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Medication for Opioid Use Disorder After Nonfatal Opioid Overdose and Association With Mortality

Supporting Files
File Language:
English


Details

  • Alternative Title:
    Ann Intern Med
  • Personal Author:
  • Description:
    Background:

    Opioid overdose survivors have an increased risk for death. Whether use of medications for opioid use disorder (MOUD) after overdose is associated with mortality is not known.

    Objective:

    To identify MOUD use after opioid overdose and its association with all-cause and opioid-related mortality.

    Design:

    Retrospective cohort study.

    Setting:

    7 individually linked data sets from Massachusetts government agencies.

    Participants:

    17 568 Massachusetts adults without cancer who survived an opioid overdose between 2012 and 2014.

    Measurements:

    Three types of MOUD were examined: methadone maintenance treatment (MMT), buprenorphine, and naltrexone. Exposure to MOUD was identified at monthly intervals, and persons were considered exposed through the month after last receipt. A multivariable Cox proportional hazards model was used to examine MOUD as a monthly time-varying exposure variable to predict time to all-cause and opioid-related mortality.

    Results:

    In the 12 months after a nonfatal overdose, 2040 persons (11%) enrolled in MMT for a median of 5 months (interquartile range, 2 to 9 months), 3022 persons (17%) received buprenorphine for a median of 4 months (interquartile range, 2 to 8 months), and 1099 persons (6%) received naltrexone for a median of 1 month (interquartile range, 1 to 2 months). Among the entire cohort, all-cause mortality was 4.7 deaths (95% CI, 4.4 to 5.0 deaths) per 100 person-years and opioid-related mortality was 2.1 deaths (CI, 1.9 to 2.4 deaths) per 100 person-years. Compared with no MOUD, MMT was associated with decreased all-cause mortality (adjusted hazard ratio [AHR], 0.47 [CI, 0.32 to 0.71]) and opioid-related mortality (AHR, 0.41 [CI, 0.24 to 0.70]). Buprenorphine was associated with decreased all-cause mortality (AHR, 0.63 [CI, 0.46 to 0.87]) and opioid-related mortality (AHR, 0.62 [CI, 0.41 to 0.92]). No associations between naltrexone and all-cause mortality (AHR, 1.44 [CI, 0.84 to 2.46]) or opioid-related mortality (AHR, 1.42 [CI, 0.73 to 2.79]) were identified.

    Limitation:

    Few events among naltrexone recipients preclude confident conclusions.

    Conclusion:

    A minority of opioid overdose survivors received MOUD. Buprenorphine and MMT were associated with reduced all-cause and opioid-related mortality.

    Primary Funding Source:

    National Center for Advancing Translational Sciences of the National Institutes of Health.

  • Subjects:
  • Source:
    Ann Intern Med. 169(3):137-145
  • Pubmed ID:
    29913516
  • Pubmed Central ID:
    PMC6387681
  • Document Type:
  • Funding:
  • Volume:
    169
  • Issue:
    3
  • Collection(s):
  • Main Document Checksum:
    urn:sha256:27202ece746515d708fd6d288f7a218bd10cea7d76f94cf8a560f4cd13ec207f
  • Download URL:
  • File Type:
    Filetype[PDF - 928.39 KB ]
File Language:
English
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