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Clinical Trials/NCT03048643
NCT03048643
Completed
Not Applicable

CATS-CARE: Combining Opioid Addiction Treatment Services With CARe for Infectious Endocarditis

Laura Fanucchi1 site in 1 country20 target enrollmentMarch 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endocarditis, Bacterial
Sponsor
Laura Fanucchi
Enrollment
20
Locations
1
Primary Endpoint
Illicit drug use
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Hospitalizations for severe infections associated with opioid use disorder (OUD), such as infective endocarditis (IE), have doubled in the US over the past decade and are frequently prolonged and resource-intensive. Once medically stabilized, persons with IE but without drug use typically enroll in outpatient parenteral antibiotic therapy (OPAT), while persons with IE and OUD are kept in the hospital for the duration of therapy (often 6 weeks or more) largely due to concerns of ongoing drug use. Unfortunately, hospitalization for IE with OUD infrequently includes evidence-based medication-assisted treatment (MAT) with buprenorphine or methadone to address the OUD, despite the strong evidence that MAT decreases illicit drug use and mortality. Enrolling hospitalized persons with IE due to OUD into comprehensive MAT (i.e., buprenorphine + counseling) while inpatient, and providing an intensive transitional outpatient care program supporting MAT, may support provision of outpatient IV antibiotic therapy and be cost effective. The primary aim of this pilot randomized clinical trial is to evaluate the equivalence of current practice plus buprenorphine (keeping patients with IE due to opioid use disorder in the hospital for the full duration of antibiotic treatment) compared to OPAT plus buprenorphine (discharge with outpatient treatment once medically stable).

Registry
clinicaltrials.gov
Start Date
March 1, 2017
End Date
October 2, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Laura Fanucchi
Responsible Party
Sponsor Investigator
Principal Investigator

Laura Fanucchi

Assistant Professor

University of Kentucky

Eligibility Criteria

Inclusion Criteria

  • meeting OUD by DSM-V criteria
  • have IE by Duke's criteria
  • candidates for outpatient treatment with buprenorphine
  • accepting of buprenorphine treatment
  • anticipated to be discharged home after medically stabilized
  • requiring ≥ 2 weeks of IV antibiotic therapy
  • having ≥ 1 week of IV antibiotic therapy remaining at the time of medical readiness for discharge (as defined by the primary clinical team),
  • and providing informed consent.

Exclusion Criteria

  • presence of stroke or central nervous system involvement
  • clinically active embolic sequelae (e.g. pulmonary sepsis, mycotic aneurysms, splenic abscesses)
  • TV treated surgically or endovascularly (AngioVac)
  • presence of osteomyelitis
  • fungal IE
  • patients who require inpatient physical rehabilitation determined by physical or occupational therapy assessment
  • current pregnancy
  • current severe methamphetamine, cocaine, alcohol or benzodiazepine use disorders by DSM-V criteria
  • currently enrolled in ongoing MAT for OUD
  • hypersensitivity or allergy to buprenorphine

Outcomes

Primary Outcomes

Illicit drug use

Time Frame: 12 weeks after discharge

Participants will be asked by their clinician to self report illicit drug use at their follow up visit 12 weeks after discharge

Secondary Outcomes

  • Completion of recommended IV antibiotic therapy(12 weeks after discharge)

Study Sites (1)

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