefits and how to deploy telehealth to improve patient outcomes. In addition to overall effectiveness,
there are additional real-world questions, including: 1) is tele-buprenorphine effective in potentially higher risk
groups (e.g. using other substances), 2) can tele-buprenorphine address existing treatment disparities, and 3)
in this new era where telehealth is an option alongside in-person visits, are hybrid approaches effective?
Traditional RCTs would be impractical and take years to address the array of important clinical questions, and
clinical and policy landscapes are evolving quickly. Emulated target trials are an innovative causal inference
approach that use existing data to emulate RCTs by carefully pre-specifying aspects of the protocol, including:
eligibility, treatment assignment, outcome and follow-up assessments, and analytic strategies. We will harness
our team’s unique expertise in causal inference, telehealth and mixed methods research to systematically
gather needed data to develop clinical guidance to optimize tele-buprenorphine care.
Quantitative aims focus on emulated target trials using national Veterans Health Administration and
Medicaid data across states, comprising the largest U.S. provider and payer for OUD services respectively, to
compare effectiveness of telehealth to in-person care, in patients starting and continuing buprenorphine. We
will first develop the target trial framework and apply this framework to analysis evaluating overall effectiveness
of tele-buprenorphine on retention and other key outcomes. We will then apply this framework to address
additional clinically relevant questions about effectiveness of tele-buprenorphine in high-risk groups and in
groups experiencing OUD treatment disparities. We will also conduct qualitative interviews with buprenorphine
patients and clinicians to obtain a nuanced understanding of experiences with telehealth compared to in-
person care to explain, contextualize and extend the quantitative findings. Finally, we will summarize
quantitative and qualitative findings, integrate with existing literature, and create joint displays that will be
provided to patient and clinician experts who will engage in an adapted Delphi process to form consensus
recommendations. Findings will be summarized and disseminated via publications and development of
Consensus Guidance on tele-buprenorphine care for clinicians and policymakers. This project will have high
public health impact by providing critical new insights on comparative effectiveness of tele-buprenorphine
treatment in order to directly inform best practice and policies to improve real-world care for patients with OUD.
Public Health Relevance Statement
Project Narrative
Telehealth is one of the most promising tools to help increase buprenorphine treatment for people with
opioid use disorder (OUD), yet we know little about effectiveness of telehealth compared to traditional in-
person care, which limits use and poses a major barrier to developing evidence-based policies and
implementing high-quality care. The overall goal of this project is to generate clinical guidance to optimize
buprenorphine care by evaluating effectiveness of telehealth-delivered buprenorphine, including for high-need
and high-risk populations, using novel target trial methods, and incorporating stakeholder perspectives and
expert consensus. This study will use national data from the Veterans Health Administration and Medicaid,
encompassing the largest U.S. provider and payer for OUD services, and incorporate novel methods to
systematically inform best practices for tele-buprenorphine care.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AddressAfrican American populationBehavioralBlack raceBuprenorphineCOVID-19CaringChronicClinicClinicalCommunitiesConsensusConsensus DevelopmentDataDecision MakingEffectivenessEligibility DeterminationGoalsHealthcareHybridsIndividualInterventionInterviewJointsLifeLiteratureMedicaidMethodsNational Institute of Drug AbuseNatureOutcomeOutcome AssessmentOverdoseOverdose reductionPatient CarePatient-Focused OutcomesPatientsPersonsPharmaceutical PreparationsPoliciesPolicy MakerProcessProtocols documentationProviderPublic HealthPublicationsQuality of CareQuality of lifeRandomized, Controlled TrialsRecommendationResearch MethodologyRiskServicesSpecific qualifier valueStrategic PlanningStructureSubgroupTechniquesVeterans Health AdministrationVisitbehavioral healthbuprenorphine treatmentclinically relevantcomorbiditycomparative effectivenesscompare effectivenessdata integrationeffectiveness evaluationevidence baseexperiencefollow up assessmenthigh riskhigh risk populationhospitalization ratesimprovedinnovationinsightinterestmedication for opioid use disordernovelopioid mortalityopioid useopioid use disorderoverdose riskprimary outcomeracial disparityrural patientsruralitystakeholder perspectivessubstance usetelehealthtooltreatment disparity
No Sub Projects information available for 1R01DA060942-01
Publications
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Outcomes
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