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      Association of Treatment With Medications for Opioid Use Disorder With Mortality After Hospitalization for Injection Drug Use–Associated Infective Endocarditis

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          Abstract

          This cohort study assess the association of receipt of medication for opioid use disorder and mortality after hospitalization for injection drug use–associated infective endocarditis in Massachusetts.

          Key Points

          Question

          Is there an association between receipt of medication for opioid use disorder (MOUD) and mortality after hospitalization for injection drug use–associated infective endocarditis?

          Findings

          In this cohort study 679 individuals hospitalized with injection drug use–associated endocarditis, 24% received MOUD within 3 months of discharge. MOUD receipt within 3 months of discharge was not associated with reduced mortality but was associated with a reduction in mortality in the month received.

          Meaning

          In this study, treatment with MOUD was uncommon and was associated with reduced mortality in the time-varying analysis but not the main analysis, possibly owing to poor treatment retention.

          Abstract

          Importance

          Although hospitalizations for injection drug use–associated infective endocarditis (IDU-IE) have increased during the opioid crisis, utilization of and mortality associated with receipt of medication for opioid use disorder (MOUD) after discharge from the hospital among patients with IDU-IE are unknown.

          Objective

          To assess the proportion of patients receiving MOUD after hospitalization for IDU-IE and the association of MOUD receipt with mortality.

          Design, Setting, and Participants

          This retrospective cohort study used a population registry with person-level medical claims, prescription monitoring program, mortality, and substance use treatment data from Massachusetts between January 1, 2011, and December 31, 2015; IDU-IE–related discharges between July 1, 2011, and June, 30, 2015, were analyzed. All Massachusetts residents aged 18 to 64 years with a first hospitalization for IDU-IE were included; IDU-IE was defined as any hospitalization with a diagnosis of endocarditis and at least 1 claim in the prior 6 months for OUD, drug use, or hepatitis C and with 2-month survival after hospital discharge. Data were analyzed from November 11, 2018, to June 23, 2020.

          Exposure

          Receipt of MOUD, defined as any treatment with methadone, buprenorphine, or naltrexone, within 3 months after hospital discharge excluding discharge month for IDU-IE.

          Main Outcomes and Measures

          The main outcome was all-cause mortality. The proportion of patients who received MOUD in the 3 months after hospital discharge was calculated. Multivariable Cox proportional hazard regression models were used to examine the association of MOUD receipt with mortality, adjusting for sex, age, medical and psychiatric comorbidities, and homelessness. In the secondary analysis, receipt of MOUD was considered as a monthly time-varying exposure.

          Results

          Of 679 individuals with IDU-IE, 413 (60.8%) were male, the mean (SD) age was 39.2 (12.1) years, 298 (43.9%) were aged 18 to 34 years, 419 (72.3) had mental illness, and 209 (30.8) experienced homelessness. A total of 134 individuals (19.7%) received MOUD in the 3 months before hospitalization and 165 (24.3%) in the 3 months after hospital discharge. Of those who received MOUD after discharge, 112 (67.9%) received buprenorphine. The crude mortality rate was 9.2 deaths per 100 person-years. MOUD receipt within 3 months after discharge was not associated with reduced mortality (adjusted hazard ratio, 1.29; 95% CI, 0.61-2.72); however, MOUD receipt was associated with reduced mortality in the month that MOUD was received (adjusted hazard ratio, 0.30; 95% CI, 0.10-0.89).

          Conclusions and Relevance

          In this cohort study, receipt of MOUD was associated with reduced mortality after hospitalization for injection drug use–associated endocarditis only in the month it was received. Efforts to improve MOUD initiation and retention after IDU-IE hospitalization may be beneficial.

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          Most cited references24

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          The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: guidelines for reporting observational studies.

          Much biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and weaknesses and of a study's generalisability. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Initiative developed recommendations on what should be included in an accurate and complete report of an observational study. We defined the scope of the recommendations to cover three main study designs: cohort, case-control, and cross-sectional studies. We convened a 2-day workshop in September 2004, with methodologists, researchers, and journal editors to draft a checklist of items. This list was subsequently revised during several meetings of the coordinating group and in e-mail discussions with the larger group of STROBE contributors, taking into account empirical evidence and methodological considerations. The workshop and the subsequent iterative process of consultation and revision resulted in a checklist of 22 items (the STROBE Statement) that relate to the title, abstract, introduction, methods, results, and discussion sections of articles. 18 items are common to all three study designs and four are specific for cohort, case-control, or cross-sectional studies. A detailed Explanation and Elaboration document is published separately and is freely available on the Web sites of PLoS Medicine, Annals of Internal Medicine, and Epidemiology. We hope that the STROBE Statement will contribute to improving the quality of reporting of observational studies.
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            Comorbidity Measures for Use with Administrative Data

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              Infective Endocarditis in Adults: Diagnosis, Antimicrobial Therapy, and Management of Complications: A Scientific Statement for Healthcare Professionals From the American Heart Association.

              Infective endocarditis is a potentially lethal disease that has undergone major changes in both host and pathogen. The epidemiology of infective endocarditis has become more complex with today's myriad healthcare-associated factors that predispose to infection. Moreover, changes in pathogen prevalence, in particular a more common staphylococcal origin, have affected outcomes, which have not improved despite medical and surgical advances.
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                Author and article information

                Journal
                JAMA Netw Open
                JAMA Netw Open
                JAMA Netw Open
                JAMA Network Open
                American Medical Association
                2574-3805
                14 October 2020
                October 2020
                14 October 2020
                : 3
                : 10
                : e2016228
                Affiliations
                [1 ]Section of General Internal Medicine, Department of Medicine, Boston Medical Center, Boston, Massachusetts
                [2 ]Section of Infectious Diseases, Department of Medicine, Boston Medical Center, Boston, Massachusetts
                [3 ]Boston University School of Medicine, Boston, Massachusetts
                [4 ]Massachusetts Department of Public Health, Boston, Massachusetts
                [5 ]Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts
                [6 ]Substance Use Disorders Division, McLean Hospital, Belmont, Massachusetts
                [7 ]Harvard Medical School, Belmont, Massachusetts
                Author notes
                Article Information
                Accepted for Publication: June 27, 2020.
                Published: October 14, 2020. doi:10.1001/jamanetworkopen.2020.16228
                Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2020 Kimmel SD et al. JAMA Network Open.
                Corresponding Author: Simeon D. Kimmel, MD, MA, Section of General Internal Medicine, Department of Medicine, Boston Medical Center, 801 Massachusetts Ave, Crosstown Center, 2nd Floor, Boston, MA, 02118 ( simeon.kimmel@ 123456bmc.org ).
                Author Contributions: Dr Kimmel had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
                Concept and design: Kimmel, Walley, Linas, Larochelle.
                Acquisition, analysis, or interpretation of data: All authors.
                Drafting of the manuscript: Kimmel.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: Kimmel, Li.
                Obtained funding: Kimmel.
                Administrative, technical, or material support: Kimmel, Linas, Bernson, Larochelle.
                Supervision: Walley, Linas, Lodi, Weiss, Larochelle.
                Conflict of Interest Disclosures: Dr Kimmel was reports receiving support through the American Society of Addiction Medicine 2017 Annual Fellowship Award, the National Institute on Drug Abuse (NIDA) including the Clinical Addiction Research and Education Unit and Fellows Immersion Training Program, Research in Addiction Medicine Scholars Program, and the National Institute of Allergy and Infectious Diseases through the Boston University Clinical HIV/AIDS Training Program and consulting for Abt Associates on a Massachusetts Department of Public Health project to improve medication for opioid use disorder access in nursing facilities. Dr Walley reports receiving support from the Clinical Addiction Research and Education Unit. Dr Linas reports receiving support from the NIDA. Dr Weiss reports receiving grants from the NIDA during the conduct of the study and receiving personal fees from Janssen Pharmaceuticals, Takeda Pharmaceuticals, Braeburn Pharmaceuticals, Cerevel, and US World Meds outside the submitted work. Dr Samet reports receiving support from the Research in Addiction Medicine Scholars Program. Dr Larochelle reports receiving support from the NIDA and a Boston University School of Medicine Department of Medicine Career Investment Award and receiving consulting funds for research on opioid use disorder treatment pathways paid to his institution from OptumLabs. No other disclosures were reported.
                Additional Contributions: The Massachusetts Department of Public Health created the cross-sector database used for this project and provided technical support for the analysis. Shapei Yan, MPH, Section of General Medicine, Boston Medical Center, Boston, Massachusetts, assisted with the analyses performed in the revision of this manuscript and was compensated for this work.
                Article
                zoi200605
                10.1001/jamanetworkopen.2020.16228
                7557514
                33052402
                b1e86359-0100-46f5-8083-4945eaf34883
                Copyright 2020 Kimmel SD et al. JAMA Network Open.

                This is an open access article distributed under the terms of the CC-BY License.

                History
                : 28 February 2020
                : 27 June 2020
                Categories
                Research
                Original Investigation
                Online Only
                Substance Use and Addiction

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