Using existing data to understand and ameliorate risk in opioid agonist therapy

Information

  • Research Project
  • 9904242
  • ApplicationId
    9904242
  • Core Project Number
    R01DA044170
  • Full Project Number
    3R01DA044170-03S1
  • Serial Number
    044170
  • FOA Number
    PA-18-591
  • Sub Project Id
  • Project Start Date
    9/15/2017 - 6 years ago
  • Project End Date
    7/31/2020 - 3 years ago
  • Program Officer Name
    DUFFY, SARAH Q
  • Budget Start Date
    9/1/2019 - 4 years ago
  • Budget End Date
    7/31/2020 - 3 years ago
  • Fiscal Year
    2019
  • Support Year
    03
  • Suffix
    S1
  • Award Notice Date
    8/29/2019 - 4 years ago

Using existing data to understand and ameliorate risk in opioid agonist therapy

PROJECT SUMMARY/ABSTRACT The United States is in the midst of an opioid epidemic, leading to unprecedented levels of overdose deaths and other harms. Effective treatment for opioid use disorders is available, in the form of opioid agonist therapy (OAT) with methadone or buprenorphine. However, there are significant questions about the risk of adverse clinical outcomes, including mortality and hospitalization during and after treatment, and unplanned treatment cessation. What is the magnitude of these risks, and what patient, treatment setting, and provider factors may contribute to or protect against risk? Additionally, it is increasingly clear that more sophisticated approaches to patient assessment and treatment planning than are currently used are needed to minimise risk. We aim to: 1. Determine the magnitude of risk for specific adverse clinical outcomes (e.g. mortality, hospitalization and ED presentation, and unplanned treatment cessation) during and after OAT with methadone and buprenorphine; 2. Identify patient, treatment setting, and provider risk factors associated with adverse clinical outcomes during and after OAT with methadone and buprenorphine; and 3. Develop a risk prediction model to identify patients at greatest risk of adverse clinical outcomes during and after OAT. To achieve these aims, this project will use existing population-based Australian data on OAT, linked to several health and criminal justice datasets to provide a rich understanding of treatment exposures and outcomes. These data will be used to inform strategies to guide the delivery of high-quality treatment for opioid use disorder in the United States. Specifically, the project will provide data about the magnitude of risk of adverse clinical outcomes during specific treatment and post-treatment periods, and identify patient, treatment setting and provider factors that influence risk. Additionally, it will use innovative machine learning techniques to demonstrate the potential for routinely collected data to be used to assess patient risk at point-of-care, allowing for the development of tailored treatment plans that minimize risk and maximize treatment retention.

IC Name
NATIONAL INSTITUTE ON DRUG ABUSE
  • Activity
    R01
  • Administering IC
    DA
  • Application Type
    3
  • Direct Cost Amount
    45000
  • Indirect Cost Amount
    3600
  • Total Cost
    48600
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    279
  • Ed Inst. Type
  • Funding ICs
    NIDA:48600\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    UNIVERSITY OF NEW SOUTH WALES
  • Organization Department
  • Organization DUNS
    751020900
  • Organization City
    SYDNEY
  • Organization State
  • Organization Country
    AUSTRALIA
  • Organization Zip Code
    2052
  • Organization District
    AUSTRALIA