The Impact of Discharge Against Medical Advice on Readmission After Opioid Use Disorder-Associated Infective Endocarditis: a National Cohort Study.
| dc.contributor.author | Schranz, Asher J | |
| dc.contributor.author | Tak, Casey | |
| dc.contributor.author | Wu, Li-Tzy | |
| dc.contributor.author | Chu, Vivian H | |
| dc.contributor.author | Wohl, David A | |
| dc.contributor.author | Rosen, David L | |
| dc.date.accessioned | 2023-09-01T17:07:30Z | |
| dc.date.available | 2023-09-01T17:07:30Z | |
| dc.date.issued | 2023-05 | |
| dc.date.updated | 2023-09-01T17:07:30Z | |
| dc.description.abstract | BackgroundHospitalizations for infective endocarditis (IE) associated with opioid use disorder (O-IE) have increased in the USA and have been linked to high rates of discharge against medical advice (DAMA). DAMA represents a truncation of care for a severe infection, yet patient outcomes after DAMA are unknown.ObjectiveThis study aimed to assess readmissions following O-IE and quantify the impact of DAMA on outcomes.DesignA retrospective study of a nationally representative dataset of persons' inpatient discharges in the USA in 2016 PARTICIPANTS: A total of 6018 weighted persons were discharged for O-IE, stratified by DAMA vs. other discharge statuses. Of these, 1331 (22%) were DAMA.Main measuresThe primary outcome of interest was 30-day readmission rates, stratified by discharge type. We also examined the total number of hospitalizations during the year and estimated the effect of DAMA on readmission.Key resultsCompared with non-DAMA, those experiencing DAMA were more commonly female, resided in metropolitan areas, lower income, and uninsured. Crude 30-day readmission following DAMA was 50%, compared with 21% for other discharge types. DAMA was strongly associated with readmission in an adjusted logistic regression model (OR 3.72, CI 3.02-4.60). Persons experiencing DAMA more commonly had ≥2 more hospitalizations during the period (31% vs. 18%, p<0.01), and were less frequently readmitted at the same hospital (49% vs 64%, p<0.01).ConclusionsDAMA occurs in nearly a quarter of patients hospitalized for O-IE and is strongly associated with short-term readmission. Interventions to address the root causes of premature discharges will enhance O-IE care, reduce hospitalizations and improve outcomes. | |
| dc.identifier | 10.1007/s11606-022-07879-6 | |
| dc.identifier.issn | 0884-8734 | |
| dc.identifier.issn | 1525-1497 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Springer Science and Business Media LLC | |
| dc.relation.ispartof | Journal of general internal medicine | |
| dc.relation.isversionof | 10.1007/s11606-022-07879-6 | |
| dc.subject | Humans | |
| dc.subject | Endocarditis, Bacterial | |
| dc.subject | Endocarditis | |
| dc.subject | Opioid-Related Disorders | |
| dc.subject | Patient Discharge | |
| dc.subject | Patient Readmission | |
| dc.subject | Retrospective Studies | |
| dc.subject | Cohort Studies | |
| dc.subject | Female | |
| dc.subject | Male | |
| dc.title | The Impact of Discharge Against Medical Advice on Readmission After Opioid Use Disorder-Associated Infective Endocarditis: a National Cohort Study. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Wu, Li-Tzy|0000-0002-5909-2259 | |
| pubs.begin-page | 1615 | |
| pubs.end-page | 1622 | |
| pubs.issue | 7 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | Sanford School of Public Policy | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Medicine | |
| pubs.organisational-group | Psychiatry & Behavioral Sciences | |
| pubs.organisational-group | Medicine, General Internal Medicine | |
| pubs.organisational-group | Medicine, Infectious Diseases | |
| pubs.organisational-group | Duke Clinical Research Institute | |
| pubs.organisational-group | Institutes and Provost's Academic Units | |
| pubs.organisational-group | University Institutes and Centers | |
| pubs.organisational-group | Duke Institute for Brain Sciences | |
| pubs.organisational-group | Psychiatry, Child & Family Mental Health & Community Psychiatry | |
| pubs.organisational-group | Center for Child and Family Policy | |
| pubs.publication-status | Published | |
| pubs.volume | 38 |
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